Exact Mass: 260.0137

Exact Mass Matches: 260.0137

Found 500 metabolites which its exact mass value is equals to given mass value 260.0137, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

BROMACIL

BROMACIL

C9H13BrN2O2 (260.016)


D010575 - Pesticides > D006540 - Herbicides D016573 - Agrochemicals CONFIDENCE standard compound; INTERNAL_ID 1265; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3915; ORIGINAL_PRECURSOR_SCAN_NO 3912 CONFIDENCE standard compound; INTERNAL_ID 1265; DATASET 20200303_ENTACT_RP_MIX504; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3781; ORIGINAL_PRECURSOR_SCAN_NO 3780 CONFIDENCE standard compound; INTERNAL_ID 1265; DATASET 20200303_ENTACT_RP_MIX504; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3766; ORIGINAL_PRECURSOR_SCAN_NO 3764 CONFIDENCE standard compound; INTERNAL_ID 1265; DATASET 20200303_ENTACT_RP_MIX504; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3789; ORIGINAL_PRECURSOR_SCAN_NO 3784 CONFIDENCE standard compound; INTERNAL_ID 1265; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3917; ORIGINAL_PRECURSOR_SCAN_NO 3915 CONFIDENCE standard compound; INTERNAL_ID 1265; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3887; ORIGINAL_PRECURSOR_SCAN_NO 3886 CONFIDENCE standard compound; EAWAG_UCHEM_ID 266

   

Aldohexose 6-phosphate

Aldohexose 6-phosphate

C6H13O9P (260.0297)


   

Glucose 6-phosphate

{[(2R,3S,4S,5R)-3,4,5,6-tetrahydroxyoxan-2-yl]methoxy}phosphonic acid

C6H13O9P (260.0297)


Glucose 6 phosphate (alpha-D-glucose 6 phosphate or G6P) is the alpha-anomer of glucose-6-phosphate. There are two anomers of glucose 6 phosphate, the alpha anomer and the beta anomer. Glucose 6 phosphate is an ester of glucose with phosphoric acid, made in the course of glucose metabolism by mammalian and other cells. It is a normal constituent of resting muscle and probably is in constant equilibrium with fructose-6-phosphate. (Stedman, 26th ed). Glucose-6-phosphate is a phosphorylated glucose molecule on carbon 6. When glucose enters a cell, it is immediately phosphorylated to G6P. This is catalyzed with hexokinase enzymes, thus consuming one ATP. A major reason for immediate phosphorylation of the glucose is so that it cannot diffuse out of the cell. The phosphorylation adds a charged group so the G6P cannot easily cross cell membranes. G6P can travel down two metabolic pathways, glycolysis and the pentose phosphate pathway. In addition to the metabolic pathways, G6P can also be stored as glycogen in the liver if blood glucose levels are high. If the body needs energy or carbon skeletons for syntheses, G6P can be isomerized to Fructose-6-phosphate and then phosphorylated to Fructose-1,6-bisphosphate. Note, the molecule now has 2 phosphoryl groups attached. The addition of the 2nd phosphoryl group is an irreversible step, so once this happens G6P will enter glycolysis and be turned into pyruvate (ATP production occurs). If blood glucose levels are high, the body needs a way to store the excess glucose. After being converted to G6P, phosphoglucose mutase (isomerase) can turn the molecule into glucose-1-phosphate. Glucose-1-phosphate can then be combined with uridine triphosphate (UTP) to form UDP-glucose. This reaction is driven by the hydrolysis of pyrophosphate that is released in the reaction. Now, the activated UDP-glucose can add to a growing glycogen molecule with the help of glycogen synthase. This is a very efficient storage mechanism for glucose since it costs the body only 1 ATP to store the 1 glucose molecule and virtually no energy to remove it from storage. It is important to note that glucose-6-phosphate is an allosteric activator of glycogen synthase, which makes sense because when the level of glucose is high the body should store the excess glucose as glycogen. On the other hand, glycogen synthase is inhibited when it is phosphorylated by protein kinase a during times of high stress or low blood glucose levels. -- Wikipedia [HMDB] Glucose 6-phosphate (G6P, sometimes called the Robison ester) is a glucose sugar phosphorylated at the hydroxy group on carbon 6. Glucose 6-phosphate (G6P) has two anomers: the alpha anomer and the beta anomer. Glucose 6-phosphate is an ester of glucose with phosphoric acid, made in the course of glucose metabolism by mammalian and other cells. It is a normal constituent of resting muscle and probably is in constant equilibrium with fructose 6-phosphate (Stedman, 26th ed). When glucose enters a cell, it is immediately phosphorylated to G6P. This is catalyzed with hexokinase enzymes, thus consuming one ATP. A major reason for immediate phosphorylation of the glucose is so that it cannot diffuse out of the cell. The phosphorylation adds a charged group so the G6P cannot easily cross cell membranes. G6P can travel down two metabolic pathways: glycolysis and the pentose phosphate pathway. In addition to the metabolic pathways, G6P can also be stored as glycogen in the liver if blood glucose levels are high. If the body needs energy or carbon skeletons for syntheses, G6P can be isomerized to fructose 6-phosphate and then phosphorylated to fructose 1,6-bisphosphate. Note, the molecule now has 2 phosphoryl groups attached. The addition of the 2nd phosphoryl group is an irreversible step, so once this happens G6P will enter glycolysis and be turned into pyruvate (ATP production occurs). If blood glucose levels are high, the body needs a way to store the excess glucose. After being converted to G6P, phosphoglucose mutase (an isomerase) can turn the molecule into glucose 1-phosphate. Glucose 1-phosphate can then be combined with uridine triphosphate (UTP) to form UDP-glucose. This reaction is driven by the hydrolysis of pyrophosphate that is released in the reaction. Now, the activated UDP-glucose can add to a growing glycogen molecule with the help of glycogen synthase. This is a very efficient storage mechanism for glucose since it costs the body only 1 ATP to store the 1 glucose molecule and virtually no energy to remove it from storage. It is important to note that glucose 6-phosphate is an allosteric activator of glycogen synthase, which makes sense because when the level of glucose is high the body should store the excess glucose as glycogen. On the other hand, glycogen synthase is inhibited when it is phosphorylated by protein kinase during times of high stress or low blood glucose levels. Acquisition and generation of the data is financially supported in part by CREST/JST. CONFIDENCE standard compound; INTERNAL_ID 237 KEIO_ID G003; [MS2] KO009109 KEIO_ID G003

   

α-D-Glucose-1-phosphate

[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

C6H13O9P (260.0297)


Glucose 1-phosphate (also called cori ester) is a glucose molecule with a phosphate group on the 1-carbon. It can exist in either the α- or β-anomeric form. Glucose 1-phosphate belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphated group linked to the carbohydrate unit. Glucose 1-phosphate is the direct product of the reaction in which glycogen phosphorylase cleaves off a molecule of glucose from a greater glycogen structure. It cannot travel down many metabolic pathways and must be interconverted by the enzyme phosphoglucomutase in order to become glucose 6-phosphate. Free glucose 1-phosphate can also react with UTP to form UDP-glucose. It can then return to the greater glycogen structure via glycogen synthase. *Found widely in both plants and animals. A precursor of starch in plants and of glycogen in animals. [CCD] Acquisition and generation of the data is financially supported in part by CREST/JST. COVID info from COVID-19 Disease Map KEIO_ID G020 Corona-virus KEIO_ID G115 Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Ifosfamide

3-(2-Chloroethyl)-2-((2-chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide

C7H15Cl2N2O2P (260.0248)


Ifosfamide is only found in individuals that have used or taken this drug. It is a positional isomer of cyclophosphamide which is active as an alkylating agent and an immunosuppressive agent. [PubChem]The exact mechanism of ifosfamide has not been determined, but appears to be similar to other alkylating agents. Ifosfamide requires biotransformation in the liver by mixed-function oxidases (cytochrome P450 system) before it becomes active. After metabolic activation, active metabolites of ifosfamide alkylate or bind with many intracellular molecular structures, including nucleic acids. The cytotoxic action is primarily through the alkylation of DNA, done by attaching the N-7 position of guanine to its reactive electrophilic groups. The formation of inter and intra strand cross-links in the DNA results in cell death. CONFIDENCE standard compound; INTERNAL_ID 895; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7346; ORIGINAL_PRECURSOR_SCAN_NO 7344 CONFIDENCE standard compound; INTERNAL_ID 895; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7289; ORIGINAL_PRECURSOR_SCAN_NO 7287 CONFIDENCE standard compound; INTERNAL_ID 895; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7327; ORIGINAL_PRECURSOR_SCAN_NO 7323 CONFIDENCE standard compound; INTERNAL_ID 895; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7274; ORIGINAL_PRECURSOR_SCAN_NO 7272 CONFIDENCE standard compound; INTERNAL_ID 895; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7310; ORIGINAL_PRECURSOR_SCAN_NO 7308 CONFIDENCE standard compound; INTERNAL_ID 895; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7330; ORIGINAL_PRECURSOR_SCAN_NO 7329 L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01A - Alkylating agents > L01AA - Nitrogen mustard analogues D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D009588 - Nitrogen Mustard Compounds D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D010752 - Phosphoramide Mustards C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent CONFIDENCE standard compound; EAWAG_UCHEM_ID 2683 CONFIDENCE standard compound; INTERNAL_ID 2723 D009676 - Noxae > D000477 - Alkylating Agents

   

Cyclophosphamide

(+,-)-2-(Bis(2-chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide monohydrate

C7H15Cl2N2O2P (260.0248)


Precursor of an alkylating nitrogen mustard antineoplastic and immunosuppressive agent that must be activated in the liver to form the active aldophosphamide. It has been used in the treatment of lymphoma and leukemia. Its side effect, alopecia, has been used for defleecing sheep. Cyclophosphamide may also cause sterility, birth defects, mutations, and cancer. [PubChem] L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01A - Alkylating agents > L01AA - Nitrogen mustard analogues D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D009588 - Nitrogen Mustard Compounds D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D010752 - Phosphoramide Mustards C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent D000970 - Antineoplastic Agents > D019653 - Myeloablative Agonists D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents C308 - Immunotherapeutic Agent > C574 - Immunosuppressant CONFIDENCE standard compound; INTERNAL_ID 4119 CONFIDENCE standard compound; INTERNAL_ID 2727 D009676 - Noxae > D000477 - Alkylating Agents D009676 - Noxae > D009153 - Mutagens D018501 - Antirheumatic Agents

   

Phosphatidylcholine O-34:2

Phosphorodithioic acid, O,O-diethyl S-((ethylthio)methyl) ester

C7H17O2PS3 (260.0128)


Phosphatidylcholine O-34:2, also known as Thimet or O,O-Diethyl S-ethylmercaptomethyl dithiophosphate, is classified as a member of the Dithiophosphate O-esters. Dithiophosphate O-esters are o-ester derivatives of dithiophosphates, with the general structure RSP(O)(O)=S (R = organyl group). Phosphatidylcholine O-34:2 is a non-carcinogenic (not listed by IARC) potentially toxic compound D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor D010575 - Pesticides > D007306 - Insecticides D004791 - Enzyme Inhibitors D016573 - Agrochemicals

   

Sorbose 1-phosphate

{[(3S,4R,5S)-3,4,5,6-tetrahydroxy-2-oxohexyl]oxy}phosphonic acid

C6H13O9P (260.0297)


Sorbose 1-phosphate is formed when extracellular sorbose is taken into the cell. The enzyme responsible for this is PTS-Sor-EIIA [EC:2.7.1.69]. Sorbose 1-phosphate has been found to be a metabolite of Klebsiella and Lactobacillus (PMID: 6361004; PMID: 12177329). Sorbose 1-phosphate is formed when extracellular sorbose is taken into the cell. The enzyme responsible for this is PTS-Sor-EIIA [EC:2.7.1.69]. [HMDB]

   

β-D-Fructose 6-phosphate

[(2R,3R,4S)-2,3,4,6-tetrahydroxy-5-oxohexyl] dihydrogen phosphate

C6H13O9P (260.0297)


Fructose 6-phosphate (F6P) belongs to the class of organic compounds known as hexose phosphates. These are carbohydrate derivatives containing a hexose substituted by one or more phosphate groups. F6P is a derivative of fructose, which has been phosphorylated at the 6-hydroxy group. Fructose 6-phosphate is a fundamental metabolite and exists in all living species, ranging from bacteria to plants to humans. The great majority of glucose is converted to fructose 6-phosphate as part of the glycolytic metabolic pathway (glycolysis). Specifically, F6P is produce is produced by the isomerisation of glucose 6-phosphate via the enzyme phosphoglucose isomerase. F6P is in turn further phosphorylated to fructose-1,6-bisphosphate by the enzyme phosphofructokinase-1. Glycolysis is the metabolic pathway that converts glucose into pyruvic acid. The free energy released in this process is used to form ATP and reduced nicotinamide adenine dinucleotide (NADH). In addition to its key involvement in glycolysis, fructose 6-phosphate can also be biosynthesized from glucosamine 6-phosphate via the enzyme glucosamine-6-phosphate isomerase 1. In addition, fructose 6-phosphate and L-glutamine can be converted into glucosamine 6-phosphate and L-glutamic acid through the action of the enzyme glutamine--fructose-6-phosphate aminotransferase. An important intermediate in the Carbohydrates pathway. The interconversion of glucose-6-phosphate and fructose-6-phosphate, the second step of the Embden-Meyerhof glycolytic pathway, is catalyzed by the enzyme phosphoglucose isomerase (PGI). In gluconeogenesis, fructose-6-phosphate is the immediate precursor of glucose-6-phosphate (wikipedia) [HMDB] Acquisition and generation of the data is financially supported in part by CREST/JST. KEIO_ID F001

   

Fructose 1-phosphate

{[(2R,3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methoxy}phosphonic acid

C6H13O9P (260.0297)


Fructose 1-phosphate, also known as D-fructose-1-p, belongs to the class of organic compounds known as hexose phosphates. These are carbohydrate derivatives containing a hexose substituted by one or more phosphate groups. Metabolism of fructose thus essentially results in intermediates of glycolysis. The final product of glycolysis (pyruvate) may then undergo gluconeogenesis, enter the TCA cycle or be stored as fatty acids. Fructose 1-phosphate exists in all living organisms, ranging from bacteria to humans. Within humans, fructose 1-phosphate participates in a number of enzymatic reactions. In particular, fructose 1-phosphate can be biosynthesized from D-fructose through the action of the enzyme ketohexokinase. In addition, fructose 1-phosphate can be converted into dihydroxyacetone phosphate and glyceraldehyde; which is catalyzed by the enzyme fructose-bisphosphate aldolase a. Because fructokinase has a high Vmax fructose entering cells is quickly phosphorylated to fructose 1-phosphate. In humans, fructose 1-phosphate is involved in fructose intolerance, hereditary. Hypoglycemia results from inhibition of glycogenolysis and gluconeogenesis. It is generated mainly by hepatic fructokinase but is also generated in smaller amounts in the small intestinal mucosa and proximal epithelium of the renal tubule. Aldolase B converts it into glyceraldehyde and dihydroxyacetone phosphate (DHAP). Symptoms of hereditary fructose intolerance are apathy, drowsiness, sweatiness and tremulousness. Fructose 1-phosphate is an intermediate metabolite in the Fructose and mannose metabolism pathway. [HMDB] KEIO_ID F009

   

Norathyriol

1,3,6,7-TETRAHYDROXY-9H-XANTHEN-9-ONE

C13H8O6 (260.0321)


A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

D-Galactose 6-sulfate

D-Galactose 6-sulfate

C6H12O9S (260.0202)


   

myo-Inositol 1-phosphate

{[(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}phosphonic acid

C6H13O9P (260.0297)


myo-Inositol 1-phosphate, also known as I1P or ins(1)p, belongs to the class of organic compounds known as inositol phosphates. Inositol phosphates are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety. myo-Inositol 1-phosphate is a metabolite of inositol phosphate metabolism and the phosphatidylinositol signalling system. Inositol phosphatases (EC:3.1.3.25) play a crucial role in the phosphatidylinositol signalling pathway. Expression is substantially higher in the subcortical regions of the brain, most prominently in the caudate. The phosphatidylinositol pathway is thought to be modified by lithium, a commonly prescribed medication in treating bipolar disorder (OMIM: 605922). Myo-inositol 1-phosphate is a metabolite of the Inositol phosphate metabolism and the Phosphatidylinositol signaling system. Inositol phosphatases [EC:3.1.3.25] play a crucial role in the phosphatidylinositol signaling pathway; in brain, the expression is substantially higher in the subcortical regions, most prominently in the caudate. The phosphatidylinositol pathway is thought to be modified by lithium, a commonly prescribed medication in treating bipolar disorder. (OMIM 605922) [HMDB]

   

Beta-D-Fructose 2-phosphate

{[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}phosphonic acid

C6H13O9P (260.0297)


beta-D-Fructose 2-phosphate is involved in the fructose eand mannose system. beta-D-Fructose 2-phosphate is produced from beta-D-Fructose 2,6-bisphosphate by the enzyme fructose-2,6-bisphosphate 6-phosphatase [EC 3.1.3.54]. [HMDB] beta-D-Fructose 2-phosphate is involved in the fructose eand mannose system. beta-D-Fructose 2-phosphate is produced from beta-D-Fructose 2,6-bisphosphate by the enzyme fructose-2,6-bisphosphate 6-phosphatase [EC 3.1.3.54].

