1776112-90-3Relevant articles and documents
Discovery of N-((3R,4R)-4-Fluoro-1-(6-((3-methoxy-1-methyl-1H-pyrazol-4-yl)amino)-9-methyl-9H-purin-2-yl)pyrrolidine-3-yl)acrylamide (PF-06747775) through Structure-Based Drug Design: A High Affinity Irreversible Inhibitor Targeting Oncogenic EGFR Mutants
Planken, Simon,Behenna, Douglas C.,Nair, Sajiv K.,Johnson, Theodore O.,Nagata, Asako,Almaden, Chau,Bailey, Simon,Ballard, T. Eric,Bernier, Louise,Cheng, Hengmiao,Cho-Schultz, Sujin,Dalvie, Deepak,Deal, Judith G.,Dinh, Dac M.,Edwards, Martin P.,Ferre, Rose Ann,Gajiwala, Ketan S.,Hemkens, Michelle,Kania, Robert S.,Kath, John C.,Matthews, Jean,Murray, Brion W.,Niessen, Sherry,Orr, Suvi T. M.,Pairish, Mason,Sach, Neal W.,Shen, Hong,Shi, Manli,Solowiej, James,Tran, Khanh,Tseng, Elaine,Vicini, Paolo,Wang, Yuli,Weinrich, Scott L.,Zhou, Ru,Zientek, Michael,Liu, Longqing,Luo, Yiqin,Xin, Shuibo,Zhang, Chengyi,Lafontaine, Jennifer
, p. 3002 - 3019 (2017/04/24)
Mutant epidermal growth factor receptor (EGFR) is a major driver of non-small-cell lung cancer (NSCLC). Marketed first generation inhibitors, such as erlotinib, effect a transient beneficial response in EGFR mutant NSCLC patients before resistance mechani
PURINE DERIVATIVES
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, (2015/05/26)
The present invention relates to compounds of formula (I) or pharmaceutically acceptable salts thereof, wherein Q, G, ring A, ring B, R1, R2, R3, R4, R5, R5a, R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18, R19, R20, R21, R22, R23, R24, and m are defined herein. The novel purine derivatives are useful in the treatment of abnormal cell growth, such as cancer, in mammals. Additional embodiments relate to pharmaceutical compositions containing the compounds and to methods of using the compounds and compositions in the treatment of abnormal cell growth in mammals.