Exact Mass: 489.1488958000001
Exact Mass Matches: 489.1488958000001
Found 222 metabolites which its exact mass value is equals to given mass value 489.1488958000001,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
4-Hydroxy duloxetine glucuronide
C24H27NO8S (489.14573020000006)
4-Hydroxy duloxetine glucuronide is a metabolite of duloxetine. Duloxetine (sold under the brand names Cymbalta, Ariclaim, Xeristar, Yentreve, Duzela) is a serotonin-norepinephrine reuptake inhibitor (SNRI) manufactured and marketed by Eli Lilly. It is effective for major depressive disorder and generalized anxiety disorder (GAD). (Wikipedia)
3-Benzyl-1-(1H-imidazol-4-ylmethyl)-4-(thien-2-ylsulfonyl)-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-7-carbonitrile
Gemigliptin
(2S)-3-[3-[(4-Carbamimidoylbenzoyl)amino]propanoylamino]-2-[(4-ethylphenyl)sulfonylamino]propanoic acid
C22H27N5O6S (489.16819620000007)
O1-[2-(2-amino-4-oxo-3,4-dihydro-pteridin-6-yl)-1-(1,2,3-dihydroxy-propyl)-ethyl]-beta-D-glucopyranuronic acid
N-(4-Acetamidophenyl)indomethacin Amide
C27H24ClN3O4 (489.14552540000005)
8-2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-deoxyguanosine
Cys Cys His Lys
Cys Cys His Gln
Cys Cys Lys His
Cys Cys Gln His
Cys His Cys Lys
Cys His Cys Gln
Cys His Lys Cys
Cys His Gln Cys
Cys Lys Cys His
Cys Lys His Cys
Cys Gln Cys His
Cys Gln His Cys
Asp Met Pro Gln
Asp Met Gln Pro
Asp Asn Asn Gln
Asp Asn Gln Asn
Asp Pro Met Gln
Asp Pro Gln Met
Asp Gln Met Pro
Asp Gln Asn Asn
Asp Gln Pro Met
Glu Met Asn Pro
Glu Met Pro Asn
Glu Asn Met Pro
Glu Asn Asn Asn
Glu Asn Pro Met
Glu Pro Met Asn
Glu Pro Asn Met
Gly His Asn Tyr
C21H27N7O7 (489.19718720000003)
Gly His Tyr Asn
C21H27N7O7 (489.19718720000003)
Gly Asn His Tyr
C21H27N7O7 (489.19718720000003)
Gly Asn Asn Trp
C21H27N7O7 (489.19718720000003)
Gly Asn Trp Asn
C21H27N7O7 (489.19718720000003)
Gly Asn Tyr His
C21H27N7O7 (489.19718720000003)
Gly Trp Asn Asn
C21H27N7O7 (489.19718720000003)
Gly Tyr His Asn
C21H27N7O7 (489.19718720000003)
Gly Tyr Asn His
C21H27N7O7 (489.19718720000003)
His Cys Cys Lys
His Cys Cys Gln
His Cys Lys Cys
His Cys Gln Cys
His Gly Asn Tyr
C21H27N7O7 (489.19718720000003)
His Gly Tyr Asn
C21H27N7O7 (489.19718720000003)
His Lys Cys Cys
His Asn Gly Tyr
C21H27N7O7 (489.19718720000003)
His Asn Tyr Gly
C21H27N7O7 (489.19718720000003)
His Gln Cys Cys
His Tyr Gly Asn
C21H27N7O7 (489.19718720000003)
His Tyr Asn Gly
C21H27N7O7 (489.19718720000003)
Lys Cys Cys His
Lys Cys His Cys
Lys His Cys Cys
Met Asp Pro Gln
Met Asp Gln Pro
Met Glu Asn Pro
Met Glu Pro Asn
Met Asn Glu Pro
Met Asn Pro Glu
Met Pro Asp Gln
Met Pro Glu Asn
Met Pro Asn Glu
Met Pro Gln Asp
Met Gln Asp Pro
Met Gln Pro Asp
Asn Asp Asn Gln
Asn Asp Gln Asn
Asn Glu Met Pro
Asn Glu Asn Asn
Asn Glu Pro Met
Asn Gly His Tyr
C21H27N7O7 (489.19718720000003)
Asn Gly Asn Trp
C21H27N7O7 (489.19718720000003)
Asn Gly Trp Asn
C21H27N7O7 (489.19718720000003)
Asn Gly Tyr His
C21H27N7O7 (489.19718720000003)
Asn His Gly Tyr
C21H27N7O7 (489.19718720000003)
Asn His Tyr Gly
C21H27N7O7 (489.19718720000003)
Asn Met Glu Pro
