Exact Mass: 244.03578519999996
Exact Mass Matches: 244.03578519999996
Found 500 metabolites which its exact mass value is equals to given mass value 244.03578519999996,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Uridine
Uridine, also known as beta-uridine or 1-beta-D-ribofuranosylpyrimidine-2,4(1H,3H)-dione, is a member of the class of compounds known as pyrimidine nucleosides. Pyrimidine nucleosides are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety. More specifically, uridine is a nucleoside consisting of uracil and D-ribose and a component of RNA. Uridine is soluble (in water) and a very weakly acidic compound (based on its pKa). Uridine can be synthesized from uracil. It is one of the five standard nucleosides which make up nucleic acids, the others being adenosine, thymidine, cytidine and guanosine. The five nucleosides are commonly abbreviated to their one-letter codes U, A, T, C and G respectively. Uridine is also a parent compound for other transformation products, including but not limited to, nikkomycin Z, 3-(enolpyruvyl)uridine 5-monophosphate, and 5-aminomethyl-2-thiouridine. Uridine can be found in most biofluids, including urine, breast milk, cerebrospinal fluid (CSF), and blood. Within the cell, uridine is primarily located in the mitochondria, in the nucleus and the lysosome. It can also be found in the extracellular space. As an essential nucleoside, uridine exists in all living species, ranging from bacteria to humans. In humans, uridine is involved in several metabolic disorders, some of which include dhydropyrimidinase deficiency, MNGIE (mitochondrial neurogastrointestinal encephalopathy), and beta-ureidopropionase deficiency. Moreover, uridine is found to be associated with Lesch-Nyhan syndrome, which is an inborn error of metabolism. Uridine is a nucleoside consisting of uracil and D-ribose and a component of RNA. Uridine plays a role in the glycolysis pathway of galactose. In humans there is no catabolic process to metabolize galactose. Therefore, galactose is converted to glucose and metabolized via the normal glucose metabolism pathways. More specifically, consumed galactose is converted into galactose 1-phosphate (Gal-1-P). This molecule is a substrate for the enzyme galactose-1-phosphate uridyl transferase which transfers a UDP molecule to the galactose molecule. The end result is UDP-galactose and glucose-1-phosphate. This process is continued to allow the proper glycolysis of galactose. Uridine is found in many foods (anything containing RNA) but is destroyed in the liver and gastrointestinal tract, and so no food, when consumed, has ever been reliably shown to elevate blood uridine levels. On the other hand, consumption of RNA-rich foods may lead to high levels of purines (adenine and guanosine) in blood. High levels of purines are known to increase uric acid production and may aggravate or lead to conditions such as gout. Uridine is a ribonucleoside composed of a molecule of uracil attached to a ribofuranose moiety via a beta-N(1)-glycosidic bond. It has a role as a human metabolite, a fundamental metabolite and a drug metabolite. It is functionally related to a uracil. Uridine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Uridine is a Pyrimidine Analog. The chemical classification of uridine is Pyrimidines, and Analogs/Derivatives. Uridine is a natural product found in Ulva australis, Synechocystis, and other organisms with data available. Uridine is a nucleoside consisting of uracil and D-ribose and a component of RNA. Uridine has been studied as a rescue agent to reduce the toxicities associated with 5-fluorouracil (5-FU), thereby allowing the administration of higher doses of 5-FU in chemotherapy regimens. (NCI04) Uridine is a metabolite found in or produced by Saccharomyces cerevisiae. A ribonucleoside in which RIBOSE is linked to URACIL. Uridine is a molecule (known as a nucleoside) that is formed when uracil is attached to a ribose ring (also known as a ribofuranose) via a b-N1-glycosidic bond. ; Uridine is a molecule (known as a nucleoside) that is formed when uracil is attached to a ribose ring (also known as a ribofuranose) via a ?-N1-glycosidic bond. Uridine is found in many foods, some of which are celery leaves, canola, common hazelnut, and hickory nut. A ribonucleoside composed of a molecule of uracil attached to a ribofuranose moiety via a beta-N(1)-glycosidic bond. [Spectral] Uridine (exact mass = 244.06954) and Adenosine (exact mass = 267.09675) and Glutathione (exact mass = 307.08381) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. [Spectral] Uridine (exact mass = 244.06954) and Glutathione (exact mass = 307.08381) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. Uridine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=58-96-8 (retrieved 2024-06-29) (CAS RN: 58-96-8). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond.
3,3',4'5-Tetrahydroxystilbene
Piceatannol is a stilbenol that is trans-stilbene in which one of the phenyl groups is substituted by hydroxy groups at positions 3 and 4, while the other phenyl group is substituted by hydroxy groups at positions 3 and 5. It has a role as a protein kinase inhibitor, a tyrosine kinase inhibitor, an antineoplastic agent, a plant metabolite, a hypoglycemic agent, an apoptosis inducer and a geroprotector. It is a stilbenol, a member of resorcinols, a member of catechols and a polyphenol. It derives from a hydride of a trans-stilbene. Piceatannol is a natural product found in Vitis amurensis, Smilax bracteata, and other organisms with data available. Piceatannol is a polyhydroxylated stilbene extract from the seeds of Euphorbia lagascae, which inhibits protein tyrosine kinase Syk and induces apoptosis. (NCI) Piceatannol is a metabolite found in or produced by Saccharomyces cerevisiae. See also: Wine grape (part of); Robinia pseudoacacia whole (part of); Tsuga canadensis bark (part of). 3,3,45-Tetrahydroxystilbene (or Piceatannol) is a phenolic stilbenoid. It is a metabolite of resveratrol found in red wine. A viral protein-tyrosine kinase (LMP2A) implicated in leukemia, non-Hodgkins lymphoma and other diseases associated with Epstein-Barr virus, was recently found to be blocked by picetannol in vitro (PMID 2590224). Therefore there is research interest in piceatannol as an anti-cancer and anti-EBV drug. Piceatannol can also act as an agonist for estrogen receptor alpha in human breast cancer cells (PMID: 16216908). [HMDB] 3,3,45-Tetrahydroxystilbene (or Piceatannol) is a phenolic stilbenoid. It is a metabolite of resveratrol found in red wine. A viral protein-tyrosine kinase (LMP2A) implicated in leukemia, non-Hodgkins lymphoma and other diseases associated with Epstein-Barr virus, was recently found to be blocked by picetannol in vitro (PMID 2590224). Therefore there is research interest in piceatannol as an anti-cancer and anti-EBV drug. Piceatannol can also act as an agonist for estrogen receptor alpha in human breast cancer cells (PMID: 16216908). A stilbenol that is trans-stilbene in which one of the phenyl groups is substituted by hydroxy groups at positions 3 and 4, while the other phenyl group is substituted by hydroxy groups at positions 3 and 5. C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor > C1967 - Tyrosine Kinase Inhibitor Piceatannol is a well-known Syk inhibitor and reduces the expression of iNOS induced by TNF. Piceatannol is an effective agent for research of acute lung injury (ALI)[1]. Piceatannol is a naturally occurring polyphenolic stilbene found in various fruits and vegetables and exhibits anticancer and anti-inflammatory properties[2]. Piceatannol induces apoptosis in DLBCL cell lines[3]. Piceatannol induces autophagy and apoptosis in MOLT-4 human leukemia cells[4]. Piceatannol is a well-known Syk inhibitor and reduces the expression of iNOS induced by TNF. Piceatannol is an effective agent for research of acute lung injury (ALI)[1]. Piceatannol is a naturally occurring polyphenolic stilbene found in various fruits and vegetables and exhibits anticancer and anti-inflammatory properties[2]. Piceatannol induces apoptosis in DLBCL cell lines[3]. Piceatannol induces autophagy and apoptosis in MOLT-4 human leukemia cells[4].
