| Weight | 161.16 g/mol |
|---|---|
| Formula | C9H7NO2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Indole-2-carboxylic acid (1477-50-5)
Score:
#18 in Medicinal chemistry
,
#4745 in Chemistry
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- Indole-2-carboxylic acid: a competitive antagonist of potentiation by glycine at the NMDA receptor. (Science, 1989)
- Effects of the excitatory amino acid receptor antagonists kynurenate and indole-2-carboxylic acid on behavioral and neurochemical outcome following experimental brain injury (The Journal of Neuroscience, 1993)
- Discovery and SAR of indole-2-carboxylic acid benzylidene-hydrazides as a new series of potent apoptosis inducers using a cell-based HTS assay. (Bioorganic & Medicinal Chemistry, 2004)
- Synthesis and biological activities of novel aryl indole-2-carboxylic acid analogs as PPAR partial agonists (Bioorganic & Medicinal Chemistry Letters, 2005)
- 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)
- Synthesis of Indole-3-carboxylic Acid Derivatives by Pd(0)-Catalyzed Intramolecular -Arylation of -(2-Iodoanilino) Esters (Journal of Organic Chemistry, 2008)
-
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)C(=O)O
-
InChIKeyHCUARRIEZVDMPT-UHFFFAOYSA-N
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