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OEM Manufacturer 2-Phenylacetophenone Powder - 3,3′- diindolylmethane – Longo Detail:

Description

3,3′-diindolylmethane is a pharmaceutical intermediate; It can be found in natural phytochemicals belonging to Cruciferae Plants, acid catalyzed reaction products, indole-3-methanol; It has the function of anti-tumor agent; Under the condition of relatively high concentration, the derivative can not only directly accelerate the apoptosis of human cancer cells, but also sensitize trail to induce the apoptosis of human cancer cells; Chemicalbookdim induces a G1 cell ring inhibition in human breast cancer MCF-7 cells through mechanism and inclusion expression; Dim is a potent inhibitor of mitochondrial h+-atpase; As a new plant growth promoter, dim and its derivatives have been used in eco-friendly system research.

Product Info

Cas No. :1968-05-4

Purity :≥98%

Formula :C17H14N2

Formula Wt. :246.31

Chemical Name :3,3′-Diindolylmethane

Synonym : :3,3′-Diindolylmethane(DIM);Di(1H-indol-3-yl);Plant:Indole;3,3′-DIINDOLYLMETHANE,>=98%(HPLC);3,3′-METHYLENEBIS-1H-INDOLE;3,3′-METHYLENEBISINDOLE;3,3′-METHYLENEDIINDOLE;3,3′-DIINDOLYLMETHANE

Melting Point :167 °C

Boiling Point :230 °C

Solubility : Chloroform (Sparingly), Methanol (Slightly)

Appearance :Off-white powder

Shipping and Storage

Storage stability Recommended storage temperature -20°C.

Preparation Place indole (1.17 g, 10 mmol), CTAB (50% mol) and oxalic acid (50% mol) in a 25 ml single-necked round-bottom flask, add 5 ml deionized water, stir thoroughly for 5 min and then add aqueous formaldehyde solution (0.38 g solution, 5 mmol formaldehyde) dropwise. React for 3 h at room temperature and stop the reaction. The reaction solution was extracted with 15 ml of ethyl acetate in three parts, and the organic phase was collected and dried with anhydrous Na2SO4 for 5 hours. The solvent was removed under reduced pressure and recrystallized from a mixture of methanol and water (methanol/H2ChemicalbookO = 10/1) to give a white solid 3,3′-diindolylmethane in 85% yield. Bioactivity3,3′-Diindolylmethane (DIM) is the main digestion product of indole-3-carbinol, which is a potential anticancer substance in cruciferous vegetables.3,3′-Diindolylmethane (DIM) is a pure strong antagonist of androgenreceptor (AR).
In vitro studies have shown that DIM is an effective radioprotector and mitigator, acting by stimulating ATM-driven DDR-like responses as well as NF-κB survival signaling.DIM can inhibit tumor cell invasion, angiogenesis, proliferation and induce apoptosis by modulating signaling pathways such as AKT, NF-κB and FOXO3. It can also inhibit estrogen-induced gene expression and induce endoplasmic reticulum stress. chemicalbookDIM can alter estrogen metabolism and antagonize estrogen and androgen receptor activity. In vivo studies have shown that DIM is effective against systemic radiation after multiple administrations. In in vivo tests, DIM provided radiation protection or mitigation. In normal tissues, DIM activates ATM. dIM can be administered to mice by oral filling (250 mg/kg) with high bioavailability and no acute t


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We strive for excellence, service the customers, hopes to become the nice cooperation team and dominator enterprise for personnel, suppliers and customers, realizes value share and continuous promotion for OEM Manufacturer 2-Phenylacetophenone Powder - 3,3′- diindolylmethane – Longo , The product will supply to all over the world, such as: Belgium, Juventus, Frankfurt, All these products are manufactured in our factory located in China. So we can guarantee our quality seriously and availably. Within these four years we sell not only our products but also our service to clients throughout the world.
Adhering to the business principle of mutual benefits, we have a happy and successful transaction, we think we will be excellent business partner.
5 Stars By Lee from Ukraine - 2017.01.28 18:53
It's really lucky to find such a professional and responsible manufacturer, the product quality is good and delivery is timely, very nice.
5 Stars By Bernice from Swedish - 2018.07.26 16:51