Gnetol
Gnetol is a natural product found in Gnetum edule, Gnetum hainanense, and other organisms with data available. Gnetol is a phenolic compound isolated from the root of Gnetum montanum . Gnetol potently inhibits COX-1 (IC50 of 0.78 μM) and HDAC. Gnetol is a potent tyrosinase inhibitor with an IC50 of 4.5 μM for murine tyrosinase and suppresses melanin biosynthesis. Gnetol has antioxidant, antiproliferative, anticancer and hepatoprotective activity. Gnetol also possesses concentration-dependent α-Amylase, α-glucosidase, and adipogenesis activities[1][2][3]. Gnetol is a phenolic compound isolated from the root of Gnetum montanum . Gnetol potently inhibits COX-1 (IC50 of 0.78 μM) and HDAC. Gnetol is a potent tyrosinase inhibitor with an IC50 of 4.5 μM for murine tyrosinase and suppresses melanin biosynthesis. Gnetol has antioxidant, antiproliferative, anticancer and hepatoprotective activity. Gnetol also possesses concentration-dependent α-Amylase, α-glucosidase, and adipogenesis activities[1][2][3].
Pseudouridine
Beta-pseudouridine, also known as p or 5-(b-D-ribofuranosyl)uracil, is a member of the class of compounds known as nucleoside and nucleotide analogues. Nucleoside and nucleotide analogues are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others. Beta-pseudouridine is soluble (in water) and a very weakly acidic compound (based on its pKa). Beta-pseudouridine can be found in a number of food items such as eggplant, wax gourd, asparagus, and garden cress, which makes beta-pseudouridine a potential biomarker for the consumption of these food products. Beta-pseudouridine can be found primarily in amniotic fluid, blood, feces, and urine. Beta-pseudouridine exists in all living species, ranging from bacteria to humans. Moreover, beta-pseudouridine is found to be associated with canavan disease. Pseudouridine, also known as psi-uridine or 5-ribosyluracil, belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides, such as phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides. Pseudouridine specifically has its uracil attached via a carbon-carbon instead of a nitrogen-carbon glycosidic bond to the ribofuranose. It is the most prevalent of the over one hundred different modified nucleosides found in RNA (PMID: 17113994). Pseudouridine is a solid that is soluble in water. Pseudouridine exists in all living species, ranging from bacteria to humans, and is in all classes of RNA except mRNA. It is formed by enzymes called pseudouridine synthases, which post-transcriptionally isomerize specific uridine residues in RNA. Pseudouridine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=1445-07-4 (retrieved 2024-07-01) (CAS RN: 1445-07-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Pseudouridine is an isomer of the nucleoside uridine, and the most abundant modified nucleoside in non-coding RNAs. Pseudouridine in rRNA and tRNA can fine-tune and stabilize the regional structure and help maintain their functions in mRNA decoding, ribosome assembly, processing and translation[1][2][3][4]. Pseudouridine is an isomer of the nucleoside uridine, and the most abundant modified nucleoside in non-coding RNAs. Pseudouridine in rRNA and tRNA can fine-tune and stabilize the regional structure and help maintain their functions in mRNA decoding, ribosome assembly, processing and translation[1][2][3][4].