   

D-Hamamelose 2(1)-phosphate

D-Hamamelose 2(1)-phosphate

C6H13O9P (260.0297)


   

alpha-D-Glucose 3-phosphate

alpha-D-Glucose 3-phosphate

C6H13O9P (260.0297)


   

5-Methylthioribose 1-phosphate

{[(2R,3R,4S,5S)-3,4-dihydroxy-5-[(methylsulfanyl)methyl]oxolan-2-yl]oxy}phosphonic acid

C6H13O7PS (260.012)


5-Methylthioribose 1-phosphate belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms. 5-Methylthioribose 1-phosphate is an intermediate in methionine biosynthesis. It is converted from 5-deoxy-5-methylthioadenosine by 5-deoxy-5-methylthioadenosine phosphorylase. Then it is converted to methionine (PMID: 2153115). In the methionine salvage pathway, 5-methylthioribose 1-phosphate isomerase (M1Pi) catalyzes the conversion of 5-methylthioribose 1-phosphate (MTR-1-P) into 5-methylthioribulose 1-phosphate (MTRu-1-P). 5-Methylthioribose 1-phosphate is an intermediate in methionine biosynthesis. It is converted from 5-Deoxy-5-methylthioadenosine by 5-Deoxy-5-methylthioadenosine phosphorylase. Then it is converted to methionine (PMID 2153115). In the methionine salvage pathway 5-methylthioribose 1-phosphate isomerase (M1Pi) catalyzes the conversion of 5-methylthioribose 1-phosphate (MTR-1-P) to 5-methylthioribulose 1-phosphate (MTRu-1-P) [HMDB]

   

S-methyl-5-thio-D-ribulose 1-phosphate(2-)

{[3,4-dihydroxy-5-(methylsulphanyl)-2-oxopentyl]oxy}phosphonic acid

C6H13O7PS (260.012)


S-methyl-5-thio-D-ribulose 1-phosphate(2-) is also known as 1-phospho-5-S-Methylthioribulose or 1-PMT-Ribulose. S-methyl-5-thio-D-ribulose 1-phosphate(2-) is considered to be soluble (in water) and acidic

   

NCIOpen2_009782

Fructose 1-phosphate(pyranose)

C6H13O9P (260.0297)


   

D-arabino-6-Phospho-hex-3-ulose

D-arabino-hex-3-ulose 6-phosphate

C6H13O9P (260.0297)


   

Suprofen

alpha-Methyl-4-(2-thienylcarbonyl)benzeneacetic acid

C14H12O3S (260.0507)


Suprofen is only found in individuals that have used or taken this drug. It is an ibuprofen-type anti-inflammatory analgesic and antipyretic. It inhibits prostaglandin synthesis and has been proposed as an anti-arthritic. [PubChem]Suprofen binds to the cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) isoenzymes, preventing the synthesis of prostaglandins and reducing the inflammatory response. Cyclooxygenase catalyses the formation of prostaglandins and thromboxane from arachidonic acid (itself derived from the cellular phospholipid bilayer by phospholipase A2). Prostaglandins act (among other things) as messenger molecules in the process of inflammation. The overall result is a reduction in pain and inflammation in the eyes and the prevention of pupil constriction during surgery. Normally trauma to the anterior segment of the eye (especially the iris) increases endogenous prostaglandin synthesis which leads to constriction of the iris sphincter. M - Musculo-skeletal system > M01 - Antiinflammatory and antirheumatic products > M01A - Antiinflammatory and antirheumatic products, non-steroids > M01AE - Propionic acid derivatives D018501 - Antirheumatic Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D016861 - Cyclooxygenase Inhibitors C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D004791 - Enzyme Inhibitors

   

1,3,5,8-Tetrahydroxyxanthone

1,3,5,8-Tetrahydroxy-9H-xanthen-9-one

C13H8O6 (260.0321)


   

Norswertianin

9H-Xanthen-9-one, 1,2,6,8-tetrahydroxy- (9CI)

C13H8O6 (260.0321)


Norswertianin is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 2, 6 and 8. It has a role as a plant metabolite. It is a member of xanthones and a polyphenol. Norswertianin is a natural product found in Swertia japonica, Swertia ciliata, and other organisms with data available. A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 2, 6 and 8.

   

Oxydeprofos

S-(2-ethylsulphinyl-1-methylethyl)-O,O-dimethyl phosphorothioate

C7H17O4PS2 (260.0306)


   

Methazole

2-(3,4-Dichlorophenyl)- 4-methyl-1,2,4-oxadiazolidine-3,5-dione

C9H6Cl2N2O3 (259.9755)


   

6-deoxy-6-sulfo-D-gluconic acid

6-Deoxy-6-sulfo-D-gluconate; 6-Deoxy-6-sulfogluconate

C6H12O9S (260.0202)


A carbohydrate sulfonate that is D-gluconic acid in which the hydroxy group at position 6 is replaced by a sulfo group.

   

Galactose 1-phosphate

{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phosphonic acid

C6H13O9P (260.0297)


Galactose 1-phosphate, also known as D-Galactose-1-phosphate or alpha-D-gal-1-P, belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphate group linked to the carbohydrate unit. Galactose-1-phosphate is an intermediate in the interconversion of glucose and uridine diphosphate galactose. Galactose 1-phosphate exists in all living species, ranging from bacteria to plants to humans. Within humans, galactose 1-phosphate participates in a number of enzymatic reactions. In particular, uridine diphosphate glucose and galactose 1-phosphate can be biosynthesized from uridine diphosphategalactose and glucose 1-phosphate; which is mediated by the enzyme galactose-1-phosphate uridylyltransferase (GALT). In addition, galactose 1-phosphate can be biosynthesized from D-galactose through the action of the enzyme galactokinase. The improper metabolism of galactose-1-phosphate is a characteristic of a condition known as galactosemia (PMID: 7671964). Type I galactosemia is a genetic disorder that is caused by the impairment of galactose-1-phosphate uridylyltransferase (EC 2.7.7.12). Evidence suggests that misfolding of the galactose 1-phosphate uridylyltransferase enzyme is the underlying cause of type I galactosemia (PMID: 23583749). Outside of the human body, galactose 1-phosphate has been detected, but not quantified in, several different foods, such as gooseberries, anises, turmerics, caraway, and cumins. COVID info from COVID-19 Disease Map Occurs in liver, milk, and yeasts Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Acquisition and generation of the data is financially supported in part by CREST/JST.

   

Mannose 6-phosphate

{[(2R,3S,4S,5S,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methoxy}phosphonic acid

C6H13O9P (260.0297)


Mannose 6-phosphate, also known as alpha-D-mannose-6-p or man-6-p, belongs to the class of organic compounds known as hexose phosphates. These are carbohydrate derivatives containing a hexose substituted by one or more phosphate groups. Mannose 6-phosphate exists in all eukaryotes, ranging from yeast to humans. Within humans, mannose 6-phosphate participates in a number of enzymatic reactions. In particular, mannose 6-phosphate can be converted into fructose 6-phosphate through its interaction with the enzyme mannose-6-phosphate isomerase. In addition, mannose 6-phosphate can be biosynthesized from D-mannose through the action of the enzyme hexokinase-1. Mannose 6-phosphate is a potent competitive inhibitor of pinocytosis of human platelet beta-glucuronidase and it is a necessary component of the recognition marker on the enzyme for pinocytosis by human fibroblasts as well (PMID 908752). In humans, mannose 6-phosphate is involved in fructose intolerance, hereditary. Mannose-6-phosphate is a potent competitive inhibitor of pinocytosis of human platelet beta-glucuronidase and it is a necessary component of the recognition marker on the enzyme for pinocytosis by human fibroblasts as well (PMID 908752). [HMDB] Acquisition and generation of the data is financially supported in part by CREST/JST. KEIO_ID M008

   

D-myo-Inositol 4-phosphate

{[(1S,2R,3S,4S,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}phosphonic acid

C6H13O9P (260.0297)


D-myo-Inositol 4-phosphate, also known as inositol 4-phosphoric acid, belongs to the class of organic compounds known as inositol phosphates. Inositol phosphates are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety. D-myo-Inositol 4-phosphate is an extremely weak basic (essentially neutral) compound (based on its pKa). Within humans, D-myo-inositol 4-phosphate participates in a number of enzymatic reactions. In particular, D-myo-inositol 4-phosphate can be biosynthesized from D-myo-inositol 1,4-bisphosphate through its interaction with the enzyme inositol polyphosphate 1-phosphatase. In addition, D-myo-inositol 4-phosphate can be converted into myo-inositol through its interaction with the enzyme inositol monophosphatase 1. D-Myo-inositol 4-phosphate is a substrate for Inositol monophosphatase, Inositol polyphosphate 1-phosphatase and Inositol monophosphatase 2. [HMDB]

   

beta-D-Glucose 6-phosphate

{[(2R,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methoxy}phosphonic acid

C6H13O9P (260.0297)


beta-D-Glucose 6 phosphate (b-G6P) is the beta-anomer of glucose-6-phosphate. There are two anomers of glucose 6 phosphate: the alpha anomer and the beta anomer. Specifically, beta-D-Glucose 6-phosphate is glucose sugar phosphorylated on carbon 6. It is a very common metabolite in cells as the vast majority of glucose entering a cell will become phosphorylated in this way. The primary reason for the immediate phosphorylation of glucose is to prevent diffusion out of the cell. The phosphorylation adds a charged phosphate group so the glucose 6-phosphate cannot easily cross the cell membrane. b-G6P is involved in glycolysis, gluconeogenesis, pentose phosphate, and glycogen and sucrose metabolic pathways. beta-D-Glucose 6 phosphate can be generated through beta-D-fructose phosphate or alpha-D-glucose 6 phosphate (via glucose-6-phosphate isomerase) or beta-D glucose (via hexokinase). It can then be sent off to the pentose phosphate pathway which generates the useful cofactor NADPH as well as ribulose 5-phosphate, a carbon source for the synthesis of other molecules. Alternately, if the cell needs energy or carbon skeletons for synthesis then glucose 6-phosphate is targeted for glycolysis. A third route is to have glucose 6 phosphate stored or converted into glycogen, especially if blood glucose levels are high. Beta-d-glucose 6-phosphate, also known as B-D-glucose 6-(dihydrogen phosphoric acid) or 6-O-phosphono-beta-D-glucopyranose, is a member of the class of compounds known as hexose phosphates. Hexose phosphates are carbohydrate derivatives containing a hexose substituted by one or more phosphate groups. Beta-d-glucose 6-phosphate is soluble (in water) and a moderately acidic compound (based on its pKa). Beta-d-glucose 6-phosphate can be found in a number of food items such as sapodilla, hickory nut, atlantic herring, and swede, which makes beta-d-glucose 6-phosphate a potential biomarker for the consumption of these food products. Beta-d-glucose 6-phosphate exists in all living species, ranging from bacteria to humans. In humans, beta-d-glucose 6-phosphate is involved in several metabolic pathways, some of which include glycolysis, glycogenosis, type IC, glycogenosis, type IB, and trehalose degradation. Beta-d-glucose 6-phosphate is also involved in several metabolic disorders, some of which include glucose-6-phosphate dehydrogenase deficiency, warburg effect, fanconi-bickel syndrome, and transaldolase deficiency.

   

Beta-D-Fructose 6-phosphate

{[(2R,3S,4S,5R)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methoxy}phosphonic acid

C6H13O9P (260.0297)


Beta-D-Fructose 6 phosphate (b-F6P) is the beta-anomer of fructose-6-phosphate. There are two anomers of fructose 6 phosphate, the alpha anomer and the beta anomer. Specifically, beta-D-fructose 6-phosphate is fructose sugar phosphorylated on carbon 6. Beta-D-Fructose 6-phosphate is a substrate for Fructose-1,6-bisphosphatase, Pyruvate kinase (isozymes R/L), Hexokinase (type I), Fructose-bisphosphate aldolase A, L-lactate dehydrogenase B chain, Glyceraldehyde-3-phosphate dehydrogenase (liver) and Transaldolase. [HMDB] Beta-D-Fructose 6 phosphate (b-F6P) is the beta-anomer of fructose-6-phosphate. There are two anomers of fructose 6 phosphate, the alpha anomer and the beta anomer. Specifically, beta-D-fructose 6-phosphate is fructose sugar phosphorylated on carbon 6. Beta-D-Fructose 6-phosphate is a substrate for Fructose-1,6-bisphosphatase, Pyruvate kinase (isozymes R/L), Hexokinase (type I), Fructose-bisphosphate aldolase A, L-lactate dehydrogenase B chain, Glyceraldehyde-3-phosphate dehydrogenase (liver) and Transaldolase.

   

D-Mannose 1-phosphate

{[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phosphonic acid

C6H13O9P (260.0297)


D-Mannose 1-phosphate (CAS: 27251-84-9) is a normal metabolite intermediate in fructose and mannose metabolism. It is a substrate of phosphomannomutase 1 (PMM, EC 5.4.2.8), an enzyme necessary for the synthesis of GDP-mannose (a substrate for dolichol-linked oligosaccharide synthesis). PMM converts mannose 6-phosphate into mannose-1-phosphate. A deficiency of phosphomannomutase in carbohydrate-deficient glycoprotein syndrome (CDGS) type I is associated with a decreased synthesis of mannose 1-phosphate. CDGS is a group of autosomal recessively transmitted disorders in which abnormally glycosylated proteins are formed (PMID: 9451026, 8549746, 12729595). α-d-mannose 1-phosphate is a member of the class of compounds known as monosaccharide phosphates. Monosaccharide phosphates are monosaccharides comprising a phosphated group linked to the carbohydrate unit. α-d-mannose 1-phosphate is soluble (in water) and a moderately acidic compound (based on its pKa). α-d-mannose 1-phosphate can be found in a number of food items such as lettuce, beech nut, red beetroot, and japanese pumpkin, which makes α-d-mannose 1-phosphate a potential biomarker for the consumption of these food products. Acquisition and generation of the data is financially supported in part by CREST/JST. KEIO_ID M080

   

D-myo-Inositol 3-phosphate

{[(1R,2S,3R,4R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}phosphonic acid

C6H13O9P (260.0297)


D-myo-Inositol 3-phosphate, also known as inositol 3-phosphoric acid, belongs to the class of organic compounds known as inositol phosphates. Inositol phosphates are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety. D-myo-Inositol 3-phosphate is an extremely weak basic (essentially neutral) compound (based on its pKa). D-myo-Inositol 3-phosphate is involved in the inositol phosphate metabolism and the phosphatidylinositol signalling systems. D-myo-Inositol 3-phosphate is created from D-myo-inositol 3,4-bisphosphate by inositol polyphosphate-4-phosphatase (EC 3.1.3.66) and is converted into myo-inositol by myo-inositol-1(or 4)-monophosphatase (EC 3.1.3.25). Myo-inositol 1-phosphate is a metabolite of the Inositol phosphate metabolism and the Phosphatidylinositol signaling system. Inositol phosphatases [EC:3.1.3.25] play a crucial role in the phosphatidylinositol signaling pathway; in brain, the expression is substantially higher in the subcortical regions, most prominently in the caudate. The phosphatidylinositol pathway is thought to be modified by lithium, a commonly prescribed medication in treating bipolar disorder. (OMIM 605922) [HMDB]

   

D-Tagatose 6-phosphate

{[(2R,3R,4S)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methoxy}phosphonic acid

C6H13O9P (260.0297)


D-Tagatose 6-phosphate is an intermediate in galactose metabolism. [HMDB] D-Tagatose 6-phosphate is an intermediate in galactose metabolism.

