3,3'-Diindolylmethane
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3,3'-Diindolylmethane
| 3,3'-Diindolylmethane | |
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3,3′-methanediylbis(1H-indole) |
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Other names
3-(1H-Indol-3-ylmethyl)-1H-indole |
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| Identifiers | |
| CAS number | 1968-05-4 |
| PubChem | 3071 |
| ChemSpider | 2963  |
| ChEBI | CHEBI:50182 |
| ChEMBL | CHEMBL446452 |
| Jmol-3D images | Image 1 Image 2 |
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| Properties | |
| Molecular formula | C17H14N2 |
| Molar mass | 246.31 g mol−1 |
 (verify) (what is:  / ?)Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
3,3′-Diindolylmethane or DIM is a compound derived from the digestion of indole-3-carbinol, found in cruciferous vegetables such as broccoli, Brussels sprouts, cabbage and kale.[1] The reputation of Brassica vegetables as healthy foods rests in part on the activities of diindolylmethane.[2][3]
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Contents
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Properties
DIM has the biological properties listed in the chart below. Because of its various potent anticancer properties, the National Cancer Institute of the United States has begun clinical trials of DIM as a therapeutic for numerous forms of cancer.[4] [5]
Uses
At the present time, DIM is used to treat recurring respiratory papillomatosis, a rare respiratory disease with tumors in the upper respiratory tracts caused by the human papilloma virus.[citation needed] In addition, DIM is in Phase III clinical trials for cervical dysplasia, a precancerous condition also caused by the human papilloma virus.[citation needed] Similarly, it has been studied and shown promising results as a immunostimulant against HPV.
See also
References
- ^ Rakel D.. Integrative Medicine.
- ^ Gong Y. Sohn H. Xue L. Firestone GL. Bjeldanes LF (2006). "3,3'-Diindolylmethane is a novel mitochondrial H(+)-ATP synthase inhibitor that can induce p21(Cip1/Waf1) expression by induction of oxidative stress in human breast cancer cells". Cancer Research 66 (9): 4880–4887. doi:10.1158/0008-5472.CAN-05-4162. PMID 16651444.
- ^ Acharya A. Das I. Singh S. Saha T. (2010). "Chemopreventive properties of indole-3-carbinol, diindolylmethane and other constituents of cardamom against carcinogenesis". Recent patents on food, nutrition & agriculture 2 (2): 166–177. doi:10.2174/1876142911002020166.
- ^ Rogan EG (2006). "The natural chemopreventive compound indole-3-carbinol: state of the science". In Vivo 20 (2): 221–228. PMID 16634522.
- ^ Kim YS. Milner JA (2005). "Targets for indole-3-carbinol in cancer prevention". Journal of Nutritional Biochemistry 16 (2): 65–73. doi:10.1016/j.jnutbio.2004.10.007. PMID 15681163.
External links
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