Asn Met Pro Glu
Asn Asn Asp Gln
Asn Asn Glu Asn
Asn Asn Gly Trp
C21H27N7O7 (489.19718720000003)
Asn Asn Asn Glu
Asn Asn Gln Asp
Asn Asn Trp Gly
C21H27N7O7 (489.19718720000003)
Asn Pro Glu Met
Asn Pro Met Glu
Asn Gln Asp Asn
Asn Gln Asn Asp
Asn Trp Gly Asn
C21H27N7O7 (489.19718720000003)
Asn Trp Asn Gly
C21H27N7O7 (489.19718720000003)
Asn Tyr Gly His
C21H27N7O7 (489.19718720000003)
Asn Tyr His Gly
C21H27N7O7 (489.19718720000003)
Pro Asp Met Gln
Pro Asp Gln Met
Pro Glu Met Asn
Pro Glu Asn Met
Pro Met Asp Gln
Pro Met Glu Asn
Pro Met Asn Glu
Pro Met Gln Asp
Pro Asn Glu Met
Pro Asn Met Glu
Pro Gln Asp Met
Pro Gln Met Asp
Gln Cys Cys His
Gln Cys His Cys
Gln Asp Met Pro
Gln Asp Asn Asn
Gln Asp Pro Met
Gln His Cys Cys
Gln Met Asp Pro
Gln Met Pro Asp
Gln Asn Asp Asn
Gln Asn Asn Asp
Gln Pro Asp Met
Gln Pro Met Asp
Trp Gly Asn Asn
C21H27N7O7 (489.19718720000003)
Trp Asn Gly Asn
C21H27N7O7 (489.19718720000003)
Trp Asn Asn Gly
C21H27N7O7 (489.19718720000003)
Tyr Gly His Asn
C21H27N7O7 (489.19718720000003)
Tyr Gly Asn His
C21H27N7O7 (489.19718720000003)
Tyr His Gly Asn
C21H27N7O7 (489.19718720000003)
Tyr His Asn Gly
C21H27N7O7 (489.19718720000003)
Tyr Asn Gly His
C21H27N7O7 (489.19718720000003)
Tyr Asn His Gly
C21H27N7O7 (489.19718720000003)
N-(4-acetamidophenyl)-Indomethacin amide
C27H24ClN3O4 (489.14552540000005)
BMS 214662
C471 - Enzyme Inhibitor > C2020 - Farnesyl Transferase Inhibitor
5-chloro-2-[2-[4-[(2-cyanoethyl)methylamino]phenyl]vinyl]-1,3,3-trimethyl-3H-indolium methyl sulphate
C24H28ClN3O4S (489.1488958000001)
3-BENZYL-1,4,5-TRIPHENYLIMIDAZOLIUM PERCHLORATE
C28H26ClN2O4 (489.15810060000007)
1,2,4-Benzotriazin-3-amine, 7-(2-chloro-5-Methoxyphenyl)-5-Methyl-N-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]-
C27H28ClN5O2 (489.19314180000003)
1-Octyl-2,3-dimethylimidazolium bis(trifluoromethanesulfonyl)imide
C15H25F6N3O4S2 (489.11906020000004)
d-galactose 1-[2-(2-azidoethoxy)ethoxyethyl]-2,3,4,6-tetra-o-acetate
3-(3-amino-3-oxopropyl)-2-[[1-methyl-2-(p-tolyl)-1H-indol-3-yl]azo]benzothiazolium chloride
C26H24ClN5OS (489.13900040000004)
(S)-AMINO-(3-NITRO-PHENYL)-ACETICACID
C21H22F3NO7S (489.10690180000006)
2-(4-METHYLUMBELLIFERYL)-α-D-N-ACETYLNEURAMINIC ACID SODIUM SALT
C21H24NNaO11 (489.12469940000005)
[(2R)-1-[6-(propan-2-yloxycarbonylamino)purin-9-yl]propan-2-yl]oxymethyl-(propan-2-yloxycarbonyloxymethoxy)phosphinic acid
C18H28N5O9P (489.16245680000003)
tert-Butyl (2S,5S)-2-(9-chloro-1,11-dihydroisochromeno[4,3:6,7]naphtho[1,2-d]imidazol-2-yl)-5-(methyl)pyrrolidine-1-carboxylate
C28H28ClN3O3 (489.1819088000001)
Gemigliptin
A - Alimentary tract and metabolism > A10 - Drugs used in diabetes > A10B - Blood glucose lowering drugs, excl. insulins > A10BH - Dipeptidyl peptidase 4 (dpp-4) inhibitors C78276 - Agent Affecting Digestive System or Metabolism > C29711 - Anti-diabetic Agent > C98086 - Dipeptidyl Peptidase-4 Inhibitor C471 - Enzyme Inhibitor > C783 - Protease Inhibitor
PRX-07034 hydrochloride
C21H29Cl2N3O4S (489.12557340000006)
