Exact Mass: 503.1692
Exact Mass Matches: 503.1692
Found 316 metabolites which its exact mass value is equals to given mass value 503.1692
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
methyl (1S,2S,3R,5S,8R,9R,10R)-10-[(2R,3E,5E,7E)-7-(2,4-dioxopyrrolidin-3-ylidene)-7-hydroxy-4-methylhepta-3,5-dien-2-yl]-3,5,9-trimethyl-7-oxo-4,11,12-trioxatricyclo[6.3.1.01,5]dodecane-2-carboxylate
[(2S,3S,4S)-4,6-Diamino-3-hydroxy-1-[[(1S)-1-[(3S)-8-hydroxy-1-oxo-3,4-dihydroisochromen-3-yl]-3-methylbutyl]amino]-1,6-dioxohexan-2-yl] dihydrogen phosphate
Gravacridonediol glucoside
Gravacridonediol glucoside is found in herbs and spices. Gravacridonediol glucoside is an alkaloid from Ruta graveolens (rue
beta-D-Galactopyranosyl-(1->4)-2-amino-2-deoxy-beta-D-glucopyranosyl-(1->6)-D-mannose
beta-D-Galactopyranosyl-(1->4)-2-amino-2-deoxy-beta-D-glucopyranosyl-(1->6)-D-mannose is a constituent of blood group substance of human milk. Constituent of blood group substance of human milk
N-(4-Acetylphenyl)-2-[4-(2,6-dioxo-1,3-dipropyl-7H-purin-8-yl)phenoxy]acetamide
D018377 - Neurotransmitter Agents > D058905 - Purinergic Agents > D058914 - Purinergic Antagonists MRS-1706 is a potent and selective adenosine A2B receptor inverse agonist. MRS-1706 has Ki values of 1.39, 112, 157, and 230 nM for human A2B, A2A, A1 and A3 receptors respectively. MRS-1706 blocks adenosine-mediated cAMP induction[1][2].
Naloxone-3-glucuronide
(3aS)-5c-[(1R,2E,4E)-6-((E)-2,4-dioxo-pyrrolidin-3-ylidene)-6-hydroxy-1,3-dimethyl-hexa-2,4-dienyl]-2c,6t,9a-trimethyl-8-oxo-(9at)-octahydro-3ar,7c-epioxido-furo[3,2-b]oxocine-3c-carboxylic acid methyl ester|antibiotic Bu-2313-B|nocamycin-I
{(2R)-2-[alpha-D-glucopyranosyl(1->6)beta-D-glucopyranosyloxy]-2-(3-hydroxy-4-methoxyphenyl)}acetonitrile
Nocamycin I
An organic heterotricyclic compound and tetramic acid derivative originally isolated from an unidentified oligosporic actinomycete strain (no. E864-861) and found to be active against both Gram-positive and Gram-negative anaerobic bacteria as well as some aerobic bacteria such as Streptococci. The methyl ester of nocamycin E.
Ala His Asn Tyr
Ala His Tyr Asn
Ala Asn His Tyr
Ala Asn Asn Trp
Ala Asn Trp Asn
Ala Asn Tyr His
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Ala Tyr His Asn
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Cys Glu Pro Arg
Cys Glu Arg Pro
Cys His Met Asn
Cys His Asn Met
Cys Met His Asn
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Cys Pro Glu Arg
Cys Pro Arg Glu
Cys Arg Glu Pro
Cys Arg Pro Glu
Asp Asn Gln Gln
Asp Pro Ser Trp
Asp Pro Trp Ser
Asp Gln Asn Gln
Asp Gln Gln Asn
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Asp Trp Ser Pro
Glu Cys Pro Arg
