The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Feb. 17, 2015

Filed:

Feb. 17, 2011
Applicants:

Christopher Thomas Brain, North Reading, MA (US);

Young Shin Cho, Cambridge, MA (US);

John William Giraldes, Quincy, MA (US);

Bharat Lagu, Acton, MA (US);

Julian Roy Levell, Arlington, MA (US);

Michael J. Luzzio, Noank, CT (US);

Lawrence Blas Perez, Hopkinton, MA (US);

Yaping Wang, Boxborough, MA (US);

Fan Yang, West Roxbury, MA (US);

Inventors:

Christopher Thomas Brain, North Reading, MA (US);

Young Shin Cho, Cambridge, MA (US);

John William Giraldes, Quincy, MA (US);

Bharat Lagu, Acton, MA (US);

Julian Roy Levell, Arlington, MA (US);

Michael J. Luzzio, Noank, CT (US);

Lawrence Blas Perez, Hopkinton, MA (US);

Yaping Wang, Boxborough, MA (US);

Fan Yang, West Roxbury, MA (US);

Assignee:

Novartis AG, Basel, CH;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 31/50 (2006.01); A61K 31/501 (2006.01); C07D 401/00 (2006.01); C07D 403/00 (2006.01); C07D 405/00 (2006.01); C07D 409/00 (2006.01); A01N 43/90 (2006.01); A61K 31/519 (2006.01); C07D 487/00 (2006.01); C07D 498/20 (2006.01); C07D 487/04 (2006.01); C07D 519/00 (2006.01); C07D 471/08 (2006.01); C07D 471/10 (2006.01); C07D 487/08 (2006.01); C07D 498/08 (2006.01);
U.S. Cl.
CPC ...
C07D 498/20 (2013.01); C07D 487/04 (2013.01); C07D 519/00 (2013.01); C07D 471/08 (2013.01); C07D 471/10 (2013.01); C07D 487/08 (2013.01); C07D 498/08 (2013.01);
Abstract

The invention is directed to novel pyrrolopyrimidine compounds of formula (I) wherein R, R, R, R-R, A and L are defined herein and to salts, including pharmaceutically acceptable salts thereof. The compounds of the present invention are CDK4/6 inhibitors and could be useful in the treatment of diseases and disorders mediated by CDK4/6, such as cancer, including mantle cell lymphoma, liposarcoma, non small cell lung cancer, melanoma, squamous cell esophageal cancer and breast cancer. The invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting CDK4/6 activity and to the treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.


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