| Weight | 194.237 g/mol |
|---|---|
| Formula | C13H10N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 1 |
2-(2-Pyridinyl)-1H-indole (13228-40-5)
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- Bis(heteroaryl)piperazine (BHAP) reverse transcriptase inhibitors: structure-activity relationships of novel substituted indole analogues and the identification of 1-[(5-methanesulfonamido-1H-indol-2-yl)-carbonyl]-4-[3- [(1-methylethyl)amino]-pyridinyl]piperazine monomethanesulfonate (U-90152S), a second-generation clinical candidate. (Journal of Medicinal Chemistry, 1993)
- Carbene complexes of cycloplatinated 1H-indole-1-methyl-2-(2-pyridine). The crystal and molecular structure of -{Pt[1H-indole-1-methyl-2-(2-pyridinyl-C3,N](DMSO)Cl} and of -{Pt[1H-indole-1-methyl-2-(2-pyridinyl-C3,N)][C(OCH2CH3)(CH2C6H5)]Cl} (Journal of Organometallic Chemistry, 2000)
- 1H-indole and benzo(b)thiophene derivatives with 4-(1,2,3,6-tetra:hydro:pyridinyl)- and 4-piperidinyl-groups bound to the heterocyclic ring as inhibitors of serotonin reuptake (1997)
- Cardiovascular properties of a 5-HT1-like receptor agonist, 5-methoxy-3(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (RU 24969) in normotensive anaesthetized rats (Archives internationales de pharmacodynamie et de thrapie, 1988)
- 3-(pyridinyl-amino)-1h-indole-2-carboxylic acid derivatives as interleukin-4 gene expression inhibitors (2003)
- 3-(pyridinyl-amino)-1h-indol-2-carbonsure-verbindungen als inhibitoren der interleukin-4 genexpression 3- (pyridinyl-amino) -1H-indole-2-carboxylic acid compounds as inhibitors of interleukin-4 gene expression (2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C=C(N2)C3=CC=CC=N3
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InChIKeyOLGGLCIDAMICTA-UHFFFAOYSA-N
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2-(2-Pyridinyl)-1H-indole
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