Dioxybenzone
C1892 - Chemopreventive Agent > C851 - Sunscreen Same as: D03853
Fucose 1-phosphate
Fucose 1-phosphate (CAS: 16562-58-6) belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphate group linked to the carbohydrate unit. Fucose 1-phosphate is an intermediate in the reversible synthesis of GDP-L-fucose catalyzed by the enzyme guanosine triphosphate fucose pyrophosphorylase (GFPP, EC 2.7.7.30). The reversible reaction is magnesium-dependent, although the enzyme is partially active when cobalt or manganese is substituted. The reaction is unusual in that, of the four canonical nucleoside triphosphates, only guanosine can be utilized efficiently to form a nucleotide-sugar. Free cytosolic fucose is phosphorylated by L-fucokinase (EC 2.7.1.52) to form fucose-1-phosphate in the salvage pathway of GDP-L-fucose (PMID: 16185085, 14686921). Fucose-1-phosphate is an intermediate in the reversible synthesis of GDP-L-fucose, in a reaction catalyzed by the enzyme guanosine triphosphate fucose pyrophosphorylase (GFPP, E.C. 2.7.7.30) . The reversible reaction is magnesium-dependent, although the enzyme is partially active when cobalt or manganese is substituted. The reaction is unusual in that, of the four canonical nucleoside triphosphates, only guanosine can be utilized efficiently to form a nucleotide-sugar. Free cytosolic fucose is phosphorylated by L-fucokinase (EC 2.7.1.52) to form fucose-1-phosphate in the salvage pathway of GDP-L-fucose. (PMID: 16185085, 14686921) [HMDB]
Apraclonidine
C9H10Cl2N4 (244.02824800000002)
Apraclonidine is only found in individuals that have used or taken this drug.Apraclonidine, also known as iopidine, is a sympathomimetic used in glaucoma therapy.Apraclonidine is a relatively selective alpha2 adrenergic receptor agonist that stimulates alpha1 receptors to a lesser extent. It has a peak ocular hypotensive effect occurring at two hours post-dosing. The exact mechanism of action is unknown, but fluorophotometric studies in animals and humans suggest that Apraclonidine has a dual mechanism of action by reducing aqueous humor production through the constriction of afferent ciliary process vessels, and increasing uveoscleral outflow. S - Sensory organs > S01 - Ophthalmologicals > S01E - Antiglaucoma preparations and miotics > S01EA - Sympathomimetics in glaucoma therapy C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists
(2E,11Z)-Wyerone acid
(2E,11Z)-Wyerone acid is found in pulses. (2E,11Z)-Wyerone acid is isolated from broad bean leaves (Vicia faba) infected with Botrytis specie Isolated from broad bean leaves (Vicia faba) infected with Botrytis subspecies (2E,11Z)-Wyerone acid is found in pulses.
Eriobofuran
Phytoalexin from the leaves of Eriobotrya japonica (loquat). Eriobofuran is found in loquat and fruits. Eriobofuran is found in fruits. Phytoalexin from the leaves of Eriobotrya japonica (loquat).
Gentisein
Gentisein is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3 and 7. It has a role as a plant metabolite. It is a member of xanthones and a polyphenol. Gentisein is a natural product found in Hypericum scabrum, Cratoxylum formosum, 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 and 7. Gentisein is found in alcoholic beverages. Gentisein is isolated from Gentiana lutea (yellow gentian Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2].
Mesuaxanthone B
A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 5 and 6.
1,3,5-Trihydroxyxanthone
A member of the class of xanthones that is xanthone substituted by hydroxy groups at positions 1, 3 and 5. It has been isolated from Anaxagorea luzonensis.
Oxyresveratrol
Oxyresveratrol (trans-Oxyresveratrol) is a potent naturally occurring antioxidant and free radical scavenger (IC50 of 28.9 μM against DPPH free radicals). Oxyresveratrol is potent and noncompetitive tyrosinase inhibitor with an IC50 value of 1.2 μM for mushroom tyrosinase. Oxyresveratrol is effective against HSV-1, HSV-2 and varicella-zoster virus, and has neuroprotective effects[1][2][3][4]. Oxyresveratrol (trans-Oxyresveratrol) is a potent naturally occurring antioxidant and free radical scavenger (IC50 of 28.9 μM against DPPH free radicals). Oxyresveratrol is potent and noncompetitive tyrosinase inhibitor with an IC50 value of 1.2 μM for mushroom tyrosinase. Oxyresveratrol is effective against HSV-1, HSV-2 and varicella-zoster virus, and has neuroprotective effects[1][2][3][4].
Penicillenic acid
C9H12N2O4S (244.05177519999998)
Cgp 52608
C8H12N4OS2 (244.04525019999997)
MCPA-thioethyl
C11H13ClO2S (244.03247480000002)
L-Rhamnulose 1-phosphate
A deoxyketohexose phosphate consisting of L-rhamnulose having a monophosphate group at the 1-position.
2-Hydroxy-2-(hydroxymethyl)-3-oxo-4-phosphonooxybutanoic acid
Urolithin C
Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2].
Graveolone
Constituent of Anethum graveolens (dill). Graveolone is found in dill, herbs and spices, and parsley. Graveolone is found in herbs and spices. Graveolone is a constituent of Anethum graveolens (dill).
p-Coumaric acid sulfate
p-Coumaric acid sulfate (CAS: 376374-66-2) is an endogenous phenolic acid metabolite. p-Coumaric 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). BioTransformer predicts that p-coumaric acid sulfate is a product of p-coumaric acid metabolism via a 4-O-sulfation-of-phenolic-compound reaction catalyzed by sulfotransferase 1A3 (P0DMM9) and sulfotransferase enzymes (PMID: 30612223).
(R)-Apiumetin
(R)-Apiumetin is found in green vegetables. (R)-Apiumetin is a constituent of the seeds of Apium graveolens. Constituent of the seeds of Apium graveolens. (R)-Apiumetin is found in green vegetables.
Suberenone
Suberenone is found in herbs and spices. Suberenone is a constituent of Ruta graveolens (rue)
9,10-Dihydro-2,3,5,7-Phenanthrenetetrol
9,10-Dihydro-2,3,5,7-Phenanthrenetetrol is found in root vegetables. 9,10-Dihydro-2,3,5,7-Phenanthrenetetrol is isolated from Dioscorea bulbifera (air potato). Isolated from Dioscorea bulbifera (air potato). 9,10-Dihydro-2,3,5,7-Phenanthrenetetrol is found in root vegetables.
Urolithin C
A polyphenol metabolite detected in biological fluids [PhenolExplorer] Urolithin C is a biomarker of nut consumption in urine. Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2].
1-O-Galloylglycerol
1-O-Galloylglycerol is found in garden rhubarb. 1-O-Galloylglycerol is isolated from commercial rhubarb. Isolated from commercial rhubarb. 1-O-Galloylglycerol is found in green vegetables and garden rhubarb.
4-phenylbutanic acid-O-sulphate
C10H12O5S (244.04054219999998)
4-phenylbutanic acid-O-sulphate is a conjugate of 4-phenylbutanic acid and sulphate. 4-phenylbutyric acid is a monocarboxylic acid the structure of which is that of butyric acid substituted with a phenyl group at C-4. It is a histone deacetylase inhibitor that displays anticancer activity. It inhibits cell proliferation, invasion and migration and induces apoptosis in glioma cells. It also inhibits protein isoprenylation, depletes plasma glutamine, increases production of foetal haemoglobin through transcriptional activation of the γ-globin gene and affects hPPARγ activation. (CHEBI:41500)
(2E)-3-[3-(sulfooxy)phenyl]prop-2-enoic acid
(2e)-3-[3-(sulfooxy)phenyl]prop-2-enoic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of (2e)-3-(3-hydroxyphenyl)prop-2-enoic acid. It is generated by Sulfotransferase 1A3 (P0DMM9) and Sulfotransferase enzymes via a -3-O-sulfation-of-phenolic-compound reaction. This -3-O-sulfation-of-phenolic-compound occurs in humans.
