Abstract: Bacterial protein synthesis-inhibiting compounds having formula (I) and salts, prodrugs, and salts of prodrugs thereof, processes for making the compounds and intermediates in the processes, compositions containing the compounds, and methods of using the compounds are disclosed.
Type:
Grant
Filed:
February 15, 2007
Date of Patent:
June 15, 2010
Assignee:
Abbott Laboratories
Inventors:
David D. Anderson, Bruce A. Beutel, Curt S. Cooper, Yu-Gui Gu, Mira M. Hinman, Douglas M. Kalvin, Robert F. Keyes, Xenia B. Searle, Rolf Wagner
Abstract: A compound of the formula is disclosed as a prodrug of an HIV protease inhibitor. Methods and compositions for inhibiting HIV protease activity and treating HIV infection are also disclosed.
Type:
Grant
Filed:
June 29, 2005
Date of Patent:
May 18, 2010
Assignee:
Abbott Laboratories
Inventors:
David A. DeGoey, William J. Flosi, David J. Grampovnik, Larry L. Klein, Dale J. Kempf, Xiu C. Wang
Abstract: Bacterial protein synthesis-inhibiting compounds having formula (I) and salts, prodrugs, and salts of prodrugs thereof, processes for making the compounds and intermediates in the processes, compositions containing the compounds, and methods of using the compounds are disclosed.
Type:
Grant
Filed:
February 4, 2005
Date of Patent:
December 15, 2009
Assignee:
Abbott Laboratories
Inventors:
Mira M Hinman, Teresa A. Rosenberg, Rolf Wagner
Abstract: The present invention is directed to a method for inducing UGT1A1 isoform expression for treatment of a disease, disorder or adverse effect caused by an elevated serum concentration of an UGT1A1 substrate comprising the step of administering to a subject an effective amount of ritonavir. In particular, the present invention is directed to a method of treating unconjugated hyperbilirubinemia by UGT1A1 induction comprising the step of administering to a subject an effective amount of ritonavir.
Type:
Grant
Filed:
January 15, 2008
Date of Patent:
June 16, 2009
Assignee:
Abbott Laboratories
Inventors:
Dale J. Kempf, Richard J. Bertz, Jeffrey F. Waring
Abstract: The present invention is directed to a method for inducing UGT1A1 isoform expression for treatment of a disease, disorder or adverse effect caused by an elevated serum concentration of an UGT1A1 substrate comprising the step of administering to a subject an effective amount of ritonavir. In particular, the present invention is directed to a method of treating unconjugated hyperbilirubinemia by UGT1A1 induction comprising the step of administering to a subject an effective amount of ritonavir.
Type:
Grant
Filed:
March 18, 2004
Date of Patent:
January 22, 2008
Assignee:
Abbott Laboratories
Inventors:
Dale J. Kempf, Richard J. Bertz, Jeffrey F. Waring
Abstract: Compounds of formula (I) are novel VR1 antagonists that are useful in treating pain, inflammatory thermal hyperalgesia, urinary incontinence and bladder overactivity, wherein X1, X2, X3, X4, X5, R5, R6, R7, R8a, R8b, R9, Z1, Z2 and L are as defined in the description.
Type:
Grant
Filed:
August 5, 2003
Date of Patent:
August 23, 2005
Assignee:
Abbott Laboratories
Inventors:
Chih-Hung Lee, Erol K. Bayburt, Stanley DiDomenico, Jr., Irene Drizin, Arthur R. Gomtsyan, John R. Koenig, Richard J. Perner, Robert G. Schmidt, Jr., Sean C. Turner, Tammie K. White, Guo Zhu Zheng
Abstract: Compounds of formula (I)
are novel P2X3 and P2X2/P2X3 antagonists which are useful in treating pain, urinary incontinence and bladder overactivity.
Type:
Grant
Filed:
May 10, 2002
Date of Patent:
December 14, 2004
Assignee:
Abbott Laboratories
Inventors:
Chih-Hung Lee, Richard J. Perner, Daniel P. Larson, John R. Koenig, Arthur R. Gomtsyan, Guo Zhu Zheng, Stanley DiDomenico, Andrew O. Stewart, Erol K. Bayburt
Abstract: Compounds of formula I
pharmaceutical compositions of these compounds, and use of said compositions to control synaptic transmission in mammals.
Type:
Grant
Filed:
April 12, 2001
Date of Patent:
October 26, 2004
Assignee:
Abbott Laboratories
Inventors:
Michael R. Schrimpf, Karin R. Tietje, Richard B. Toupence, Jianguo Ji, Anwer Basha, William H. Bunnelle, Jerome F. Daanen, Jennifer M. Pace, Kevin B. Sippy
Abstract: Cyanide-free reagents for the determination of hemoglobin and leukocytes present in a blood sample comprise an aqueous solutions of at least one quaternary ammonium salt, preferably selected from the group of alkyltrimethylammonium salts, alkyldimethylbenzylammonium salts or alkylpyridium salts consisting of tetradecyltrimethyl ammonium bromide (TTAB), dodecyltrimethyl ammonium chloride, cetyltrimethyl ammonium bromide, hexadecyltrimethyl ammonium bromide and benzalkonium chlorides, and hydroxylamine salts, especially hydrochloride, sulfate and phosphates and other acid salts. The method involves mixing the reagent with a diluent-diluted blood sample, presenting it to an absorbance spectrophotometer and measuring the resulting optical density as an indicator of hemoglobin concentration. This cyanide-free reagent could be used solely for hemoglobin determinations, or, it can also be used in leukocyte counting and sizing using hematology instrumentation.
