Divergent synthesis of a pochonin library targeting HSP90 and in vivo efficacy of an identified inhibitor

被引:48
作者
Barluenga, Sofia [1 ]
Wang, Cuihua [1 ]
Fontaine, Jean-Gonzague [1 ]
Aouadi, Kaiss [1 ]
Beebe, Kristin [2 ]
Tsutsumi, Shinji [2 ]
Neckers, Len [2 ]
Winssinger, Nicolas [1 ]
机构
[1] Univ Strasbourg 1, Inst Sci & Ingn Supramol, F-67000 Strasbourg, France
[2] NCI, Urol Oncol Branch, Bethesda, MD 20892 USA
关键词
antitumor agents; bioorganic chemistry; natural products; solid-phase synthesis; synthesis design;
D O I
10.1002/anie.200800233
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Chemical Equation Presented) Make a clean breast of it: The generation of a library of pochonin Dderivatives by a solid-phase approach has led to the discovery of pochoxime (see scheme), a potent inhibitor of the heat-shock protein 90, with over 100-fold improved incellular activity. Pochoxime was found to be effective in breast tumor xenografts, leading to a reduction in the tumor size. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:4432 / 4435
页数:4
相关论文
共 37 条
[1]   Halohydrin and oxime derivatives of radicicol: Synthesis and antitumor activities [J].
Agatsuma, T ;
Ogawa, H ;
Akasaka, K ;
Asai, A ;
Yamashita, Y ;
Mizukami, T ;
Akinaga, S ;
Saitoh, Y .
BIOORGANIC & MEDICINAL CHEMISTRY, 2002, 10 (11) :3445-3454
[2]   Pharmacological prevention of Parkinson disease in Drosophila [J].
Auluck, PK ;
Bonini, NM .
NATURE MEDICINE, 2002, 8 (11) :1185-1186
[3]   Solution- and solid-phase synthesis of radicicol (monorden) and pochonin C [J].
Barluenga, S ;
Moulin, E ;
Lopez, P ;
Winssinger, N .
CHEMISTRY-A EUROPEAN JOURNAL, 2005, 11 (17) :4935-4952
[4]   Ansamycin antibiotics inhibit Akt activation and cyclin D expression in breast cancer cells that overexpress HER2 [J].
Basso, AD ;
Solit, DB ;
Munster, PN ;
Rosen, N .
ONCOGENE, 2002, 21 (08) :1159-1166
[5]   A small molecule designed to bind to the adenine nucleotide pocket of Hsp90 causes Her2 degradation and the growth arrest and differentiation of breast cancer cells [J].
Chiosis, G ;
Timaul, MN ;
Lucas, B ;
Munster, PN ;
Zheng, FF ;
Sepp-Lorenzino, L ;
Rosen, N .
CHEMISTRY & BIOLOGY, 2001, 8 (03) :289-299
[6]   Tumor selectivity of Hsp90 inhibitors: The explanation remains elusive [J].
Chiosis, Gabriela ;
Neckers, Len .
ACS CHEMICAL BIOLOGY, 2006, 1 (05) :279-284
[7]  
Chiosis G, 2006, CURR OPIN INVEST DR, V7, P534
[8]   Novel, potent small-molecule inhibitors of the molecular chaperone Hsp90 discovered through structure-based design [J].
Dymock, BW ;
Barril, X ;
Brough, PA ;
Cansfield, JE ;
Massey, A ;
McDonald, E ;
Hubbard, RE ;
Surgenor, A ;
Roughley, SD ;
Webb, P ;
Workman, P ;
Wright, L ;
Drysdale, MJ .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (13) :4212-4215
[9]   A biochemical rationale for the anticancer effects of Hsp90 inhibitors: Slow, tight binding inhibition by geldanamycin and its analogues [J].
Gooljarsingh, Lata T. ;
Fernandes, Christine ;
Yan, Kang ;
Zhang, Hong ;
Grooms, Michael ;
Johanson, Kyung ;
Sinnamon, Robert H. ;
Kirkpatrick, Robert B. ;
Kerrigan, John ;
Lewis, Tia ;
Arnone, Marc ;
King, Alastair J. ;
Lai, Zhihong ;
Copeland, Robert A. ;
Tummino, Peter J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (20) :7625-7630
[10]   BCR-ABL point mutants isolated from patients with imatinib mesylate-resistant chronic myeloid leukemia remain sensitive to inhibitors of the BCR-ABL chaperone heat shock protein 90 [J].
Gorre, ME ;
Ellwood-Yen, K ;
Chiosis, G ;
Rosen, N ;
Sawyers, CL .
BLOOD, 2002, 100 (08) :3041-3044