   

[(2R,3R,4S,5S)-3,4,5,6-Tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

[(2R,3R,4S,5S)-3,4,5,6-Tetrahydroxyoxan-2-yl]methyl dihydrogen phosphoric acid

C6H13O9P (260.0297)


   

beta-D-Glucose 1-phosphate

{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phosphonic acid

C6H13O9P (260.0297)


   

Tiazofurin

Tiazofurin

C9H12N2O5S (260.0467)


C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite C471 - Enzyme Inhibitor > C2087 - Inosine Monophosphate Dehydrogenase Inhibitor L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents

   

alpha-D-Glucose 6-phosphate

6-O-phosphono-alpha-D-glucopyranose

C6H13O9P (260.0297)


A D-glucopyranose 6-phosphate where alpha-D-glucose is the sugar component. [Spectral] alpha-D-Glucose 6-phosphate (exact mass = 260.02972) and L-Isoleucine (exact mass = 131.09463) and 3-Sulfino-L-alanine (exact mass = 153.00958) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. [Spectral] alpha-D-Glucose 6-phosphate (exact mass = 260.02972) and 3-Sulfino-L-alanine (exact mass = 153.00958) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions.

   

D-Galactose 6-phosphate

D-galactopyranose 6-phosphate

C6H13O9P (260.0297)


   

beta-D-Glucose 1-phosphate

β-D-Glucose 1-phosphate

C6H13O9P (260.0297)


The beta-anomer of D-glucose 1-phosphate.

   

1D-myo-inositol 5-phosphate

1D-myo-inositol 5-phosphate

C6H13O9P (260.0297)


   

Galactose 1-phosphate

alpha-D-Galactose-1-phosphate dipotassium salt pentahydrate

C6H13O9P (260.0297)


A D-galactopyranose 1-phosphate having alpha-configuration at the anomeric centre. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS α-d-galactose 1-phosphate, also known as alpha-D-galactopyranosyl phosphate or A-D-galactopyranose 1-phosphoric acid, is a member of the class of compounds known as monosaccharide phosphates. Monosaccharide phosphates are monosaccharides comprising a phosphated group linked to the carbohydrate unit. α-d-galactose 1-phosphate is soluble (in water) and a moderately acidic compound (based on its pKa). α-d-galactose 1-phosphate can be found in a number of food items such as kai-lan, cinnamon, macadamia nut (m. tetraphylla), and durian, which makes α-d-galactose 1-phosphate a potential biomarker for the consumption of these food products. α-d-galactose 1-phosphate can be found primarily in blood, as well as in human erythrocyte and red blood cell tissues. α-d-galactose 1-phosphate exists in all living species, ranging from bacteria to humans. In humans, α-d-galactose 1-phosphate is involved in few metabolic pathways, which include galactose metabolism, lactose synthesis, and nucleotide sugars metabolism. α-d-galactose 1-phosphate is also involved in several metabolic disorders, some of which include GLUT-1 deficiency syndrome, congenital disorder of glycosylation cdg-iid, galactosemia III, and galactosemia.

   

[(2R,3S,4R)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

[(2R,3S,4R)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

(3S,4R)-Ketose 1-phosphate

(3S,4R)-Ketose 1-phosphate

C6H13O9P (260.0297)


   

D-Glucose 6-sulfate

[(2R,3S,4S,5R)-3,4,5,6-tetrahydroxytetrahydropyran-2-yl]methyl hydrogen sulfate

C6H12O9S (260.0202)


   

L-tagatofuranose 6-phosphate

L-tagatofuranose 6-phosphate

C6H13O9P (260.0297)


The furanose form of L-tagatose 6-phosphate.

   

b-D-Mannose 6-phosphate

[(6S)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

alpha-D-Hexose 1-phosphate

alpha-D-Hexose 1-phosphate

C6H13O9P (260.0297)


   

D-Allopyranose 6-phosphate

D-Allopyranose 6-phosphate

C6H13O9P (260.0297)


   

L-Galactose 1-phosphate

beta-L-galactose 1-phosphate

C6H13O9P (260.0297)


A galactose phosphate compound with undefined anomeric stereochemistry having L-configuration and the phosphate group at the 1-position. A L-galactose 1-phosphate compound having beta-configuration about the anomeric centre.

   

Tiaprofenic acid

5-Benzoyl-alpha-methylthiophene-2-acetic acid

C14H12O3S (260.0507)


Tiaprofenic acid is only found in individuals that have used or taken this drug. It is a non-steroidal anti-inflammatory drug of the arylpropionic acid (profen) class, used to treat pain, especially arthritic pain.Tiaprofenic acid belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). It works by blocking the production of a chemical (prostaglandin) which the body produces in response to injury or certain diseases. This prostaglandin would otherwise go on to cause swelling, pain and inflammation. M - Musculo-skeletal system > M01 - Antiinflammatory and antirheumatic products > M01A - Antiinflammatory and antirheumatic products, non-steroids > M01AE - Propionic acid derivatives C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents

   

D-Tagatose 1-phosphate

{[(3S,4S,5R)-3,4,5,6-tetrahydroxy-2-oxohexyl]oxy}phosphonic acid

C6H13O9P (260.0297)


D-tagatose is a stereoisomer of D-fructose, which is phosphorylated to D-tagatose-1-phosphate by fructokinase in the liver. Slow degradation rate of D-tagatose-1-phosphate, cause accumulation, and ingested D-tagatose may therefore cause a longer lasting reduction in inorganic phosphate (Pi) and adenosine triphosphate (ATP) levels in the liver compared with D-fructose. It is also seen in patients with hereditary fructose intolerance, this may increase purine nucleotide degradation and thereby increase uric acid production. (PMID: 11079825) [HMDB] D-tagatose is a stereoisomer of D-fructose, which is phosphorylated to D-tagatose-1-phosphate by fructokinase in the liver. Slow degradation rate of D-tagatose-1-phosphate, cause accumulation, and ingested D-tagatose may therefore cause a longer lasting reduction in inorganic phosphate (Pi) and adenosine triphosphate (ATP) levels in the liver compared with D-fructose. It is also seen in patients with hereditary fructose intolerance, this may increase purine nucleotide degradation and thereby increase uric acid production. (PMID: 11079825).

   

5-Methylthioribulose 1-phosphate

{[(3R,4S)-3,4-dihydroxy-5-(methylsulfanyl)-2-oxopentyl]oxy}phosphonic acid

C6H13O7PS (260.012)


5-Methylthioribulose 1-phosphate is an intermediate in the methionine salvage pathway. It is a microbial metabolite produced by gut microbes during methionine generation from methylthioadenosine. The first step is the phosphorolysis of methylthioadenosine to 5-methylthioribose-1-phosphate and adenine by the enzyme 5-deoxy- 5-methylthioadenosine phosphorylase (methylthioadenosine phosphorylase); 5-methylthioribose-1-phosphate is then converted to 5-methylthioribulose-1-phosphate (PMID: 6725268). 5-Deoxy-5-methylthioadenosine (methylthioadenosine) is a metabolite of S-adenosyl-L-methionine formed during the synthesis of the polyamines, spermidine and spermine. [HMDB]. 5-Methylthioribulose 1-phosphate is found in many foods, some of which are fireweed, lemon verbena, parsley, and fox grape. 5-Methylthioribulose 1-phosphate is an intermediate in the methionine salvage pathway. It is a microbial metabolite produced by gut microbes during methionine generation from methylthioadenosine. The first step is the phosphorolysis of methylthioadenosine to 5-methylthioribose-1-phosphate and adenine by the enzyme 5-deoxy- 5-methylthioadenosine phosphorylase (methylthioadenosine phosphorylase); 5-methylthioribose-1-phosphate is then converted to 5-methylthioribulose-1-phosphate (PMID: 6725268). 5-Deoxy-5-methylthioadenosine (methylthioadenosine) is a metabolite of S-adenosyl-L-methionine formed during the synthesis of the polyamines, spermidine and spermine.

   

Caffeic acid 4-O-sulfate

(2E)-3-[3-Hydroxy-4-(sulphooxy)phenyl]prop-2-enoic acid

C9H8O7S (259.9991)


Caffeic acid 4-sulfate, also known as caffeate 4-sulphate or caffeic acid 4-sulphuric acid, is a member of the class of compounds known as hydroxycinnamic acids. Hydroxycinnamic acids are compounds containing an cinnamic acid where the benzene ring is hydroxylated. Caffeic acid 4-sulfate is practically insoluble (in water) and an extremely strong acidic compound (based on its pKa). Caffeic acid 4-sulfate can be found primarily in blood and urine. Within the cell, caffeic acid 4-sulfate is primarily located in the cytoplasm. It can also be found in the extracellular space. Caffeic acid 4-O-sulfate (CAS: 1213651-94-5) is a polyphenol metabolite detected in biological fluids (PMID: 20428313). Caffeic acid sulfate was found to be elevated in rat urine after whole rye consumption which makes this compound a potential urinary biomarker of whole grain intake (PMID: 26862900).

   

Caffeic acid 3-O-sulfate

(2E)-3-[4-Hydroxy-3-(sulfooxy)phenyl]-2-propenoic acid

C9H8O7S (259.9991)


Caffeic acid 3-O-sulfate (CAS: 1208232-16-9) is a polyphenol metabolite detected in biological fluids (PMID: 20428313). Caffeic acid sulfate was found to be elevated in rat urine after whole rye consumption which makes this compound a potential urinary biomarker of whole grain intake (PMID: 26862900).

   

Dolichyl phosphate D-mannose

{[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phosphonic acid

C6H13O9P (260.0297)


Dolichyl phosphate D-mannose (DPM) is an intermediate in the biosynthesis of N-glycans. It is a substrate for dolichol-phosphate mannosyltransferase (PMID: 10835346). Dolichol-phosphate mannosyltransferase is a heterotrimeric protein embedded in the endoplasmic reticulum membrane. The first subunit of the heterotrimer appears to be the actual catalyst, and the other two subunits appear to stabilize it. More specifically, dolichol-phosphate-mannose is the donor of mannose groups in the synthesis of the dolichol pyrophosphate-linked precursor oligosaccharide in asparagine-linked glycosylation, in the synthesis of glycosyl phosphatidylinositol (GPI) anchor precursors, in protein O-mannosylation and in protein C-mannosylation. Its synthesis proceeds in two steps. First, cytosolic GDP-mannose reacts with dolichol phosphate exposed on the cytosolic face of the endoplasmic reticulum membrane to form DPM with its mannose moiety oriented toward the cytosol. The DPM molecule then flips in the endoplasmic reticulum membrane, so that its mannose moiety is in the endoplasmic reticulum lumen, accessible to the enzymes that catalyze its transfer to growing glycolipids and glycoproteins. (PMID: 11102867). Dolichyl phosphate D-mannose is also a substrate for protein O-mannosyl-transferase 2 and protein O-mannosyl-transferase 1. [HMDB] Dolichyl phosphate D-mannose (DPM) is an intermediate in the biosynthesis of N-glycans. It is a substrate for dolichol-phosphate mannosyltransferase (PMID: 10835346). Dolichol-phosphate mannosyltransferase is a heterotrimeric protein embedded in the endoplasmic reticulum membrane. The first subunit of the heterotrimer appears to be the actual catalyst, and the other two subunits appear to stabilize it. More specifically, dolichol-phosphate-mannose is the donor of mannose groups in the synthesis of the dolichol pyrophosphate-linked precursor oligosaccharide in asparagine-linked glycosylation, in the synthesis of glycosyl phosphatidylinositol (GPI) anchor precursors, in protein O-mannosylation and in protein C-mannosylation. Its synthesis proceeds in two steps. First, cytosolic GDP-mannose reacts with dolichol phosphate exposed on the cytosolic face of the endoplasmic reticulum membrane to form DPM with its mannose moiety oriented toward the cytosol. The DPM molecule then flips in the endoplasmic reticulum membrane, so that its mannose moiety is in the endoplasmic reticulum lumen, accessible to the enzymes that catalyze its transfer to growing glycolipids and glycoproteins. (PMID: 11102867). Dolichyl phosphate D-mannose is also a substrate for protein O-mannosyl-transferase 2 and protein O-mannosyl-transferase 1.

   

myo-Inositol 6-phosphate

{[(1R,2R,3R,4R,5R,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}phosphonic acid

C6H13O9P (260.0297)


myo-Inositol 6-phosphate, also known as I6P or Ins(6)P, belongs to the class of organic compounds known as inositol phosphates. Inositol phosphates are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety. Inositol phosphate is an intermediate step in the metabolism of glucose-6-phosphate into myo-inositol. myo-Inositol is synthesized from glucose-6-phosphate (G-6-P) in two steps. First, G-6-P is isomerized by INYNA1 into myo-inositol 1-phosphate, which is then dephosphorylated by IMPA1 to give myo-inositol. An intermediate step in the metabolism of glucose-6-phosphate to myo-inositol. myo-Inositol is synthesized from glucose-6-phosphate (G-6-P) in two steps. First, G-6-P is isomerised by INYNA1 to myo-inositol 1-phosphate, which is then dephosphorylated by IMPA1 to give myo-inositol [HMDB]

   

Urolithin D

3,4,8,9-tetrahydroxy-6H-benzo[c]chromen-6-one

C13H8O6 (260.0321)


Urolithin D is a biomarker of nut consumption in urine. Urolithin D is competitive and reversible antagonist of EphA receptors. Urolithin D exhibits intra-classes selectivity[1].

   

D-fructose 1-phosphate

{[(3S,4R,5R)-3,4,5,6-tetrahydroxy-2-oxohexyl]oxy}phosphonic acid

C6H13O9P (260.0297)


D-fructose 1-phosphate, also known as 1-O-phosphono-D-fructose or fructose-1-phosphate, barium salt, (D)-isomer, is a member of the class of compounds known as monosaccharide phosphates. Monosaccharide phosphates are monosaccharides comprising a phosphated group linked to the carbohydrate unit. D-fructose 1-phosphate is soluble (in water) and a moderately acidic compound (based on its pKa). D-fructose 1-phosphate can be found in a number of food items such as rye, ucuhuba, sugar apple, and spelt, which makes D-fructose 1-phosphate a potential biomarker for the consumption of these food products. D-fructose 1-phosphate exists in all eukaryotes, ranging from yeast to humans. This compound belongs to the family of Monosaccharide Phosphates. These are monosaccharides comprising a phosphated group linked tot he carbohydrate unit.