2-Deoxy-D-arabino-hexose 6-(dihydrogen phosphate)
1-[(2R,3S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione
1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2]. 1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2]. 1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2].
7-Methoxy-4-(trifluoromethyl)coumarin
C11H7F3O3 (244.03472680000002)
(5R,6S)-3-(Aminomethyl)-6-[(1R)-1-hydroxyethyl]-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
C9H12N2O4S (244.05177519999998)
3-Pyroglutamylthiazolidine-4-carboxylic acid
C9H12N2O4S (244.05177519999998)
D007155 - Immunologic Factors
1-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxypyrimidin-2-one
Piceatannol
Piceatannol, also known as (Z)-3,5,3,4-tetrahydroxystilbene, is a member of the class of compounds known as stilbenes. Stilbenes are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. Piceatannol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Piceatannol can be synthesized from cis-stilbene. Piceatannol can also be synthesized into cis-astringin. Piceatannol can be found in common grape and grape wine, which makes piceatannol a potential biomarker for the consumption of these food products. Piceatannol is a stilbenoid, a type of phenolic compound .
Uridine
C26170 - Protective Agent > C2459 - Chemoprotective Agent > C2080 - Cytoprotective Agent COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond.
Pseudouridine
Pseudouridine is an isomer of the nucleoside uridine, and the most abundant modified nucleoside in non-coding RNAs. Pseudouridine in rRNA and tRNA can fine-tune and stabilize the regional structure and help maintain their functions in mRNA decoding, ribosome assembly, processing and translation[1][2][3][4]. Pseudouridine is an isomer of the nucleoside uridine, and the most abundant modified nucleoside in non-coding RNAs. Pseudouridine in rRNA and tRNA can fine-tune and stabilize the regional structure and help maintain their functions in mRNA decoding, ribosome assembly, processing and translation[1][2][3][4].
4-Hydroxydehydrokawain
6-[(e)-2-(4-Hydroxyphenyl)ethenyl]-4-methoxypyran-2-one is a natural product found in Alpinia blepharocalyx, Anaphalis sinica, and Alpinia roxburghii with data available.
Oxyresveratrol
Oxyresveratrol is a stilbenoid. Oxyresveratrol is a natural product found in Spirotropis longifolia, Melaleuca leucadendra, and other organisms with data available. Oxyresveratrol (trans-Oxyresveratrol) is a potent naturally occurring antioxidant and free radical scavenger (IC50 of 28.9 μM against DPPH free radicals). Oxyresveratrol is potent and noncompetitive tyrosinase inhibitor with an IC50 value of 1.2 μM for mushroom tyrosinase. Oxyresveratrol is effective against HSV-1, HSV-2 and varicella-zoster virus, and has neuroprotective effects[1][2][3][4]. Oxyresveratrol (trans-Oxyresveratrol) is a potent naturally occurring antioxidant and free radical scavenger (IC50 of 28.9 μM against DPPH free radicals). Oxyresveratrol is potent and noncompetitive tyrosinase inhibitor with an IC50 value of 1.2 μM for mushroom tyrosinase. Oxyresveratrol is effective against HSV-1, HSV-2 and varicella-zoster virus, and has neuroprotective effects[1][2][3][4].
Cearoin
(2,5-dihydroxy-4-methoxyphenyl)-phenylmethanone is a member of benzophenones. Cearoin is a natural product found in Dalbergia cochinchinensis, Pterocarpus santalinus, and other organisms with data available.
2-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,3-diol
5-Hydroxyseselin
5-Hydroxyseselin is a natural product found in Metrodorea flavida, Citrus sulcata, and Citrus tamurana with data available.
1,2,5-Trihydroxyxanthone
A member of the class of xanthones that is 9H-xanthen-9-one substituted bybhydroxy groups at positions 1, 2 and 5. It is isolated from Garcinia subelliptica.
8-Chloro-5,10-dihydro-11H-dibenzo[b,e][1,4]-diazepin-11-one
C13H9ClN2O (244.04033739999997)
1-(beta-D-ribofuranosyl)imidazolin-2-one-4-carboxaldehyde|ribofuranosyl-4-formyl-4-imidazolin-2-one|RT 2.0
4-chloro-3,4-dihydro-5,6,8-trihydroxy-3-methylisocoumarin
C10H9ClO5 (244.01384939999997)
3-(hydroxyprop-1-ynyl)-6-(5-hexen-3-yn-1-ynyl)-1,2-dithiacyclohexa-3,5-diene|4,7-Epidithio-4,6,12-tridecatriene-2,8,10-triyn-1-ol
7,8-Dihydroxy-1-methylnaphtho[2,3-c]furan-4,9-dione
1,2,3,4-Tetrahydro-6-hydroxy-2-methyl-1,3,4-trioxo-pyrazino<1,2-a>indol|6-Hydroxy-1,3,4-trioxo-2-methyl-1,2,3,4-tetrahydro-pyrazino<1,2-a>indol|6-hydroxy-2-methyl-pyrazino[1,2-a]indole-1,3,4-trione
Ketone-2,3-Dihydro-5-[[5-(1-propynyl)-2-thienyl]ethynyl]thiophen-3-ol
3-(1-propynyl)-6-(5-hexen-3-yn-1-ynyl)-cyclohexa-3,5-diene-1,2-thiosulphinate|Thiarubrin 1-oxide
5-hydroxy-6-methoxynaphtho<2,3-b>furan-4,9-quinone
3-(1-propynyl)-6-(5,6-epoxyhex-3-yn-1-ynyl)-1,2-dithiacyclohexa-3,5-diene|3-[4-(2-Oxiranyl)-1,3-butadiynyl]-6-(1-propynyl)-1,2-dithiin|thiarubrine D
L-Uridine
L-Uridine, isolated from the Polyporaceae fungus Poria cocos (Schw.), is an enantiomer of the normal RNA constituent D-uridine. L-uridine acts as a phosphate acceptor for nucleoside phosphotransferases[1]. L-Uridine, isolated from the Polyporaceae fungus Poria cocos (Schw.), is an enantiomer of the normal RNA constituent D-uridine. L-uridine acts as a phosphate acceptor for nucleoside phosphotransferases[1]. L-Uridine, isolated from the Polyporaceae fungus Poria cocos (Schw.), is an enantiomer of the normal RNA constituent D-uridine. L-uridine acts as a phosphate acceptor for nucleoside phosphotransferases[1].
