Shashidhar U Rao, Age 80301 Wingate Dr, Schaumburg, IL 60193

Shashidhar Rao Phones & Addresses

301 Wingate Dr, Schaumburg, IL 60193 (847) 352-3597

Washington, DC

Elk Grove Village, IL

Mentions for Shashidhar U Rao

Shashidhar Rao resumes & CV records

Resumes

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Quality Analyst

Work:
Ags Health
Quality Analyst
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Shashidhar Rao

Location:
Washington, DC
Industry:
Computer Software
Shashidhar Rao Photo 26

Shashidhar Rao

Shashidhar Rao Photo 27

Shashidhar Rao

Shashidhar Rao Photo 28

Shashidhar Rao

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Shashidhar Rao

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Shashidhar Rao

Publications & IP owners

Us Patents

Substituted Pyrazoles As P38 Kinase Inhibitors

US Patent:
6525059, Feb 25, 2003
Filed:
Feb 24, 2000
Appl. No.:
09/513351
Inventors:
Ashok Anantanarayan - Hainesville IL
Michael Clare - Skokie IL
Paul W. Collins - Deerfield IL
Joyce Zuowu Crich - Glenview IL
Rajesh Devraj - Chesterfield MO
Daniel L. Flynn - Clarkson Valley MO
Lifeng Geng - Skokie IL
Matthew J. Graneto - Chesterfield MO
Cathleen E. Hanau - Chesterfield MO
Gunnar J. Hanson - Skokie IL
Susan J. Hartmann - Kirkwood MO
Michael Hepperle - St. Charles MO
He Huang - Chicago IL
Francis J. Koszyk - Prospect Heights IL
Shuyuan Liao - Northbrook IL
Suzanne Metz - Chesterfield MO
Richard A. Partis - Evanston IL
Thao D. Perry - Chesterfield MO
Shashidhar N. Rao - Mundelein IL
Shaun Raj Selness - St. Louis MO
Michael S. South - St. Louis MO
Michael A. Stealey - Libertyville IL
John Jeffrey Talley - St. Louis MO
Michael L. Vazquez - Ballwin MO
Richard M. Weier - Lake Bluff IL
Xiangdong Xu - Gurnee IL
Ish K. Khanna - Libertyville IL
Yi Yu - Skokie IL
Assignee:
G. D. Searle Company - Skokie IL
International Classification:
A61K 31506
US Classification:
514256, 544333, 544335
Abstract:
A class of pyrazole derivatives is described for use in treating p38 kinase mediated disorders. Compounds of particular interest are defined by Formula IA wherein R , R , R and R are as described in the specification.

Heterocyclic Glycyl -Alanine Derivatives

US Patent:
6689754, Feb 10, 2004
Filed:
Apr 8, 1999
Appl. No.:
09/289140
Inventors:
Nizal Samuel Chandrakumar - Vernon Hills IL
Bipinchandra Nanubhai Desai - Vernon Hills IL
Balekudru Devadas - Chesterfield MO
Alan Frank Gasiecki - Vernon Hills IL
Renee Huff - Park Ridge IL
Ish K. Khanna - Vernon Hills IL
James W. Malecha - Libertyville IL
Julie M. Miyashiro - Skokie IL
Shashidhar N. Rao - Mundelein IL
Joseph Gerace Rico - Ballwin MO
Thomas Edward Rogers - Ballwin MO
Peter Gerrard Ruminski - Dardenne Prairie MO
Mark Andrew Russell - Gurnee IL
Yi Yu - Skokie IL
Assignee:
G. D. Searle Co. - Chicago IL
International Classification:
C07K 506
US Classification:
514 20, 514 19, 546304
Abstract:
The present invention relates to a class of compounds represented by the Formula I or a pharmaceutically acceptable salts thereof, pharmaceutical compositions containing such compounds and methods of treating conditions mediated by the integrin.

Sulfonyl Aryl Hydroxamates And Their Use As Matrix Metalloprotease Inhibitors

US Patent:
6696449, Feb 24, 2004
Filed:
Jul 19, 2001
Appl. No.:
09/909227
Inventors:
Thomas E. Barta - Evanston IL
Daniel P. Becker - Glenview IL
Louis J. Bedell - Prospect Heights IL
Gary A. DeCrescenzo - St. Charles MO
John N Freskos - Clayton MO
Daniel P. Getman - Chesterfield MO
Joseph J. McDonald - Wildwood MO
Brent V. Mischke - Defiance MO
Shashidhar N. Rao - Saint Louis MO
Clara I. Villamil - Glenview IL
Assignee:
Pharmacia Corporation - St. Louis MO
International Classification:
A61K 31496
US Classification:
51425503, 51425212, 51425218, 514309, 514312, 514331, 514469, 514575, 544360, 544383, 546141, 546153, 546233, 546234, 546331
Abstract:
This invention is directed to sulfonyl aromatic hydroxamic acid compounds and salts thereof that, inter alia, inhibit matrix metalloprotease (MMP) activity and/or aggrecanase activity. In some particularly preferred embodiments, the compound corresponds in structure to one of the following formulas: wherein W , the R groups, and âAâRâEâY are described in more detail in Applicants specification. This invention also is directed to a process that comprises administering such a compound or pharmaceutically acceptable salt thereof to a host animal having a condition associated with MMP activity.