   

3,5-Dihydroxycinnamic acid sulfate

(2E)-3-[3-Hydroxy-5-(sulphooxy)phenyl]prop-2-enoic acid

C9H8O7S (259.9991)


   

(2,3,4,5,6-Pentahydroxycyclohexyl) dihydrogen phosphate

(2,3,4,5,6-Pentahydroxycyclohexyl) dihydrogen phosphoric acid

C6H13O9P (260.0297)


   

(2R,3R,4S,5R)-2,3,4,5-Tetrahydroxy-6-oxohexyl dihydrogen phosphate

(2R,3R,4S,5R)-2,3,4,5-Tetrahydroxy-6-oxohexyl dihydrogen phosphoric acid

C6H13O9P (260.0297)


   

(3S,4R)-Ketose 1-phosphate

[(3,4,5,6-tetrahydroxy-2-oxohexyl)oxy]phosphonic acid

C6H13O9P (260.0297)


   

beta-D-Fructopyranose 1-phosphate

[(2,3,4,5-tetrahydroxyoxan-2-yl)methoxy]phosphonic acid

C6H13O9P (260.0297)


   

3-Thiacytidine

3-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-imino-3,6-dihydro-2H-1,3-thiazin-2-one

C9H12N2O5S (260.0467)


   

3,4,5,6-Tetrahydroxyxanthone

3,4,5,6-tetrahydroxy-9H-xanthen-9-one

C13H8O6 (260.0321)


   

2-Mercapto-3-phenylthieno[3,2-d]pyrimidin-4(3H)-one

3-phenyl-2-sulfanylidene-1H,2H,3H,4H-thieno[3,2-d]pyrimidin-4-one

C12H8N2OS2 (260.0078)


   

2-(Bis(2-chloroethyl)amino)-4-hydroxytetrahydro-2H-1,3,2-oxazaphosphorine

2-(Bis(2-chloroethyl)amino)-4-hydroxytetrahydro-2H-1,3,2-oxazaphosphorine

C7H15Cl2N2O2P (260.0248)


   

4-Thiouridine

1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylidene-1,2,3,4-tetrahydropyrimidin-2-one

C9H12N2O5S (260.0467)


   

D-Glucose 2-phosphate

[(3,4,5,6-tetrahydroxy-1-oxohexan-2-yl)oxy]phosphonic acid

C6H13O9P (260.0297)


   

Fructose 3-phosphate

(1,4,5,6-Tetrahydroxy-2-oxohexan-3-yl) dihydrogen phosphate

C6H13O9P (260.0297)


   

Fructose-6-Phosphate (closed form)

{[3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methoxy}phosphonic acid

C6H13O9P (260.0297)


   

Benzonitrile, 3-fluoro-5-(2-(2-(fluoromethyl)-4-thiazolyl)ethynyl)-

3-fluoro-5-{2-[2-(fluoromethyl)-1,3-thiazol-4-yl]ethynyl}benzonitrile

C13H6F2N2S (260.022)


   

Tiazofurin

2-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3-thiazole-4-carboximidate

C9H12N2O5S (260.0467)


   

D-mannose 6-phosphate

{[(2R,3S,4S,5S)-3,4,5,6-tetrahydroxyoxan-2-yl]methoxy}phosphonic acid

C6H13O9P (260.0297)


D-mannose 6-phosphate, also known as mannose-6-phosphate disodium salt, is a member of the class of compounds known as hexose phosphates. Hexose phosphates are carbohydrate derivatives containing a hexose substituted by one or more phosphate groups. D-mannose 6-phosphate is soluble (in water) and a moderately acidic compound (based on its pKa). D-mannose 6-phosphate can be found in a number of food items such as bog bilberry, wild celery, common pea, and breadnut tree seed, which makes D-mannose 6-phosphate a potential biomarker for the consumption of these food products. D-mannose 6-phosphate may be a unique S.cerevisiae (yeast) metabolite. The M6P-tagged lysosomal enzymes are shipped to the late endosomes via vesicular transport. Enzyme replacement therapy (ERT) for several lysosomal storage diseases relies on this pathway to efficiently direct synthetic enzymes to the lysosome where each can metabolize its particular substrate. The pH in the late endosome can reach 6.0, which causes dissociation of M6P from its receptor. Upon release, the enzymes are ferried to their final destination in the lysosomes. The MPRs are packed into vesicles that bud off the late endosome and return to the "trans"-Golgi network. In this way, the MPRs can be recycled . D-mannose 6-phosphate, also known as mannose-6-phosphate disodium salt, is a member of the class of compounds known as hexose phosphates. Hexose phosphates are carbohydrate derivatives containing a hexose substituted by one or more phosphate groups. D-mannose 6-phosphate is soluble (in water) and a moderately acidic compound (based on its pKa). D-mannose 6-phosphate can be found in a number of food items such as bog bilberry, wild celery, common pea, and breadnut tree seed, which makes D-mannose 6-phosphate a potential biomarker for the consumption of these food products. D-mannose 6-phosphate may be a unique S.cerevisiae (yeast) metabolite. The M6P-tagged lysosomal enzymes are shipped to the late endosomes via vesicular transport. Enzyme replacement therapy (ERT) for several lysosomal storage diseases relies on this pathway to efficiently direct synthetic enzymes to the lysosome where each can metabolize its particular substrate. The pH in the late endosome can reach 6.0, which causes dissociation of M6P from its receptor. Upon release, the enzymes are ferried to their final destination in the lysosomes. The MPRs are packed into vesicles that bud off the late endosome and return to the "trans"-Golgi network. In this way, the MPRs can be recycled.

   

Bellidin

1,3,5,8-Tetrahydroxyxanthone; Desmethylbellidifolin

C13H8O6 (260.0321)


Bellidin is a member of the class of xanthones that is xanthone which is substituted by hydroxy groups at positions 1, 3, 5, and 8. A natural product found particularly in Iris nigricans and Gentiana campestris. It has a role as a metabolite, an EC 3.1.1.7 (acetylcholinesterase) inhibitor, a mutagen, an antioxidant and a radical scavenger. It is a member of xanthones and a tetrol. It is functionally related to a xanthone. 1,3,5,8-Tetrahydroxyxanthone is a natural product found in Gentiana orbicularis, Swertia teres, and other organisms with data available. A member of the class of xanthones that is xanthone which is substituted by hydroxy groups at positions 1, 3, 5, and 8. A natural product found particularly in Iris nigricans and Gentiana campestris.

   

Uridine, 4-thio-

Uridine, 4-thio-

C9H12N2O5S (260.0467)


   

1,3,5,6-Tetrahydroxyxanthone

1,3,5,6-Tetrahydroxyxanthone

C13H8O6 (260.0321)


   
   

2,3,4,5-tetramethoxybenzoyl chloride

2,3,4,5-tetramethoxybenzoyl chloride

C11H13ClO5 (260.0451)


   

1,3,5,7-Tetrahydroxyxanthone

1,3,5,7-Tetrahydroxyxanthone

C13H8O6 (260.0321)


   

1,4,5,6-Tetrahydroxy xanthone

1,4,5,6-Tetrahydroxy xanthone

C13H8O6 (260.0321)


   

beta-D-Glucopyranosyl-1-phosphate

beta-D-Glucopyranosyl-1-phosphate

C6H13O9P (260.0297)


   

Glucose 6-phosphate

D-Glucose 6-phosphate

C6H13O9P (260.0297)


   

Glucose 1-phosphate

[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

C6H13O9P (260.0297)


COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

2-(Phenylsulfonyl)acetophenone

2-(Phenylsulfonyl)acetophenone

C14H12O3S (260.0507)


   

2-[(phenylsulfinyl)methyl]benzoic acid

2-[(phenylsulfinyl)methyl]benzoic acid

C14H12O3S (260.0507)


   

Maybridge1_006456

Maybridge1_006456

C14H12O3S (260.0507)


   
   

1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-sulfanylidenepyrimidin-4-one

1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-sulfanylidenepyrimidin-4-one

C9H12N2O5S (260.0467)


   

D-fructofuranose 6-phosphate

D-Fructose-6-phosphate disodium salt hydrate

C6H13O9P (260.0297)


The five-membered ring form of D-fructose 6-phosphate.

   

glucose 3-sulfate

glucose 3-sulfate

C6H12O9S (260.0202)


   

coniferyl alcohol 4-O-sulphate

coniferyl alcohol 4-O-sulphate

C10H12O6S (260.0355)


   

(E)-Hymenoquinone|Hymenochinon

(E)-Hymenoquinone|Hymenochinon

C13H8O6 (260.0321)


   

1,3,5,7-Tetrahydroxyxanthon

1,3,5,7-Tetrahydroxyxanthon

C13H8O6 (260.0321)


   

phelligridin A

phelligridin A

C13H8O6 (260.0321)


   

1,3,6,8-Tetrahydroxy-9H-xanthen-9-one

1,3,6,8-Tetrahydroxy-9H-xanthen-9-one

C13H8O6 (260.0321)


   

5-(1-Naphthyl)-3H-1,2-dithiol-3-thione

5-(1-Naphthyl)-3H-1,2-dithiol-3-thione

C13H8S3 (259.9788)


   

Lamellicolic anhydride

Lamellicolic anhydride

C13H8O6 (260.0321)


   

8-Hydroxypenillic acid

8-Hydroxypenillic acid

C9H12N2O5S (260.0467)


   

3,4,5,6-tetrahydroxyxanthone

3,4,5,6-tetrahydroxyxanthone

C13H8O6 (260.0321)


   

3,4,6,7-tetrahydroxyxanthone

3,4,6,7-tetrahydroxyxanthone

C13H8O6 (260.0321)


   

CHEMBL12700

CHEMBL12700

C13H8O6 (260.0321)


   

1,2,3,5-Tetrahydroxyxanthone

1,2,3,5-Tetrahydroxyxanthone

C13H8O6 (260.0321)


   

9-hydroxyacetoxy-furo[3,2-g]chromen-7-one

9-hydroxyacetoxy-furo[3,2-g]chromen-7-one

C13H8O6 (260.0321)


   

1,3,6,7-Tetrahydroxyxanthon|2,4,6,7-tetrahydroxyxanthone

1,3,6,7-Tetrahydroxyxanthon|2,4,6,7-tetrahydroxyxanthone

C13H8O6 (260.0321)


   

6-bromo-1-methyl-9H-pyrido[3,4-b]indole

6-bromo-1-methyl-9H-pyrido[3,4-b]indole

C12H9BrN2 (259.9949)


   

5,8-dihydroxy-1-hydroxymethylnaphtho[2,3-c]furan-4,9-dione

5,8-dihydroxy-1-hydroxymethylnaphtho[2,3-c]furan-4,9-dione

C13H8O6 (260.0321)


   

p-sulfooxyphenylpyruvic acid

p-sulfooxyphenylpyruvic acid

C9H8O7S (259.9991)


   

1,5,6,7-tetrahydroxyxanthone

1,5,6,7-tetrahydroxyxanthone

C13H8O6 (260.0321)


   
   

SCHEMBL12640196

SCHEMBL12640196

C6H14O7P2 (260.0215)


   

1-(methylsulfanyl)xylulose 5-phosphate

1-(methylsulfanyl)xylulose 5-phosphate

C6H13O7PS (260.012)


   

Norathyriol

9H-Xanthen-9-one, 1,3,6,7-tetrahydroxy-

C13H8O6 (260.0321)


Norathyriol is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3, 6 and 7. Isolated from Garcinia mangostana and Maclura pomifera, it exhibits inhibitory activity against protein kinase C. It has a role as an antineoplastic agent, an EC 2.7.11.13 (protein kinase C) inhibitor and a plant metabolite. It is a member of xanthones and a polyphenol. Norathyriol is a natural product found in Hypericum aucheri, Hypericum elegans, and other organisms with data available. A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3, 6 and 7. Isolated from Garcinia mangostana and Maclura pomifera, it exhibits inhibitory activity against protein kinase C.

   

1,3,5,6-Tetrahydroxyxantone

1,3,5,6-TETRAHYDROXY-9H-XANTHEN-9-ONE

C13H8O6 (260.0321)


1,3,5,6-Tetrahydroxyxanthone is a natural product found in Hypericum scabrum, Hypericum androsaemum, and other organisms with data available.

   

cyclophosphamide

cyclophosphamide

C7H15Cl2N2O2P (260.0248)


L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01A - Alkylating agents > L01AA - Nitrogen mustard analogues D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D009588 - Nitrogen Mustard Compounds D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D010752 - Phosphoramide Mustards C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent D000970 - Antineoplastic Agents > D019653 - Myeloablative Agonists D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents C308 - Immunotherapeutic Agent > C574 - Immunosuppressant D009676 - Noxae > D000477 - Alkylating Agents D009676 - Noxae > D009153 - Mutagens D018501 - Antirheumatic Agents CONFIDENCE standard compound; EAWAG_UCHEM_ID 2579

   

D-Fructose 1-phosphate

D-Fructose 1-phosphate

C6H13O9P (260.0297)


CONFIDENCE standard compound; ML_ID 35

   
   

Clafen (Cyclophosphamide)

Clafen (Cyclophosphamide)

C7H15Cl2N2O2P (260.0248)


   

ifosfamide

ifosfamide

C7H15Cl2N2O2P (260.0248)


L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01A - Alkylating agents > L01AA - Nitrogen mustard analogues D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D009588 - Nitrogen Mustard Compounds D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D010752 - Phosphoramide Mustards C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent D009676 - Noxae > D000477 - Alkylating Agents

   

suprofen

Suprofen (Profenal)

C14H12O3S (260.0507)


M - Musculo-skeletal system > M01 - Antiinflammatory and antirheumatic products > M01A - Antiinflammatory and antirheumatic products, non-steroids > M01AE - Propionic acid derivatives D018501 - Antirheumatic Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D016861 - Cyclooxygenase Inhibitors C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D004791 - Enzyme Inhibitors

   

MLS002154021-01!Ifosfamide3778-73-2

MLS002154021-01!Ifosfamide3778-73-2

C7H15Cl2N2O2P (260.0248)


   

D-Glucose 6-phosphate

D-Glucose-6-phosphate sodium salt

C6H13O9P (260.0297)


The open-chain form of D-glucose 6-phosphate.

   

D-Glucose-6-phosphate

D-Glucose-6-phosphate

C6H13O9P (260.0297)


   

alpha-D-Galactose 1-phosphate

alpha-D-Galactose 1-phosphate

C6H13O9P (260.0297)


   

D-Fructose 6-phosphate

D-Fructose 6-phosphate

C6H13O9P (260.0297)


   

D-Mannose-6-phosphate mono sodium salt

D-Mannose-6-phosphate mono sodium salt

C6H13O9P (260.0297)


   

D-Mannose-6-phosphate barium salt hydrate

D-Mannose-6-phosphate barium salt hydrate

C6H13O9P (260.0297)


   

alpha-D-(+)-mannose-1-phosphate sodium salt hydrate

alpha-D-(+)-mannose-1-phosphate sodium salt hydrate

C6H13O9P (260.0297)


   

alpha-D-glucose-1-phosphate dipotassium salt dihydate

[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

C6H13O9P (260.0297)


   

Galactose-1P

alpha-D-Galactose-1-phosphate Dipotassium Salt

C6H13O9P (260.0297)


   

Fructose 6-phosphate

D-fructofuranose 6-phosphate

C6H13O9P (260.0297)


   

Mannose 6-phosphate

Mannose 6-phosphate

C6H13O9P (260.0297)


   
   

4-thiouridine

4-thiouridine

C9H12N2O5S (260.0467)


D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D000345 - Affinity Labels D009676 - Noxae > D000963 - Antimetabolites 4-Thiouridine is a ribonucleoside analog, it is widely used in RNA analysis and (m)RNA labeling. 4-Thiouridine inhibits rRNA synthesis and causes a nucleolar stress response[1].

   

Glucose-1-phosphate

Glucose-1-phosphate

C6H13O9P (260.0297)


   

Glucose-6-phosphate

Glucose-6-phosphate

C6H13O9P (260.0297)


   

Fructose-1-phosphate

Fructose-1-phosphate

C6H13O9P (260.0297)


   

petunidin-3-glucoside

petunidin-3-glucoside

C7H17O2PS3 (260.0128)


   

tiaprofenic acid

tiaprofenic acid

C14H12O3S (260.0507)


M - Musculo-skeletal system > M01 - Antiinflammatory and antirheumatic products > M01A - Antiinflammatory and antirheumatic products, non-steroids > M01AE - Propionic acid derivatives C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents

   
   

D-Mannose 6-phosphate

D-Mannose 6-phosphate

C6H13O9P (260.0297)


   

alpha-D-Glucose 1-phosphate

alpha-D-Glucose 1-phosphate

C6H13O9P (260.0297)


A D-glucopyranose 1-phosphate in which the anomeric centre has alpha-configuration.

