Synthesis and antiproliferativeactivity of new vinca alkaloids containing an α,β-unsaturated aromatic side chain
摘要:
A new series of vinca-alkaloids derivatives containing various alpha,beta-unsaturated aromatic side chains was synthesized. Four new vinca-alkaloids derivatives showed selective cytotoxicities against KB tumor cell lines with IC50 value below 0.1 mu M, thus comparable with vinblastine. (C) 2015 Elsevier Ltd. All rights reserved.
Synthesis of dimeric indole alkaloids by cell free extracts from cell suspension cultures of Catharanthus roseus
作者:Masanaru Misawa、Tsuyoshi Endo、Anne Goodbody、John Vukovic、Clint Chapplet、Lewis Choi、James P. Kutney
DOI:10.1016/0031-9422(88)80193-6
日期:1988.1
Abstract Crude enzyme obtained from suspension cultures of Catharanthusroseus catalysed the coupling of vindoline and catharanthine to form dimeric indole alkaloids. Substantially improved yields were realized through the use of flavin mononucleotide and manganous ion in the reaction mixture. With the optimized conditions, ca 25% of the substrates were converted to 3′,4′-anhydrovinblastine.
Battersby, Alan R.; Westcott, Neil D.; Gluesenkamp, Karl-Heinz, Chemische Berichte, 1981, vol. 114, # 10, p. 3439 - 3447
作者:Battersby, Alan R.、Westcott, Neil D.、Gluesenkamp, Karl-Heinz、Tietze, Lutz-F.
DOI:——
日期:——
Battersby, Alan R.; Thompson, Mervyn; Gluesenkamp, Karl-Heinz, Chemische Berichte, 1981, vol. 114, # 10, p. 3430 - 3438
作者:Battersby, Alan R.、Thompson, Mervyn、Gluesenkamp, Karl-Heinz、Tietze, Lutz-F.
DOI:——
日期:——
CN116768898
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Synthesis and antiproliferativeactivity of new vinca alkaloids containing an α,β-unsaturated aromatic side chain
作者:Quoc Anh Ngo、Le Anh Nguyen、Ngoc Binh Vo、Thuy Hang Nguyen、Fanny Roussi、The Hung Nguyen、Van Tuyen Nguyen
DOI:10.1016/j.bmcl.2015.10.040
日期:2015.12
A new series of vinca-alkaloids derivatives containing various alpha,beta-unsaturated aromatic side chains was synthesized. Four new vinca-alkaloids derivatives showed selective cytotoxicities against KB tumor cell lines with IC50 value below 0.1 mu M, thus comparable with vinblastine. (C) 2015 Elsevier Ltd. All rights reserved.