Uridine
C26170 - Protective Agent > C2459 - Chemoprotective Agent > C2080 - Cytoprotective Agent COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; DRTQHJPVMGBUCF_STSL_0179_Uridine_8000fmol_180506_S2_LC02_MS02_83; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. relative retention time with respect to 9-anthracene Carboxylic Acid is 0.088 Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond.
alpha-L-(-)-Fucose 1-phosphate bis(cyclohexylammonium) salt
Pidotimod
C9H12N2O4S (244.05177519999998)
L - Antineoplastic and immunomodulating agents > L03 - Immunostimulants > L03A - Immunostimulants C308 - Immunotherapeutic Agent > C2139 - Immunostimulant D007155 - Immunologic Factors
Pseudouridine
A C-glycosyl pyrimidine that consists of uracil having a beta-D-ribofuranosyl residue attached at position 5. The C-glycosyl isomer of the nucleoside uridine. Pseudouridine is an isomer of the nucleoside uridine, and the most abundant modified nucleoside in non-coding RNAs. Pseudouridine in rRNA and tRNA can fine-tune and stabilize the regional structure and help maintain their functions in mRNA decoding, ribosome assembly, processing and translation[1][2][3][4]. Pseudouridine is an isomer of the nucleoside uridine, and the most abundant modified nucleoside in non-coding RNAs. Pseudouridine in rRNA and tRNA can fine-tune and stabilize the regional structure and help maintain their functions in mRNA decoding, ribosome assembly, processing and translation[1][2][3][4].
Arabinofuranosyluracil
1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2]. 1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2]. 1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2].
8-Chloro-11-oxo-10,11-dihydro-5H-dibenzo-1,4-diazepine
C13H9ClN2O (244.04033739999997)
CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 1093
(6-P-TOLYL-IMIDAZO[2,1-B]THIAZOL-2-YL)-METHANOL
C13H12N2OS (244.06703019999998)
4-(7-Chloropyrazolo[1,5-a]pyridin-2-yl)phenol
C13H9ClN2O (244.04033739999997)
methyl 5-(trifluoromethyl)-1H-pyrrolo[3,2-b]pyridine-2-carboxylate
C10H7F3N2O2 (244.04595980000002)
5-amino-2-chloro-10h-acridin-9-one
C13H9ClN2O (244.04033739999997)
2-(3-Chloropropyl)-2-(4-fluorophenyl)-1,3-dioxolane
C12H14ClFO2 (244.06663060000002)
N-(3-Chlorophenyl)-1H-pyrazolo[4,3-b]pyridin-3-amine
C12H9ClN4 (244.05157039999997)
4-AMINO-N-CYCLOPROPYL-3,5-DICHLOROBENZAMIDE
C10H10Cl2N2O (244.01701500000001)
2-Amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carbonitrile
C13H12N2OS (244.06703019999998)
3-(4-METHANESULFONYLOXOPHENYL)-PROPANOIC ACID
C10H12O5S (244.04054219999998)
4-CYANO-2-(TRIFLUOROMETHOXY)ACETANILIDE
C10H7F3N2O2 (244.04595980000002)
2-Boc-Aminothiazole-5-carboxylic acid
C9H12N2O4S (244.05177519999998)
Naphthalene-1-sulfonic acid hydrate,
C10H12O5S (244.04054219999998)
1,2-BIS(PHENYLTHIO)ETHYLENE (CIS- AND TRANS- MIXTURE)
3-(3,4-DICHLORO-PHENYL)-TETRAHYDRO-PYRAN-2-ONE
C11H10Cl2O2 (244.00578200000004)
2-PYRIDINECARBOXAMIDE, N-[2-(METHYLTHIO)PHENYL]-
C13H12N2OS (244.06703019999998)
3-FLUORO-2-FORMYL-[1,1-BIPHENYL]-4-CARBOXYLIC ACID
3-FLUORO-4-FORMYL-[1,1-BIPHENYL]-4-CARBOXYLIC ACID
N-((5-bromopyridin-3-yl)methyl)-2-methoxyethanamine
C9H13BrN2O (244.02111879999998)
3-AMINO-3-(5-CHLORO-2-NITRO-PHENYL)-PROPIONIC ACID
methyl 2-[(4-aminophenyl)sulfonylamino]acetate
C9H12N2O4S (244.05177519999998)
METHYL 4-ACETYL-3-METHYL-5-(METHYLTHIO)THIOPHENE-2-CARBOXYLATE
Mesulfen
P - Antiparasitic products, insecticides and repellents > P03 - Ectoparasiticides, incl. scabicides, insecticides and repellents > P03A - Ectoparasiticides, incl. scabicides > P03AA - Sulfur containing products D - Dermatologicals > D10 - Anti-acne preparations > D10A - Anti-acne preparations for topical use > D10AB - Preparations containing sulfur C308 - Immunotherapeutic Agent > C574 - Immunosuppressant
1-bromo-2-(1,1-dimethoxyethyl)benzene
C10H13BrO2 (244.00988580000003)
Boc-2-Amino-4-thiazole-carboxylic acid
C9H12N2O4S (244.05177519999998)
3-[(4-METHOXYPHENYL)SULFONYL]PROPANOIC ACID