   

ALPHA-GLUCOSE 1-PHOSPHATE

ALPHA-GLUCOSE 1-PHOSPHATE

C6H13O9P (260.0297)


   

ALPHA-GALACTOSE 1-PHOSPHATE

ALPHA-GALACTOSE 1-PHOSPHATE

C6H13O9P (260.0297)


   

Protionamide sulfate

Protionamide sulfate

C9H12N2O3S2 (260.0289)


   

b-D-Mannopyranosyl phosphate

b-D-Mannopyranosyl phosphate

C6H13O9P (260.0297)


   

D-Myo-inositol-3-phosphate

D-myo-inositol-3-hydrogen phosphate, monosodium salt

C6H13O9P (260.0297)


   

D-Tagatose 1-phosphate

D-Tagatose 1-phosphate

C6H13O9P (260.0297)


   

Methylthioribosyl phosphate

Methylthioribosyl phosphate

C6H13O7PS (260.012)


   

(E)-C-HDMAPP

P-[(3E)-5-hydroxy-4-methyl-3-penten-1-yl]-isohypophosphoric acid, triammonium salt

C6H14O7P2 (260.0215)


   

Urolithin D

3,4,8,9-tetrahydroxy-6H-benzo[c]chromen-6-one

C13H8O6 (260.0321)


Urolithin D is competitive and reversible antagonist of EphA receptors. Urolithin D exhibits intra-classes selectivity[1].

   

Caffeic acid 3-sulfate

(2E)-3-[4-hydroxy-3-(sulfooxy)phenyl]prop-2-enoic acid

C9H8O7S (259.9991)


An aryl sulfate that is trans-caffeic acid in which the phenolic hydrogen at position 3 is replaced by a sulfo group. A metabolite from coffee.

   

Caffeic acid 4-sulfate

(2E)-3-[3-hydroxy-4-(sulfooxy)phenyl]prop-2-enoic acid

C9H8O7S (259.9991)


   

4,4,4-Trifluorobutyl trifluoromethanesulfonate

4,4,4-Trifluorobutyl trifluoromethanesulfonate

C5H6F6O3S (259.9942)


   

1-(2-PROPYNYL)-1H-BENZOTRIAZOLE

1-(2-PROPYNYL)-1H-BENZOTRIAZOLE

C11H8N4O2S (260.0368)


   

3-CHLORO-4-FORMYL-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

3-CHLORO-4-FORMYL-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

C14H9ClO3 (260.024)


   

5-(3,5-DICHLOROPHENYL)-5-OXOVALERIC ACID

5-(3,5-DICHLOROPHENYL)-5-OXOVALERIC ACID

C11H10Cl2O3 (260.0007)


   

3-Bromobenzophenone

3-Bromobenzophenone

C13H9BrO (259.9837)


   

1,1,1,3,3,3-Hexafluoro-2-(4-Hydroxyphenyl)Propan-2-ol

1,1,1,3,3,3-Hexafluoro-2-(4-Hydroxyphenyl)Propan-2-ol

C9H6F6O2 (260.0272)


   

1-Iodo-4-(2-methyl-2-propanyl)benzene

1-Iodo-4-(2-methyl-2-propanyl)benzene

C10H13I (260.0062)


   

sodium,formaldehyde,naphthalene-1-sulfonate

sodium,formaldehyde,naphthalene-1-sulfonate

C11H9NaO4S (260.0119)


   

1-chloro-7-iodoheptane

1-chloro-7-iodoheptane

C7H14ClI (259.9829)


   

1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarbonyl chloride

1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarbonyl chloride

C11H7ClF2O3 (260.0052)


   

5-BENZOTHIAZOL-2-YL-2-CHLOROPHENYLAMINE

5-BENZOTHIAZOL-2-YL-2-CHLOROPHENYLAMINE

C13H9ClN2S (260.0175)


   

2,2-dimethyl-3,4-dihydrochromene-6-sulfonyl chloride

2,2-dimethyl-3,4-dihydrochromene-6-sulfonyl chloride

C11H13ClO3S (260.0274)


   

2-[1-Methyl-3-(trifluoromethyl)pyrazol-5-yl]-thiophene-5-carboxaldehyde

2-[1-Methyl-3-(trifluoromethyl)pyrazol-5-yl]-thiophene-5-carboxaldehyde

C10H7F3N2OS (260.0231)


   

4-CHLORO-3,5-DINITROPHENYLACETIC ACID

4-CHLORO-3,5-DINITROPHENYLACETIC ACID

C8H5ClN2O6 (259.9836)


   
   

7-METHOXY-4,5-DIHYDRONAPHTHO[1,2-B]THIOPHENE-2-CARBOXYLIC ACID

7-METHOXY-4,5-DIHYDRONAPHTHO[1,2-B]THIOPHENE-2-CARBOXYLIC ACID

C14H12O3S (260.0507)


   

1,2,4,5-Cyclohexanetetracarboxylic Acid

1,2,4,5-Cyclohexanetetracarboxylic Acid

C10H12O8 (260.0532)


   

Ethyl bromo(4-fluorophenyl)acetate

Ethyl bromo(4-fluorophenyl)acetate

C10H10BrFO2 (259.9848)


   

Bismuth(3+) trihydroxide

Bismuth(3+) trihydroxide

BiH3O3 (259.9886)


   

Uridine, 2-deoxy-5-mercapto-

Uridine,2-deoxy-5-mercapto- (9CI)

C9H12N2O5S (260.0467)


D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents D000890 - Anti-Infective Agents > D000998 - Antiviral Agents

   

1-((4-BROMOTHIOPHEN-2-YL)METHYL)PIPERAZINE

1-((4-BROMOTHIOPHEN-2-YL)METHYL)PIPERAZINE

C9H13BrN2S (259.9983)


   

2,3-bis(2-sulfanylethylsulfanyl)propane-1-thiol

2,3-bis(2-sulfanylethylsulfanyl)propane-1-thiol

C7H16S5 (259.9856)


   

2-(3-chlorobenzoyl)benzoic acid

2-(3-chlorobenzoyl)benzoic acid

C14H9ClO3 (260.024)


   

carbarsone

carbarsone

C7H9AsN2O4 (259.9778)


C254 - Anti-Infective Agent > C276 - Antiparasitic Agent > C277 - Antiprotozoal Agent

   

4-CHLORO-5-P-TOLYL-THIENO[2,3-D]PYRIMIDINE

4-CHLORO-5-P-TOLYL-THIENO[2,3-D]PYRIMIDINE

C13H9ClN2S (260.0175)


   

TRIMETHYL 4-BROMOORTHOBENZOATE

TRIMETHYL 4-BROMOORTHOBENZOATE

C10H13BrO3 (260.0048)


   

1-(4-iodophenyl)butane

1-(4-iodophenyl)butane

C10H13I (260.0062)


   

Methyl 5H-perfluoropentanoate

Methyl 5H-perfluoropentanoate

C6H4F8O2 (260.0084)


   

1-(2-AMINOETHYL)-2-METHYL-5-NITROIMIDAZOLE DIHYDROCHLORIDE MONOHYDRATE

1-(2-AMINOETHYL)-2-METHYL-5-NITROIMIDAZOLE DIHYDROCHLORIDE MONOHYDRATE

C6H14Cl2N4O3 (260.0443)


   

Methyl 5-(Trifluoromethyl)-1-Benzothiophene-2-Carboxylate

Methyl 5-(Trifluoromethyl)-1-Benzothiophene-2-Carboxylate

C11H7F3O2S (260.0119)


   

2-Bromobenzophenone

2-Bromobenzophenone

C13H9BrO (259.9837)


   

3-CHLORO-2-FORMYL-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

3-CHLORO-2-FORMYL-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

C14H9ClO3 (260.024)


   

4-CHLORO-2-FORMYL-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

4-CHLORO-2-FORMYL-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

C14H9ClO3 (260.024)


   

5-CHLORO-4-FORMYL-[1,1-BIPHENYL]-2-CARBOXYLIC ACID

5-CHLORO-4-FORMYL-[1,1-BIPHENYL]-2-CARBOXYLIC ACID

C14H9ClO3 (260.024)


   

diethylmercury

diethylmercury

C4H10Hg (260.0489)


   

4-CHLORO-4-FLUOROCHALCONE

4-CHLORO-4-FLUOROCHALCONE

C15H10ClFO (260.0404)


   

4-Bromo-[1,1-biphenyl]-4-carboxaldehyde

4-Bromo-[1,1-biphenyl]-4-carboxaldehyde

C13H9BrO (259.9837)


   

sodium,1,4-dioxonaphthalene-2-sulfonate

sodium,1,4-dioxonaphthalene-2-sulfonate

C10H5NaO5S (259.9755)


   

4-(3-TRIFLUOROMETHOXYPHENYL)THIAZOL-2-YLAMINE

4-(3-TRIFLUOROMETHOXYPHENYL)THIAZOL-2-YLAMINE

C10H7F3N2OS (260.0231)


   

ethyl 2-broMo-2-(2-fluorophenyl)acetate

ethyl 2-broMo-2-(2-fluorophenyl)acetate

C10H10BrFO2 (259.9848)


   

Chloro(dimethyl)(pentafluorophenyl)silane

Chloro(dimethyl)(pentafluorophenyl)silane

C8H6ClF5Si (259.9847)


   

2-[(4-Bromo-2-nitrophenyl)amino]ethanol

2-[(4-Bromo-2-nitrophenyl)amino]ethanol

C8H9BrN2O3 (259.9797)


   
   

Sulfonium,dimethyl(2-oxo-2-phenylethyl)-, bromide (1:1)

Sulfonium,dimethyl(2-oxo-2-phenylethyl)-, bromide (1:1)

C10H13BrOS (259.987)


   

4-chloro-5-methyl-6-phenylthieno[2,3-d]pyrimidine

4-chloro-5-methyl-6-phenylthieno[2,3-d]pyrimidine

C13H9ClN2S (260.0175)


   

2,3,5,6-Tetramethyliodobenzene

2,3,5,6-Tetramethyliodobenzene

C10H13I (260.0062)


   

Phorate sulfoxide

Phorate sulfoxide

C7H17O4PS2 (260.0306)


   

4-Bromobenzophenone

4-Bromobenzophenone

C13H9BrO (259.9837)


   
   

1-IODO-3-TERT-BUTYLBENZENE

1-IODO-3-TERT-BUTYLBENZENE

C10H13I (260.0062)


   

(S)-N-(1-hydroxypropan-2-yl)-2-nitrobenzenesulfonamide

(S)-N-(1-hydroxypropan-2-yl)-2-nitrobenzenesulfonamide

C9H12N2O5S (260.0467)


   

Nonyl trichlorosilane

Nonyl trichlorosilane

C9H19Cl3Si (260.0322)


   

thiouridine

2-Thiouridine

C9H12N2O5S (260.0467)


   

3-amino-4-(4-chlorophenyl)sulfanylbenzonitrile

3-amino-4-(4-chlorophenyl)sulfanylbenzonitrile

C13H9ClN2S (260.0175)


   

4-Chloro-2-methyl-6-phenylthieno[3,2-d]pyrimidine

4-Chloro-2-methyl-6-phenylthieno[3,2-d]pyrimidine

C13H9ClN2S (260.0175)


   

1,2,4,5-(2H2)Benzene(2H4)tetracarboxylic acid

1,2,4,5-(2H2)Benzene(2H4)tetracarboxylic acid

C10D6O8 (260.0439)


   

N-(2-Chlorophenyl)-1,3-benzothiazol-2-amine

N-(2-Chlorophenyl)-1,3-benzothiazol-2-amine

C13H9ClN2S (260.0175)


   

(4R,6S)-6-METHYL-7,7-DIOXIDO-5,6-DIHYDRO-4H-THIENO[2,3-B]THIOPYRAN-4-YL ACETATE

(4R,6S)-6-METHYL-7,7-DIOXIDO-5,6-DIHYDRO-4H-THIENO[2,3-B]THIOPYRAN-4-YL ACETATE

C10H12O4S2 (260.0177)


   

5,6-dichloro-N-(2-oxobutyl)pyridine-3-carboxamide

5,6-dichloro-N-(2-oxobutyl)pyridine-3-carboxamide

C10H10Cl2N2O2 (260.0119)


   

5-NITRO-2-(2-PYRIDYLITHIO)BENZALDEHYDE

5-NITRO-2-(2-PYRIDYLITHIO)BENZALDEHYDE

C12H8N2O3S (260.0256)


   

[2,4-dichloro-5-(cyclopropylmethoxy)phenyl]boronic acid

[2,4-dichloro-5-(cyclopropylmethoxy)phenyl]boronic acid

C10H11BCl2O3 (260.0178)


   

4-(heptafluoroisopropyl)toluene

4-(heptafluoroisopropyl)toluene

C10H7F7 (260.0436)


   

oxybis[4-nitrobenzene]

oxybis[4-nitrobenzene]

C12H8N2O5 (260.0433)


   

BIS(2 2 2-TRIFLUOROETHYL)METHYLPHOSPHON&

BIS(2 2 2-TRIFLUOROETHYL)METHYLPHOSPHON&

C5H7F6O3P (260.0037)


   

1-Thianthrenylboronic acid

1-Thianthrenylboronic acid

C12H9BO2S2 (260.0137)


   

2,4-bis(trifluoromethyl)pyrimidine-5-carboxylic acid

2,4-bis(trifluoromethyl)pyrimidine-5-carboxylic acid

C7H2F6N2O2 (260.002)


   

4-BROMO-1-(TERT-BUTYL)-3-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID

4-BROMO-1-(TERT-BUTYL)-3-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID

C9H13BrN2O2 (260.016)


   

4-BROMO-3-ETHYL-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID ETHYL ESTER

4-BROMO-3-ETHYL-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID ETHYL ESTER

C9H13BrN2O2 (260.016)


   

Benzene,2-(2-bromoethoxy)-1,3-dimethoxy-

Benzene,2-(2-bromoethoxy)-1,3-dimethoxy-

C10H13BrO3 (260.0048)


   

Benzene,1-nitro-3-(4-nitrophenoxy)-

Benzene,1-nitro-3-(4-nitrophenoxy)-

C12H8N2O5 (260.0433)


   

5-BROMOMETHYL-1,2,3-TRIMETHOXY-BENZENE

5-BROMOMETHYL-1,2,3-TRIMETHOXY-BENZENE

C10H13BrO3 (260.0048)


   

Famotidine propionic acid

3-[[[2-[(Aminoiminomethyl)amino]-4-thiazolyl]methyl]thio]propanoic acid

C8H12N4O2S2 (260.0402)


   

1-(4-Fluorobenzyl)-2-chloro-benzimidazole

1-(4-Fluorobenzyl)-2-chloro-benzimidazole

C14H10ClFN2 (260.0517)


   

3-(2-chloro-3,4-dimethoxyphenyl)prop-2-enoyl chloride

3-(2-chloro-3,4-dimethoxyphenyl)prop-2-enoyl chloride

C11H10Cl2O3 (260.0007)


   

4-Bromo-1-methoxy-2-(2-methoxyethoxy)benzene

4-Bromo-1-methoxy-2-(2-methoxyethoxy)benzene

C10H13BrO3 (260.0048)


   

2-[1-Methyl-5-(trifluoromethyl)pyrazol-3-yl]-thiophene-5-carboxaldehyde

2-[1-Methyl-5-(trifluoromethyl)pyrazol-3-yl]-thiophene-5-carboxaldehyde

C10H7F3N2OS (260.0231)


   

1-(3-PYRIDINYLSULFONYL)-1H-BENZOTRIAZOLE

1-(3-PYRIDINYLSULFONYL)-1H-BENZOTRIAZOLE

C11H8N4O2S (260.0368)


   

2-methyl-4-oxo-4-(3,4-dichlorophenyl)butyric acid

2-methyl-4-oxo-4-(3,4-dichlorophenyl)butyric acid

C11H10Cl2O3 (260.0007)


