Exact Mass: 503.2075
Exact Mass Matches: 503.2075
Found 237 metabolites which its exact mass value is equals to given mass value 503.2075
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 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
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].
(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
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
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Cys Glu Pro Arg
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Cys Arg Pro Glu
Asp Asn Gln Gln
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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
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Gly His Gln Tyr
Gly His Tyr Gln
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Gly Gln Tyr His
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Gly Tyr Gln His
His Ala Asn Tyr
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Met Gln Pro Glu
Asn Ala His Tyr
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Asn Asn Glu Gln
Asn Asn Gln Glu
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Asn Gln Asp Gln
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Asn Gln Gly Trp
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Asn Ser Phe His
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Pro Cys Glu Arg
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Pro Glu Met Gln
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Pro Met Gln Glu
Pro Gln Glu Met
Pro Gln Met Glu
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Gln Asp Asn Gln
Gln Asp Gln Asn
Gln Glu Met Pro
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Gln Glu Pro Met
Gln Gly His Tyr
Gln Gly Asn Trp
Gln Gly Trp Asn
Gln Gly Tyr His
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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
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Ser Phe His Asn
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Trp Gly Asn Gln
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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].