Weight | 118.139 g/mol |
---|---|
Formula | C7H6N2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
5-AZAINDOLE (271-34-1)
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- Discovery of 1-[4-(3-Chlorophenylamino)-1-methyl-1H-pyrrolo[3,2-c]pyridin-7-yl]-1-morpholin-4-ylmethanone (GSK554418A), a Brain Penetrant 5-Azaindole CB2 Agonist for the Treatment of Chronic Pain (Journal of Medicinal Chemistry, 2009)
- Potent 4-amino-5-azaindole factor VIIa inhibitors (Bioorganic & Medicinal Chemistry Letters, 2006)
- Novel blue luminescent/electroluminescent 7-azaindole derivatives: 1,3-Di(N-7-azaindolyl)benzene, 1-bromo-3,5-Di(N-7-azaindolyl)benzene, 1,3,5-Tri(N-7-azaindolyl)benzene, and 4,4'-Di(N-7-azaindolyl)biphenyl (Chemistry of Materials, 2001)
- Design and synthesis of a C-2-symmetric self-complementary hydrogen-bonding cleft molecule based on the bicyclo 3.3.1 nonane and 4-oxo-5-azaindole framework. Formation of channels and inclusion complexes in the solid state (Journal of Organic Chemistry, 2004)
- Novel 5-azaindole factor VIIa inhibitors. (Bioorganic & Medicinal Chemistry Letters, 2006)
- 7-Azaindole. VI. Preparation of 5- and 6-Substituted 7-Azaindoles1 (Journal of the American Chemical Society, 1959)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CNC2=C1C=NC=C2
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InChIKeySRSKXJVMVSSSHB-UHFFFAOYSA-N
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