   

1,3-Propanediol,2,2-dimethyl-, 1,3-dimethanesulfonate

1,3-Propanediol,2,2-dimethyl-, 1,3-dimethanesulfonate

C7H16O6S2 (260.0388)


   

Ethyl 3-(2,5-dichlorophenyl)-3-oxopropanoate

Ethyl 3-(2,5-dichlorophenyl)-3-oxopropanoate

C11H10Cl2O3 (260.0007)


   

4-(2,2-DIMETHOXYETHOXY)BROMOBENZENE

4-(2,2-DIMETHOXYETHOXY)BROMOBENZENE

C10H13BrO3 (260.0048)


   

methyl 4-chloro-2,6-dinitrobenzoate

methyl 4-chloro-2,6-dinitrobenzoate

C8H5ClN2O6 (259.9836)


   

(E)-2-(2-TOSYLHYDRAZONO)ACETYL CHLORIDE

(E)-2-(2-TOSYLHYDRAZONO)ACETYL CHLORIDE

C9H9ClN2O3S (260.0022)


   

1-chloro-6,6-dimethyl-3-methylsulfanyl-5,7-dihydro-2-benzothiophen-4-one

1-chloro-6,6-dimethyl-3-methylsulfanyl-5,7-dihydro-2-benzothiophen-4-one

C11H13ClOS2 (260.0096)


   

methyl 4-amino-5-chloro-2-methoxy-3-nitrobenzoate

methyl 4-amino-5-chloro-2-methoxy-3-nitrobenzoate

C9H9ClN2O5 (260.02)


   

N-(2-acetamido-4,5-dichlorophenyl)acetamide

N-(2-acetamido-4,5-dichlorophenyl)acetamide

C10H10Cl2N2O2 (260.0119)


   
   

6,8-DICHLORO-CHROMAN-3-CARBOXYLIC ACID METHYL ESTER

6,8-DICHLORO-CHROMAN-3-CARBOXYLIC ACID METHYL ESTER

C11H10Cl2O3 (260.0007)


   

[1,1-Biphenyl]-4-ol,3,5-dinitro-

[1,1-Biphenyl]-4-ol,3,5-dinitro-

C12H8N2O5 (260.0433)


   

Ethyl 3-(3,5-dichlorophenyl)-3-oxopropanoate

Ethyl 3-(3,5-dichlorophenyl)-3-oxopropanoate

C11H10Cl2O3 (260.0007)


   

2-Hexanol,3,3,4,4,5,5,6,6-octafluoro-2-methyl-

2-Hexanol,3,3,4,4,5,5,6,6-octafluoro-2-methyl-

C7H8F8O (260.0447)


   

Propanoic acid,2-hydroxy-, zinc salt, hydrate (2:1:1)

Propanoic acid,2-hydroxy-, zinc salt, hydrate (2:1:1)

C6H12O7Zn (259.9874)


   

4-Bromo-2-methoxy-1-(2-methoxyethoxy)benzene

4-Bromo-2-methoxy-1-(2-methoxyethoxy)benzene

C10H13BrO3 (260.0048)


   

7-CHLORO-5-(THIOPHEN-2-YL)PYRAZOLO[1,5-A]PYRIMIDINE-3-CARBONITRILE

7-CHLORO-5-(THIOPHEN-2-YL)PYRAZOLO[1,5-A]PYRIMIDINE-3-CARBONITRILE

C11H5ClN4S (259.9923)


   

1-[4-(Phenylsulfonyl)phenyl]ethanone

1-[4-(Phenylsulfonyl)phenyl]ethanone

C14H12O3S (260.0507)


   

4-[(5-nitroindazol-1-yl)methyl]-1,3-thiazole

4-[(5-nitroindazol-1-yl)methyl]-1,3-thiazole

C11H8N4O2S (260.0368)


   

(5-BROMO-2-HYDROXY)BENZENEBORONICACID

(5-BROMO-2-HYDROXY)BENZENEBORONICACID

C9H13BrN2O2 (260.016)


   

1,3-adamantanedicarbonyl dichloride

1,3-adamantanedicarbonyl dichloride

C12H14Cl2O2 (260.0371)


   

Dimethyl diacetoxyfumarate

Dimethyl diacetoxyfumarate

C10H12O8 (260.0532)


   

1,5-Pentanediol bis(methanesulfonate)

1,5-Pentanediol bis(methanesulfonate)

C7H16O6S2 (260.0388)


   

3-(1,3-Benzothiazol-2-yl)-4-chloroaniline

3-(1,3-Benzothiazol-2-yl)-4-chloroaniline

C13H9ClN2S (260.0175)


   

4-Bromo-5-ethoxy-2-nitroaniline

4-Bromo-5-ethoxy-2-nitroaniline

C8H9BrN2O3 (259.9797)


   

TERT-BUTYL 4-BROMO-3-METHYL-1H-PYRAZOLE-1-CARBOXYLATE

TERT-BUTYL 4-BROMO-3-METHYL-1H-PYRAZOLE-1-CARBOXYLATE

C9H13BrN2O2 (260.016)


   

Ethyl 4-chloro-3-cyano-6-quinolinecarboxylate

Ethyl 4-chloro-3-cyano-6-quinolinecarboxylate

C13H9ClN2O2 (260.0353)


   

3-Chloro-2,6-dimethoxy-5-nitrobenzamide

3-Chloro-2,6-dimethoxy-5-nitrobenzamide

C9H9ClN2O5 (260.02)


   

4-CHLORO-1-(4-METHOXYPHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDINE

4-CHLORO-1-(4-METHOXYPHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDINE

C12H9ClN4O (260.0465)


   

2-Pentafluorophenyl-acetamidine HCl

2-Pentafluorophenyl-acetamidine HCl

C8H6ClF5N2 (260.014)


   

2-(1,1,2,3,3,3-Hexafluoropropoxy)phenol

2-(1,1,2,3,3,3-Hexafluoropropoxy)phenol

C9H6F6O2 (260.0272)


   

4-(BENZO[D]OXAZOL-4-YLOXY)-3-CHLOROANILINE

4-(BENZO[D]OXAZOL-4-YLOXY)-3-CHLOROANILINE

C13H9ClN2O2 (260.0353)


   

4-chloro-2-(3-fluorophenyl)-2H-chromene

4-chloro-2-(3-fluorophenyl)-2H-chromene

C15H10ClFO (260.0404)


   

4-BENZOTHIAZOL-2-YL-3-CHLOROPHENYLAMINE

4-BENZOTHIAZOL-2-YL-3-CHLOROPHENYLAMINE

C13H9ClN2S (260.0175)


   

Guaiacolsulfonate

Guaiacolsulfonate

C7H9KO6S (259.9757)


   

(3S)-7-Hydroxy-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid

(3S)-7-Hydroxy-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid

C5H13N2O4PS2 (260.0054)


   

3-BROMO-[1,1-BIPHENYL]-4-CARBALDEHYDE

3-BROMO-[1,1-BIPHENYL]-4-CARBALDEHYDE

C13H9BrO (259.9837)


   

1-(4-Chloro-benzenesulfonyl)-piperazine

1-(4-Chloro-benzenesulfonyl)-piperazine

C10H13ClN2O2S (260.0386)


   

(4-Bromo-2,5-dimethoxyphenyl)boronic acid

(4-Bromo-2,5-dimethoxyphenyl)boronic acid

C8H10BBrO4 (259.9855)


   

4-(2-Naphthyl)-1,3-dithiol-2-thione

4-(2-Naphthyl)-1,3-dithiol-2-thione

C13H8S3 (259.9788)


   

2-CHLORO-5-(PIPERIDINE-1-SULFONYL)-PYRIDINE

2-CHLORO-5-(PIPERIDINE-1-SULFONYL)-PYRIDINE

C10H13ClN2O2S (260.0386)


   

1-iodo-2,3,4,5-tetramethylbenzene

1-iodo-2,3,4,5-tetramethylbenzene

C10H13I (260.0062)


   

[2-(4-CHLOROPHENYL)-1,3-THIAZOL-4-YL]METHANAMINE HYDROCHLORIDE

[2-(4-CHLOROPHENYL)-1,3-THIAZOL-4-YL]METHANAMINE HYDROCHLORIDE

C10H10Cl2N2S (259.9942)


   

N-cyclopropyl-3-iodopyridin-2-amine

N-cyclopropyl-3-iodopyridin-2-amine

C8H9IN2 (259.981)


   

Ethyl 4-chloro-8-cyano-3-quinolinecarboxylate

Ethyl 4-chloro-8-cyano-3-quinolinecarboxylate

C13H9ClN2O2 (260.0353)


   

2-(4-bromophenyl)-2-(hydroxymethyl)propane-1,3-diol

2-(4-bromophenyl)-2-(hydroxymethyl)propane-1,3-diol

C10H13BrO3 (260.0048)


   

2-(4-chloro-2,6-dinitrophenyl)acetic acid

2-(4-chloro-2,6-dinitrophenyl)acetic acid

C8H5ClN2O6 (259.9836)


   

8-Chlorodibenzo[b,f]thiepin-10(11H)-one

8-Chlorodibenzo[b,f]thiepin-10(11H)-one

C14H9ClOS (260.0063)


   

3-(3,5-Dichloro-4-methylbenzoyl)propionic acid

3-(3,5-Dichloro-4-methylbenzoyl)propionic acid

C11H10Cl2O3 (260.0007)


   

3-(4-methylsulfanylphenyl)-1-thiophen-2-ylprop-2-en-1-one

3-(4-methylsulfanylphenyl)-1-thiophen-2-ylprop-2-en-1-one

C14H12OS2 (260.033)


   

tert-Butyl 3-(bromomethyl)pyrazole-1-carboxylate

tert-Butyl 3-(bromomethyl)pyrazole-1-carboxylate

C9H13BrN2O2 (260.016)


   

3-(4-Methanesulfonylphenyl)benzaldehyde

3-(4-Methanesulfonylphenyl)benzaldehyde

C14H12O3S (260.0507)


   

2-beta-Carboxyethylamino-4-aminobenzenesulfonicacid

2-beta-Carboxyethylamino-4-aminobenzenesulfonicacid

C9H12N2O5S (260.0467)


   

6-Bromo-2-fluoro-3-propoxybenzaldehyde

6-Bromo-2-fluoro-3-propoxybenzaldehyde

C10H10BrFO2 (259.9848)


   

2,2,2-trifluoro-1-(4-methylsulfonylpiperazin-1-yl)ethanone

2,2,2-trifluoro-1-(4-methylsulfonylpiperazin-1-yl)ethanone

C7H11F3N2O3S (260.0442)


   

(6E)-6-[(4-fluorophenyl)methylidene]-7H-[1,3]thiazolo[3,2-a]pyrimidin-5-one

(6E)-6-[(4-fluorophenyl)methylidene]-7H-[1,3]thiazolo[3,2-a]pyrimidin-5-one

C13H9FN2OS (260.042)


   

6-[(4-fluorophenyl)methyl]-[1,3]thiazolo[3,2-a]pyrimidin-5-one

6-[(4-fluorophenyl)methyl]-[1,3]thiazolo[3,2-a]pyrimidin-5-one

C13H9FN2OS (260.042)


   

Benzoic acid,4-chloro-3,5-dinitro-, methyl ester

Benzoic acid,4-chloro-3,5-dinitro-, methyl ester

C8H5ClN2O6 (259.9836)


   

N-(2-Thiophenesulfonyl)-L-prolinamide Trifluoroacetate

N-(2-Thiophenesulfonyl)-L-prolinamide Trifluoroacetate

C9H12N2O3S2 (260.0289)


   

ethyl 3-(3,4-dichlorophenyl)-3-oxopropanoate

ethyl 3-(3,4-dichlorophenyl)-3-oxopropanoate

C11H10Cl2O3 (260.0007)


   

3-(Methylsulfonyl)benzophenone

3-(Methylsulfonyl)benzophenone

C14H12O3S (260.0507)


   

Ethyl 5,7-dichloro-1H-pyrazolo[4,3-d]pyrimidine-3-carboxylate

Ethyl 5,7-dichloro-1H-pyrazolo[4,3-d]pyrimidine-3-carboxylate

C8H6Cl2N4O2 (259.9868)


   

pyridostigmine bromide

pyridostigmine bromide

C9H13BrN2O2 (260.016)


D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

1-(4-Chlorophenoxy)-3,3-dimethyl-1-chloro-2-butanone

1-(4-Chlorophenoxy)-3,3-dimethyl-1-chloro-2-butanone

C12H14Cl2O2 (260.0371)


   
   

1-(1,1-DIMETHYL-3-BUTYL-1H-BENZOEINDOL-2-YLIDENEMETHYL)-3-(1,1-DIMETHYL-3-BUTYL-1H-BENZOEINDOLIUM-2-YL-METHYLENE)-CYCLOBUTEN-2-ONE-4-OLATE

1-(1,1-DIMETHYL-3-BUTYL-1H-BENZOEINDOL-2-YLIDENEMETHYL)-3-(1,1-DIMETHYL-3-BUTYL-1H-BENZOEINDOLIUM-2-YL-METHYLENE)-CYCLOBUTEN-2-ONE-4-OLATE

C11H7F3O4 (260.0296)


   

6-(5-Chloro-2-pyridyl)-5H-pyrrolo[3,4-b]pyrazine-5,7(6H)-dione

6-(5-Chloro-2-pyridyl)-5H-pyrrolo[3,4-b]pyrazine-5,7(6H)-dione

C11H5ClN4O2 (260.0101)


   

1-Ethyl-3-methylimidazolium trifluoromethanesulfonate

1-Ethyl-3-methylimidazolium trifluoromethanesulfonate

C7H11F3N2O3S (260.0442)


   

urolithin M6

Urolithin M-6

C13H8O6 (260.0321)


   

(3-Fluorooxetan-3-yl)methyl 4-methylbenzenesulfonate

(3-Fluorooxetan-3-yl)methyl 4-methylbenzenesulfonate

C11H13FO4S (260.0519)


   

2-(4-Chlorobenzoyl)benzoic acid

2-(4-Chlorobenzoyl)benzoic acid

C14H9ClO3 (260.024)


   

[2-(quinolin-8-yloxy)ethyl]amine dihydrochloride

[2-(quinolin-8-yloxy)ethyl]amine dihydrochloride

C11H14Cl2N2O (260.0483)


   

4-BromophenylMethylDimethoxysilane

4-BromophenylMethylDimethoxysilane

C9H13BrO2Si (259.9868)


   

Methyl 4-(trifluoromethyl)-1-benzothiophene-2-carboxylate

Methyl 4-(trifluoromethyl)-1-benzothiophene-2-carboxylate

C11H7F3O2S (260.0119)


   

Diethyl 3,4-dihydroxy-2,5-thiophenedicarboxylate

Diethyl 3,4-dihydroxy-2,5-thiophenedicarboxylate

C10H12O6S (260.0355)


   

5-Methoxy-2-nitro-4-(trifluoroMethyl)phenylacetonitrile

5-Methoxy-2-nitro-4-(trifluoroMethyl)phenylacetonitrile

C10H7F3N2O3 (260.0409)


   

5-Bromo-2-ethoxy-4-methyl-3-nitropyridine

5-Bromo-2-ethoxy-4-methyl-3-nitropyridine

C8H9BrN2O3 (259.9797)


   

4-Chloro-N-(2-nitrobenzylidene)aniline

4-Chloro-N-(2-nitrobenzylidene)aniline

C13H9ClN2O2 (260.0353)


   

(4-BOC-AMINO-PIPERIDIN-1-YL)-PYRIDIN-3-YL-ACETICACID

(4-BOC-AMINO-PIPERIDIN-1-YL)-PYRIDIN-3-YL-ACETICACID

C9H13BrN2O2 (260.016)


   

1-bromo-4-(4-ethylphenyl)benzene

1-bromo-4-(4-ethylphenyl)benzene

C14H13Br (260.0201)


   

Ethyl 2,6-dichlorobenzoylacetate

Ethyl 2,6-dichlorobenzoylacetate

C11H10Cl2O3 (260.0007)


