Development of Yondelis® (trabectedin, ET-743). A semisynthetic process solves the supply problem

被引:254
作者
Cuevas, Carmen [1 ]
Francesch, Andres [1 ]
机构
[1] PharmaMar SA, Madrid 28770, Spain
关键词
TUNICATE ECTEINASCIDIA-TURBINATA; TETRAHYDROISOQUINOLINE ANTITUMOR ANTIBIOTICS; ASYMMETRIC TOTAL SYNTHESES; ANTI-TUMOR ANTIBIOTICS; FORMAL TOTAL-SYNTHESIS; CARIBBEAN TUNICATE; ENANTIOSELECTIVE SYNTHESIS; HOMOLOGOUS RECOMBINATION; NUCLEOTIDE-EXCISION; CYANOSAFRACIN-B;
D O I
10.1039/b808331m
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ecteinascidins are marine natural products consisting of two or three linked tetrahydroisoquinoline subunits and an active carbinolamine functional group. Their potent antiproliferative activity against a variety of tumor cells makes them attractive candidates for development as anticancer agents. The lead compound, Yondelis(R) (trabectedin, ET-743) is the first marine anticancer agent approved in the European Union for patients with soft tissue sarcoma (STS). Positive results of a large randomized Phase III clinical trial in ovarian cancer have recently been presented. The low amounts present in its natural source, the tunicate Ecteinascidia turbinata, made it necessary to develop efficient synthetic procedures. The original total synthesis is reviewed as well as a new semisynthetic process from the readily available cyanosafracin B, which has solved the supply problem.
引用
收藏
页码:322 / 337
页数:16
相关论文
共 90 条
[1]   Ecteinascidin 743: a novel anticancer drug with a unique mechanism of action [J].
Aune, GJ ;
Furuta, T ;
Pommier, Y .
ANTI-CANCER DRUGS, 2002, 13 (06) :545-555
[2]  
Barton D. H. R., 1997, ORG SYNTH, V74, P101
[3]   SYNTHESIS OF ISOQUINOLINES .3. A NEW SYNTHESIS OF 1,2,3,4-TETRAHYDROISOQUINOLINES [J].
BOBBITT, JM ;
KIELY, JMN ;
KHANNA, KL ;
EBERMANN, R .
JOURNAL OF ORGANIC CHEMISTRY, 1965, 30 (07) :2247-+
[4]   MILD AND SIMPLE BIOMIMETIC CONVERSION OF AMINES TO CARBONYL-COMPOUNDS [J].
BUCKLEY, TF ;
RAPOPORT, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (16) :4446-4450
[5]  
Carballo JL, 1999, B MAR SCI, V65, P755
[6]   Larval ecology of an ascidian tropical population in a Mediterranean enclosed ecosystem [J].
Carballo, JL .
MARINE ECOLOGY PROGRESS SERIES, 2000, 195 :159-167
[7]  
Carballo JL, 2000, J WORLD AQUACULT SOC, V31, P481
[8]  
CARDONA L, 1986, TETRAHEDRON, V42, P2725
[9]   Synthesis of ecteinascidin 743 analogues from cyanosafracin B:: Isolation of a kinetically stable quinoneimine tautomer of a 5-hydroxyindole [J].
Ceballos, PA ;
Pérez, M ;
Cuevas, C ;
Francesch, A ;
Manzanares, I ;
Echavarren, AM .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2006, 2006 (08) :1926-1933
[10]   The solution to a deep stereochemical conundrum: Studies toward the tetrahydroisoquinoline alkaloids [J].
Chan, C ;
Zheng, SP ;
Zhou, BS ;
Guo, J ;
Heid, RM ;
Wright, BJD ;
Danishefsky, S .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (11) :1749-1754