PRX-07034 hydrochloride is a highly selective and potent 5-HT6 receptor antagonist with a Ki= 4-8 nM and an IC50 of 19 nM. PRX-07034 can be used for the research of enhancing working memory and cognitive flexibility[1].
(2S,3S,4R,5R)-2-(5-tert-Butyl-1,3,4-oxadiazol-2-yl)-5-(6-(4-chloro-2-fluoro-anilino)purin-9-yl)tetrahydrofuran-3,4-diol
C21H21ClFN7O4 (489.13275080000005)
1-((1H-Imidazol-5-yl)methyl)-3-benzyl-4-(thiophen-2-ylsulfonyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile
4-Hydroxy Duloxetine b-D-Glucuronide
C24H27NO8S (489.14573020000006)
5-(benzenesulfonyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-ethylbenzenesulfonamide
C24H27NO6S2 (489.12797220000004)
N-[4-bromo-2-[[(2-hydrazinyl-2-oxoethyl)amino]-phenylmethyl]phenyl]-3-(4-morpholinyl)propanamide
[9-(4-Ethoxyphenyl)sulfonyl-2,3-dihydro-[1,4]dioxino[2,3-g]quinolin-8-yl]-(4-methylphenyl)methanone
C27H23NO6S (489.12460180000005)
2-[5-Methanesulfonylamino-2-(4-aminophenyl)-6-oxo-1,6-dihydro-1-pyrimidinyl]-n-(3,3,3-trifluoro-1-isopropyl-2-oxopropyl)acetamide
C19H22F3N5O5S (489.12936780000007)
Citicoline
C14H27N4O11P2+ (489.11515119999996)
Citicoline is an essential intermediate in the biosynthetic pathway of structural phospholipids in cell membranes, particularly phosphatidylcholine. Once absorbed, citicoline is widely distributed throughout the body, crosses the blood-brain barrier and reaches the central nervous system (CNS), where it is incorporated into the membrane and microsomal phospholipid fraction. Citicoline activates biosynthesis of structural phospholipids of neuronal membranes, increases brain metabolism, and acts upon the levels of different neurotransmitters. Thus, citicoline has been experimentally shown to increase norepinephrine and dopamine levels in the CNS. Owing to these pharmacological mechanisms, citicoline has a neuroprotective effect in hypoxic and ischemic conditions, decreasing the volume of ischemic lesion, and also improves learning and memory performance in animal models of brain aging. In addition, citicoline has been shown to restore the activity of mitochondrial ATPase and membrane Na+/K+ATPase, to inhibit activation of certain phospholipases, and to accelerate reabsorption of cerebral edema in various experimental models. Citicoline has also been shown to be able to inhibit mechanisms of apoptosis associated to cerebral ischemia and in certain neurodegeneration models, and to potentiate neuroplasticity mechanisms. Citicoline is a safe drug, as shown by the toxicological tests conducted, that has no significant systemic cholinergic effects and is a well tolerated product. (PMID: 17171187) [HMDB]. Citicoline is found in many foods, some of which are chives, black walnut, kohlrabi, and abiyuch. Citicoline is an essential intermediate in the biosynthetic pathway of structural phospholipids in cell membranes, particularly phosphatidylcholine. Once absorbed, citicoline is widely distributed throughout the body, crosses the blood-brain barrier and reaches the central nervous system (CNS), where it is incorporated into the membrane and microsomal phospholipid fraction. Citicoline