Drug Information
Drug General Information | Top | |||
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Drug ID |
D0D9OC
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Former ID |
DNC007394
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Drug Name |
2-chloro-6(methylamino)purine
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Synonyms |
2-Chloro-6(methylamino)purine; 82499-02-3; 2-CHLORO-N-METHYL-9H-PURIN-6-AMINE; 2-chloro-N-methyl-7H-purin-6-amine; CHEMBL446449; 2-Chloro-6-(methylamino)purine; 2-CHLORO-6-(N-METHYLAMINO)-9H-PURINE; ACMC-20anyt; PubChem9784; 2-chloro-6-methylaminopurine; SCHEMBL130696; AC1NE105; CTK5E9746; DTXSID00404544; RIAVUEFUPHOGJY-UHFFFAOYSA-N; 2-Chloro-6-methylamino-9H-purine; NSC15416; ZINC4429067; NSC-15416; BDBM50208873; AKOS006283488; AKOS015894684; 2-Chloro-6(methylamino)purine, 97%; AB44277; TC-170732
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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 |
C6H6ClN5
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Canonical SMILES |
CNC1=NC(=NC2=C1NC=N2)Cl
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InChI |
1S/C6H6ClN5/c1-8-4-3-5(10-2-9-3)12-6(7)11-4/h2H,1H3,(H2,8,9,10,11,12)
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InChIKey |
RIAVUEFUPHOGJY-UHFFFAOYSA-N
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CAS Number |
CAS 82499-02-3
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Xanthine dehydrogenase/oxidase (XDH) | Target Info | Inhibitor | [1] |
BioCyc | Purine nucleotides degradation | |||
Urate biosynthesis/inosine 5'-phosphate degradation | ||||
Guanosine nucleotides degradation | ||||
Adenosine nucleotides degradation | ||||
Retinoate biosynthesis II | ||||
KEGG Pathway | Purine metabolism | |||
Caffeine metabolism | ||||
Drug metabolism - other enzymes | ||||
Metabolic pathways | ||||
Peroxisome | ||||
Panther Pathway | Adenine and hypoxanthine salvage pathway | |||
Purine metabolism | ||||
Pathwhiz Pathway | Caffeine Metabolism | |||
Purine Metabolism | ||||
Reactome | Purine catabolism | |||
WikiPathways | Oxidative Stress | |||
Effects of Nitric Oxide | ||||
Metabolism of nucleotides | ||||
Selenium Micronutrient Network |
References | Top | |||
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REF 1 | The screening and characterization of 6-aminopurine-based xanthine oxidase inhibitors. Bioorg Med Chem. 2007 May 15;15(10):3450-6. |
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