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:
Jun. 28, 2011

Filed:

Oct. 31, 2007
Applicants:

Bingwei Vera Yang, Belle Mead, NJ (US);

Lidia M. Doweyko, Long Valley, NJ (US);

Wayne Vaccaro, Yardley, PA (US);

Tram N. Huynh, Pennington, NJ (US);

David R. Tortolani, Skillman, NJ (US);

T. G. Murali Dhar, Newtown, PA (US);

Inventors:

Bingwei Vera Yang, Belle Mead, NJ (US);

Lidia M. Doweyko, Long Valley, NJ (US);

Wayne Vaccaro, Yardley, PA (US);

Tram N. Huynh, Pennington, NJ (US);

David R. Tortolani, Skillman, NJ (US);

T. G. Murali Dhar, Newtown, PA (US);

Assignee:

Bristol-Myers Squibb Company, Princeton, NJ (US);

Attorneys:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61K 31/5377 (2006.01); A61K 31/5375 (2006.01); A61K 31/505 (2006.01); A61K 31/50 (2006.01); A61K 31/4965 (2006.01); A61K 31/496 (2006.01); A61K 31/4709 (2006.01); A61K 31/454 (2006.01); A61K 31/4439 (2006.01); A61K 31/433 (2006.01); A61K 31/426 (2006.01); A61K 31/427 (2006.01); A61K 31/428 (2006.01); A61K 31/421 (2006.01); A61K 31/4168 (2006.01); A61K 31/415 (2006.01); A61K 31/165 (2006.01); C07D 417/04 (2006.01); C07D 417/12 (2006.01); C07D 277/46 (2006.01); C07D 285/135 (2006.01); C07D 263/48 (2006.01); C07D 241/20 (2006.01); C07D 239/42 (2006.01); C07D 233/88 (2006.01); C07D 231/44 (2006.01);
U.S. Cl.
CPC ...
Abstract

Novel non-steroidal compounds are provided which are useful in treating diseases associated with modulation of the glucocorticoid receptor, AP-1, and/or NF-κB activity including inflammatory and immune diseases, obesity and diabetes having the structure of formula (I) an enantiomer, diastereomer, tautomer, solvate (e.g. a hydrate), or a pharmaceutically-acceptable salt, thereof, wherein: M is selected from alkyl, substituted alkyl, cycloalkyl, aryl, heterocyclo, and heteroaryl, provided that if M is alkyl then Rand Rtaken together with the carbon atom to which they are both attached are selected from a group other than cycloalkyl; Q is selected from (i) hydrogen, C-Calkyl, and substituted C-Calkyl; or (ii) Q and Rare combined with the carbon atoms to which they are attached to form a 3- to 6-membered cycloalkyl; or (iii) Q and MM are combined with the carbon atom(s) to which they are attached to form a 3- to 7-membered ring containing 1-2 heteroatoms which are independently selected from the group consisting of O, S, SO, and N which ring may be optionally substituted with 0-2 Rgroups or carbonyl; Z is selected from cycloalkyl, heterocyclo, aryl, or heteroaryl; and M, Z, R, R, R, R, R, R, and Rare as defined herein. Also provided are pharmaceutical compositions and methods of treating metabolic and inflammatory- or immune-associated diseases or disorders using said compounds.


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