Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0RC9T
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| Former ID |
DNC003992
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| Drug Name |
2-Phenyl-3-piperidin-3-yl-1H-indole
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| Synonyms |
CHEMBL42557; 2-Phenyl-3-piperidin-3-yl-1H-indole; 2-phenyl-3-(3-piperidinyl)-1H-Indole; SCHEMBL8525019; BDBM50099262; AKOS022450446; 3-(3-Piperidinyl)-2-phenyl-1H-indole; 244086-74-6; 3-(Piperidin-3-yl)-2-phenyl-1H-indole; DA-07759
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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 |
C19H20N2
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| Canonical SMILES |
C1CC(CNC1)C2=C(NC3=CC=CC=C32)C4=CC=CC=C4
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| InChI |
1S/C19H20N2/c1-2-7-14(8-3-1)19-18(15-9-6-12-20-13-15)16-10-4-5-11-17(16)21-19/h1-5,7-8,10-11,15,20-21H,6,9,12-13H2
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| InChIKey |
FYHCOUIJWCQUMZ-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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