Abstract: The present invention relates to the design, synthesis, and the peptidyl-prolyl isomerase (PPIase or rotamase) inhibitory activity of novel &agr;,&agr;-difluoroacetamido compounds that are neurotrophic agents (i.e. compounds capable of stimulating growth or proliferation of nervous tissue) and that bind to immunophilins such as FKBP12 and inhibit their rotamase activity. This invention also relates to pharmaceutical compositions comprising these compounds.
Type:
Grant
Filed:
June 9, 2000
Date of Patent:
May 29, 2001
Assignee:
Bristol-Myers Squibb Company
Inventors:
Vivekananda M. Vrudhula, Gene M. Dubowchik, Bireshwar Dasgupta, Dolatrai M. Vyas
Abstract: The present invention relates to the design, synthesis, and the peptidyl-prolyl isomerase (PPIase or rotamase) inhibitory activity of novel pyrrolidinemethyl diamide and carbamate compounds that are neurotrophic agents (i.e. compounds capable of stimulating growth or proliferation of nervous tissue) and that bind to immunophilins such as FKBP12 and inhibit their rotamase activity. This invention also relates to pharmaceutical compositions comprising these compounds.
Type:
Grant
Filed:
November 8, 1999
Date of Patent:
May 8, 2001
Assignee:
Bristol-Myers Squibb Company
Inventors:
Gene M. Dubowchik, Jonathan L. Ditta, David P. Provencal, Derek J. Denhart
Abstract: Novel thiazolyl peptide antibiotic compounds, including nocathiacin I, II and III, are disclosed. Also, novel microorganism ATCC-202099 is disclosed.
Type:
Grant
Filed:
July 13, 1999
Date of Patent:
April 17, 2001
Assignee:
Bristol-Myers Squibb Company
Inventors:
John E. Leet, Helen A. Ax, Donald R. Gustavson, Daniel M. Brown, Laura Turner, Kimberly Brown, Wenying Li, Kin S. Lam
Abstract: The present invention concerns novel 7-ethers of taxane derivatives, their use as antitumor agents and pharmaceutical compositions containing the novel compounds.
Abstract: The present invention relates to the design, synthesis, and the peptidyl-prolyl isomerase (PPIase or rotamase) inhibitory activity of novel .alpha.,.alpha.-difluoroacetamido compounds that are neurotrophic agents (i.e. compounds capable of stimulating growth or proliferation of nervous tissue) and that bind to immunophilins such as FKBP12 and inhibit their rotamase activity. This invention also relates to pharmaceutical compositions comprising these compounds.
Type:
Grant
Filed:
May 21, 1999
Date of Patent:
August 1, 2000
Assignee:
Bristol-Myers Squibb Company
Inventors:
Vivekananda M. Vrudhula, Gene M. Dubowchik, Bireshwar Dasgupta, Dolatrai M. Vyas
Abstract: This invention relates to uncoated direct compression tablets containing cefadroxil monohydrate as the active ingredient, which are capable of oral administration to human beings by swallowing, chewing or disintegrating in water resulting in a drinkable dispersion.
Abstract: The present invention relates to novel taxane derivatives wherein, the taxol ring is substituted by sulfur groups on the C-7, their use as antitumor agents and pharmaceutical formulations.
Abstract: The present invention provides novel cis-N-iminomethyl-3,4-disubstituted-2-azetidinones, and their use in the preparation of N-acyl-2-azetidinones, intermediates in the semi-synthesis of taxol and taxol derivatives.
Type:
Grant
Filed:
January 10, 1995
Date of Patent:
December 28, 1999
Assignee:
Bristol-Myers Squibb Company
Inventors:
Allan W. Rey, Purushotham Vemishetti, Roberto Droghini
Abstract: The present invention is directed to the use of pharmaceutical compositions containing anti-retroviral effective amounts of (a) d4T and (b) 5-fluorouracil or a prodrug, or salt thereof.
Abstract: This invention relates to a stable, easy to constitute, injectable formulation of anticancer agent BMY-25067. More specifically, the present invention concerns a formulation of BMY-25067 obtained from lyophilizing a solution comprising up to 4 mg of BMY-25067 per mL of 65% t-butanol/water, further comprising about 2% PVP (K-12 or K-17), optionally comprising pharmaceutically acceptable carrier(s).
Type:
Grant
Filed:
December 4, 1996
Date of Patent:
December 30, 1997
Assignee:
Bristol-Myers Squibb Company
Inventors:
Uday S. Gogate, Shreeram N. Agharkar, Lawan Phusanti
Abstract: Etoposide phosphate is prepared by coupling dibenzyl 4'-demethyl-4-epipodophyllotoxin-4'-phosphate with 2,3-di-O-benzyl-4,6-O-ethylidene-.alpha.,.beta.-D-glucopyranose in a solvent and subsequently removing the protecting groups. The tetra-benzyl protected etoposide phosphate is recrystallized from methanol or directly crystallized from acetonitrile by adding methanol to yield substantially the pure C-1"-.beta. form. The benzyl protecting groups are simultaneously removed by hydrogenation to produce etoposide phosphate in high yields. In a further embodiment, etoposide phosphate is treated with a phosphatase enzyme to yield etoposide.
Type:
Grant
Filed:
June 7, 1995
Date of Patent:
November 18, 1997
Assignee:
Bristol-Myers Squibb Company
Inventors:
Lee J. Silverberg, Purushotham Vemishetti, John L. Dillon, Jr., John J. Usher
Abstract: The present invention concerns antitumor compounds. More particularly, the invention provides novel taxane derivatives, pharmaceutical compositions thereof, and their use as antitumor agents.
Type:
Grant
Filed:
May 19, 1995
Date of Patent:
July 8, 1997
Assignee:
Bristol-Myers Squibb Company
Inventors:
Jerzy Golik, Dolatrai Vyas, John J. Wright, Henry Wong, John F. Kadow, John K. Thottathil, Wen-Sen Li, Murray A. Kaplan, Robert K. Perrone, Mark D. Wittman