532935-96-9

Upstream product

• 108-24-7 acetic anhydride 
• 532935-95-8 2α-benzoyloxy-5β,20-epoxy-4α,9α,10β-trihydroxy-11-taxen-13-one 
• 222844-42-0 C₃₉H₄₄O₇ 
• 931422-00-3 C₃₀H₃₈O₆ 
• 931422-01-4 C₃₀H₄₀O₈ 
• 931422-02-5 C₃₆H₅₄O₈Si 
• 931422-03-6 C₃₇H₅₆O₁₀SiS 
• 931422-04-7 C₃₁H₄₂O₁₀S 
• 15135-57-6 9α,10β-dihydroxy-2α-acetoxy-5α-cinnamoyloxy-taxa-4(20),11-dien-13-one 
• 172304-02-8 5α-cinnamoyloxy-9α,10β-(dimethylmethylenedioxy)-2α-hydroxytaxa-4(20),11-dien-13-one 
• 2571-73-5 2α-acetoxy-5α-cinnamoyloxy-9α,10β-(dimethylmethylenedioxy)taxa-4(20),11-dien-13-one 
• 532935-93-6 2α-benzoyloxy-5β,20-epoxy-4α-hydroxy-9α,10β-isopropylidenedioxy-11-taxen-13-one 
• 532936-05-3 20-t-butyldimethylsilyloxy-2α-(1-ethoxyethoxy)-4α,5α-dihydroxy-9α,10β-isopropylidenedioxy-11-taxen-13-one 
• 532936-03-1 C₃₃H₅₆O₆Si 

Relevant academic research and scientific papers

Structure-activity relationships of some taxoids as multidrug resistance modulator

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

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

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