Recent developments in the chemistry, biology and medicine of the epothilones

被引:136
作者
Nicolaou, KC
Ritzén, A
Namoto, K
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[3] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
关键词
D O I
10.1039/b104949f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The epothilones have occupied center stage on the scenes of total synthesis, chemical biology and medicine for the last five years, no doubt because of their intriguing mode of action and unusually high potency against tumor cells, including multidrug-resistant cell lines. This article highlights the most recent advances within this exciting field. Thus, an overview of recent synthetic endeavors culminating in a new generation of total syntheses and analogues, some with higher potencies than the naturally occurring substances, will be given, and the chemical biology, in particular the current understanding of structure-activity relationships of the epothilones, will also be discussed in light of the latest biological results. In addition, the recently elucidated biosynthetic machinery of the natural epothilone-producing myxobacterium Sorangium cellulosum, as it is now understood, will be described. Finally, some preclinical and clinical studies will be summarized.
引用
收藏
页码:1523 / 1535
页数:13
相关论文
共 93 条
[1]   Epothilones and related structures - a new class of microtubule inhibitors with potent in vivo antitumor activity [J].
Altmann, KH ;
Wartmann, M ;
O'Reilly, T .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2000, 1470 (03) :M79-M91
[2]   Microtubule-stabilizing agents: a growing class of important anticancer drugs [J].
Altmann, KH .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2001, 5 (04) :424-431
[3]  
Altmann KH, 2000, CHIMIA, V54, P612
[4]   Synthesis and biological evaluation of highly potent analogues of epothilones B and D [J].
Altmann, KH ;
Bold, G ;
Caravatti, G ;
Flörsheimer, A ;
Guagnano, V ;
Wartmann, M .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2000, 10 (24) :2765-2768
[5]  
ALTMANN KH, COMMUNICATION
[6]  
[Anonymous], [No title captured], Patent No. [DE 4138042, 4138042]
[7]   A density functional study of a new family of anticancer drugs: Paclitaxel, taxotere, epothilone, and discodermolide [J].
Ballone, P ;
Marchi, M .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (16) :3097-3102
[8]   Stereoselective syntheses of epothilones A and B via directed nitrile oxide cycloaddition [J].
Bode, JW ;
Carreira, EM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (15) :3611-3612
[9]  
BOLLAG DM, 1995, CANCER RES, V55, P2325
[10]   A novel application of a Pd(0)-catalyzed nucleophilic substitution reaction to the regio- and stereoselective synthesis of lactam analogues of the epothilone natural products [J].
Borzilleri, RM ;
Zheng, XP ;
Schmidt, RJ ;
Johnson, JA ;
Kim, SH ;
DiMarco, JD ;
Fairchild, CR ;
Gougoutas, JZ ;
Lee, FYF ;
Long, BH ;
Vite, GD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (37) :8890-8897