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
  • [21] Inhibition of heat shock protein 90 prolongs survival of mice with BCR-ABL-T315I-induced leukemia and suppresses leukemic stem cells
    Peng, Cong
    Brain, Julia
    Hu, Yiguo
    Goodrich, Ami
    Kong, Linghong
    Grayzel, David
    Pak, Roger
    Read, Margaret
    Li, Shaoguang
    [J]. BLOOD, 2007, 110 (02) : 678 - 685
  • [22] Inhibition of Hsp90 with synthesis macrolactones: Synthesis and structural and biological evaluation of ring and conformational analogs of radicicol
    Proisy, Nicolas
    Sharp, Swee Y.
    Boxall, Kathy
    Connelly, Stephen
    Roe, S. Mark
    Prodromou, Chrisostomos
    Slawin, Alexandra M. Z.
    Pearl, Laurence H.
    Workman, Paul
    Moody, Christopher J.
    [J]. CHEMISTRY & BIOLOGY, 2006, 13 (11): : 1203 - 1215
  • [23] Schulte TW, 1998, CELL STRESS CHAPERON, V3, P100, DOI 10.1379/1466-1268(1998)003<0100:ARBTTN>2.3.CO
  • [24] 2
  • [25] Targeting of the protein chaperone, HSP90, by the transformation suppressing agent, radicicol
    Sharma, SV
    Agatsuma, T
    Nakano, H
    [J]. ONCOGENE, 1998, 16 (20) : 2639 - 2645
  • [26] Geldanamycin activates a heat shock response and inhibits huntingtin aggregation in a cell culture model of Huntington's disease
    Sittler, A
    Lurz, R
    Lueder, G
    Priller, J
    Hayer-Hartl, MK
    Hartl, FU
    Lehrach, H
    Wanker, EE
    [J]. HUMAN MOLECULAR GENETICS, 2001, 10 (12) : 1307 - 1315
  • [27] Soga S, 1999, CANCER RES, V59, P2931
  • [28] Solit DB, 2003, CANCER RES, V63, P2139
  • [29] Development of 17-allylamino-17-demethoxygeldanamycin hydroquinone hydrochloride (IPI-504), an anti-cancer agent directed against Hsp90
    Sydor, Jens R.
    Normant, Emmanuel
    Pien, Christine S.
    Porter, James R.
    Ge, Jie
    Grenier, Louis
    Pak, Roger H.
    Ali, Janid A.
    Dembski, Marlene S.
    Hudak, Jebecka
    Patterson, Jon
    Penders, Courtney
    Pink, Melissa
    Read, Margaret A.
    Sang, Jim
    Woodward, Caroline
    Zhang, Yilong
    Grayzel, David S.
    Wright, Jim
    Barrett, John A.
    Palombella, Vito J.
    Adams, Julian
    Tong, Jeffrey K.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (46) : 17408 - 17413
  • [30] Targeting wide-range oncogenic transformation via PU24FCI, a specific inhibitor of tumor Hsp90
    Vilenchik, M
    Solit, D
    Basso, A
    Huezo, H
    Lucas, B
    He, HZ
    Rosen, N
    Spampinato, C
    Modrich, P
    Chiosis, G
    [J]. CHEMISTRY & BIOLOGY, 2004, 11 (06): : 787 - 797