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

Author:

Folkes Adrian J.1,Ahmadi Khatereh1,Alderton Wendy K.1,Alix Sonia1,Baker Stewart J.1,Box Gary1,Chuckowree Irina S.1,Clarke Paul A.1,Depledge Paul1,Eccles Suzanne A.1,Friedman Lori S.1,Hayes Angela1,Hancox Timothy C.1,Kugendradas Arumugam1,Lensun Letitia1,Moore Pauline1,Olivero Alan G.1,Pang Jodie1,Patel Sonal1,Pergl-Wilson Giles H.1,Raynaud Florence I.1,Robson Anthony1,Saghir Nahid1,Salphati Laurent1,Sohal Sukhjit1,Ultsch Mark H.1,Valenti Melanie1,Wallweber Heidi J.A.1,Wan Nan Chi1,Wiesmann Christian1,Workman Paul1,Zhyvoloup Alexander1,Zvelebil Marketa J.1,Shuttleworth Stephen J.1

Affiliation:

1. Piramed Pharma, 957 Buckingham Avenue, Slough, Berks SL1 4NL, United Kingdom, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, Cancer Research UK Centre for Cancer Therapeutics, The Institute of Cancer Research, Haddon Laboratories, Sutton, Surrey, SN2 5NG, United Kingdom and Breakthrough Breast Cancer Research Centre, The Institute of Cancer Research, London, SW3 6JB, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

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