Patents Represented by Attorney, Agent or Law Firm John D. Conway
  • Patent number: 7091227
    Abstract: The present invention is directed to a compound of formula (I), racemic-diastereomeric mixtures thereof, optical isomers thereof, prodrugs thereof, isotopes thereof or pharmaceutically-acceptable salts of said compound, isomers, prodrugs and isotopes, wherein the variables are defined herein. The compounds of this invention are useful as inhibitors of serine/threonine and tyrosine kinases. In particular, compounds of this invention are useful as inhibitors of tyrosine kinases that are important in hyperproliferative diseases, especially in cancer and in the process of angiogenesis.
    Type: Grant
    Filed: February 6, 2001
    Date of Patent: August 15, 2006
    Assignee: Abbott GmbH & Co. KG
    Inventors: Barbara Scott, Lee D. Arnold, Anna M. Ericsson, Kevin P. Cusack
  • Patent number: 7071199
    Abstract: The present application is directed to a compound of Formula (I) as defined herein which are useful as kinase inhibitors.
    Type: Grant
    Filed: September 15, 2000
    Date of Patent: July 4, 2006
    Assignee: Abbott GmbH & CCo. KG
    Inventors: Gavin C. Hirst, Paul Rafferty, Kurt Ritter, David Calderwood, Helen Twigger, Stephen St. Gallay
  • Patent number: 7060822
    Abstract: Chemical compounds having structural formula I and physiologically acceptable salts thereof, are inhibitors of serine/threonine and tyrosine kinase activity. Several of the tyrosine kinases, whose activity is inhibited by these chemical compounds, are involved in angiogenic processes. Thus, these chemical compounds can ameliorate disease states where angiogenesis or endothelial cell hyperproliferation is a factor. These compounds can be used to treat cancer and hyperproliferative disorders.
    Type: Grant
    Filed: July 24, 2000
    Date of Patent: June 13, 2006
    Assignee: Abbott GmbH & Co. KG
    Inventors: Lee Arnold, Marina Moran Moset, Jose Maria Castellano Berlanga, Isabel Fernandez, David J. Calderwood, Paul Rafferty
  • Patent number: 6992216
    Abstract: A method for reducing the particle size of amino acid crystals using ultrasound is discussed.
    Type: Grant
    Filed: January 7, 2003
    Date of Patent: January 31, 2006
    Assignee: Abbott GmbH & Co. KG
    Inventors: Siegfried Bechtel, Matthias Rauls, Richard Van Gelder, Seth C. Simpson
  • Patent number: 6803387
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl) cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for treating fibromyalgia or neuropathic pain, such as pain associated with diabetes mellitus, shingles, nerve injury and varied peripheral neuropathies.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: October 12, 2004
    Assignee: Abbott GmbH & Co. KG
    Inventors: Carl M. Mendel, Timothy B. Seaton, Steve P. Weinstein, Edward Chong
  • Patent number: 6713474
    Abstract: Chemical compounds having structural formula I and physiologically acceptable salts and metabolites thereof, are inhibitors of serine/threonine and tyrosine kinase activity. Several of the kinases, whose activity is inhibited by these chemical compounds, are involved in immunologic, hyperproliferative, or angiogenic processes. Thus, these chemical compounds can ameliorate disease states where angiogenesis or endothelial cell hyperproliferation is a factor. These compounds can be used to treat cancer and hyper proliferative disorders, rheumatiod arthritis, disorders of the immune system, trasplant rejections and imflammatory disorders.
    Type: Grant
    Filed: March 29, 2000
    Date of Patent: March 30, 2004
    Assignee: Abbott GmbH & Co. KG
    Inventors: Gavin C. Hirst, David Calderwood, Rainer Munschauer, Lee D. Arnold, David N. Johnston, Paul Rafferty
  • Patent number: 6660744
    Abstract: The present invention is directed to pyrazolopyrimidine derivatives which are useful as kinase inhibitors and as such are useful for affecting angiogenesis and diseases and conditions associated with angiogenesis.
