Abstract: A class of novel phenyl acetamides is disclosed together with the use of such compounds for inhibiting sPLA2 mediated release of fatty acids for treatment of conditions such as septic shock.
Type:
Grant
Filed:
November 24, 1997
Date of Patent:
March 5, 2002
Assignee:
Eli Lilly and Company
Inventors:
Theodore Goodson, Jr., Richard Waltz Harper, David Kent Herron
Abstract: The present invention provides the compounds of the following formula (I):
and a method for inhibiting the reuptake of seretonin, antagonizing the 5-HT1A receptor and antagonizing the 5-HT2A receptor which comprises administering to a subject in need of such treatment an effective amount of formula (I).
Abstract: This invention provides compounds and their pharmaceutically-acceptable salts, pharmaceutical formulations of said compounds, and methods for treating hyperglycemia associated with non-insulin dependent diabetes and for treating hyperlipidemia.
Type:
Grant
Filed:
March 3, 2000
Date of Patent:
March 5, 2002
Assignee:
Eli Lilly and Company
Inventors:
Samuel James Dominianni, Margaret Mary Faul, Russell Dean Stucky, Leonard Larry Winneroski, Jr.
Abstract: The current invention relates to a method for decreasing levels of homocysteine and/or C-reactive protein in humans comprising administering to a mammal in need thereof an effective amount of a compound of formula I:
or a pharmaceutical salt or solvate thereof.
Abstract: The invention provides isolated nucleic acid compounds encoding FtsZ of Streptococcus pneumoniae. Also provided are vectors and transformed host cells for expressing the encoded protein, and a method for identifying compounds that bind and/or inhibit said protein.
Type:
Grant
Filed:
December 8, 1997
Date of Patent:
February 26, 2002
Assignee:
Eli Lilly and Company
Inventors:
Paul Luther Skatrud, Robert Brown Peery, Q May Wang, Paul Robert Rosteck, Jr., Pamela Kay Rockey
Abstract: This invention is directed to a class of acrylic and propionic acid compounds and their use in the treatment of post-menopausal symptoms and restenosis. In other embodiments, the invention is directed to intermediates and to processes for the preparation of the acrylic and propionic acid compounds.
Type:
Grant
Filed:
September 30, 1997
Date of Patent:
February 26, 2002
Assignee:
Eli Lilly and Company
Inventors:
Charles David Jones, Alan David Palkowitz, Kenneth Jeff Thrasher
Abstract: This application relates to novel compounds of formula (I) (and their pharmaceutically acceptable salts), as defined herein, processes and intermediates for their preparation, pharmaceutical formulations comprising the novel compounds of formula (I), and the use of the compounds of formula (I) as thrombin inhibitors.
Type:
Grant
Filed:
January 24, 2000
Date of Patent:
February 26, 2002
Assignee:
Eli Lilly And Company
Inventors:
Nicholas J Bach, Jolie A. Bastian, Nickolay Y Chirgadze, Michael L Denney, Robert J. Foglesong, Richard W Harper, Mary G Johnson, Ho-Shen Lin, Michael P Lynch, Jefferson R McCowan, Alan D Palkowitz, Daniel J Sall, Gerald F Smith, Kumiko Takeuchi, Minsheng Zhang
Abstract: The present invention provides a method of treatment for patients with sepsis. The claimed treatment is a combination therapy with protein C and BPI protein. Combining protein C, with its anti-coagulant/anti-inflammatory properties, and BPI, with its bactericidal and endotoxin neutralizing activities, provides an effective, synergistic therapy for sepsis that will reduce or ameliorate the adverse events and improve the clinical outcome of septic patients.
Abstract: Anylpiperazines of formula (1) useful as serotonin reuptake inhibitors and 5-HT1D&agr; receptor antagonists are disclosed herein:
wherein
R1 and R2 are each independently hydrogen, halo, —(C1-C6)alkyl or —(C1-C6)alkoxy;
R3 is hydrogen or —(C1-C6)alkyl;
Y is —CO— or —CH2—;
Z is —NH—, —N(COR)— or —CH2— where R is —(C1-C6)alkyl or —(C3-C8)cycloalkyl;
represents a double or single bond;
n and m are an each independently integer from 1 to 3, both inclusive; or a pharmaceutically acceptable salt thereof.
Type:
Grant
Filed:
March 31, 2000
Date of Patent:
January 29, 2002
Assignee:
Eli Lilly and Company
Inventors:
Clint Duane Walker, David Taiwai Wong, Yao-Chang Xu
Abstract: Safer pediculicidal formulations comprising a spinosyn, or a physiologically acceptable derivative or salt thereof, and a physiologically acceptable carrier, and methods of controlling lice infestations in a human with these formulations are provided.
