| Weight | 118.139 g/mol |
|---|---|
| Formula | C7H6N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
6-AZAINDOLE (271-29-4)
271-29-4 · 1H-pyrrolo[2,3-c]pyridine
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- NOVEL OXO-BRIDGED BLUE LUMINESCENT ORGANOALUMINUM COMPLEXES : AL4(CH3)6(MU3-O)2(DPA)2 AND AL3(7-AZAIN)4(OCH(CF3)2)2(CH3)(MU 3-O) (DPA = DEPROTONATED DI-2-PYRIDYLAMINE, 7-AZAIN = DEPROTONATED 7-AZAINDOLE) (Organometallics, 1997)
- Blue Luminescent Organoaluminum Compounds: Al2(CH3)4(7-azain)2, Al2(CH3)2(7-azain)4, Al2(CH3)(OCH(CF3)2)3(7-azain)2, Al2(-OCH(CF3)2)(CH3)(7-azain)2((OCH(CF3)2)2, Al3(3-O)(CH3)(7-azain)4(OCH(CF3)2)2, and Al4(3-O)2(7-azain)6(OCH(CF3)2)2 (7-azain = Deprotonated 7-Azaindole) (Organometallics, 1998)
- Structure-based design of orally bioavailable 1H-pyrrolo[3,2-c]pyridine inhibitors of mitotic kinase monopolar spindle 1 (MPS1). (Journal of Medicinal Chemistry, 2013)
- Total syntheses of 6- and 7-azaindole derived GnRH antagonists (Tetrahedron Letters, 2001)
- Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment. 12. Structure-activity relationships associated with 4-fluoro-6-azaindole derivatives leading to the identification of 1-(4-benzoylpiperazin-1-yl)-2-(4-fluoro-7-[1,2,3]triazol-1-yl-1h-pyrrolo[2,3-c]pyridin-3-yl)ethane-1,2-dione (BMS-585248). (Journal of Medicinal Chemistry, 2013)
- Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines (European Journal of Medicinal Chemistry, 2011)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 271-29-4
- 1H-pyrrolo[2,3-c]pyridine
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SMILESC1=CNC2=C1C=CN=C2
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InChIKeyXLKDJOPOOHHZAN-UHFFFAOYSA-N
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