activates biosynthesis of structural phospholipids of neuronal membranes, increases brain metabolism, and acts upon the levels of different neurotransmitters. Thus, citicoline has been experimentally shown to increase norepinephrine and dopamine levels in the CNS. Owing to these pharmacological mechanisms, citicoline has a neuroprotective effect in hypoxic and ischemic conditions, decreasing the volume of ischemic lesion, and also improves learning and memory performance in animal models of brain aging. In addition, citicoline has been shown to restore the activity of mitochondrial ATPase and membrane Na+/K+ATPase, to inhibit activation of certain phospholipases, and to accelerate reabsorption of cerebral edema in various experimental models. Citicoline has also been shown to be able to inhibit mechanisms of apoptosis associated to cerebral ischemia and in certain neurodegeneration models, and to potentiate neuroplasticity mechanisms. Citicoline is a safe drug, as shown by the toxicological tests conducted, that has no significant systemic cholinergic effects and is a well tolerated product. (PMID:17171187). N - Nervous system > N06 - Psychoanaleptics > N06B - Psychostimulants, agents used for adhd and nootropics D002491 - Central Nervous System Agents > D018697 - Nootropic Agents
(2R,3R,4S,7S)-7-(2-bromo-5-hydroxyphenyl)-3-[(3R,4R)-3,4-dihydroxypentanoyl]oxy-7-methoxy-2,4-dimethylheptanoate
4-Amino-1-{5-O-[hydroxy({hydroxy[2-(trimethylazaniumyl)ethoxy]phosphoryl}oxy)phosphoryl]pentofuranosyl}pyrimidin-2(1H)-one
C14H27N4O11P2+ (489.11515119999996)
(2S)-3-[3-[(4-Carbamimidoylbenzoyl)amino]propanoylamino]-2-[(4-ethylphenyl)sulfonylamino]propanoic acid
C22H27N5O6S (489.16819620000007)
4-[(2-bromophenoxy)methyl]-N-[4-[(3,5-dimethyl-1-pyrazolyl)methyl]phenyl]benzamide
4-[[3-[(4-Chlorophenyl)sulfonylamino]-2-quinoxalinyl]amino]-1-piperidinecarboxylic acid ethyl ester
C22H24ClN5O4S (489.1237454000001)
N-(3-hydroxyphenyl)-2-[[4-methyl-5-[4-(4-morpholinylsulfonyl)phenyl]-1,2,4-triazol-3-yl]thio]acetamide
3-[[4-(1-benzotriazolyl)-1-piperidinyl]sulfonyl]-N-cyclopentylbenzenesulfonamide
C22H27N5O4S2 (489.15043820000005)
4-[3-[(3-chloro-4-fluoroanilino)-oxomethyl]-7-oxo-1H-pyrazolo[1,5-a]pyrimidin-5-yl]-1-piperidinecarboxylic acid tert-butyl ester
1-[(4-chlorophenyl)-oxomethyl]-N-[4-(1-piperidinylsulfonyl)phenyl]-3-piperidinecarboxamide
C24H28ClN3O4S (489.1488958000001)
N-[[3-(4-carboxybutyl)-5-chloro-3,4-dihydro-8-hydroxy-1-oxo-1H-2-benzopyran-7-yl]carbonyl]-L-phenylalanine
(1R,9S,10S,11S)-5-(3-fluorophenyl)-10-(hydroxymethyl)-12-methylsulfonyl-11-(piperidine-1-carbonyl)-7,12-diazatricyclo[7.2.1.02,7]dodeca-2,4-dien-6-one
C24H28FN3O5S (489.17336100000006)
(1S,9R,10R,11R)-5-(3-fluorophenyl)-10-(hydroxymethyl)-12-methylsulfonyl-11-(piperidine-1-carbonyl)-7,12-diazatricyclo[7.2.1.02,7]dodeca-2,4-dien-6-one
C24H28FN3O5S (489.17336100000006)
4-fluoro-N-[(2R,3S,6R)-2-(hydroxymethyl)-6-[2-oxo-2-(4-phenyl-1-piperazinyl)ethyl]-3,6-dihydro-2H-pyran-3-yl]benzenesulfonamide
C24H28FN3O5S (489.17336100000006)