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: This invention provides a series of substituted propanamines useful as tachykinin receptor antagonists. This invention also provides methods employing these substituted propanamines as well as pharmaceutical formulations comprising these compounds.
Type:
Grant
Filed:
January 27, 2000
Date of Patent:
January 15, 2002
Assignee:
Eli Lilly and Company
Inventors:
James E Fritz, Philip A Hipskind, Stephen W Kaldor, Karen L Lobb, James A Nixon
Abstract: The invention relates to a method of administering a fatty acid-acylated insulin or insulin analog by inhalation, a method for treating diabetes by administering a fatty acid-acylated insulin or insulin analog by inhalation, and a method for treating hyperglycemia by administering a fatty acid-acylated insulin or insulin analog by inhalation.
Type:
Grant
Filed:
March 10, 2000
Date of Patent:
January 1, 2002
Assignee:
Eli Lilly and Company
Inventors:
Benjamin Lee Hughes, Ronald Keith Wolff
Abstract: Disclosed are compounds which inhibit &bgr;-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed pharmaceutical compositions comprising a compound which inhibits &bgr;-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.
Type:
Grant
Filed:
May 3, 1999
Date of Patent:
December 25, 2001
Assignees:
Athena Neurosciences, Inc., Eli Lilly & Company
Inventors:
Jing Wu, Eugene D. Thorsett, Jeffrey S. Nissen, Thomas E. Mabry, Lee H. Latimer, Varghese John, Lawrence Y. Fang, James E. Audia
Abstract: A pharmaceutical compound of the formula
in which R1 and R2 are each hydrogen, halo, cyano or methyl,
the dotted line represents an optional double bond,
where R4 and R5 are each hydrogen, C1-6 alkyl, cyclopropyl or cyclopropyl-C1-6 alkyl,
n is 0 or 1, and
R3 is —SR6, —SOR6, —SO2R6, —COR6, —CH2OH or —CONHR7, where R6 is C1-6 alkyl and R7 is hydrogen or C1-6 alkyl;
provided that when one of R1 and R2 is hydrogen and the other is fluoro,
R4 and R5 are each hydrogen or C1-6 alkyl,
and n is 0,
then R3 is not —COR6 or —CONHR7;
and salts thereof.
Type:
Grant
Filed:
November 18, 1999
Date of Patent:
December 11, 2001
Assignee:
Eli Lilly and Company Limited
Inventors:
John Fairhurst, Peter Thaddeus Gallagher, Martin Victor Miles
Abstract: A physical form of (R)-7-acetyl-5-(4-aminophenyl)-8,9-dihydro-8-methyl-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine having an X-ray powder diffraction pattern with d spacings at 12.78, 9.48, 8.99, 8.64, 8.23, 6.39, 6.27. 5.73, 4.01 and 3.96 Å. The compound is useful as an AMPA antagonist.
Abstract: The present invention is directed to methods for the modulation of cardiac function which comprise the administration of certain compounds, as defined herein, having growth hormone secretagogue activity.
Abstract: The invention provides new fluorinated cephalosporin antibiotics and methods of preventing or treating infection, particularly mastitis in ruminants, using these antibiotics, and veterinary and pharmaceutical formulations comprising these antibiotics.
Abstract: The present invention provides DNA compounds that encode ACV synthetase activity of Cephalosporium acremonium. The compounds can be used to construct recombinant DNA expression vectors for a wide variety of host cells, including E. coli, Penicillium, Cephalosporium, and Aspergillus.
Type:
Grant
Filed:
October 29, 1992
Date of Patent:
November 27, 2001
Assignee:
Eli Lilly and Company
Inventors:
Cathleen A. Cantwell, Roland L. Hodges, JoAnn Hoskins, Stephen W. Queener, Paul L. Skatrud
Abstract: The invention provides isolated nucleic acids, vectors, transformed host cells, analogs, functional fragments, and fusion proteins, related to beta-lipotropin. Also provided are pharmaceutical compositions comprising beta-lipotropin or fragments and/or analogs thereof, and methods for treating diabetes and complications associated therewith by administration of an effective amount of beta-lipotropin.
Type:
Grant
Filed:
December 21, 1998
Date of Patent:
November 27, 2001
Assignee:
Eli Lilly and Company
Inventors:
John Edward Hale, Mark Louis Heiman, Brigitte Elisabeth Schoner, William Francis Heath, Jr.