Heterocyclic Glycyl Beta-Alanine Derivatives

US Patent:
2004012, Jul 1, 2004
Filed:
Nov 20, 2003
Appl. No.:
10/718328
Inventors:
Nizal Chandrakumar - Vernon Hills IL, US
Bipinchandra Desai - Vernon Hills IL, US
Balekudru Devadas - Chesterfield MO, US
Alan Gasiecki - Vernon Hills IL, US
Renee Huff - Park Ridge IL, US
Ish Khanna - Vernon Hills IL, US
James Malecha - Libertyville IL, US
Julie Miyashiro - Skokie IL, US
Shashidhar Rao - Mundelein IL, US
Joseph Rico - Ballwin MO, US
Thomas Rogers - Ballwin MO, US
Peter Ruminski - Dardenne Prairie MO, US
Mark Russell - Gurnee IL, US
Yi Yu - Skokie IL, US
Assignee:
G. D. Searle & Co. - Chicago IL
International Classification:
A61K031/54
A61K031/537
A61K031/495
A61K031/44
A61K031/426
A61K031/421
A61K031/401
US Classification:
514/183000, 514/217110, 514/227500, 514/237500, 514/255010, 514/317000, 514/370000, 514/374000, 514/377000, 514/398000, 514/423000, 544/059000, 544/162000, 544/382000, 546/306000, 548/190000, 548/230000, 548/531000
Abstract:
The present invention relates to a class of compounds represented by the Formula I or a pharmaceutically acceptable salts thereof, pharmaceutical compositions containing such compounds and methods of treating conditions mediated by the integrin.

Sulfonyl Aryl Or Heteroaryl Hydroxamic Acid Compounds

US Patent:
2005007, Apr 7, 2005
Filed:
Jun 14, 2004
Appl. No.:
10/867391
Inventors:
Louis Bedell - Prospect Heights IL, US
Joseph McDonald - Wildwood MO, US
Thomas Barta - Chapel Hill NC, US
Daniel Becker - Glenview IL, US
Shashidhar Rao - Plainsboro NJ, US
John Freskos - Clayton MO, US
Brent Mischke - Defiance MO, US
Daniel Getman - Chesterfield MO, US
Gary DeCrescenzo - St. Charles MO, US
Clara Villamil - Glenview IL, US
International Classification:
C07D211/84
A61K031/44
A61K031/4015
US Classification:
514345000, 514424000, 546294000, 548530000
Abstract:
A sulfonyl aromatic or heteroaromatic ring hydroxamic acid compound that inter alia inhibits matrix metalloprotease activity is disclosed as are a treatment process that comprises administering a contemplated sulfonyl aromatic or heteroaromatic ring hydroxamic acid compound in a MMP enzyme-inhibiting effective amount to a host having a condition associated with pathological matrix metalloprotease activity.

Cyclopropyl Alkanoic Acid Derivatives

US Patent:
5773644, Jun 30, 1998
Filed:
Mar 27, 1997
Appl. No.:
8/825040
Inventors:
Barbara B. Chen - Glenview IL
Helen Y. Chen - Livingston NJ
Michael Clare - Skokie IL
Shashidhar N. Rao - Mundelein IL
Mark A. Russell - Gurnee IL
Assignee:
G. D. Searle & Co. - Chicago IL
International Classification:
C07C24100
C07C22900
C07D23900
US Classification:
562439
Abstract:
The present invention relates to a class of compounds represented by the Formula I ##STR1## or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising compounds of the Formula I, and methods of selectively inhibiting or antagonizing the. alpha. sub. v. beta. sub. 3 integrin.

2-,3-,5-, And/Or 8-Substituted Dibenzoxazepine Compounds, Pharmaceutical Compositions And Methods For Treating Pain

US Patent:
5449674, Sep 12, 1995
Filed:
Mar 3, 1994
Appl. No.:
8/204175
Inventors:
Timothy J. Hagen - Gurnee IL
Nizal S. Chandrakumar - Vernon Hills IL
E. Ann Hallinan - Evanston IL
Shashidhar N. Rao - Mundelein IL
Barnett S. Pitzele - Skokie IL
Assignee:
G. D. Searle & Co. - Chicago IL
International Classification:
A61K 3155
C07D26720
C07D28116
US Classification:
514211
Abstract:
The present invention provides substituted dibenzoxazepine compounds of Formula I: ##STR1## which are useful as analgesic agents for the treatment of pain, pharmaceutical compositions comprising a therapeutically-effective amount of a compound of Formula I in combination with a pharmaceutically-acceptable carrier, and a method for eliminating or ameliorating pain in an animal comprising administering a therapeutically-effective amount of a compound of Formula I to the animal.

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