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3,3'-Diindolylmethane

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    3,3'-Diindolyl<wbr/>methane
  • 3,3'-Diindolyl<wbr/>methane
Cat No: 15927
Biochemicals - Small Molecule Inhibitors
Cayman

3,3’-Diindolylmethane (DIM) is a bioactive metabolite of indole-3-carbinol, a phytochemical produced by the breakdown of the glucosinolate glucobrassicin found in cruciferous vegetables. At 10-30 µM, it demonstrates anticancer and chemopreventative ef...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 3,3'-methylenebis-1H-indole
Correlated keywords:
  • phytochemicals indole-3-carbinol indoles 3 three carbinol glucosinolate glucobrassicin cruciferous vegetables broccoli anticancers anti-cancer anti cancers chemoprevention Nrf2 Phase 2 enzymes apoptosis epigenetics radioprotectors radiomitigators antioxidants anti-oxidants oxidants intracellular signaling signals inhibitors inhibits inhibitions epigenetics DNAs damages repairs natural products transduction AhR agonists arundine HBs 236 HB236 HB-236 antiradiation anti-radiation chemopreventative metabolites cells cycles arrests proliferation histones deacetylases methylation Bis(3-indolyl)methane
Product Overview:
3,3’-Diindolylmethane (DIM) is a bioactive metabolite of indole-3-carbinol, a phytochemical produced by the breakdown of the glucosinolate glucobrassicin found in cruciferous vegetables. At 10-30 µM, it demonstrates anticancer and chemopreventative effects involving Nrf2 induction of Phase 2 enzymes, promotion of apoptosis, induction of cell cycle arrest, inhibition of cell proliferation, and inhibition of histone deacetylases and DNA methylation activities.{25951,25954,25953} Furthermore, at 0.3 µM DIM was shown to act as a potent radioprotector and mitigator of the effects of ionizing radiation exposure by stimulating an ATM-driven DNA damage-like response and NF-κB survival signaling in cultured epithelial cells.{25952}
Size 100 mg
Shipping dry ice
CAS Number 04/05/1968 00:00
Molecular Formula C17H14N2
SMILES C12=CC=CC=C1C(CC3=CNC4=C3C=CC=C4)=CN2
Molecular Weight 246,3
Formulation A crystalline solid
Purity ≥98%
Custom Code 2933.49
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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