4-fluoro-N-[(2S,3S,6S)-2-(hydroxymethyl)-6-[2-oxo-2-(4-phenyl-1-piperazinyl)ethyl]-3,6-dihydro-2H-pyran-3-yl]benzenesulfonamide
C24H28FN3O5S (489.17336100000006)
[(3aR,4R,9bR)-1-(3-methoxyphenyl)sulfonyl-5-methyl-8-[2-(3-pyridinyl)ethynyl]-3,3a,4,9b-tetrahydro-2H-pyrrolo[3,2-c]quinolin-4-yl]methanol
C27H27N3O4S (489.1722182000001)
[(3aS,4S,9bS)-1-(3-methoxyphenyl)sulfonyl-5-methyl-8-[2-(3-pyridinyl)ethynyl]-3,3a,4,9b-tetrahydro-2H-pyrrolo[3,2-c]quinolin-4-yl]methanol
C27H27N3O4S (489.1722182000001)
(6R,7R,8R)-N-(2,5-difluorophenyl)-8-(hydroxymethyl)-2-oxo-7-[4-[(E)-2-phenylethenyl]phenyl]-1,4-diazabicyclo[4.2.0]octane-4-carboxamide
C28H25F2N3O3 (489.18638839999994)
(6S,7S,8S)-N-(2,5-difluorophenyl)-8-(hydroxymethyl)-2-oxo-7-[4-[(E)-2-phenylethenyl]phenyl]-1,4-diazabicyclo[4.2.0]octane-4-carboxamide
C28H25F2N3O3 (489.18638839999994)
N-[[(2R,3S)-8-[2-(3-fluorophenyl)ethynyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-pyrido[2,3-b][1,5]oxazocin-2-yl]methyl]-N-methylmethanesulfonamide
C24H28FN3O5S (489.17336100000006)
4-fluoro-N-[(2S,3R,6R)-2-(hydroxymethyl)-6-[2-oxo-2-(4-phenyl-1-piperazinyl)ethyl]-3,6-dihydro-2H-pyran-3-yl]benzenesulfonamide
C24H28FN3O5S (489.17336100000006)
4-fluoro-N-[(2R,3S,6S)-2-(hydroxymethyl)-6-[2-oxo-2-(4-phenyl-1-piperazinyl)ethyl]-3,6-dihydro-2H-pyran-3-yl]benzenesulfonamide
C24H28FN3O5S (489.17336100000006)
4-fluoro-N-[(2S,3R,6S)-2-(hydroxymethyl)-6-[2-oxo-2-(4-phenyl-1-piperazinyl)ethyl]-3,6-dihydro-2H-pyran-3-yl]benzenesulfonamide
C24H28FN3O5S (489.17336100000006)
4-fluoro-N-[(2S,3S,6R)-2-(hydroxymethyl)-6-[2-oxo-2-(4-phenyl-1-piperazinyl)ethyl]-3,6-dihydro-2H-pyran-3-yl]benzenesulfonamide
C24H28FN3O5S (489.17336100000006)
4-fluoro-N-[(2R,3R,6S)-2-(hydroxymethyl)-6-[2-oxo-2-(4-phenyl-1-piperazinyl)ethyl]-3,6-dihydro-2H-pyran-3-yl]benzenesulfonamide
C24H28FN3O5S (489.17336100000006)
4-fluoro-N-[(2R,3R,6R)-2-(hydroxymethyl)-6-[2-oxo-2-(4-phenyl-1-piperazinyl)ethyl]-3,6-dihydro-2H-pyran-3-yl]benzenesulfonamide
C24H28FN3O5S (489.17336100000006)
[(3aS,4R,9bS)-1-(3-methoxyphenyl)sulfonyl-5-methyl-8-[2-(3-pyridinyl)ethynyl]-3,3a,4,9b-tetrahydro-2H-pyrrolo[3,2-c]quinolin-4-yl]methanol
C27H27N3O4S (489.1722182000001)
(6R,7S,8S)-N-(2,5-difluorophenyl)-8-(hydroxymethyl)-2-oxo-7-[4-[(E)-2-phenylethenyl]phenyl]-1,4-diazabicyclo[4.2.0]octane-4-carboxamide
C28H25F2N3O3 (489.18638839999994)
(6S,7R,8R)-N-(2,5-difluorophenyl)-8-(hydroxymethyl)-2-oxo-7-[4-[(E)-2-phenylethenyl]phenyl]-1,4-diazabicyclo[4.2.0]octane-4-carboxamide
C28H25F2N3O3 (489.18638839999994)
[(2R,3S,4R,5R)-5-[2-amino-5-[[[(1S,4S,5R)-4,5-dihydroxycyclopent-2-en-1-yl]amino]methyl]-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-7-yl]-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
C17H24N5O10P (489.12607340000005)
JNJ-42226314
JNJ-42226314 is a competitive, highly selective and reversible non-covalent monoacylglycerol lipase (MAGL) inhibitor. JNJ-42226314 demonstrates dose-dependent enhancement of the major endocannabinoid 2-arachidonoylglycerol (2-AG) as well as efficacy in models of neuropathic and inflammatory pain[1].
