Drug Information
Drug General Information | Top | |||
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Drug ID |
D01PSS
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Former ID |
DNC002972
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Drug Name |
Deoxyuridine-5'-Triphosphate
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Synonyms |
dUTP; Deoxyuridine triphosphate; deoxy-UTP; DEOXYURIDINE-5'-TRIPHOSPHATE; 2'-Deoxyuridine 5'-triphosphate; Deoxyuridine 5'-triphosphate; 2'-deoxy-UTP; 2'-Deoxyuracil 5'-triphosphate; 1173-82-6; 102814-08-4; CHEMBL374361; CHEBI:17625; N(4)-Methoxydeoxycytidine triphosphate; 2'-deoxyuridine 5'-(tetrahydrogen triphosphate); Uridine 5'-(tetrahydrogen triphosphate), 2'-deoxy-; 2'-Deoxyuridine-5'-triphosphate trisodium salt; [[(2R,3S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl] phosp
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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 |
C9H15N2O14P3
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Canonical SMILES |
C1C(C(OC1N2C=CC(=O)NC2=O)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O
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InChI |
1S/C9H15N2O14P3/c12-5-3-8(11-2-1-7(13)10-9(11)14)23-6(5)4-22-27(18,19)25-28(20,21)24-26(15,16)17/h1-2,5-6,8,12H,3-4H2,(H,18,19)(H,20,21)(H,10,13,14)(H2,15,16,17)/t5-,6+,8+/m0/s1
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InChIKey |
AHCYMLUZIRLXAA-SHYZEUOFSA-N
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CAS Number |
CAS 1173-82-6
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PubChem Compound ID | ||||
PubChem Substance ID |
3744, 583870, 621212, 838635, 841374, 7887228, 8017226, 8019733, 8144074, 8189485, 14858482, 24277306, 29211984, 43121910, 57315284, 76309464, 81065683, 103509228, 104332788, 126523870, 126664447, 127334184, 127334185, 127406060, 135021810, 135102503, 135242350, 144187016, 144187213, 144235010, 152198982, 160655027, 164797312, 164797314, 211786605, 223653187, 223953725, 226399282, 242659242, 252225432, 252400708
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ChEBI ID |
CHEBI:17625
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Target and Pathway | Top | |||
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Target(s) | Bacterial Deoxyuridine triphosphate nucleotidohydrolase (Bact dut) | Target Info | Inhibitor | [1] |
Panther Pathway | De novo pyrimidine deoxyribonucleotide biosynthesis |
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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