Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0B3GP
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| Former ID |
DNC010182
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| Drug Name |
6-amino-N-(2,4-dichlorobenzyl)nicotinamide
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| Synonyms |
CHEMBL567109; 6-amino-N-(2,4-dichlorobenzyl)nicotinamide
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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 |
C13H11Cl2N3O
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| Canonical SMILES |
C1=CC(=C(C=C1Cl)Cl)CNC(=O)C2=CN=C(C=C2)N
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| InChI |
1S/C13H11Cl2N3O/c14-10-3-1-8(11(15)5-10)6-18-13(19)9-2-4-12(16)17-7-9/h1-5,7H,6H2,(H2,16,17)(H,18,19)
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| InChIKey |
PWGDOYQXBPVPGB-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Soluble epoxide hydrolase (EPHX2) | Target Info | Inhibitor | [1] |
| KEGG Pathway | Arachidonic acid metabolism | |||
| Metabolic pathways | ||||
| Peroxisome | ||||
| Pathwhiz Pathway | Arachidonic Acid Metabolism | |||
| WikiPathways | Metapathway biotransformation | |||
| Arachidonate Epoxygenase / Epoxide Hydrolase | ||||
| Arachidonic acid metabolism | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Design and synthesis of substituted nicotinamides as inhibitors of soluble epoxide hydrolase. Bioorg Med Chem Lett. 2009 Oct 15;19(20):5864-8. | |||
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