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(2E,2′E)-3,3′-(1,4-phenylene)bis(1-(2,4-dimethoxyphenyl)prop-2-en-1-one) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26483-86-3

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26483-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26483-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,8 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26483-86:
(7*2)+(6*6)+(5*4)+(4*8)+(3*3)+(2*8)+(1*6)=133
133 % 10 = 3
So 26483-86-3 is a valid CAS Registry Number.

26483-86-3Relevant academic research and scientific papers

Analogues of xanthones——Chalcones and bis-chalcones as α-glucosidase inhibitors and anti-diabetes candidates

Cai, Chao-Yun,Rao, Li,Rao, Yong,Guo, Jin-Xuan,Xiao, Zhi-Zun,Cao, Jing-Yu,Huang, Zhi-Shu,Wang, Bo

, p. 51 - 59 (2017/03/01)

Two series of compounds (chalcones and bis-chalcones) were designed, synthesized, and evaluated as α-glucosidase inhibitors (AGIs) with 1-deoxynojirimycin as positive control in vitro. Most of the compounds with two or four hydroxyl groups showed better inhibitory activities than 1-deoxynojirimycin towards α-glucosidase with noncompetitive mechanism. Moreover, most of the hydroxy bis-chalcones exhibit good α-glucosidase inhibitory activities in enzyme test. Inspiringly, bis-chalcones 2g (at 1 μM concentration) has stronger effect than 1-deoxynojirimycin on reducing the glucose level in HepG-2 cells (human liver cancer cell line).

Symmetric bis-chalcones as a new type of breast cancer resistance protein inhibitors with a mechanism different from that of chromones

Winter, Evelyn,Devantier Neuenfeldt, Patrícia,Chiaradia-Delatorre, Louise Domeneghini,Gauthier, Charlotte,Yunes, Rosendo Augusto,Nunes, Ricardo J.,Creczynski-Pasa, Tania Beatriz,Di Pietro, Attilio

, p. 2930 - 2941 (2014/05/06)

Potent ABCG2 inhibitors were recently identified as asymmetric chromones with different types of substituents. We here synthesized symmetric bis-chalcones that were differently substituted and screened for their ability to inhibit mitoxantrone efflux from

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