Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0Z9TM
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| Former ID |
DNC002971
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| Drug Name |
2'-Deoxyuridine 5'-Alpha,Beta-Imido-Triphosphate
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| Synonyms |
2'-DEOXYURIDINE 5'-ALPHA,BETA-IMIDO-TRIPHOSPHATE; CHEMBL1232397; DUP; alpha,beta-Imino-dUTP; AC1L9LWH; BDBM50386619; DB01965; 2'-deoxy-5'-O-[(S)-hydroxy{[(R)-hydroxy(phosphonooxy)phosphoryl]amino}phosphoryl]uridine; [(2R,3S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-hydroxyoxolan-2-yl]methoxy-N-[hydroxy(phosphonooxy)phosphoryl]phosphonamidic acid
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C9H16N3O13P3
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| Canonical SMILES |
C1C(C(OC1N2C=CC(=O)NC2=O)COP(=O)(NP(=O)(O)OP(=O)(O)O)O)O
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| InChI |
1S/C9H16N3O13P3/c13-5-3-8(12-2-1-7(14)10-9(12)15)24-6(5)4-23-26(16,17)11-27(18,19)25-28(20,21)22/h1-2,5-6,8,13H,3-4H2,(H,10,14,15)(H2,20,21,22)(H3,11,16,17,18,19)/t5-,6+,8+/m0/s1
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| InChIKey |
XZLLMTSKYYYJLH-SHYZEUOFSA-N
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| PubChem Compound ID | ||||
| PubChem Substance ID |
583746, 583748, 832523, 7887226, 8027805, 17422139, 24423623, 24697999, 24771153, 26715958, 36890251, 49737983, 50086966, 53812495, 78398328, 85747847, 85747905, 85747909, 99226729, 99226860, 99432267, 104248575, 104639365, 109816975, 113584931, 125264748, 125299908, 125310691, 125310975, 125310976, 125310979, 125310981, 125311010, 125311013, 125311076, 125311084, 125311088, 125311091, 125311095, 135642792, 152256036, 160649996, 160661246, 160779668, 160865702, 162108286, 162108289, 162108292, 162108299, 162108302
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| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Bacterial Deoxyuridine triphosphate nucleotidohydrolase (Bact dut) | Target Info | Inhibitor | [1] |
| Panther Pathway | De novo pyrimidine deoxyribonucleotide biosynthesis | |||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6. | |||
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