| Weight | 201.273 g/mol |
|---|---|
| Formula | C12H15N3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
4-(1-Piperazinyl)-1H-indole (84807-09-0)
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- Process Development of 5-Fluoro-3-[3-[4-(5-methoxy-4-pyrimidinyl)-1- piperazinyl]propyl]-1H-indole Dihydrochloride (Organic Process Research & Development, 1997)
- Synthesis, 5-hydroxytryptamine1A receptor affinity and docking studies of 3-[3-(4-aryl-1-piperazinyl)-propyl]-1H-indole derivatives. (Chemical & Pharmaceutical Bulletin, 2012)
- Discovery and Development of 1-[(2-Bromophenyl)sulfonyl]-5-methoxy-3-[(4-methyl-1-piperazinyl)methyl]-1H-indole Dimesylate Monohydrate (SUVN-502): A Novel, Potent, Selective and Orally Active Serotonin 6 (5-HT6) Receptor Antagonist for Potential Treatment of Alzheimers Disease (Journal of Medicinal Chemistry, 2017)
- Synthesis of H3 labeled 5fluoro3[3[4(5methoxy4pyrimidinyl)1piperazinyl]propyl]1Hindole, a serotonergic agent with potential antidepressant activity (Journal of Labelled Compounds and Radiopharmaceuticals, 1995)
- MESYLATDIHYDRATSALZE von 5-(2-(4-(1,2-BENZISOTHIAZOL-3-yl)-1-PIPERAZINYL)-ETHYL)-6-CHLORO-1,3-DIHYDRO-2(1H)-INDOL-2-ON (=ZIPRASIDONE), DESSEN HERSTELLUNG UND VERWENDUNG ALS DOPAMIN-D2-ANTAGONIST MESYLATDIHYDRATSALZE of 5- (2- (4- (1,2-benzisothiazol-3-yl) -1-piperazinyl) ethyl) -6-chloro-1,3-dihydro-2 (1H) -indole-2-ON (= ziprasidone), THE PRODUCTION AND USE AS DOPAMINE D2 ANTAGONIST (1997)
- MESYLATDIHYDRATSALZE of 5- (2- (4- (1,2-benzisothiazol-3-yl) -1-piperazinyl) ethyl) -6-chloro-1,3-dihydro-2 (1H) -indole-2-ON (= ziprasidone), ITS PRODUCTION AND USE AS DOPAMINE D2 ANTAGONIST (1997)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CN(CCN1)C2=CC=CC3=C2C=CN3
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InChIKeyYZKSXUIOKWQABW-UHFFFAOYSA-N
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