   

Ethyl 3-(2,4-dichlorophenyl)-3-oxopropanoate

Ethyl 3-(2,4-dichlorophenyl)-3-oxopropanoate

C11H10Cl2O3 (260.0007)


   

Galactose-6-phosphate

D-Galactose,6-(dihydrogen phosphate)

C6H13O9P (260.0297)


   

2-Propen-1-one,3-(2-chlorophenyl)-1-(4-fluorophenyl)-

2-Propen-1-one,3-(2-chlorophenyl)-1-(4-fluorophenyl)-

C15H10ClFO (260.0404)


   

7-TRIFLUOROMETHYL-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER

7-TRIFLUOROMETHYL-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER

C11H7F3O2S (260.0119)


   

6-TRIFLUOROMETHYL-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER

6-TRIFLUOROMETHYL-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER

C11H7F3O2S (260.0119)


   

4-AMINO-5-BROMO-6-ETHOXYPICOLINIC ACID

4-AMINO-5-BROMO-6-ETHOXYPICOLINIC ACID

C8H9BrN2O3 (259.9797)


   

Chlorflurecol

Chlorflurecol

C14H9ClO3 (260.024)


   

5-(3,4-dichlorophenyl)-5-oxopentanoic acid

5-(3,4-dichlorophenyl)-5-oxopentanoic acid

C11H10Cl2O3 (260.0007)


   

LEAD CYANATE

LEAD CYANATE

C2N2Pb (259.9828)


   

4-(5-Bromo-3-fluoro-2-pyridinyl)morpholine

4-(5-Bromo-3-fluoro-2-pyridinyl)morpholine

C9H10BrFN2O (259.996)


   

ETHYL 2-(4-BROMO-3,5-DIMETHYL-1H-PYRAZOL-1-YL)ACETATE

ETHYL 2-(4-BROMO-3,5-DIMETHYL-1H-PYRAZOL-1-YL)ACETATE

C9H13BrN2O2 (260.016)


   

2-(Phenylsulfonylmethyl)benzaldehyde

2-(Phenylsulfonylmethyl)benzaldehyde

C14H12O3S (260.0507)


   

9H-Pyrido[3,4-b]indole, 6-bromo-1-methyl-

9H-Pyrido[3,4-b]indole, 6-bromo-1-methyl-

C12H9BrN2 (259.9949)


   

alpha-D-mannose 6-phosphate

alpha-D-mannose 6-phosphate

C6H13O9P (260.0297)


The alpha-anomer of D-mannose 6-phosphate.

   

3-chloro-2-(4-hydroxyphenyl)-2H-indazol-5-ol

3-chloro-2-(4-hydroxyphenyl)-2H-indazol-5-ol

C13H9ClN2O2 (260.0353)


   

6-O-phosphono-D-tagatose

6-O-phosphono-D-tagatose

C6H13O9P (260.0297)


   

3-O-sulfo-beta-D-galactopyranose

3-O-sulfo-beta-D-galactopyranose

C6H12O9S (260.0202)


   

4-(HYDROGEN SULFATE)-beta-D-GALACTOPYRANOSE

4-(HYDROGEN SULFATE)-beta-D-GALACTOPYRANOSE

C6H12O9S (260.0202)


   

3,6-Dimethyl-1,4-dioxane-2,5-dione;1,4-dioxane-2,5-dione

3,6-Dimethyl-1,4-dioxane-2,5-dione;1,4-dioxane-2,5-dione

C10H12O8 (260.0532)


D001697 - Biomedical and Dental Materials

   

1D-myo-inositol 6-phosphate

1D-myo-inositol 6-phosphate

C6H13O9P (260.0297)


A myo-inositol monophosphate in which the phosphate group is located at position 6.

   

D-Sorbitol 6-phosphate

D-Sorbitol 6-phosphate

C6H13O9P-2 (260.0297)


   

beta-L-galactose 1-phosphate

beta-L-galactose 1-phosphate

C6H13O9P (260.0297)


   

2-Deoxy-6-phosphogluconate

2-Deoxy-6-phosphogluconate

C6H13O9P (260.0297)


   

D-sorbose 1-phosphate

D-sorbose 1-phosphate

C6H13O9P (260.0297)


   

Urolithin E

Urolithin E

C13H8O6 (260.0321)


   

6-o-Phosphonohexose

6-o-Phosphonohexose

C6H13O9P (260.0297)


   

2-beta-D-Ribofuranosyl-4-thiazolecarboxamide

2-beta-D-Ribofuranosyl-4-thiazolecarboxamide

C9H12N2O5S (260.0467)


   

1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylidenepyrimidin-2-one

1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylidenepyrimidin-2-one

C9H12N2O5S (260.0467)


   

Benzonitrile, 3-fluoro-5-(2-(2-(fluoromethyl)-4-thiazolyl)ethynyl)-

Benzonitrile, 3-fluoro-5-(2-(2-(fluoromethyl)-4-thiazolyl)ethynyl)-

C13H6F2N2S (260.022)


   

Propyl paraben sulfate

Propyl paraben sulfate

C10H12O6S (260.0355)


   

Lawrencium

Lawrencium

Lr (260)


   

D-psicose 6-phosphate

D-psicose 6-phosphate

C6H13O9P (260.0297)


   

N-(1,3-benzothiazol-2-yl)-2-thiophenecarboxamide

N-(1,3-benzothiazol-2-yl)-2-thiophenecarboxamide

C12H8N2OS2 (260.0078)


   

6-[(Phenylmethylthio)methyl]imidazo[2,1-b]thiazole

6-[(Phenylmethylthio)methyl]imidazo[2,1-b]thiazole

C13H12N2S2 (260.0442)


   

2-(5-Ethylthiophene-2-carbonyl)benzoic acid

2-(5-Ethylthiophene-2-carbonyl)benzoic acid

C14H12O3S (260.0507)


   

Galactose 6-sulfate

Galactose 6-sulfate

C6H12O9S (260.0202)


   

alpha-D-tagatofuranose 6-phosphate

alpha-D-tagatofuranose 6-phosphate

C6H13O9P (260.0297)


A D-tagatofuranose 6-phosphate with an alpha-configuration at the anomeric position.

   

Glucose 6-(hydrogen sulfate)

Glucose 6-(hydrogen sulfate)

C6H12O9S (260.0202)


   

D-Mannose 1-phosphate

D-Mannose 1-phosphate

C6H13O9P (260.0297)


A mannose phosphate that is D-mannose carrying a phosphate group at position 1.

   
   

beta-Galactose-6-phosphate

beta-Galactose-6-phosphate

C6H13O9P (260.0297)


   

4-(2-Hydroxyphenylthio)-1-butenylphosphonic acid

4-(2-Hydroxyphenylthio)-1-butenylphosphonic acid

C10H13O4PS (260.0272)


   

AIDS-011165

1,3,5,6-tetrahydroxy-9-xanthenone

C13H8O6 (260.0321)


   

phorate

6Z-8-Hydroxygeraniol 8-O-glucoside

C7H17O2PS3 (260.0128)


D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor D010575 - Pesticides > D007306 - Insecticides D004791 - Enzyme Inhibitors D016573 - Agrochemicals Constituent of fresh ginger (Zingiber officinale). 6Z-8-Hydroxygeraniol 8-O-glucoside is found in herbs and spices.

   

α-D-Glucose 1-phosphate

[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

C6H13O9P (260.0297)


Alpha-d-glucose-1-phosphate, also known as D-glucose 1-phosphoric acid or alpha-D-glucopyranosyl phosphate, is a member of the class of compounds known as monosaccharide phosphates. Monosaccharide phosphates are monosaccharides comprising a phosphated group linked to the carbohydrate unit. Alpha-d-glucose-1-phosphate is soluble (in water) and a moderately acidic compound (based on its pKa). Alpha-d-glucose-1-phosphate can be found in a number of food items such as guava, purple mangosteen, cocoa bean, and fig, which makes alpha-d-glucose-1-phosphate a potential biomarker for the consumption of these food products. Alpha-d-glucose-1-phosphate exists in E.coli (prokaryote) and yeast (eukaryote).

   

(2,3,5,6-Tetrahydroxy-4-oxohexyl) dihydrogen phosphate

(2,3,5,6-Tetrahydroxy-4-oxohexyl) dihydrogen phosphate

C6H13O9P (260.0297)


   

D-mannitol 1-phosphate(2-)

D-mannitol 1-phosphate(2-)

C6H13O9P-2 (260.0297)


   

beta-D-Fructopyranose 1-phosphate

beta-D-Fructopyranose 1-phosphate

C6H13O9P (260.0297)


   

Galactitol 1-phosphate(2-)

Galactitol 1-phosphate(2-)

C6H13O9P-2 (260.0297)


   

6-O-Phosphono-Alpha-D-Fructofuranose

6-O-Phosphono-Alpha-D-Fructofuranose

C6H13O9P (260.0297)


   

1-(Methylthio)ribulose 5-phosphate

1-(Methylthio)ribulose 5-phosphate

C6H13O7PS (260.012)


A ketopentose phosphate that is D-ribulose 5-phosphate in which the 1-hydroxy group is replaced by a methylthio group.

   

2-Amino-2-deoxyglucitol 6-phosphate

2-Amino-2-deoxyglucitol 6-phosphate

C6H15NO8P- (260.0535)


   

[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

C6H13O9P (260.0297)


   

keto-L-tagatose 6-phosphate

keto-L-tagatose 6-phosphate

C6H13O9P (260.0297)


The open chain form of L-tagatose 6-phosphate

   

alpha-D-galactose 6-phosphate

alpha-D-galactose 6-phosphate

C6H13O9P (260.0297)


   

2-Hydroxy-6-(2-carboxyphenyl)-6-oxo-2,4-hexadienoate

2-Hydroxy-6-(2-carboxyphenyl)-6-oxo-2,4-hexadienoate

C13H8O6-2 (260.0321)


   

[(2S,3S,4S)-2,3,4,6-tetrahydroxy-5-oxohexyl] dihydrogen phosphate

[(2S,3S,4S)-2,3,4,6-tetrahydroxy-5-oxohexyl] dihydrogen phosphate

C6H13O9P (260.0297)


   

[(2S,3S,4S,5S)-2,3,4,5-tetrahydroxy-6-oxohexyl] dihydrogen phosphate

[(2S,3S,4S,5S)-2,3,4,5-tetrahydroxy-6-oxohexyl] dihydrogen phosphate

C6H13O9P (260.0297)


   

[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

C6H13O9P (260.0297)


   

[(2S,3S,4R,5R)-2,3,4,5-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

[(2S,3S,4R,5R)-2,3,4,5-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

6-O-Sulfo-beta-D-glucopyranose

6-O-Sulfo-beta-D-glucopyranose

C6H12O9S (260.0202)


   

4-Pyridoxate 5-phosphate

4-Pyridoxate 5-phosphate

C8H7NO7P-3 (259.996)


   

2-(2-phenylethyl)-thiohydroximate-O-sulfate

2-(2-phenylethyl)-thiohydroximate-O-sulfate

C9H10NO4S2- (260.0051)


   

[(3R,4R,5R)-2,4,5-trihydroxy-3-(hydroxymethyl)oxan-3-yl] dihydrogen phosphate

[(3R,4R,5R)-2,4,5-trihydroxy-3-(hydroxymethyl)oxan-3-yl] dihydrogen phosphate

C6H13O9P (260.0297)


   

[(2S,3S,4R,5S)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

[(2S,3S,4R,5S)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

alpha-D-Fructofuranose 1-phosphoric acid

alpha-D-Fructofuranose 1-phosphoric acid

C6H13O9P (260.0297)


   

[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

C6H13O9P (260.0297)


   

[(2S,3S,4R,5S)-2,3,4,5-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

[(2S,3S,4R,5S)-2,3,4,5-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

[(2R,3S)-2,3-dihydroxy-5-methylsulfanyl-4-oxopentyl] dihydrogen phosphate

[(2R,3S)-2,3-dihydroxy-5-methylsulfanyl-4-oxopentyl] dihydrogen phosphate

C6H13O7PS (260.012)


   

[(2S,3S,4S,5S)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

[(2S,3S,4S,5S)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

[(2R,3S,4R,5S)-2,3,4,5-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

[(2R,3S,4R,5S)-2,3,4,5-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

[(2R,3S,4S,5S)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

[(2R,3S,4S,5S)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

[(3S,4S,5S)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

[(3S,4S,5S)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

[(3S,4R,5S)-2,3,4,5-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

[(3S,4R,5S)-2,3,4,5-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

3-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-imino-1,3-thiazin-2-one

3-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-imino-1,3-thiazin-2-one

C9H12N2O5S (260.0467)


   

3,5-Dihydroxycinnamic acid sulfate

3,5-Dihydroxycinnamic acid sulfate

C9H8O7S (259.9991)


   

D-Allose 6-phosphate

D-Allose 6-phosphate

C6H13O9P (260.0297)


An allose phosphate consisting of D-allose having a monophosphate group at the 6-position.

   

5-Methylthioribose 1-phosphate

5-Methylthioribose 1-phosphate

C6H13O7PS (260.012)


   

6-O-phosphono-beta-D-tagatofuranose

6-O-phosphono-beta-D-tagatofuranose

C6H13O9P (260.0297)


   

D-Fructofuranose 2-phosphate

D-Fructofuranose 2-phosphate

C6H13O9P (260.0297)


   

(2S)-2-azaniumyl-3-[4-(sulfonatooxy)phenyl]propanoate

(2S)-2-azaniumyl-3-[4-(sulfonatooxy)phenyl]propanoate

C9H10NO6S- (260.0229)


   

aldehydo-D-glucose 3-phosphate

aldehydo-D-glucose 3-phosphate

C6H13O9P (260.0297)


   

L-fructose 1-phosphate

L-fructose 1-phosphate

C6H13O9P (260.0297)


   

D-galactopyranose 4-sulfate

D-galactopyranose 4-sulfate

C6H12O9S (260.0202)


   

6-O-Sulfo-D-galactopyranose

6-O-Sulfo-D-galactopyranose

C6H12O9S (260.0202)


   

3-O-Sulfo-D-glucopyranose

3-O-Sulfo-D-glucopyranose

C6H12O9S (260.0202)


   

D-glucopyranose 3-phosphate

D-glucopyranose 3-phosphate

C6H13O9P (260.0297)


   

L-Gulose 1-phosphate

L-Gulose 1-phosphate

C6H13O9P (260.0297)


   
   

alpha-L-galactose 1-phosphate

alpha-L-galactose 1-phosphate

C6H13O9P (260.0297)


A L-galactose 1-phosphate compound having beta-configuration about the anomeric centre.

   

3-O-sulfo-beta-D-glucopyranose

3-O-sulfo-beta-D-glucopyranose

C6H12O9S (260.0202)


   

beta-D-galactofuranose 6-phosphate

beta-D-galactofuranose 6-phosphate

C6H13O9P (260.0297)


   

D-tagatopyranose 1-phosphate

D-tagatopyranose 1-phosphate

C6H13O9P (260.0297)


   

(9-Oxo-2-fluorenyl)phosphonic acid

(9-Oxo-2-fluorenyl)phosphonic acid

C13H9O4P (260.0238)


   

2-Oxo-3-(4-sulooxyphenyl)propanoic acid

2-Oxo-3-(4-sulooxyphenyl)propanoic acid

C9H8O7S (259.9991)


   
   

D-hamamelose 2(1)-(dihydrogen phosphate)

D-hamamelose 2(1)-(dihydrogen phosphate)

C6H13O9P (260.0297)


   

D-hexopyranose 6-phosphate

D-hexopyranose 6-phosphate

C6H13O9P (260.0297)


   

alpha-D-hexose 1-phosphates

alpha-D-hexose 1-phosphates

C6H13O9P (260.0297)


   

4-Acetamido-3-methoxyphenyl sulfate

4-Acetamido-3-methoxyphenyl sulfate

C9H10NO6S- (260.0229)


   

[2,3,4-Trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl hydrogen sulate

[2,3,4-Trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl hydrogen sulate

C6H12O9S (260.0202)


   

[3,4,5-Trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl hydrogen sulate

[3,4,5-Trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl hydrogen sulate

C6H12O9S (260.0202)


   

[3-(4-Methoxyphenyl)oxiran-2-yl]methyl hydrogen sulate

[3-(4-Methoxyphenyl)oxiran-2-yl]methyl hydrogen sulate

C10H12O6S (260.0355)


   

[(2S,3S,4S,5R)-2,3,4,5-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

[(2S,3S,4S,5R)-2,3,4,5-tetrahydroxyoxan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

[(3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

[(3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

C6H13O9P (260.0297)


   

3,8-Dioxa-4,7-dioxocyclooctane-1,2-dicarboxylic acid dimethyl ester

3,8-Dioxa-4,7-dioxocyclooctane-1,2-dicarboxylic acid dimethyl ester

C10H12O8 (260.0532)


   
   

alpha-D-Glucose-1-phosphate

[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] dihydrogen phosphate

C6H13O9P (260.0297)


   

Mannose-6-phosphate

D-mannopyranose 6-phosphate

C6H13O9P (260.0297)


The pyranose form of D-mannose 6-phosphate.

