| Weight | 161.16 g/mol |
|---|---|
| Formula | C9H7NO2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Indole-7-carboxylic acid (1670-83-3)
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- Cellular Inhibition of Checkpoint Kinase 2 (Chk2) and Potentiation of Camptothecins and Radiation by the Novel Chk2 Inhibitor PV1019 [7-Nitro-1H-indole-2-carboxylic acid {4-[1-(guanidinohydrazone)-ethyl]-phenyl}-amide] (Journal of Pharmacology and Experimental Therapeutics, 2009)
- Design, synthesis and biological evaluation of 7-nitro-1H-indole-2-carboxylic acid derivatives as allosteric inhibitors of fructose-1,6-bisphosphatase (Bioorganic & Medicinal Chemistry, 2014)
- One-step template-free electrodeposition of novel poly(indole-7-carboxylic acid) nanowires and their high capacitance properties (RSC Advances, 2015)
- 1,7-fused 1H-indole-2-carboxylic acid-N-(1,4-benzodiazepin-3-yl)amides (1990)
- Facile Synthesis of 2,3,6,11-Tetrahydro-1H,5H-indolizino[8,7-b]indole-11b-Carboxylic Acid Methyl Ester via a 9-BBN-Mediated Tertiary Lactam Reduction (Synthetic Communications, 2008)
- 4-Chloro-7-trifluoromethyl-10H- benzo[4,5]furo[3,2-b]indole-1-carboxylic acid (TBIC), a putative BK(Ca) channel opener with uterine relaxant activities. (Pharmacology, 2011)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C(=C1)C(=O)O)NC=C2
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InChIKeyIPDOBVFESNNYEE-UHFFFAOYSA-N
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