| Weight | 117.151 g/mol |
|---|---|
| Formula | C8H7N |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
indole (120-72-9)
indole hydrochloride · indole, 14C-labeled
Score:
#612 in Biochemistry
,
#1769 in Biology
,
#2094 in Chemistry
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- Indole-3-acetic acid in microbial and microorganism-plant signaling (Fems Microbiology Reviews, 2007)
- Indole Metabolism in the Pineal Gland: A Circadian Rhythm in N-Acetyltransferase (Science, 1970)
- Bacterial biosynthesis of indole-3-acetic acid (Canadian Journal of Microbiology, 1996)
- Asymmetric Syntheses of Oxindoleand Indole Spirocyclic Alkaloid Natural Products (Synthesis, 2009)
- Marine indole alkaloids: potential new drug leads for the control of depression and anxiety (Chemical Reviews, 2010)
- Characterization of an Arabidopsis Enzyme Family That Conjugates Amino Acids to Indole-3-Acetic Acid (The Plant Cell, 2005)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H319: Causes serious eye irritation
Warning Serious eye damage/eye irritation - Category 2A - indole hydrochloride
- indole, 14C-labeled
-
SMILESC1=CC=C2C(=C1)C=CN2
-
InChIKeySIKJAQJRHWYJAI-UHFFFAOYSA-N
- Pubchem - indole
- Wikipedia - indole
Indole is an aromatic heterocyclic organic compound with formula C8H7N. It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. Indole is widely distributed in the natural environment and can be produced by a variety of bacteria.
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