Chung-Pin Chen - Madison CT Timothy Paul Connolly - Meriden CT Laxma Reddy Kolla - Rocky Hill CT John D. Matiskella - Wallingford CT Richard H. Mueller - Ringoes NJ Yadagiri Pendri - South Glastonbury CT Dejah T. Petsch - Mansfield Center CT
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
C07F 902
US Classification:
544243, 544337, 548112, 558 87
Abstract:
An improved process is provided for preparing water-soluble prodrugs of triazole antifungal compounds containing a secondary or tertiary hydroxyl group. More particularly, the improved process is directed toward preparation of water-soluble triazole antifungal compounds are provided having the general formula wherein A is the non-hydroxy portion of a triazole antifungal compound of the type containing a secondary or tertiary hydroxyl group and R and R are as defined in the specification.
Thomas W. Hudyma - Durham CT, US Xiaofan Zheng - Cheshire CT, US B. Narasimhulu Naidu - Durham CT, US Margaret E. Sorenson - Meriden CT, US Alicia Regueiro-Ren - Middletown CT, US Timothy P. Connolly - Middletown CT, US John D. Matiskella - Wallingford CT, US Oak K. Kim - Cambridge MA, US Yunhui Zhang - Glastonbury CT, US Dane M. Springer - North Haven CT, US Jason Goodrich - Meriden CT, US Yasutsugu Ueda - Clinton CT, US Joanne J. Bronson - Durham CT, US
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
A61K 38/16
US Classification:
514 8, 514 9, 530317
Abstract:
The present invention provides compounds of formula I having potent antibiotic activity, including activity towards Gram-positive bacteria and mycobacteria.
B. Narasimhulu Naidu - Durham CT, US Jacques Banville - St-Hubert, CA Francis Beaulieu - Laprairie, CA Timothy P. Connolly - Portland CT, US Mark R. Krystal - Westport CT, US John D. Matiskella - Wallingford CT, US Carl Ouellet - Boucherville, CA Serge Plamondon - Ste-Catherine, CA Roger Remillard - Napierville, CA Margaret E. Sorenson - Meriden CT, US Yasutsugu Ueda - Clinton CT, US Michael A. Walker - Durham CT, US
The invention encompasses a series bicyclic pyrimidinone compounds of Formula I which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses pharmaceutical compositions and methods for treating those infected with HIV.
B. Narasimhulu Naidu - Durham CT, US Jacques Banville - St-Hubert, CA Francis Beaulieu - Laprairie, CA Timothy P. Connolly - Portland CT, US Mark R. Krystal - Westport CT, US John D. Matiskella - Wallingford CT, US Carl Ouellet - Boucherville, CA Serge Plamondon - Ste-Catherine, CA Roger Remillard - Napierville, CA Margaret E. Sorenson - Meriden CT, US Yasutsugu Ueda - Clinton CT, US Michael A. Walker - Durham CT, US
The invention encompasses a series cyclic bicyclic pyrimidinone compounds of Formula I which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses pharmaceutical compositions and methods for treating those infected with HIV.
Hiv Integrase Inhibitors: Cyclic Pyrimidinone Compounds
The invention encompasses a series of pyrimidinone compounds which inhibit HIV integrase and thereby prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses intermediates useful for making the pyrimidone compounds. Additionally, pharmaceutical compositions and methods for treating those infected with HIV are encompassed.
N-[[4-Fluoro-2-(5-Methy-1H-1,2,4-Triazol-1-Yl)Phenyl]Methyl]-4-,6,7,9-Tetrahydro-3-Hydroxy-9,9-Dimethyl-4-Oxo-Pyrimido[2,1-C][1,4]Oxazine-2-Carboxamide As An Hiv Integrase Inhibitor
B. Narasimhulu Naidu - Durham CT, US Jacques Banville - St-Hubert, CA Francis Beaulieu - Laprairie, CA Timothy P. Connolly - Portland CT, US Mark R. Krystal - Westport CT, US John D. Matiskella - Wallingford CT, US Carl Ouellet - Boucherville, CA Serge Plamondon - Ste-Catherine, CA Roger Remillard - Napierville, CA Margaret E. Sorenson - Meriden CT, US Yasutsugu Ueda - Clinton CT, US Michael A. Walker - Durham CT, US
The invention encompasses a series of bicyclic pyrimidinone compounds of Formula I which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses pharmaceutical compositions and methods for treating those infected with HIV.
Prodrugs Of Piperazine And Substituted Piperidine Antiviral Agents
Yasutsugu Ueda - Clinton CT, US Timothy P. Connolly - Portland CT, US John F. Kadow - Wallingford CT, US Nicholas A. Meanwell - East Hampton CT, US Tao Wang - Middletown CT, US Chung-Pin H. Chen - Madison CT, US Kap-Sun Yeung - Madison CT, US Zhongxing Zhang - Madison CT, US David Kenneth Leahy - Somerset NJ, US Shawn K. Pack - Plainsboro NJ, US Nachimuthu Soundararajan - Kendall Park NJ, US Pierre Sirard - St. Jean sur Richelieu, CA Kathia Levesque - Ste-Catherine, CA Dominique Thoraval - Candiac, CA
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
C07D 401/00
US Classification:
544362
Abstract:
This invention provides for prodrug Compounds I, pharmaceutical compositions thereof, and their use in treating HIV infection. Also, this invention provides for intermediate Compounds II useful in making prodrug Compounds I.
Francis Beaulieu - Quebec, CA Carl Ouellet - Boucherville, CA B. Narasimhulu Naidu - Durham CT, US Manoj Patel - Berlin CT, US Yasutsugu Ueda - Clinton CT, US Timothy P. Connolly - Portland CT, US Jonathan R. Weiss - Boston MA, US Michael A. Walker - Durham CT, US Nicholas A. Meanwell - East Hampton CT, US Kevin M. Peese - Haddam CT, US Margaret E. Sorenson - Meriden CT, US Chen Li - South Glastonbury CT, US
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
A61K 31/505 C07D 487/12
US Classification:
514267, 544252
Abstract:
The disclosure generally relates to the novel compounds of formula I, including their salts, which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses pharmaceutical compositions and methods for treating those infected with HIV.
Dr. Connolly graduated from the Georgetown University School of Medicine in 1998. He works in Houston, TX and specializes in Pulmonary Critical Care Medicine and Sleep Medicine. Dr. Connolly is affiliated with Baylor St Lukes Medical Center and Houston Methodist Hospital.
Name / Title
Company / Classification
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Timothy J. Connolly Director
Hdr Environmental, Operations and Construction, Inc Business Consulting Services · Engineering Services & Environmental Consultant
(610)9499699, (916)8527792, (830)4384720
Timothy Connolly President, Principal
Connolly Construction Company, LLC Single-Family House Construction
134 Main St S, Southbury, CT 06488
Timothy Connolly Managing
Connolly Squared, LLC
Timothy Connolly
BIG CREEK DISTRIBUTION LLC
Timothy Connolly
Timothy J Connolly Broker
134 Main St S, Southbury, CT 06488 (203)3941979
Timothy Connolly President, Principal
SADDLE ROCK ASSOCIATES, LLC General Warehouse/Storage