C10H12O5S (244.04054219999998)
4-Chloro-6-phenyl-5H-pyrrolo[3,2-d]pyrimidin-2-amine
C12H9ClN4 (244.05157039999997)
4-Chloro-2-methyl-6-phenylfuro[3,2-d]pyrimidine
C13H9ClN2O (244.04033739999997)
2-(4-(METHOXYCARBONYL)PHENYL)ETHANESULFONIC ACID
C10H12O5S (244.04054219999998)
3 7-DIMETHYLOCTYLMAGNESIUM BROMIDE 1.0&
C10H21BrMg (244.06770260000002)
7-Methoxy-2-(trifluoromethyl)-4H-chromen-4-one
C11H7F3O3 (244.03472680000002)
4-(2-Bromoethyl)-1,2-dimethoxybenzene
C10H13BrO2 (244.00988580000003)
[3-(3-bromopropoxy)phenyl]methanol
C10H13BrO2 (244.00988580000003)
1-(Bromomethyl)-4-(trifluoromethyl)cyclohexane
C8H12BrF3 (244.00744079999998)
Methyl 2-methoxy-5-(methylsulfonyl)benzoate
C10H12O5S (244.04054219999998)
Benzoyl chloride,4-(2-phenyldiazenyl)-
C13H9ClN2O (244.04033739999997)
Benzenesulfonamide,4-nitro-N-propyl-
C9H12N2O4S (244.05177519999998)
[4-(3-bromopropoxy)phenyl]methanol
C10H13BrO2 (244.00988580000003)
1-Bromo-2-(3-methoxypropoxy)benzene
C10H13BrO2 (244.00988580000003)
(3-((N,N-DIMETHYLSULFAMOYL)AMINO)PHENYL)BORONIC ACID
C8H13BN2O4S (244.06890479999998)
2-benzylsulfanylpyridine-4-carboxamide
C13H12N2OS (244.06703019999998)
2-AMINO-6-CHLORO-4,7-DIMETHOXYBENZOTHIAZOLE
C9H9ClN2O2S (244.00732440000002)
4-(2,2-Dichlorocyclopropyl)phenol 1-acetate
C11H10Cl2O2 (244.00578200000004)
1-Bromo-3-(2-methoxyethoxy)methylbenzene
C10H13BrO2 (244.00988580000003)
1-Bromo-4-[(2-methoxyethoxy)methyl]benzene
C10H13BrO2 (244.00988580000003)
2-(4-methylphenyl)sulfanylpyridine-3-carboxamide
C13H12N2OS (244.06703019999998)
2-thiophen-3-yl-3H-benzimidazole-5-carboxylic acid
2-THIOPHEN-2-YL-3H-BENZOIMIDAZOLE-4-CARBOXYLIC ACID
4-Chloro-2-(4-oxo-piperidinyl)-5-thiazolecarboxaldehyde
C9H9ClN2O2S (244.00732440000002)
3-Chlorothiophene-2-boronic acid pinacol ester
C10H14BClO2S (244.04960440000002)
[4-(trifluoromethyl)thiophen-2-yl]hydrazine,hydrochloride
C7H8ClF3N2S (244.00487939999996)
4-bromo-1-methoxy-2-propan-2-yloxybenzene
C10H13BrO2 (244.00988580000003)
2-Bromo-4-(dimethoxymethyl)-1-methylbenzene
C10H13BrO2 (244.00988580000003)
2-(4-Chlorophenyl)-1,3-benzoxazol-4-amine
C13H9ClN2O (244.04033739999997)
2,5-Furandicarboxylicacid, 3,4-dihydroxy-, 2,5-diethyl ester
5-Hydroxy-2-deoxyuridine
5-Hydroxy-2'-deoxyuridine (5-OHdU) is a major stable oxidation product of 2'-Deoxycytidine. 5-Hydroxy-2'-deoxyuridine can be incorporated into DNA in vitro by DNA polymerase[1].
2-THIOPHEN-2-YL-1H-BENZOIMIDAZOLE-5-CARBOXYLIC ACID
ETHYL 2-CHLORO-2-[2-(2-FLUOROPHENYL)HYDRAZONO]-ACETATE
Carnidazole
C8H12N4O3S (244.06300819999998)
C254 - Anti-Infective Agent > C276 - Antiparasitic Agent > C277 - Antiprotozoal Agent
(4-(Benzylthio)phenyl)boronic acid
C13H13BO2S (244.07292680000003)
magnesium hypophosphite hexahydrate
C11H9NaO3S (244.01700839999998)
4-CHLORO-1-(P-TOLYL)-1H-PYRAZOLO[3,4-D]PYRIMIDINE
C12H9ClN4 (244.05157039999997)
2-(Methylsulfonyl)-6-propylpyrimidine-4-carboxylic acid
C9H12N2O4S (244.05177519999998)
(2R)-3-amino-2-(benzenesulfonamido)propanoic acid
C9H12N2O4S (244.05177519999998)
methyl 6-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylate
C10H7F3N2O2 (244.04595980000002)
5-(1H-BENZOIMIDAZOL-2-YLSULFANYL)-FURAN-2-CARBALDEHYDE
2-(CHLOROMETHYL)-5-(2-NAPHTHYL)-1,3,4-OXADIAZOLE
C13H9ClN2O (244.04033739999997)
3-(3,4-dichlorophenyl)piperazin-2-one
C10H10Cl2N2O (244.01701500000001)
1-Bromo-3-(3-methoxypropoxy)benzene
C10H13BrO2 (244.00988580000003)
3-bromo-5-tert-butylbenzene-1,2-diol
C10H13BrO2 (244.00988580000003)
N-(5-bromo-2-pyrimidinyl)-N,N-dimethylethane-1,2-diamine
2-Bromo-6-(3-methoxypropylamino)pyridine
C9H13BrN2O (244.02111879999998)
6-(5-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-2-pyridinamine
C12H9ClN4 (244.05157039999997)
Benzenemethanol, alpha,alpha-bis(trifluoromethyl)-
8-(2-AMINOETHYL)-5-HYDROXY-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE HYDROCHLORIDE
2,6-Dichloro-9-isopropyl-8-methyl-9H-purine
C9H10Cl2N4 (244.02824800000002)
(S)-2-(DIBENZYLAMINO)-3-METHYL-1-BUTANOL
C10H12O5S (244.04054219999998)
