Abstract: The invention relates to novel heterocycle substituted diphenyl leukotriene B4 (LTB4) antagonists, to compositions containing such compounds, and to methods of using such compounds for treatment of inflammatory diseases.
Type:
Grant
Filed:
April 24, 2002
Date of Patent:
September 28, 2004
Assignee:
Eli Lilly and Company
Inventors:
Jason Scott Sawyer, Douglas Wade Beight, Edward C R Smith, William Thomas McMillen
Abstract: A class of novel indolizine-1-functional compounds and indolizine-3-functional compounds is disclosed together with the use of such indolizine compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of conditions such as septic shock. The compounds are indolizine-1-acetamides, indolizine-1-acetic acid hydrazides, indolizine-1-glyoxylamides, indolizine-3-acetamides, indolizine-3-acetic acid hydraxides, and indolizine-3-glyoxylasides.
Type:
Grant
Filed:
April 28, 1997
Date of Patent:
November 11, 2003
Assignees:
Eli Lilly and Company, Shiongi and Company, Ltd.
Inventors:
Robert D. Dillard, Sanji Hagishita, Mitsuaki Ohtani
Abstract: A method is disclosed for the treatment of non-rheumatoid arthritis by administering to a mammal in need thereof a therapeutically effective amount of an sPLA2 inhibitor.
Abstract: A class of novel acylsulfonamide substituted indole compounds is disclosed together with the use of such compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of inflammatory diseases.
Type:
Grant
Filed:
January 30, 2001
Date of Patent:
August 19, 2003
Assignee:
Eli Lilly and Company
Inventors:
Edward David Mihelich, Michael LeRoy Phillips, Alan M Warshawsky
Abstract: A method is disclosed for the treatment of cystic fibrosis by administering to a human in need thereof a therapeutically effective amount of an sPLA2 inhibitor, such as a 1H-indole-3-glyoxylamide.
Abstract: A method is disclosed for the prevention and treatment of Alzheimer's disease by administering to a human in need thereof an effective amount of a substituted tricyclic sPLA2 inhibitor.
Abstract: This invention relates to a method of making N-benzyl indoles, and to intermediates for use in the method, and to certain substantially optically pure N-benzyl indoles obtained by the method.
Type:
Grant
Filed:
August 11, 2000
Date of Patent:
January 21, 2003
Assignees:
The University of East Anglia, Eli Lilly and Company
Inventors:
Nicholas James Bach, Stephen Richard Baker, Jeremy Gilmore, Russell Andrew Lewthwaite, Alexander McKillop, Jason Scott Sawyer, George Richard Stephenson, Michael William John Urquhart
Abstract: A class of novel indole is disclosed together with the use of such compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of inflammatory diseases such as septic shock.
Type:
Grant
Filed:
January 30, 2001
Date of Patent:
September 17, 2002
Assignee:
Eli Lilly and Company
Inventors:
Nicholas James Bach, Robert Delane Dillard, Susan Elizabeth Draheim, Edward David Mihelich, Tulio Suarez
Abstract: This invention is a method of treating a mammal, including a human, susceptible to having Alzheimer's disease, to prevent or delay the onset of Alzheimer's disease; said method comprising administering to said mammal a prophylactically effective amount of 1H-indole-3-glycoxyamide sPLA2 inhibitor or a pharmaceutically acceptable salt, solvate or prodrug derivative thereof.
Abstract: A class of novel 1H-indole-3-glyoxylamides is disclosed together with the use of such indole compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of conditions such as septic shock.
Type:
Grant
Filed:
November 16, 2000
Date of Patent:
August 13, 2002
Assignee:
Eli Lilly and Company
Inventors:
Nicholas J. Bach, Robert D. Dillard, Susan E. Draheim
Abstract: A class of novel oxime indoles is disclosed together with the use of such compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of inflammatory diseases such as septic shock.
