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2α-benzoyloxy-5β,20-epoxy-4α-hydroxy-9α,10β-isopropylidenedioxy-11-taxen-13-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

532935-93-6

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532935-93-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 532935-93-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,2,9,3 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 532935-93:
(8*5)+(7*3)+(6*2)+(5*9)+(4*3)+(3*5)+(2*9)+(1*3)=166
166 % 10 = 6
So 532935-93-6 is a valid CAS Registry Number.

532935-93-6Relevant academic research and scientific papers

Synthesis and antitumor activity of 2-(m-substituted-benzoyl)baccatin III analogs from taxinine

Horiguchi, Tohru,Oritani, Takayuki,Kiyota, Hiromasa

, p. 1529 - 1538 (2003)

2-m-Azidobenzoyl and 2-m-chlorobenzoyl baccatin III analogs were prepared from taxinine, a major component in Japanese yew leaves. In this study, a novel acetyl migration from 13- to 4-hydroxyl group was observed. The antitumor activity of these compounds

Structure-activity relationships of some taxoids as multidrug resistance modulator

Hasegawa, Toshiaki,Bai, Jao,Zhang, Shujun,Wang, Jinlan,Matsubara, Junichi,Kawakami, Junichi,Tomida, Akihiro,Tsuruo, Takashi,Hirose, Katsutoshi,Sakai, Junichi,Kikuchi, Midori,Abe, Mariko,Ando, Masayoshi

, p. 1122 - 1126 (2008/01/27)

1,7-Deoxy-4-deacetylbaccatin III (12) and its five analogues 6-9, 13, and their oxetane ring opened derivatives 14, 16, and 17, which were synthesized from taxinine, showed significant activity as MDR reversal agent by the assay of the calcein accumulatio

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