Exact Mass: 244.01384939999997
Exact Mass Matches: 244.01384939999997
Found 500 metabolites which its exact mass value is equals to given mass value 244.01384939999997
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
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
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.
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].
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).
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)
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
1,2,5-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)
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
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
8-Chloro-11-oxo-10,11-dihydro-5H-dibenzo-1,4-diazepine
C13H9ClN2O (244.04033739999997)
CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 1093
4-(7-Chloropyrazolo[1,5-a]pyridin-2-yl)phenol
C13H9ClN2O (244.04033739999997)
(3-Bromophenyl)(tert-butyl)sulfane
C10H13BrS (243.99212780000002)
methyl 5-(trifluoromethyl)-1H-pyrrolo[3,2-b]pyridine-2-carboxylate
C10H7F3N2O2 (244.04595980000002)
acetazolamide sodium
C471 - Enzyme Inhibitor > C29577 - Carbonic Anhydrase Inhibitor C78275 - Agent Affecting Blood or Body Fluid > C448 - Diuretic
5-amino-2-chloro-10h-acridin-9-one
C13H9ClN2O (244.04033739999997)
N-(3-Chlorophenyl)-1H-pyrazolo[4,3-b]pyridin-3-amine
C12H9ClN4 (244.05157039999997)
3-(1H-Tetrazol-1-yl)benzenesulfonyl chloride
C7H5ClN4O2S (243.98217400000001)
(S)-(6-BROMO-2,3-DIHYDROBENZO[B][1,4]DIOXIN-2-YL)METHANOL
4-AMINO-N-CYCLOPROPYL-3,5-DICHLOROBENZAMIDE
C10H10Cl2N2O (244.01701500000001)
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)
6-CHLORO-2-METHYL-1,2,3,4-TETRAHYDRO-1LAMBDA6-BENZOTHIINE-1,1,4-TRIONE
C10H9ClO3S (243.99609139999998)
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)
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
4-Chlorobenzenesulfonic acid but-3-ynyl ester
C10H9ClO3S (243.99609139999998)
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
2,4-dichloro-6-(trifluoromethyl)phenylhydrazine
C7H5Cl2F3N2 (243.97818660000002)
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)
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-(3-bromo-5-fluorophenyl)-2-methylpropan-1-one
C10H10BrFO (243.98990019999997)
1-(Bromomethyl)-4-(trifluoromethyl)cyclohexane
C8H12BrF3 (244.00744079999998)
Methyl 2-methoxy-5-(methylsulfonyl)benzoate
C10H12O5S (244.04054219999998)
2,6-Dichloro-4-(trifluoromethyl)phenylhydrazine
C7H5Cl2F3N2 (243.97818660000002)
Benzoyl chloride,4-(2-phenyldiazenyl)-
C13H9ClN2O (244.04033739999997)
Benzenesulfonamide,4-nitro-N-propyl-
C9H12N2O4S (244.05177519999998)
7-CHLORO-3-OXO-3,4-DIHYDRO-2H-PYRIDO[3,2-B][1,4]THIAZINE-6-CARBOXYLIC ACID
4-Bromo-1-(4-fluorophenyl)-1-butanone
C10H10BrFO (243.98990019999997)
[4-(3-bromopropoxy)phenyl]methanol
C10H13BrO2 (244.00988580000003)
1-Bromo-2-(3-methoxypropoxy)benzene
C10H13BrO2 (244.00988580000003)
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)
(R)-(6-BROMO-2,3-DIHYDROBENZO[B][1,4]DIOXIN-2-YL)METHANOL
1-Bromo-4-[(2-methoxyethoxy)methyl]benzene
C10H13BrO2 (244.00988580000003)
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)
4-(2H-Tetrazol-5-yl)benzenesulfonyl chloride
C7H5ClN4O2S (243.98217400000001)
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
2-THIOPHEN-2-YL-1H-BENZOIMIDAZOLE-5-CARBOXYLIC ACID
ETHYL 2-CHLORO-2-[2-(2-FLUOROPHENYL)HYDRAZONO]-ACETATE
