Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D07ETF
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| Former ID |
DNC003988
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| Drug Name |
3-(1-Methyl-piperidin-3-yl)-2-phenyl-1H-indole
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| Synonyms |
CHEMBL43819; 3-(1-Methyl-piperidin-3-yl)-2-phenyl-1H-indole; SCHEMBL8525408; BDBM50099264; 3-(1-methylpiperidin-3-yl)-2-phenyl-1H-indole
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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 |
C20H22N2
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| Canonical SMILES |
CN1CCCC(C1)C2=C(NC3=CC=CC=C32)C4=CC=CC=C4
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| InChI |
1S/C20H22N2/c1-22-13-7-10-16(14-22)19-17-11-5-6-12-18(17)21-20(19)15-8-3-2-4-9-15/h2-6,8-9,11-12,16,21H,7,10,13-14H2,1H3
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| InChIKey |
JRFXDRYERZNJFJ-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Voltage-gated potassium channel Kv11.1 (KCNH2) | Target Info | Inhibitor | [1] |
| Pathwhiz Pathway | Muscle/Heart Contraction | |||
| Reactome | Voltage gated Potassium channels | |||
| WikiPathways | SIDS Susceptibility Pathways | |||
| Hematopoietic Stem Cell Differentiation | ||||
| Potassium Channels | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | 3-(4-Fluoropiperidin-3-yl)-2-phenylindoles as high affinity, selective, and orally bioavailable h5-HT(2A) receptor antagonists. J Med Chem. 2001 May 10;44(10):1603-14. | |||
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