Synthesis and Evaluation of Water-Soluble Non-Prodrug Analogs of Docetaxel Bearing sec-Aminoethyl Group at the C-10 Position
| Autor: | Shuichi Ando, Tsunehiko Soga, Ikuo Mitsui, Hirofumi Terasawa, Kouichi Uoto, Haruhiro Takenoshita, Yasuhide Hirota, Toshiharu Yoshino |
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| Rok vydání: | 1998 |
| Předmět: |
Chemical Phenomena
Paclitaxel Tertiary amine Swine Stereochemistry Docetaxel Microtubules Chemical synthesis Methanesulfonic acid chemistry.chemical_compound Tubulin In vivo Drug Discovery medicine Animals Humans Cytotoxicity Chemistry Physical General Chemistry General Medicine Prodrug Antineoplastic Agents Phytogenic Solubility chemistry Taxoids Drug Screening Assays Antitumor medicine.drug |
| Zdroj: | Chemical and Pharmaceutical Bulletin. 46:770-776 |
| ISSN: | 1347-5223 0009-2363 |
| Popis: | To develop non-prodrugs of taxoids with satisfactory stability in vivo, high water-solubility, and potent antitumor activity, we prepared several 10-O-sec-aminoethyl docetaxel analogs (3) and evaluated their cytotoxicity against mouse leukemia and human tumor cell lines, microtubule disassembly-inhibitory activity, and water-solubility. These analogs were synthesized from the 10-O-allyl baccatin derivatives (5a-c) using the beta-lactam synthon method. Among these analogs, the 10-O-(2-morpholinoethyl) (18, 21) and 10-O-(2-thiomorpholinoethyl) (19, 24) analogs exhibited cytotoxicity comparable or superior to that of docetaxel (2). In addition, the methanesulfonic acid salt (18a) had a high water-solubility. |
| Databáze: | OpenAIRE |
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