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)
1-bromo-4-tert-butylsulfanylbenzene
C10H13BrS (243.99212780000002)
methyl 6-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylate
C10H7F3N2O2 (244.04595980000002)
5-(1H-BENZOIMIDAZOL-2-YLSULFANYL)-FURAN-2-CARBALDEHYDE
1,3,5-TRIMETHYL-1H-PYRAZOLE-4-SULFONYL CHLORIDE
C6H10Cl2N2O2S (243.98400200000003)
2-(CHLOROMETHYL)-5-(2-NAPHTHYL)-1,3,4-OXADIAZOLE
C13H9ClN2O (244.04033739999997)
3-(3,4-dichlorophenyl)piperazin-2-one
C10H10Cl2N2O (244.01701500000001)
2-chloro-N-(6-fluoro-1,3-benzothiazol-2-yl)acetamide
1-Bromo-3-(3-methoxypropoxy)benzene
C10H13BrO2 (244.00988580000003)
3-bromo-5-tert-butylbenzene-1,2-diol
C10H13BrO2 (244.00988580000003)
4-fluoronaphthalene-1-sulfonyl chloride
C10H6ClFO2S (243.97610580000003)
N-(5-bromo-2-pyrimidinyl)-N,N-dimethylethane-1,2-diamine
2-Bromo-6-(3-methoxypropylamino)pyridine
C9H13BrN2O (244.02111879999998)
2-chloro-1-(2,3-dihydro-1,4-benzodithiin-6-yl)ethanone
C10H9ClOS2 (243.97833339999997)
6-(5-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-2-pyridinamine
C12H9ClN4 (244.05157039999997)
Benzenemethanol, alpha,alpha-bis(trifluoromethyl)-
2,6-Dichloro-9-isopropyl-8-methyl-9H-purine
C9H10Cl2N4 (244.02824800000002)
2-[(4-chlorophenyl)sulfonyl]-2-hydroxyiminoacetonitrile
Methyl 2-(2,6-dichloro-3-cyanopyridin-4-yl)acetate
(S)-2-(DIBENZYLAMINO)-3-METHYL-1-BUTANOL
C10H12O5S (244.04054219999998)
2-(2-chloro-phenyl)-benzooxazol-5-ylamine
C13H9ClN2O (244.04033739999997)
methyl 3-chloro-6-fluorobenzo(b)thiophe&
C10H6ClFO2S (243.97610580000003)
methyl 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate
methyl 2-(trifluoromethyl)-1H-benzo[d]imidazole-7-carboxylate
C10H7F3N2O2 (244.04595980000002)
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)
2-Bromo-1-(4-fluorophenyl)-1-butanone
C10H10BrFO (243.98990019999997)
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)
1H-Pyrrolo[2,3-b]pyridine-1-carboxylic acid, 4,6-dichloro-, methyl ester
(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)
ethyl 4-(chlorocarbonothioyloxy)benzoate
C10H9ClO3S (243.99609139999998)
(2-Chloro-4-methoxy-5-(methoxycarbonyl)phenyl)boronic acid
1-(difluoromethyl)-3,5-dimethylpyrazole-4-sulfonyl chloride
6-Fluoro-2-naphthalenesulfonyl chloride
C10H6ClFO2S (243.97610580000003)
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)
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)
5,11-bisthio-(R,R)-1,7-diazatricyclo[7.3.0.07,11]dodecane-2,8-diketone
Methyl 7-(trifluoromethyl)-1-benzofuran-2-carboxylate
C11H7F3O3 (244.03472680000002)
Iron,tricarbonyl[(1,2,3,4-h)-1,3,5,7-cyclooctatetraene]-
C11H8FeO3 (243.98228079999998)
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)
1-Methyl-3-oxo-1,3-dihydro-benzo[c]isothiazole-5-sulfonic acid amide
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
Trisilane, 1,3-dichloro-1,1,2,2,3,3-hexamethyl-
C6H18Cl2Si3 (244.00933280000004)
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
[Phosphonoamino-(2-sulfoethylamino)methylene]ammonium
[(2S,4S,5S)-4-hydroxy-5-(methylsulfanylmethyl)oxolan-2-yl] dihydrogen phosphate
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)
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.
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.
ZAPA (sulfate)
ZAPA sulfate is an agonist at low affinity GABAA-receptors. ZAPA sulfate induces membrane hyperpolarization of the Ascaris muscle cell with an EC50 of 10.3 μM[1][2].