Dibenzosuberone

CAS: 1210-35-1

Ref. 3D-ID21532

Product Information

• Name: Dibenzosuberone
• Synonyms: 10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-one10,11-Dihydro-5H-dibenzo[a,d]cycloheptatrien-5-one10,11-Dihydrodibenzo[a,d]cyclohept en-5-oneAmitriptyline Impurity A, 10,11-Dihydro-5H-dibenzo[a,d]cycloheptan-5-one, 10,11-Dihydro-5H-dibenzo[a,d]cycloheptatrien-5-one, 10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-one, 10,11-Dihydrodibenzo[a,d]cycloheptanone, 10,11-Dihydrodibenzo[a,d]cyclohepten-5-one, 10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-one, 2,3:6,7-Dibenzosuberone, 5H-Dibenzo[a,d]cyclohepten-5-one, 10,11-dihydro-, D)Cyclohepten-5-One,10,11-Dihydro-5H-Dibenzo(, DBS, Dibenzo(A,D)Cycloheptadien-5-One, Dibenzo[a,d]cyclohepta[1,4]dien-5-one, Dibenzocycloheptadienone, Dibenzocycloheptenone, Dibenzosuberan-5-one, Dibenzosuberone 98%, NSC 49727, d]cyclohepten-5-one,10,11-dihydro-5H-Dibenzo[a

Description

Dibenzosuberone is a reactive, surfactant, and β-catenin inhibitor that has been shown to have anti-cancer activity against solid tumours. It is synthesized by the asymmetric synthesis of dibenzoyl-L-tartaric acid with sodium dodecylsulfate in the presence of light. The substrate film is used to increase the rate of reactivity. Dibenzosuberone inhibits the growth of cancer cells by inhibiting cyclic peptide synthesis and blocking light emission from these cells. Dibenzosuberone also has an effect on cell migration and proliferation through its interactions with β-catenin. Dibenzosuberone hydrolyzes in aqueous solution to form benzene, which can be removed by adding hydrochloric acid or hydrogen bonding with anhydrous sodium.

• Brand: Biosynth

Chemical properties

• Molecular weight: 208.26 g/mol
• Formula: C₁₅H₁₂O
• Purity: Min. 95%
• Color/Form: Solidified Mass
• InChI: InChI=1S/C15H12O/c16-15-13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)15/h1-8H,9-10H2
• InChI key: InChIKey=BMVWCPGVLSILMU-UHFFFAOYSA-N
• SMILES: O=C1c2ccccc2CCc2ccccc21