Abstract: Compounds of formula I:
are useful in treating diseases prevented by or ameliorated with potassium channel openers. Also disclosed are potassium channel opening compositions and a method of opening potassium channels in a mammal.
Type:
Grant
Filed:
February 5, 2001
Date of Patent:
November 11, 2003
Assignee:
Abbott Laboratories
Inventors:
Robert J. Altenbach, Hao Bai, Jorge D. Brioni, William A. Carroll, Murali Gopalakrishnan, Robert J. Gregg, Mark W. Holladay, Peggy P. Huang, John F. Kincaid, Michael E. Kort, Philip R. Kym, John K. Lynch, Arturo Perez-Medrano, Henry Q. Zhang
Abstract:
The present invention provides novel compounds of formula I which may be useful in hyperpolarizing cell membranes, opening potassium channels, relaxing smooth muscle cells, and inhibiting bladder contractions.
Type:
Grant
Filed:
May 3, 2000
Date of Patent:
November 4, 2003
Assignee:
Abbott Laboratories
Inventors:
William A. Carroll, Konstantinos A. Agrios, Robert J. Altenbach, Irene Drizin, Michael E. Kort
Abstract: Compounds having the formula I:
are useful in treating diseases prevented by or ameliorated with potassium channel openers. Also disclosed are potassium channel opening compositions and a method of opening potassium channels in a mammal.
Type:
Grant
Filed:
June 23, 1999
Date of Patent:
July 15, 2003
Assignee:
Abbott Laboratories
Inventors:
William A. Carroll, Yiyuan Chen, Mark W. Holladay, Michael E. Kort, Philip R. Kym, James P. Sullivan, Rui Tang, Lin Yi, Henry Q. Zhang, Irene Drizin
Abstract: Compounds of formula I
are useful in treating diseases prevented by or ameliorated with potassium channel openers. Also disclosed are potassium channel opening compositions and a method of opening potassium channels in a mammal.
Type:
Grant
Filed:
February 7, 2001
Date of Patent:
March 25, 2003
Assignee:
Abbott Laboratories
Inventors:
Irene Drizin, Robert J. Altenbach, William A. Carroll
Abstract: Compounds of formula (I)
are useful in treating diseases prevented by or ameliorated with potassium channel openers. Also disclosed are potassium channel opening compositions and a method of opening potassium channels in a mammal.
Type:
Grant
Filed:
November 10, 2000
Date of Patent:
March 25, 2003
Assignee:
Abbott Laboratories
Inventors:
Mark W. Holladay, William A. Carroll, Irene Drizin, Lin Yi, Henry Q. Zhang
Abstract: The present invention describes pyridazione compounds having the formula (I), which are cyclooxygenase (COX) inhibitors The compounds are selective inhibitors of cyclooxygenase-2-(COX-2), which is the inducible isoform associated with inflammation, as opposed to the constitutive isoform, cyclooxygenase-1 (COX-1), which is an important “housekeeping” enzyme in many tissues, including the gastrointestinal (GI) tract and the kidneys. The selectivity of these compounds for COX-2 minimizes the unwanted GI and renal side-effects seen with currently marketed non-steroidal anti-inflammatory drugs (NSAIDS).
Abstract: The present invention relates to a process for preparing a cross-linked pollyallylamine hydrochloride. The process involves mixing polyallylamine hydrochloride, water, a hydroxide or alkoxide, and a water-miscible organic solvent or co-solvents, to a reaction mixture and adding a cross-linking agent to the reaction mixture to form a cross-linked polyallylamine.
Type:
Grant
Filed:
July 11, 2001
Date of Patent:
February 25, 2003
Assignee:
Abbott Laboratories
Inventors:
Russell C. Klix, Jufang H. Barkalow, William T. Monte
Abstract: Compounds of formula I
are useful in treating diseases prevented by or ameliorated with potassium channel openers. Also disclosed are potassium channel opening compositions and a method of opening potassium channels in a mammal.
Type:
Grant
Filed:
March 4, 1999
Date of Patent:
February 11, 2003
Assignee:
Abbott Laboratories
Inventors:
William A. Carroll, Yiyuan Chen, Irene Drizin, James F. Kerwin, Jimmie L. Moore
Abstract: Compounds of formula I
are useful in treating diseases or conditions prevented by or ameliorated with histamine-3 receptor ligands. Also disclosed are histamine-3 receptor ligand compositions and methods of antagonizing or agonizing histamine-3 receptors.
Type:
Grant
Filed:
July 11, 2001
Date of Patent:
February 4, 2003
Assignee:
Abbott Laboratories
Inventors:
Youssef L. Bennani, Ramin Faghih, Wesley J. Dwight, Anil Vasudevan, Scott E. Conner
Abstract: Compounds having formula I:
are useful in treating diseases prevented by or ameliorated with &agr;1A agonists. Also disclosed are &agr;1A agonist compositions and a method of activating &agr;1 adrenoceptors in a mammal.
Type:
Grant
Filed:
July 29, 1999
Date of Patent:
January 7, 2003
Assignee:
Abbott Laboratories
Inventors:
Robert J. Altenbach, Michael D. Meyer, James F. Kerwin, Jr., Mark W. Holladay, Albert Khilevich, Teodozyj Kolasa, Jeffrey Rohde, William A. Carroll