2-(2-chloro-phenyl)-benzooxazol-5-ylamine
C13H9ClN2O (244.04033739999997)
methyl 2-(trifluoromethyl)-1H-benzo[d]imidazole-7-carboxylate
C10H7F3N2O2 (244.04595980000002)
2-PROPEN-1-ONE, 1-(2,5-DIFLUOROPHENYL)-3-PHENYL-, (2E)-
4-(5-Chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)-2-pyridinamine
C12H9ClN4 (244.05157039999997)
2-Pyridinamine, 4-(4-chloro-1H-pyrrolo[2,3-b]pyridin-2-yl)-
C12H9ClN4 (244.05157039999997)
5,6-Dichloro-2-(3-hydroxypropyl)benzimidazole
C10H10Cl2N2O (244.01701500000001)
2-FLUORO-4-FORMYL-[1,1-BIPHENYL]-4-CARBOXYLIC ACID
(2-trifluoromethyl-benzoimidazol-1-yl)-acetic acid
C10H7F3N2O2 (244.04595980000002)
4-chloro-6-(1,3-dihydrobenzimidazol-2-ylidene)cyclohexa-2,4-dien-1-one
C13H9ClN2O (244.04033739999997)
(3-(3-CHLOROPHENYL)ISOXAZOL-5-YL)METHANAMINE HYDROCHLORIDE
C10H10Cl2N2O (244.01701500000001)
6-TRIFLUOROMETHYL-1H-INDAZOLE-3-CARBOXYLIC ACID METHYL ESTER
C10H7F3N2O2 (244.04595980000002)
Imidazo[1,2-a]pyridine-7-carboxylic acid, 2-(2-thienyl)
1-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)-3,5-DIMETHYL-1H-PYRAZOLE HYDROBROMIDE
2-chloro-6-(4-methoxyphenyl)nicotinonitrile
C13H9ClN2O (244.04033739999997)
5-Chlorothiophene-2-boronic acid pinacol ester
C10H14BClO2S (244.04960440000002)
poassium 3-methoxyethylether phenyl trifluoroborate
3-Bromo-6-(methoxymethoxy)-o-xylene
C10H13BrO2 (244.00988580000003)
[R-(R*,R*)]-3-[(5-Oxo-2-pyrrolidinyl)carbonyl]-4-thiazolidinecarboxylic acid
C9H12N2O4S (244.05177519999998)
[S-(R*,R*)]-3-[(5-Oxo-2-pyrrolidinyl)carbonyl]-4-thiazolidinecarboxylic acid
C9H12N2O4S (244.05177519999998)
Hexahydro-5,8-dioxo-3H-thiazolo[3,4-a]pyrazine-6-propanoic acid
C9H12N2O4S (244.05177519999998)
(2-Chloro-4-methoxy-5-(methoxycarbonyl)phenyl)boronic acid
1-(2-BROMOETHYL)-2,3,4,5,6-PENTAMETHYLBENZENE
C10H13BrO2 (244.00988580000003)
2-(4-AMINOBENZAMIDO)ETHANESULFONIC ACID
C9H12N2O4S (244.05177519999998)
methyl 4-(trifluoromethyl)-1H-pyrrolo[3,2-c]pyridine-2-carboxylate
C10H7F3N2O2 (244.04595980000002)
5-phenyl-thieno[2,3-d]pyrimidine-4-thiol
C12H8N2S2 (244.01288879999998)
N-[(1-ETHYL-1H-PYRAZOL-4-YL)METHYL]-N-ISOPROPYLAMINE
3-AMINO-3-(4-CHLORO-3-NITRO-PHENYL)-PROPIONIC ACID
5-(Ethylsulfonyl)-2-methoxybenzoic acid
C10H12O5S (244.04054219999998)
N-ISOPROPYL-4-NITROBENZENESULFONAMIDE
C9H12N2O4S (244.05177519999998)
Methyl 7-(trifluoromethyl)-1-benzofuran-2-carboxylate
C11H7F3O3 (244.03472680000002)
1-(BENZO[B]THIOPHEN-5-YL)-4-VINYLIMIDAZOLIDIN-2-ONE
C13H12N2OS (244.06703019999998)
n-(2-formyl-5,8-dioxo-5,8-dihydroquinolin-7-yl)acetamide
potassium O-(2-ethylhexyl) dithiocarbonate
C9H17KOS2 (244.03578519999996)
(PHENYLSELENOMETHYL)TRIMETHYLSILANE
C10H16SeSi (244.01864259999996)
2-(4-chloro-phenyl)-benzooxazol-5-ylamine
C13H9ClN2O (244.04033739999997)
Benzenesulfonamide, N-(1-methylethyl)-3-nitro-
C9H12N2O4S (244.05177519999998)
potassium (4-ethylthiophenyl)trifluoroborate
C8H9BF3KS (244.01071599999997)
6-Formamidopenicillanic acid
C9H12N2O4S (244.05177519999998)
The N-formyl derivative of 6-aminopenicillanic acid.
6-fluoro-N-phenyl-1,3-benzothiazol-2-amine
C13H9FN2S (244.04704459999996)
2-{[(2-chloro-6-fluorophenyl)methyl]sulfanyl}-4,5-dihydro-1H-imidazole
C10H10ClFN2S (244.02372219999998)
[(3S,4R,5S)-3,4,5-trihydroxy-2-keto-hexyl] dihydrogen phosphate
Trimethylsilyl p-toluenesulphonate
C10H16O3SSi (244.05893859999998)
Trisilane, 1,3-dichloro-1,1,2,2,3,3-hexamethyl-
C6H18Cl2Si3 (244.00933280000004)
3-(5-Amino-3-imino-3H-pyrazol-4-ylazo)-benzoic acid
Gentisein
Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2].
(2-Hydroxypropyl)phenylarsinic acid
C9H13AsO3 (244.00806079999998)
alpha-oxo-1-carboxy-5,6-dihydrothiopyranpropanoate S-oxide
[(2S,4S,5S)-4-hydroxy-5-(methylsulfanylmethyl)oxolan-2-yl] dihydrogen phosphate
1-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxypyrimidin-2-one
Spongouridine
1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2]. 1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2]. 1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2].
