Discovery of GSK2126458, a Highly Potent Inhibitor of PI3K and the Mammalian Target of Rapamycin

被引:328
作者
Knight, Steven D. [1 ]
Adams, Nicholas D. [1 ]
Burgess, JoeIle L. [1 ]
Chaudhari, Amita M. [1 ]
Darcy, Michael G. [1 ]
Donatelli, Carla A. [1 ]
Luengo, Juan I. [1 ]
Newlander, Ken A. [1 ]
Parrish, Cynthia A. [1 ]
Ridgers, Lance H. [1 ]
Sarpong, Martha A. [1 ]
Schmidt, Stanley J. [1 ]
Van Aller, Glenn S. [1 ]
Carson, Jeffrey D. [1 ]
Diamond, Melody A. [1 ]
Elkins, Patricia A. [1 ]
Gardiner, Christine M. [1 ]
Garver, Eric [1 ]
Gilbert, Seth A. [1 ]
Gontarek, Richard R. [1 ]
Jackson, Jeffrey R. [1 ]
Kershner, Kevin L. [1 ]
Luo, Lusong [1 ]
Raha, Kaushik [1 ]
Sherk, Christian S. [1 ]
Sung, Chiu-Mei [1 ]
Sutton, David [1 ]
Tummino, Peter J. [1 ]
Wegrzyn, Ronald J. [1 ]
Auger, Kurt R. [1 ]
Dhanak, Dashyant [1 ]
机构
[1] GlaxoSmithKline Inc, Collegeville, PA 19426 USA
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2010年 / 1卷 / 01期
关键词
GSK2126458; phosphoinositide 3-kinase alpha; mammalian target of rapamycin; PI3K/AKT pathway; CANCER-SPECIFIC MUTATIONS; PHOSPHATIDYLINOSITOL; 3-KINASES; PIK3CA; PHOSPHORYLATION; IDENTIFICATION; P110-ALPHA; PATHWAY; CELL;
D O I
10.1021/ml900028r
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Phosphomositide 3-kinase alpha (PI3K alpha) is a critical regulator of cell growth and transformation, and its signaling pathway is the most commonly mutated pathway in human cancers The mammalian target of rapamycin (mTOR), a class IV PI3K protein kinase, is also a central regulator of cell growth, and mTOR inhibitors are believed to augment the antiproliferative efficacy of PI3K/AKT pathway inhibition 2,4-Difluoro-N-{2-(methyloxy)-5-[4-(4-pyridazinyl)-6-quinolinyl]-3-pyridinyl}benzenesulfonamide (GSK2126458, 1) has been identified as a highly potent, orally bioavailable inhibitor of PI3K alpha and mTOR with in vivo activity in both pharrnacodynamic and tumor growth efficacy models Compound 1 is currently being evaluated in human clinical trials for the treatment of cancer.
引用
收藏
页码:39 / 43
页数:5
相关论文
共 27 条
  • [1] ADAMS ND, 2008, Patent No. 2008144463
  • [2] ADAMS ND, 2008, Patent No. 2008144464
  • [3] [Anonymous], EORTC NCI AACR INT C
  • [4] PDGF-DEPENDENT TYROSINE PHOSPHORYLATION STIMULATES PRODUCTION OF NOVEL POLYPHOSPHOINOSITIDES IN INTACT-CELLS
    AUGER, KR
    SERUNIAN, LA
    SOLTOFF, SP
    LIBBY, P
    CANTLEY, LC
    [J]. CELL, 1989, 57 (01) : 167 - 175
  • [5] Cancer-specific mutations in PIK3CA are oncogenic in vivo
    Bader, AG
    Kang, SY
    Vogt, PK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (05) : 1475 - 1479
  • [6] Beyond PTEN mutations: the PI3K pathway as an integrator of multiple inputs during tumorigenesis
    Cully, M
    You, H
    Levine, AJ
    Mak, TW
    [J]. NATURE REVIEWS CANCER, 2006, 6 (03) : 184 - 192
  • [7] Delano W.L., 2002, CCP4 NEWSL PROTEIN C, V4, P82
  • [8] The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism
    Engelman, Jeffrey A.
    Luo, Ji
    Cantley, Lewis C.
    [J]. NATURE REVIEWS GENETICS, 2006, 7 (08) : 606 - 619
  • [9] The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer
    Folkes, Adrian J.
    Ahmadi, Khatereh
    Alderton, Wendy K.
    Alix, Sonia
    Baker, Stewart J.
    Box, Gary
    Chuckowree, Irina S.
    Clarke, Paul A.
    Depledge, Paul
    Eccles, Suzanne A.
    Friedman, Lori S.
    Hayes, Angela
    Hancox, Timothy C.
    Kugendradas, Arumugam
    Lensun, Letitia
    Moore, Pauline
    Olivero, Alan G.
    Pang, Jodie
    Patel, Sonal
    Pergl-Wilson, Giles H.
    Raynaud, Florence I.
    Robson, Anthony
    Saghir, Nahid
    Salphati, Laurent
    Sohal, Sukhjit
    Ultsch, Mark H.
    Valenti, Melanie
    Wallweber, Heidi J. A.
    Wan, Nan Chi
    Wiesmann, Christian
    Workman, Paul
    Zhyvoloup, Alexander
    Zvelebil, Marketa J.
    Shuttleworth, Stephen J.
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (18) : 5522 - 5532
  • [10] Nonradioactive methods for the assay of phosphoinositide 3-kinases and phosphoinositide phosphatases and selective detection of signaling lipids in cell and tissue extracts
    Gray, A
    Olsson, H
    Batty, IH
    Priganica, L
    Downes, CP
    [J]. ANALYTICAL BIOCHEMISTRY, 2003, 313 (02) : 234 - 245