Weight | 147.177 g/mol |
---|---|
Formula | C9H9NO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 1 |
Indole-3-carbinol (700-06-1)
I3C cpd · 3-hydroxymethylindole · 1H-indole-3-methanol
Score:
#1774 in Biochemistry
,
#3890 in Biology
,
#4900 in Chemistry
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- Aromatic hydrocarbon responsiveness-receptor agonists generated from indole-3-carbinol in vitro and in vivo: comparisons with 2,3,7,8-tetrachlorodibenzo-p-dioxin. (Proceedings of the National Academy of Sciences of the United States of America, 1991)
- Molecular targets and anticancer potential of indole-3-carbinol and its derivatives (Cell Cycle, 2005)
- Effects of dietary indole-3-carbinol on estradiol metabolism and spontaneous mammary tumors in mice. (Carcinogenesis, 1991)
- Indole-3-carbinol (I3C) induced cell growth inhibition, G1 cell cycle arrest and apoptosis in prostate cancer cells (Oncogene, 2001)
- Indole-3-carbinol Inhibits the Expression of Cyclin-dependent Kinase-6 and Induces a G1 Cell Cycle Arrest of Human Breast Cancer Cells Independent of Estrogen Receptor Signaling (Journal of Biological Chemistry, 1998)
- Chemoprevention of chemically-induced mammary carcinogenesis by indole-3-carbinol. (Anticancer Research, 1995)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - I3C cpd
- 3-hydroxymethylindole
- 1H-indole-3-methanol
- indole-3-methanol
-
SMILESC1=CC=C2C(=C1)C(=CN2)CO
-
InChIKeyIVYPNXXAYMYVSP-UHFFFAOYSA-N
- Pubchem - Indole-3-carbinol
- Wikipedia - indole-3-carbinol
Indole-3-carbinol (C9H9NO) is produced by the breakdown of the glucosinolate glucobrassicin, which can be found at relatively high levels in cruciferous vegetables such as broccoli, cabbage, cauliflower, brussels sprouts, collard greens and kale. It is also available in dietary supplements. Indole-3-carbinol is the subject of on-going biomedical research into its possible anticarcinogenic, antioxidant, and anti-atherogenic effects.
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