Synthesis, in vitro, and in vivo evaluation of phosphate ester derivatives of combretastatin A-4

التفاصيل البيبلوغرافية
العنوان: Synthesis, in vitro, and in vivo evaluation of phosphate ester derivatives of combretastatin A-4
المؤلفون: Rajendra P. Tanpure, Yezhou Sheng, Kevin G. Pinney, Jianxing Zhang, Robert R. Kane, Jianyi Hua, Mallinath B. Hadimani, Klaus Edvardsen, Aimee Weiser, Adrian O. Olivares, Raymond J. Kessler, M.Devan Jonklaas
المصدر: Bioorganicmedicinal chemistry letters. 13(9)
سنة النشر: 2003
مصطلحات موضوعية: Combretastatin, Combretastatin A-4, Natural product, Stereochemistry, Aryl, Organic Chemistry, Clinical Biochemistry, Pharmaceutical Science, Angiogenesis Inhibitors, Prodrug, Biochemistry, Chemical synthesis, Organophosphates, chemistry.chemical_compound, chemistry, In vivo, Cell Line, Tumor, Drug Discovery, Stilbenes, Molecular Medicine, Humans, Prodrugs, Drug Screening Assays, Antitumor, Cytotoxicity, Molecular Biology
الوصف: Combretastatin A-4 disodiumphosphate (CA4P), a prodrug formulation of the natural product combretastatin A-4 (CA4), is currently in clinical investigation for the treatment of cancer. In vivo, CA4P is rapidly enzymatically converted to CA4, a potent inhibitor of tubulin polymerization (IC50 = 1-2 muM), and rapidly causes bloodflow shutdown in tumor tissues. A variety of alkyl and aryl di- and triesters of CA4P have been synthesized and evaluated as potential CA4 prodrugs and/or stable CAV analogues. (C) 2003 Elsevier Science Ltd. All rights reserved.
تدمد: 0960-894X
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7118a11f10c60fb03c9617146ffaa0f1
https://pubmed.ncbi.nlm.nih.gov/12699742
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....7118a11f10c60fb03c9617146ffaa0f1
قاعدة البيانات: OpenAIRE