Glu Cys Arg Pro
Glu Met Pro Gln
Glu Met Gln Pro
Glu Asn Asn Gln
Glu Asn Gln Asn
Glu Pro Cys Arg
Glu Pro Met Gln
Glu Pro Gln Met
Glu Pro Arg Cys
Glu Gln Met Pro
Glu Gln Asn Asn
Glu Gln Pro Met
Glu Arg Cys Pro
Glu Arg Pro Cys
Phe His Asn Ser
Phe His Ser Asn
Phe Asn His Ser
Phe Asn Ser His
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Phe Ser Asn His
Gly His Gln Tyr
Gly His Tyr Gln
Gly Asn Gln Trp
Gly Asn Trp Gln
Gly Gln His Tyr
Gly Gln Asn Trp
Gly Gln Trp Asn
Gly Gln Tyr His
Gly Trp Asn Gln
Gly Trp Gln Asn
Gly Tyr His Gln
Gly Tyr Gln His
His Ala Asn Tyr
His Ala Tyr Asn
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His Phe Asn Ser
His Phe Ser Asn
His Gly Gln Tyr
His Gly Tyr Gln
His Met Cys Asn
His Met Asn Cys
His Asn Ala Tyr
His Asn Cys Met
His Asn Phe Ser
His Asn Met Cys
His Asn Ser Phe
His Asn Tyr Ala
His Gln Gly Tyr
His Gln Tyr Gly
His Ser Phe Asn
His Ser Asn Phe
His Tyr Ala Asn
His Tyr Gly Gln
His Tyr Asn Ala
His Tyr Gln Gly
Met Cys His Asn
Met Cys Asn His
Met Glu Pro Gln
Met Glu Gln Pro
Met His Cys Asn
Met His Asn Cys
Met Asn Cys His
Met Asn His Cys
Met Pro Glu Gln
Met Pro Gln Glu
Met Gln Glu Pro
Met Gln Pro Glu
Asn Ala His Tyr
Asn Ala Asn Trp
Asn Ala Trp Asn
Asn Ala Tyr His
Asn Cys His Met
Asn Cys Met His
Asn Asp Gln Gln
Asn Glu Asn Gln
Asn Glu Gln Asn
Asn Phe His Ser
Asn Phe Ser His
Asn Gly Gln Trp
Asn Gly Trp Gln
Asn His Ala Tyr
Asn His Cys Met
Asn His Phe Ser
Asn His Met Cys
Asn His Ser Phe
Asn His Tyr Ala
Asn Met Cys His
Asn Met His Cys
Asn Asn Ala Trp
Asn Asn Glu Gln
Asn Asn Gln Glu
Asn Asn Trp Ala
Asn Gln Asp Gln
Asn Gln Glu Asn
Asn Gln Gly Trp
Asn Gln Asn Glu
Asn Gln Gln Asp
Asn Gln Trp Gly
Asn Ser Phe His
Asn Ser His Phe
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Asn Trp Gly Gln
Asn Trp Asn Ala
Asn Trp Gln Gly
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Asn Tyr His Ala
Pro Cys Glu Arg
Pro Cys Arg Glu
Pro Asp Ser Trp
Pro Asp Trp Ser
Pro Glu Cys Arg
Pro Glu Met Gln
Pro Glu Gln Met
Pro Glu Arg Cys
Pro Met Glu Gln
Pro Met Gln Glu
Pro Gln Glu Met
Pro Gln Met Glu
Pro Arg Cys Glu
Pro Arg Glu Cys
Pro Ser Asp Trp
Pro Ser Trp Asp
Pro Trp Asp Ser
Pro Trp Ser Asp
Gln Asp Asn Gln
Gln Asp Gln Asn
Gln Glu Met Pro
Gln Glu Asn Asn
Gln Glu Pro Met
Gln Gly His Tyr
Gln Gly Asn Trp
Gln Gly Trp Asn
Gln Gly Tyr His
Gln His Gly Tyr
Gln His Tyr Gly
Gln Met Glu Pro
Gln Met Pro Glu
Gln Asn Asp Gln
Gln Asn Glu Asn
Gln Asn Gly Trp
Gln Asn Asn Glu
Gln Asn Gln Asp
Gln Asn Trp Gly
Gln Pro Glu Met
Gln Pro Met Glu
Gln Gln Asp Asn
Gln Gln Asn Asp
Gln Trp Gly Asn
Gln Trp Asn Gly
Gln Tyr Gly His
Gln Tyr His Gly
Arg Cys Glu Pro
Arg Cys Pro Glu
Arg Glu Cys Pro
Arg Glu Pro Cys
Arg Pro Cys Glu
Arg Pro Glu Cys
Ser Asp Pro Trp