3,4,5-trihydroxy-6-{[1,3,4,5-tetrahydroxy-1-(4-hydroxy-2-imino-1h-pteridin-6-yl)pentan-2-yl]oxy}oxane-2-carboxylic acid
methyl 4-[(7s)-7-(acetyloxy)-5-chloro-3-[(5s)-3,5-dimethylhepta-1,3-dien-1-yl]-7-methyl-6,8-dioxoisoquinolin-2-yl]butanoate
C26H32ClNO6 (489.19180420000004)
(2e)-3-(4-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-3-methoxyphenyl)-n-[2-(4-hydroxyphenyl)ethyl]prop-2-enimidic acid
C28H27NO7 (489.17874320000004)
Cytidine 5'-diphosphocholine sodium salt dihydrate
C14H27N4O11P2+ (489.11515119999996)
3-(4-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-3-methoxyphenyl)-n-[2-(4-hydroxyphenyl)ethyl]prop-2-enimidic acid
C28H27NO7 (489.17874320000004)
(2s,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[(1r,2s,3r,4r)-1,3,4,5-tetrahydroxy-1-(4-hydroxy-2-imino-1h-pteridin-6-yl)pentan-2-yl]oxy}oxane-2-carboxylic acid
10-(3-hydroxyphenyl)-19-azahexacyclo[20.2.2.1⁸,¹⁹.0²,⁷.0¹⁰,¹⁸.0¹¹,¹⁶]heptacosa-1(25),2,4,6,8(27),11,13,15,22(26),23-decaene-5,12,24-triol
C32H27NO4 (489.19399820000007)
(2z)-3-(4-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-3-methoxyphenyl)-n-[2-(4-hydroxyphenyl)ethyl]prop-2-enimidic acid
C28H27NO7 (489.17874320000004)
methyl 4-[(7r)-7-(acetyloxy)-5-chloro-3-[(5s)-3,5-dimethylhepta-1,3-dien-1-yl]-7-methyl-6,8-dioxoisoquinolin-2-yl]butanoate
C26H32ClNO6 (489.19180420000004)
2-(hydroxymethyl)-6-[(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}-1h-indol-3-yl)oxy]oxane-3,4,5-triol
C20H27NO11S (489.1304752000001)
2-({1-hydroxy-2-[(2r)-2-hydroxy-n-methyl-3-phenylpropanamido]ethylidene}amino)-n-[2-(methoxycarbonyl)phenyl]benzenecarboximidic acid
C27H27N3O6 (489.18997620000005)
(10s,18s)-10-(3-hydroxyphenyl)-19-azahexacyclo[20.2.2.1⁸,¹⁹.0²,⁷.0¹⁰,¹⁸.0¹¹,¹⁶]heptacosa-1(25),2,4,6,8(27),11,13,15,22(26),23-decaene-5,12,24-triol
C32H27NO4 (489.19399820000007)
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-[(2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}-1h-indol-3-yl)oxy]oxane-3,4,5-triol
C20H27NO11S (489.1304752000001)