   

Inositol 1-phosphate

Inositol 1-phosphate

C6H13O9P (260.0297)


   

beta-D-Glucose 6-phosphate

beta-D-Glucose 6-phosphate

C6H13O9P (260.0297)


A D-glucopyranose 6-phosphate in which the anomeric centre has beta-configuration.

   

alpha-D-Mannose 1-phosphate

alpha-D-Mannose 1-phosphate

C6H13O9P (260.0297)


A D-mannose 1-phosphate with an alpha-configuration at the anomeric position.

   

6-O-Phosphono-beta-D-fructofuranose

6-O-Phosphono-beta-D-fructofuranose

C6H13O9P (260.0297)


   

6-o-Phosphonohexopyranose

6-o-Phosphonohexopyranose

C6H13O9P (260.0297)


   

Beta-D-Fructose 2-phosphate

Beta-D-Fructose 2-phosphate

C6H13O9P (260.0297)


   

1D-Myo-inositol 4-phosphate

1D-Myo-inositol 4-phosphate

C6H13O9P (260.0297)


   

D-Tagatose 6-phosphate

D-Tagatose 6-phosphate

C6H13O9P (260.0297)


   

S-Methyl-5-thio-D-ribulose 1-phosphate

S-Methyl-5-thio-D-ribulose 1-phosphate

C6H13O7PS (260.012)


   

S-Methyl-5-thio-alpha-D-ribose 1-phosphate

S-Methyl-5-thio-alpha-D-ribose 1-phosphate

C6H13O7PS (260.012)


   

D-fructofuranose 1-phosphate

D-fructofuranose 1-phosphate

C6H13O9P (260.0297)


The furanose form of D-fructose 1-phosphate.

   

D-galactopyranose 6-phosphate

D-galactopyranose 6-phosphate

C6H13O9P (260.0297)


The pyranose form of D-galactose 6-phosphate.

   

1D-myo-inositol 3-phosphate

1D-myo-inositol 3-phosphate

C6H13O9P (260.0297)


   

D-arabino-hex-3-ulose 6-phosphate

D-arabino-hex-3-ulose 6-phosphate

C6H13O9P (260.0297)


   

L-Sorbose 1-phosphate

L-Sorbose 1-phosphate

C6H13O9P (260.0297)


The L-stereoisomer of sorbose 1-phosphate.

   

1-O-phosphonohexopyranose

1-O-phosphonohexopyranose

C6H13O9P (260.0297)


   

D-Galactopyranose 1-phosphate

D-Galactopyranose 1-phosphate

C6H13O9P (260.0297)


A D-galactose phosphate that consists of D-galactopyranose having a single phospho substituent located at the 1-position. It is an intermediate obtained during the the galactose metabolism.

   

D-fructopyranose 1-phosphate

D-fructopyranose 1-phosphate

C6H13O9P (260.0297)


   

[(2R,3S,4S,5R)-3,4,5,6-tetrahydroxytetrahydropyran-2-yl]methyl hydrogen sulfate

[(2R,3S,4S,5R)-3,4,5,6-tetrahydroxytetrahydropyran-2-yl]methyl hydrogen sulfate

C6H12O9S (260.0202)


   

alpha-D-Hexose 6-phosphate

alpha-D-Hexose 6-phosphate

C6H13O9P (260.0297)


   

Fructose-6-phosphate

D-fructofuranose 6-phosphate

C6H13O9P (260.0297)


   

beta-D-mannose 6-phosphate

beta-D-mannose 6-phosphate

C6H13O9P (260.0297)


A D-mannopyranose 6-phosphate with a beta-configuration at the anomeric position.

   

keto-D-fructose 1-phosphate

keto-D-fructose 1-phosphate

C6H13O9P (260.0297)


The open chain form of D-fructose 1-phosphate.

   

beta-D-fructofuranose 1-phosphate

beta-D-fructofuranose 1-phosphate

C6H13O9P (260.0297)


A D-fructofuranose 1-phosphate in which the anomeric centre has beta-configuration.

   

D-mannitol 1-phosphate(2-)

D-mannitol 1-phosphate(2-)

C6H13O9P (260.0297)


An organophosphate oxoanion arising from deprotonation of the phosphate OH groups of D-mannitol.

   

D-glucitol 6-phosphate(2-)

D-glucitol 6-phosphate(2-)

C6H13O9P (260.0297)


Dianion of D-glucitol 1-phosphate arising from deprotonation of the phosphate OH groups; major species at pH 7.3.

   

beta-D-tagatofuranose 6-phosphate

beta-D-tagatofuranose 6-phosphate

C6H13O9P (260.0297)


A D-tagatofuranose 6-phosphate with a beta-configuration at the anomeric position.

   

O(4)-sulfo-L-tyrosinate(1-)

O(4)-sulfo-L-tyrosinate(1-)

C9H10NO6S (260.0229)


An L-alpha-amino acid anion that is the conjugate base of O(4)-sulfo-L-tyrosine; major species ar pH 7.3.

   

6-O-phosphono-beta-D-galactofuranose

6-O-phosphono-beta-D-galactofuranose

C6H13O9P (260.0297)


A D-galactose 6-phosphate that is beta-D-galactofuranose in which the hydroxy group at position 6 has been converted into the corresponding dihydrogen phosphate derivative.

   

2-methoxyacetaminophen sulfate(1-)

2-methoxyacetaminophen sulfate(1-)

C9H10NO6S (260.0229)


A phenyl sulfate oxoanion that is the conjugate base of 2-methoxyacetaminophen sulfate, obtained by deprotonation of the sulfo group; major species at pH 7.3.

   

aldehydo-D-galactose 6-phosphate

aldehydo-D-galactose 6-phosphate

C6H13O9P (260.0297)


The ring-opened aldehydo-form of D-galactose 6-phosphate.

   

aldehydo-D-mannose 6-phosphate

aldehydo-D-mannose 6-phosphate

C6H13O9P (260.0297)


   

1D-myo-Inositol 1-phosphate

1D-myo-Inositol 1-phosphate

C6H13O9P (260.0297)


An inositol having myo- configuration substituted at position 1 by a phosphate group.

   

keto-D-tagatose 6-phosphate

keto-D-tagatose 6-phosphate

C6H13O9P (260.0297)


A D-tagatose 6-phosphate that is in the open-chain keto-form.

   

Galactitol 1-phosphate(2-)

Galactitol 1-phosphate(2-)

C6H13O9P (260.0297)


Dianion of D-galactitol 1-phosphate arising from deprotonation of the phosphate OH groups; major species at pH 7.3.

   

beta-D-galactose 6-phosphate

beta-D-galactose 6-phosphate

C6H13O9P (260.0297)


   

D-glucopyranose 6-phosphate

D-glucopyranose 6-phosphate

C6H13O9P (260.0297)


A glucopyranose ring with a phosphate replacing the hydroxy in the hydroxymethyl group at position 6.

   

keto-D-fructose 6-phosphate

keto-D-fructose 6-phosphate

C6H13O9P (260.0297)


The open chain form of D-fructose 6-phosphate.

   

D-Glucopyranose 1-phosphate

D-Glucopyranose 1-phosphate

C6H13O9P (260.0297)


A D-glucose monophosphate in which the phosphate group is located at position 1.

   

beta-D-fructofuranose 6-phosphate

beta-D-fructofuranose 6-phosphate

C6H13O9P (260.0297)


A D-fructofuranose 6-phosphate with a beta-configuration at the anomeric position.

   

D-tagatofuranose 6-phosphate

D-tagatofuranose 6-phosphate

C6H13O9P (260.0297)


The furanose form of D-tagatose 6-phosphate.

   

S-Methyl-1-thio-D-xylulose 5-phosphate

S-Methyl-1-thio-D-xylulose 5-phosphate

C6H13O7PS (260.012)


   

S-Methyl-1-thio-D-ribulose 5-phosphate

S-Methyl-1-thio-D-ribulose 5-phosphate

C6H13O7PS (260.012)


   

1D-myo-Inositol 2-phosphate

1D-myo-Inositol 2-phosphate

C6H13O9P (260.0297)


   

Galactose 6-phosphate

Galactose 6-phosphate

C6H13O9P (260.0297)


   

Hexose 6-phosphate

Hexose 6-phosphate

C6H13O9P (260.0297)


   

Methylthioribose phosphate

Methylthioribose phosphate

C6H13O7PS (260.012)


   

myo-Inositol 2-phosphate

myo-Inositol 2-phosphate

C6H13O9P (260.0297)


   

SUVN-911

SUVN-911

C11H14Cl2N2O (260.0483)


SUVN-911 is a potent, selective, brain penetrated and orally bioavailable neuronal nicotinic acetylcholine α4β2 receptor antagonist, with a Ki of 1.5 nM. SUVN-911 has antidepressant activity[1].

   

fructose -6-phosphate

fructose -6-phosphate

C6H13O9P (260.0297)


   

6,10,12-trihydroxy-8-methyl-3-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),5,7,9,11-pentaene-2,4-dione

6,10,12-trihydroxy-8-methyl-3-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),5,7,9,11-pentaene-2,4-dione

C13H8O6 (260.0321)


   

(2z)-2-hydroxy-3-[4-(sulfooxy)phenyl]prop-2-enoic acid

(2z)-2-hydroxy-3-[4-(sulfooxy)phenyl]prop-2-enoic acid

C9H8O7S (259.9991)


   

[(2r,3r,5s,6r)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid

[(2r,3r,5s,6r)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid

C6H13O9P (260.0297)


   

2,3,6,7-tetrahydroxyxanthen-9-one

2,3,6,7-tetrahydroxyxanthen-9-one

C13H8O6 (260.0321)


   

5,8-dihydroxy-1-(hydroxymethyl)naphtho[2,3-c]furan-4,9-dione

5,8-dihydroxy-1-(hydroxymethyl)naphtho[2,3-c]furan-4,9-dione

C13H8O6 (260.0321)


   

[(1r,2r,3r,4r,5r,6r)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid

[(1r,2r,3r,4r,5r,6r)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid

C6H13O9P (260.0297)


   

[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphosphonic acid

[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphosphonic acid

C6H13O9P (260.0297)


   

2,3,5,7-tetrahydroxyxanthen-9-one

2,3,5,7-tetrahydroxyxanthen-9-one

C13H8O6 (260.0321)


   

2,3,5,6-tetrahydroxyxanthen-9-one

2,3,5,6-tetrahydroxyxanthen-9-one

C13H8O6 (260.0321)


   

α-d-glucose 6-phosphate

α-d-glucose 6-phosphate

C6H13O9P (260.0297)


   

2,4,12-trihydroxy-8-methyl-3-oxatricyclo[7.3.1.0⁵,¹³]trideca-1,4,7,9(13),11-pentaene-6,10-dione

2,4,12-trihydroxy-8-methyl-3-oxatricyclo[7.3.1.0⁵,¹³]trideca-1,4,7,9(13),11-pentaene-6,10-dione

C13H8O6 (260.0321)


   

1-[(2r,3s,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylpyrimidin-2-one

1-[(2r,3s,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylpyrimidin-2-one

C9H12N2O5S (260.0467)


   

2-hydroxy-3-[4-(sulfooxy)phenyl]prop-2-enoic acid

2-hydroxy-3-[4-(sulfooxy)phenyl]prop-2-enoic acid

C9H8O7S (259.9991)


   

8,9-dihydroxy-3-methylpyrano[4,3-c]isochromene-1,6-dione

8,9-dihydroxy-3-methylpyrano[4,3-c]isochromene-1,6-dione

C13H8O6 (260.0321)


   

4-[2-(3-chloro-1h-pyrrol-2-yl)-1,3-oxazol-5-yl]phenol

4-[2-(3-chloro-1h-pyrrol-2-yl)-1,3-oxazol-5-yl]phenol

C13H9ClN2O2 (260.0353)


   

{4-[(1e)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenyl}oxidanesulfonic acid

{4-[(1e)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenyl}oxidanesulfonic acid

C10H12O6S (260.0355)


   

1,2,5,7-tetrahydroxyxanthen-9-one

1,2,5,7-tetrahydroxyxanthen-9-one

C13H8O6 (260.0321)


   

1-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylpyrimidin-2-one

1-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylpyrimidin-2-one

C9H12N2O5S (260.0467)


   

(2e)-3-[(1s,3s,4r)-3-bromo-4-hydroxy-4-methylcyclohexyl]but-2-enal

(2e)-3-[(1s,3s,4r)-3-bromo-4-hydroxy-4-methylcyclohexyl]but-2-enal

C11H17BrO2 (260.0412)


   

[(2r,3r,5r,6s)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid

[(2r,3r,5r,6s)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid

C6H13O9P (260.0297)


   

[4-(3-hydroxyprop-1-en-1-yl)-2-methoxyphenyl]oxidanesulfonic acid

[4-(3-hydroxyprop-1-en-1-yl)-2-methoxyphenyl]oxidanesulfonic acid

C10H12O6S (260.0355)


   

[(2s,3r,4s,5r,6r)-3,4,5,6-tetrahydroxyoxan-2-yl]methoxyphosphonic acid

[(2s,3r,4s,5r,6r)-3,4,5,6-tetrahydroxyoxan-2-yl]methoxyphosphonic acid

C6H13O9P (260.0297)


   

[(2r,3s,4r,5r)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methoxyphosphonic acid

[(2r,3s,4r,5r)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methoxyphosphonic acid

C6H13O9P (260.0297)


   

2-hydroxy-5-[(1e)-2-(4-hydroxy-6-oxopyran-2-yl)ethenyl]cyclohexa-2,5-diene-1,4-dione

2-hydroxy-5-[(1e)-2-(4-hydroxy-6-oxopyran-2-yl)ethenyl]cyclohexa-2,5-diene-1,4-dione

C13H8O6 (260.0321)


   

6-o-phosphono-d-mannose

6-o-phosphono-d-mannose

C6H13O9P (260.0297)


   

β-d-galactose 6-phosphate

β-d-galactose 6-phosphate

C6H13O9P (260.0297)


   

2-hydroxy-5-[2-(4-hydroxy-6-oxopyran-2-yl)ethenyl]cyclohexa-2,5-diene-1,4-dione

2-hydroxy-5-[2-(4-hydroxy-6-oxopyran-2-yl)ethenyl]cyclohexa-2,5-diene-1,4-dione

C13H8O6 (260.0321)


   

(2r,3s,4s,5s)-2,3,4,5-tetrahydroxy-6-sulfohexanoic acid

(2r,3s,4s,5s)-2,3,4,5-tetrahydroxy-6-sulfohexanoic acid

C6H12O9S (260.0202)


   

6,7,8-trihydroxy-1-methylnaphtho[2,3-c]furan-4,9-dione

6,7,8-trihydroxy-1-methylnaphtho[2,3-c]furan-4,9-dione

C13H8O6 (260.0321)