Ser Asp Trp Pro
Ser Phe His Asn
Ser Phe Asn His
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Ser His Asn Phe
Ser Asn Phe His
Ser Asn His Phe
Ser Pro Asp Trp
Ser Pro Trp Asp
Ser Trp Asp Pro
Ser Trp Pro Asp
Trp Ala Asn Asn
Trp Asp Pro Ser
Trp Asp Ser Pro
Trp Gly Asn Gln
Trp Gly Gln Asn
Trp Asn Ala Asn
Trp Asn Gly Gln
Trp Asn Asn Ala
Trp Asn Gln Gly
Trp Pro Asp Ser
Trp Pro Ser Asp
Trp Gln Gly Asn
Trp Gln Asn Gly
Trp Ser Asp Pro
Trp Ser Pro Asp
Tyr Ala His Asn
Tyr Ala Asn His
Tyr Gly His Gln
Tyr Gly Gln His
Tyr His Ala Asn
Tyr His Gly Gln
Tyr His Asn Ala
Tyr His Gln Gly
Tyr Asn Ala His
Tyr Asn His Ala
Tyr Gln Gly His
Tyr Gln His Gly
Gravacridonediol glucoside
beta-D-Galactopyranosyl-(1->4)-2-amino-2-deoxy-beta-D-glucopyranosyl-(1->6)-D-mannose
Rosuvastatin calcium
Rosuvastatin Sodium is a competitive HMG-CoA reductase (HMGCR) inhibitor, with an IC50 of 11 nM. Rosuvastatin Sodium potently blocks hERG current with an IC50 of 195 nM[2]. Rosuvastatin Sodium reduces the expression of the mature hERG and the interaction of heat shock protein 70 (Hsp70) with the hERG protein. Rosuvastatin Sodium effectively lowers low-density lipoprotein (LDL) cholesterol, triglycerides, and C-reactive protein levels[1][2][3].
4-methoxyphenyl 4,6-o-benzylidene-2-deoxy-2-phthalimido-beta-d-glucopyranoside
1-Decyl-3-Methylimidazolium Bis(Trifluoromethylsulfonyl)Imide
Trimebutine Maleate
D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D010276 - Parasympatholytics D005765 - Gastrointestinal Agents Trimebutine maleate is an orally anti-tumor agent. Trimebutine maleate selectively suppresses stemness and proliferation of ovarian cancer stem cells (CSCs). Trimebutine maleate reduces the colonic muscle hypercontractility, modulates gastrointestinal motility, induces apoptosis and can be used for the research of glioma/glioblastoma and irritable bowel syndrome[1][2][3][4][5][6].
5,5,5′,5′,5′′,5′′-Hexamethyltris(1,2,3-Dioxaphosphorinanemethan)-Amin 2,2′,2′′-Trioxid
((hydroxy((2-(6-pivalaMido-9H-purin-9-yl)ethoxy)Methyl)phosphoryl)oxy)Methyl pivalate
4-Methylphenyl 2-O-(phenylmethyl)-1-thio-beta-D-galactopyranoside triacetate
4-methyl-3-(1-methyl-6-(pyridin-3-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino)-N-(3-(trifluoromethyl)phenyl)benzamide
3-(1h-Indol-3-yl)-2-[4-(4-phenyl-piperidin-1-yl)-benzenesulfonylamino]-propionic acid
methyl (3R,5S,9R,10R)-10-[(2R,3E,5E,7Z)-7-(2,4-dioxopyrrolidin-3-ylidene)-7-hydroxy-4-methylhepta-3,5-dien-2-yl]-3,5,9-trimethyl-7-oxo-4,11,12-trioxatricyclo[6.3.1.01,5]dodecane-2-carboxylate
3-L-arginyl-AMP
An L-arginyl ester obtained by formal condensation of the carboxy group of L-arginine with the 3-hydroxy group of AMP.
