Weight | 145.161 g/mol |
---|---|
Formula | C9H7NO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 1 |
INDOLE-3-CARBOXALDEHYDE (487-89-8)
indole-3-aldehyde · indole-3-carbaldehyde · 3-indolemethanal
Score:
#1723 in Biochemistry
,
#4805 in Chemistry
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- Synthesis, characterization and biological activity of Schiff base analogues of indole-3-carboxaldehyde (European Journal of Medicinal Chemistry, 2008)
- Studies on organic indole-3-aldehyde single crystals (Journal of Crystal Growth, 2000)
- Excited indole-3-aldehyde from the peroxidase-catalyzed aerobic oxidation of indole-3-acetic acid. Reaction with and energy transfer to transfer ribonucleic acid. (Biochemistry, 1980)
- Identification of 4-chloroindole-3-acetic acid and indole-3-aldehyde in seeds of Pinus sylvestris. (Physiologia Plantarum, 1986)
- Improved Syntheses of Indole-3-aldehyde (Journal of the American Chemical Society, 1946)
- Investigation of Antimicrobial Activities of Indole-3-Aldehyde Hydrazide/Hydrazone Derivatives (Chemotherapy, 2009)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - indole-3-aldehyde
- indole-3-carbaldehyde
- 3-indolemethanal
-
SMILESC1=CC=C2C(=C1)C(=CN2)C=O
-
InChIKeyOLNJUISKUQQNIM-UHFFFAOYSA-N
- Pubchem - INDOLE-3-CARBOXALDEHYDE
- Wikipedia - indole-3-carboxaldehyde
Indole-3-carboxaldehyde (I3A), also known as indole-3-aldehyde and 3-formylindole, is a metabolite of dietary L-tryptophan which is synthesized by human gastrointestinal bacteria, particularly species of the Lactobacillus genus. I3A is a biologically active metabolite which acts as a receptor agonist at the aryl hydrocarbon receptor in intestinal immune cells, in turn stimulating the production of interleukin-22 which facilitates mucosal reactivity.
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Similar Compounds
6-methyl-1H-indole-3-carbaldehyde
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7-Methylindole
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