Weight | 145.205 g/mol |
---|---|
Formula | C10H11N |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
2,5-Dimethyl-1H-indole (1196-79-8)
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- RS-17053 (N-[2-(2-cyclopropylmethoxyphenoxy)ethyl]-5-chloro-alpha, alpha-dimethyl-1H-indole-3-ethanamine hydrochloride), a selective alpha 1A-adrenoceptor antagonist, displays low affinity for functional alpha 1-adrenoceptors in human prostate: implications for adrenoceptor classification. (Molecular Pharmacology, 1996)
- Plasma concentration, tissue distribution and excretion of the prospective cardioprotective agent cis-(-)-2,3,4,4a,5,9b-hexahydro-2,8-dimethyl-1H-pyrido-[4,3-b]indole dihydrochloride in rats. (Drug Research, 1990)
- Synthesis of 1H-Pyrrolo [1, 2-] indole Derivatives. III. Synthesis of 2, 3-Dihydro-7-hydroxy-6, 9-dimethyl-5, 8-dioxo-1H-pyrrolo [1, 2-] indole (Chemical & Pharmaceutical Bulletin, 1972)
- Reproductive toxicity studies with cis-(-)-2,3,4,4a,5,9b-hexahydro-2,8-dimethyl-1H-pyrido-[4,3-b]indole dipalmitate in rats. (Drug Research, 1991)
- 5,5-Dimethyl-3-(5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-1-phenyl-3-(trifluoromethyl)-3,5,6,7-tetrahydro-1H-indole-2,4-dione, a potent inhibitor for mammalian elongase of long-chain fatty acids family 6: examination of its potential utility as a pharmacological tool. (Journal of Pharmacology and Experimental Therapeutics, 2009)
- Synthesis of 1,2-Diaryl-6,6-dimethyl-5,6-dihydro-1H-indole-4,7-diones from Arylglyoxals and Enamines through Domino Condensation and Allylic Hydroxylation (Synthesis, 2013)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC2=C(C=C1)NC(=C2)C
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InChIKeyZFLFWZRPMDXJCW-UHFFFAOYSA-N
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Similar Compounds
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