Drug Information
Drug General Information | Top | |||
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Drug ID |
D06UGK
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Former ID |
DNC002544
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Drug Name |
Uridine-Diphosphate-N-Acetylgalactosamine
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Synonyms |
UDP-N-acetyl-D-galactosamine; uridine 5'-[3-(2-acetamido-2-deoxy-D-galactopyranosyl) dihydrogen diphosphate]; Uridine 5'-(trihydrogen diphosphate), P'-(2-(acetylamino)-2-deoxy-alpha-D-galactopyranosyl) ester; AC1O4WBS; CHEBI:16650; [(3R,4R,5R,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate
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Drug Type |
Small molecular drug
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Structure |
Download2D MOL |
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Formula |
C17H27N3O17P2
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Canonical SMILES |
CC(=O)NC1C(C(C(OC1OP(=O)(O)OP(=O)(O)OCC2C(C(C(O2)N3C=CC(=O)NC3=O)O)O)CO)O)O
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InChI |
1S/C17H27N3O17P2/c1-6(22)18-10-13(26)11(24)7(4-21)35-16(10)36-39(31,32)37-38(29,30)33-5-8-12(25)14(27)15(34-8)20-3-2-9(23)19-17(20)28/h2-3,7-8,10-16,21,24-27H,4-5H2,1H3,(H,18,22)(H,29,30)(H,31,32)(H,19,23,28)/t7-,8-,10-,11+,12-,13-,14-,15-,16-/m1/s1
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InChIKey |
LFTYTUAZOPRMMI-NESSUJCYSA-N
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CAS Number |
CAS 7277-98-7
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PubChem Compound ID | ||||
PubChem Substance ID | ||||
ChEBI ID |
CHEBI:67168
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Target and Pathway | Top | |||
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Target(s) | Bacterial Glycosyltransferase MurG (Bact murG) | Target Info | Inhibitor | [1] |
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 | Peptidoglycan biosynthesis | |||
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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