Drug Information
Drug General Information | Top | |||
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Drug ID |
D0Z9JO
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Former ID |
DNC003169
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Drug Name |
Uridine-5'-Diphosphate-Mannose
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Synonyms |
URIDINE-5'-DIPHOSPHATE-MANNOSE; CHEMBL227711; UFM; UDP-Mannose; AC1L9MFS; SCHEMBL1520993; BDBM50209666; DB02421; URIDINE-5''-DIPHOSPHATE-MANNOSE; [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] hydrogen phosphate; [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl dihydrogen diphosphat
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C15H24N2O17P2
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Canonical SMILES |
C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OC3C(C(C(C(O3)CO)O)O)O)O)O
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InChI |
1S/C15H24N2O17P2/c18-3-5-8(20)10(22)12(24)14(32-5)33-36(28,29)34-35(26,27)30-4-6-9(21)11(23)13(31-6)17-2-1-7(19)16-15(17)25/h1-2,5-6,8-14,18,20-24H,3-4H2,(H,26,27)(H,28,29)(H,16,19,25)/t5-,6-,8-,9-,10+,11-,12+,13-,14-/m1/s1
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InChIKey |
HSCJRCZFDFQWRP-NYYOCOOHSA-N
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CAS Number |
CAS 16375-64-7
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PubChem Compound ID | ||||
PubChem Substance ID |
Target and Pathway | Top | |||
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Target(s) | UDP-glucose 4-epimerase (GALE) | Target Info | Inhibitor | [1] |
BioCyc | D-galactose degradation V (Leloir pathway) | |||
UDP-N-acetyl-D-galactosamine biosynthesis I | ||||
UDP-N-acetyl-D-galactosamine biosynthesis II | ||||
KEGG Pathway | Galactose metabolism | |||
Amino sugar and nucleotide sugar metabolism | ||||
Metabolic pathways | ||||
NetPath Pathway | IL2 Signaling Pathway | |||
Panther Pathway | Fructose galactose metabolism | |||
Pathwhiz Pathway | Nucleotide Sugars Metabolism | |||
Galactose Metabolism | ||||
WikiPathways | Metabolism of carbohydrates |
References | Top | |||
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REF 1 | How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6. |
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