Drug Information
| Drug General Information | |||||
|---|---|---|---|---|---|
| Drug ID |
D08RNW
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| Former ID |
DNC011881
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| Drug Name |
2-Hydroxy-2-phenyl-nonanoic acid amide
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent | Investigative | [1] | ||
| Structure |
|
Download2D MOL |
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| Formula |
C15H23NO2
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| Canonical SMILES |
CCCCCCCC(C1=CC=CC=C1)(C(=O)N)O
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| InChI |
1S/C15H23NO2/c1-2-3-4-5-9-12-15(18,14(16)17)13-10-7-6-8-11-13/h6-8,10-11,18H,2-5,9,12H2,1H3,(H2,16,17)
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| InChIKey |
FXKCDILPUXRDAT-UHFFFAOYSA-N
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| PubChem Compound ID | |||||
| Target and Pathway | |||||
| Target(s) | Voltage-gated sodium channel subunit alpha Nav1.3 | Target Info | Inhibitor | [1] | |
| Sodium channel | Target Info | Inhibitor | [1] | ||
| KEGG Pathway | Dopaminergic synapse | ||||
| Reactome | Interaction between L1 and AnkyrinsR-HSA-445095:Interaction between L1 and Ankyrins | ||||
| References | |||||
| REF 1 | J Med Chem. 1999 May 6;42(9):1537-45.Comparative molecular field analysis of hydantoin binding to the neuronal voltage-dependent sodium channel. | ||||
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