Drug Information
Drug General Information | Top | |||
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Drug ID |
D0IZ1A
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Former ID |
DNC000905
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Drug Name |
LY309887
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Drug Type |
Small molecular drug
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Indication | Solid tumour/cancer [ICD-11: 2A00-2F9Z; ICD-10: C76-C80; ICD-9: 140-229] | Phase 1 | [1] | |
Structure |
Download2D MOL |
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Formula |
C19H23N5O6S
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Canonical SMILES |
C1C(CNC2=C1C(=O)NC(=N2)N)CCC3=CC=C(S3)C(=O)NC(CCC(=O)O)C(=O)O
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InChI |
1S/C19H23N5O6S/c20-19-23-15-11(16(27)24-19)7-9(8-21-15)1-2-10-3-5-13(31-10)17(28)22-12(18(29)30)4-6-14(25)26/h3,5,9,12H,1-2,4,6-8H2,(H,22,28)(H,25,26)(H,29,30)(H4,20,21,23,24,27)/t9-,12+/m1/s1
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InChIKey |
GQCXGHHHNACOGE-SKDRFNHKSA-N
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CAS Number |
CAS 127228-54-0
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PubChem Compound ID | ||||
PubChem Substance ID |
Target and Pathway | Top | |||
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Target(s) | Glycinamide ribonucleotide formyltransferase (GART) | Target Info | Inhibitor | [2], [3] |
BioCyc | Purine nucleotides de novo biosynthesis | |||
5-aminoimidazole ribonucleotide biosynthesis | ||||
Tetrahydrofolate salvage from 5,10-methenyltetrahydrofolate | ||||
KEGG Pathway | Purine metabolism | |||
One carbon pool by folate | ||||
Metabolic pathways | ||||
Biosynthesis of antibiotics | ||||
NetPath Pathway | TCR Signaling Pathway | |||
Panther Pathway | De novo purine biosynthesis | |||
Pathwhiz Pathway | Purine Metabolism | |||
Reactome | Purine ribonucleoside monophosphate biosynthesis | |||
WikiPathways | One Carbon Metabolism | |||
Metabolism of nucleotides | ||||
Folate Metabolism |
References | Top | |||
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REF 1 | Phase I and pharmacokinetic study of LY309887: a specific inhibitor of purine biosynthesis. Cancer Chemother Pharmacol. 2001 Jun;47(6):525-31. | |||
REF 2 | New antimetabolites in cancer chemotherapy and their clinical impact. Br J Cancer. 1998;78 Suppl 3:1-7. | |||
REF 3 | Cellular pharmacology of MTA: a correlation of MTA-induced cellular toxicity and in vitro enzyme inhibition with its effect on intracellular folate and nucleoside triphosphate pools in CCRF-CEM cells. Semin Oncol. 1999 Apr;26(2 Suppl 6):48-54. |
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