(1R)-N-(3,5-dimethyl-4-isoxazolyl)-1-ethylsulfonyl-1-(hydroxymethyl)-7-methoxy-2-spiro[3,9-dihydro-1H-pyrido[3,4-b]indole-4,3-azetidine]carboxamide
N-[(1S,3S,4aS,9aR)-1-(hydroxymethyl)-3-[2-[(2-methoxyphenyl)methylamino]-2-oxoethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-3-pyridinecarboxamide
N-[(1S,3R,4aS,9aR)-1-(hydroxymethyl)-3-[2-[(2-methoxyphenyl)methylamino]-2-oxoethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b][1]benzofuran-6-yl]pyridine-3-carboxamide
N-[(1S,3S,4aR,9aS)-1-(hydroxymethyl)-3-[2-[(2-methoxyphenyl)methylamino]-2-oxoethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b][1]benzofuran-6-yl]pyridine-3-carboxamide
N-[(1R,3S,4aS,9aR)-1-(hydroxymethyl)-3-[2-[(2-methoxyphenyl)methylamino]-2-oxoethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b][1]benzofuran-6-yl]pyridine-3-carboxamide
N-[(1S,3R,4aR,9aS)-1-(hydroxymethyl)-3-[2-[(2-methoxyphenyl)methylamino]-2-oxoethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-3-pyridinecarboxamide
2-[(2R,4aS,12aS)-8-(methanesulfonamido)-5-methyl-6-oxo-2,3,4,4a,12,12a-hexahydropyrano[2,3-c][1,5]benzoxazocin-2-yl]-N-(2-methoxyphenyl)acetamide
N-[(2S,3R)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-[[methyl(methylsulfonyl)amino]methyl]-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-8-yl]-2-phenylacetamide
N-[(2S,3S)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-[[methyl(methylsulfonyl)amino]methyl]-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-8-yl]-2-phenylacetamide
N-[(1R,3S,4aR,9aS)-1-(hydroxymethyl)-3-[2-[(2-methoxyphenyl)methylamino]-2-oxoethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-3-pyridinecarboxamide
N-[(1R,3R,4aS,9aR)-1-(hydroxymethyl)-3-[2-[(2-methoxyphenyl)methylamino]-2-oxoethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-3-pyridinecarboxamide
2-[(3S,6aR,8S,10aR)-1-(4-chlorophenyl)sulfonyl-3-hydroxy-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocin-8-yl]-N-[3-(dimethylamino)propyl]acetamide
[(1S)-2-[(3-chlorophenyl)methyl]-1-ethylsulfonyl-7-methoxy-9-methyl-1-spiro[1,3-dihydropyrido[3,4-b]indole-4,3-azetidine]yl]methanol
N-[(2S,3S)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-[[methyl(methylsulfonyl)amino]methyl]-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-8-yl]-2-phenylacetamide
N-[(2S,3R)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-[[methyl(methylsulfonyl)amino]methyl]-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-8-yl]-2-phenylacetamide
N-[(1R,3R,4aR,9aS)-1-(hydroxymethyl)-3-[2-[(2-methoxyphenyl)methylamino]-2-oxoethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-3-pyridinecarboxamide
2-[(3R,6aR,8S,10aR)-1-(4-chlorophenyl)sulfonyl-3-hydroxy-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocin-8-yl]-N-[3-(dimethylamino)propyl]acetamide
[(1R)-2-[(3-chlorophenyl)methyl]-1-ethylsulfonyl-7-methoxy-9-methyl-1-spiro[1,3-dihydropyrido[3,4-b]indole-4,3-azetidine]yl]methanol
(1S)-N-(3,5-dimethyl-4-isoxazolyl)-1-ethylsulfonyl-1-(hydroxymethyl)-7-methoxy-2-spiro[3,9-dihydro-1H-pyrido[3,4-b]indole-4,3-azetidine]carboxamide
4-[7-[Ethyl(5-carboxypentyl)amino]-2-oxo-2H-1-benzopyran-3-yl]-1-(3-sulfonatopropyl)pyridinium
YH239-EE
YH239-EE, ethyl ester of the free carboxylic acid compound YH239, is a potent p53-MDM2 antagonizing and apoptosis-inducing agent. IC50 value: Target: MDM2/p53 YH239-EE inhibits the growth of OCI-AML-3 cells with wild type p53 by inhibiting the p53-MDM2 interaction. YH239-EE induces cell cycle arrest and causes potent cell apoptosis via activation of p53 and downstream targets in four AML cells (OCI-AML-3 and MOLM-13 with wt p53, NB4 with p53 mutation, and HL60 with p53 deletion).