Drug Information
Drug General Information | Top | |||
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Drug ID |
D08NRK
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Former ID |
DNC000502
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Drug Name |
Cyclopropyl
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Synonyms |
Cyclopropyl; Cyclopropyl radical; cyclopropan-1-yl; 2417-82-5; AC1L3VZL; AC1Q1GU5; DTXSID30178882; 16084-EP2281563A1; 16084-EP2275401A1; 16084-EP2316459A1
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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 |
C3H5
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Canonical SMILES |
C1C[CH]1
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InChI |
1S/C3H5/c1-2-3-1/h1H,2-3H2
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InChIKey |
XIPUIGPNIDKXJU-UHFFFAOYSA-N
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CAS Number |
CAS 2417-82-5
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PubChem Compound ID | ||||
PubChem Substance ID |
Target and Pathway | Top | |||
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Target(s) | Entamoeba Alcohol dehydrogenase 2 (Entamo ADH2) | Target Info | Inhibitor | [1] |
BioCyc | Superpathway of tryptophan utilization | |||
Tryptophan degradation via tryptamine | ||||
KEGG Pathway | Glycolysis / Gluconeogenesis | |||
Pentose and glucuronate interconversions | ||||
Glycerolipid metabolism | ||||
Metabolic pathways | ||||
Biosynthesis of antibiotics | ||||
Degradation of aromatic compounds | ||||
WikiPathways | Metapathway biotransformation | |||
Benzo(a)pyrene metabolism |
References | Top | |||
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REF 1 | Entamoeba histolytica alcohol dehydrogenase 2 (EhADH2) as a target for anti-amoebic agents. J Antimicrob Chemother. 2004 Jul;54(1):56-9. |
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