Type:
Grant
Filed:
May 30, 2001
Date of Patent:
May 21, 2002
Assignee:
Eli Lilly and Company
Inventors:
Nicholas James Bach, Richard Waltz Harper, Michael Dean Kinnick, Ho-Shen Lin, John Michael Morin, Jr., Michael Enrico Richett
Abstract: The compounds are of the class of pyrrolo[2,3-d]pyrimidines useful for inhibiting sPLA2 mediated release of fatty acids for treatment of diseases such as septic shock.
Type:
Grant
Filed:
December 11, 2000
Date of Patent:
May 7, 2002
Assignee:
Eli Lilly and Company
Inventors:
Darrell Robert Hutchison, Michael John Martinelli, Thomas Michael Wilson
Abstract: The present invention is directed to compounds for treating inflammatory bowel disease. More specifically, the present invention is directed to 1H-indole-3-glyoxyamide compounds a sPLA2 inhibitors for treating inflammatory bowel disease.
Abstract: The compound, ((3-(2-amino-1,2-dioxoethyl)-1-((1,1′-biphenyl-3-ylmethyl)-2-methyl-1H-indol-4-yl)oxy)acetic acid N,N-diethylglycolamido ester, is disclosed together with its use as a highly bioavailable indole compound for inhibiting sPLA2 mediated release of fatty acids for treatment of conditions such as septic shock.
Type:
Grant
Filed:
March 29, 2000
Date of Patent:
August 14, 2001
Assignee:
Eli Lilly and Company
Inventors:
Michael L Denney, John M Morin, Jr., Daniel J Sall, Jason S Sawyer
Abstract: The compound, ((3(2-amino-1,2-dioxoethyl)-2-methyl-1-(phenylmethyl)-1H-indol-4-yl)oxy)acetic acid N-morpholino ester, is disclosed together with its use as a highly bioavailable indole sPLA2 inhibitor compound.
Type:
Grant
Filed:
October 17, 2000
Date of Patent:
August 14, 2001
Assignee:
Eli Lilly and Company
Inventors:
Michael Lyle Denney, John Michael Morin, Daniel Jon Sall, Jason Scott Sawyer
Abstract: A class of novel 1H-indole-3-acetamides is disclosed together with the use of such indole compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of conditions such as septic shock.
Type:
Grant
Filed:
October 31, 1997
Date of Patent:
June 26, 2001
Assignee:
Eli Lilly and Company
Inventors:
Nicholas J. Bach, Robert D. Dillard, Susan E. Draheim, Robert B. Hermann, Richard W. Schevitz
Abstract: Indene-1-acetamide compounds of the general formula (I) below;
inhibit sPLA2 mediated release of fatty acids and are useful for treatment of conditions such as septic shock.
Type:
Grant
Filed:
July 21, 1994
Date of Patent:
April 10, 2001
Assignees:
Eli Lilly and Company, Shionogi & Company, Ltd.
Inventors:
Robert D. Dillard, Sanji Hagishita, Mitsuaki Ohtani
Abstract: The compound, ((3(2-amino-1,2-dioxoethyl)-1-((1,1′-biphenyl)-3-ylmethyl)-2-methyl-1H-indol-4-yl)oxy)acetic acid morpholino-ethyl ester, is disclosed together with its use as a highly bioavailable indole compound for inhibiting sPLA2 mediated release of fatty acids for treatment of conditions such as septic shock.
Type:
Grant
Filed:
March 29, 2000
Date of Patent:
January 23, 2001
Assignee:
Eli Lilly and Company
Inventors:
Michael L Denney, John M Morin, Daniel J Sall, Jason S Sawyer
Abstract: A class of novel 1H-indole-3-glyoxylamides is disclosed together with the use of such indole compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of conditions such as septic shock.
Type:
Grant
Filed:
February 26, 1999
Date of Patent:
January 16, 2001
Assignee:
Eli Lilly and Company
Inventors:
Nicholas J. Bach, Robert D. Dillard, Susan E. Draheim