Ribavirin carboxylate
A monocarboxylic acid anion that is the conjugate base of ribavirin carboxylic acid arising from the deprotonation of the carboxy group. Major species at pH 7.3.
1-methyl-3-[(Z)-(4-oxo-3-prop-2-enyl-1,3-thiazolidin-2-ylidene)amino]thiourea
C8H12N4OS2 (244.04525019999997)
(3,3-Diethoxy-2-hydroxypropyl) dihydrogen phosphate
2-(3-Pyridinyl)-4-thiophen-2-ylthiazole
C12H8N2S2 (244.01288879999998)
8-chloro-1-methyl-2,6-dioxo-7H-purine-3-carboxylic acid
[(2S,3S,4S,5S)-3,4,5,6-tetrahydroxyoxan-2-yl]methanesulfonic acid
[(2S,3S,4S,5S,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methanesulfonic acid
5-Chloro-2-hydroxy-3,7-bis(methoxymethyl)cyclohepta-2,4,6-trien-1-one
apraclonidine
C9H10Cl2N4 (244.02824800000002)
S - Sensory organs > S01 - Ophthalmologicals > S01E - Antiglaucoma preparations and miotics > S01EA - Sympathomimetics in glaucoma therapy C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists
6-deoxy-6-sulfo-D-fructofuranose
A carbohydrate sulfonate that is D-fructofuranose in which the hydroxy group at at position 6 is replaced by a sulfo group.
2-Deoxy-D-glucose 6-phosphate
A deoxyaldohexose phosphate comprising 2-deoxy-D-glucose having the phosphate group at the 6-position.
4-(sulfooxy)-cinnamic acid
An aryl sulfate that is (2E)-3-phenylprop-2-enoic acid which is substituted by a sulfooxy group at position 4. It is produced by the seagrass Zostera marina and has very promising antifouling potential against several micro- and macrofouling organisms.
3-Pyroglutamylthiazolidine-4-carboxylic acid
C9H12N2O4S (244.05177519999998)
D007155 - Immunologic Factors
3-(3-sulfooxyphenyl)propanoate(2-)
A 3-(3-sulfooxyphenyl)propanoic acid anion obtained by deprotonation of the carboxy and sulfo groups of 3-(3-sulfooxyphenyl)propanoic acid.
6-sulfo-beta-D-quinovose
A 6-sulfo-D-quinovose (6-deoxy-6-sulfo-D-glucopyranose) that has beta configuration at the anomeric centre.
6-sulfo-alpha-D-quinovose
A 6-sulfo-D-quinovose that has alpha configuration at the anomeric centre.
6-Sulfo-d-quinovose
A carbohydrate sulfonate that is D-quinovose (6-deoxy-D-glucose) in which one of the methyl hydrogens at position 6 is replaced by a sulfo group.
N-(3-carboxylatopropanoyl)-L-glutamate(3-)
Trianion of N(2)-succinyl-L-glutamic acid arising from global deprotonation of the carboxy groups.
1-(a-D-ribofuranosyl)uracil
1-(a-D-ribofuranosyl)uracil is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
4-Thio-2'-deoxyuridine
C9H12N2O4S (244.05177519999998)
4-Thio-2'-deoxyuridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.
(2s)-2-{4-[6-(prop-1-yn-1-yl)-1,2-dithiin-3-yl]buta-1,3-diyn-1-yl}oxirane
4-hydroxy-1-[(3,4,5-trihydroxyoxolan-2-yl)methyl]pyrimidin-2-one
5-[(2r,3r,4r,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-diol
n-[(5z)-2-hydroxy-4-(methylsulfanyl)-5-[(methylsulfanyl)methylidene]pyrrol-3-yl]ethanimidic acid
2-{4-[6-(prop-1-yn-1-yl)-1,2-dithiin-3-yl]buta-1,3-diyn-1-yl}oxirane
(1s)-3-(hex-5-en-1,3-diyn-1-yl)-6-(prop-1-yn-1-yl)-1,2-dithiin-1-ium-1-olate
3-[(2s,3r,4r,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-hydroxypyrimidin-4-one
(3s,4s)-4-chloro-5,6,8-trihydroxy-3-methyl-3,4-dihydro-2-benzopyran-1-one
C10H9ClO5 (244.01384939999997)
1-[(2s,3s,4s,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-hydroxypyrimidin-2-one
(3r,4r)-5-chloro-4,6,8-trihydroxy-3-methyl-3,4-dihydro-2-benzopyran-1-one
C10H9ClO5 (244.01384939999997)
4-chloro-5,6,8-trihydroxy-3-methyl-3,4-dihydro-2-benzopyran-1-one
C10H9ClO5 (244.01384939999997)
1,6-dihydroxy-5-oxo-5h-5λ⁵-phenazin-5-ylium-10-olate
3-(hex-5-en-1,3-diyn-1-yl)-6-(prop-1-yn-1-yl)-1,2-dithiin-1-ium-1-olate
3-[6-(hex-5-en-1,3-diyn-1-yl)-1,2-dithiin-3-yl]prop-2-yn-1-ol
5,8-dihydroxy-1-methylnaphtho[2,3-c]furan-4,9-dione
(2r)-2-{2-[6-(penta-1,3-diyn-1-yl)-1,2-dithiin-3-yl]ethynyl}oxirane
1-[(2s,3s,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-hydroxypyrimidin-2-one
4-hydroxy-1-{[(2r,3s,4r,5r)-3,4,5-trihydroxyoxolan-2-yl]methyl}pyrimidin-2-one
2-{2-[6-(penta-1,3-diyn-1-yl)-1,2-dithiin-3-yl]ethynyl}oxirane
4-acetyl-3-chloro-2,6-dihydroxy-5-methoxybenzaldehyde
C10H9ClO5 (244.01384939999997)
5-chloro-4,6,8-trihydroxy-3-methyl-3,4-dihydro-2-benzopyran-1-one
C10H9ClO5 (244.01384939999997)
1-[(2r,3s,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-hydroxypyrimidin-2-one
(2s,5r,6r)-6-[(hydroxymethylidene)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
C9H12N2O4S (244.05177519999998)