    Type: Grant
    Filed: September 15, 2000
    Date of Patent: December 9, 2003
    Assignee: Abbott GmbH & Co. KG
    Inventors: Gavin C. Hirst, Paul Rafferty, Kurt Ritter, David Calderwood, Neil Wishart, Lee D. Arnold, Michael M. Friedman
  • Patent number: 6617360
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for reducing Insulin resistance in humans in whom Impaired Glucose Tolerance and Non-Insulin Dependent Diabetes Mellitus have not presented.
    Type: Grant
    Filed: October 30, 2000
    Date of Patent: September 9, 2003
    Assignee: Knoll Aktiengesellschaft
    Inventors: Clifford James Bailey, Robert Brian Jones, Helen Christine Jackson
  • Patent number: 6462036
    Abstract: This invention relates to certain 3-aryl or 3-heteroaryl pyrazoles with 4,5(3,4)-bicyclic ring fusion which are inhibitors of protein kinase activity, of which some are novel compounds, to pharmaceutical compositions containing these pyrazoles and to processes for preparing these pyrazoles.
    Type: Grant
    Filed: May 17, 2000
    Date of Patent: October 8, 2002
    Assignee: BASF Aktiengesellschaft
    Inventors: Kevin J. Doyle, Paul Rafferty, Robert W. Steele, David J. Wilkins, Lee D. Arnold, Michael Hockley, Anna M. Ericsson, Nobuhiko Iwasaki, Nobuo Ogawa
  • Patent number: 6451834
    Abstract: Chemical compounds that are derivatives of indeno[1,2-c]-, naphtho[1,2-c]- and benzo[6,7]cyclohepta[1,2-c]pyrazole are inhibitors of tyrosine kinase activity. Several of the tyrosine kinases, whose activity is inhibited by these chemical compounds, are involved in hyperproliferative, angiogenic or in vascular hyperpermeability processes. Thus, these chemical compounds can ameliorate disease states where tumor formation, metastasis, angiogenesis, vascular hyperpermeability or endothelial cell proliferation is a factor.
    Type: Grant
    Filed: April 3, 2000
    Date of Patent: September 17, 2002
    Assignee: BASF Aktiengesellschaft
    Inventors: Lee D. Arnold, Yajun Xu, Teresa Barlozzari
  • Patent number: 6441046
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl)cyclobutyl ]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for treating metabolic disorders, such as increased non-exercise activity thermogenesis or increased metabolic rate.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: August 27, 2002
    Assignee: Abbott GmbH & Co. KG
    Inventors: Carl M. Mendel, Timothy B. Seaton, Steve P. Weinstein
  • Patent number: 6433020
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for treating cardiovascular disease, such as dyslipidaemia or carotid intimal medial thickening.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: August 13, 2002
    Assignee: Knoll Pharmaceutical Company
    Inventors: Carl M. Mendel, Timothy B. Seaton, Steve P. Weinstein
  • Patent number: 6403650
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-4chlorophenyl)cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for treating pulmonary hypertension, particularly in patients who take certain anorectic medications.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: June 11, 2002
    Assignee: Knoll Pharmaceutical Company
    Inventors: Carl M. Mendel, Timothy B. Seaton, Steve P. Weinstein
  • Patent number: 6380260
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl) cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for decreasing platelet adhesiveness.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: April 30, 2002
    Assignee: Knoll Pharmaceutical Company
    Inventors: Carl M. Mendel, Timothy B. Seaton, Steve P. Weinstein
  • Patent number: 6376554
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate), including individual enantiomers and racemates thereof, is used for treating sexual dysfunction.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: April 23, 2002
    Assignee: Knoll Pharmaceutical Company
    Inventors: Sharon C. Cheetham, David J. Heal
  • Patent number: 6376551
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for treating chronic fatigue syndrome.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: April 23, 2002
    Assignee: Knoll Pharmaceutical Company
    Inventors: Carl M. Mendel, Timothy B. Seaton, Steve P. Weinstein
  • Patent number: 6376553
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for treating pain such as low back pain.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: April 23, 2002
    Assignee: Knoll Pharmaceutical Company
    Inventors: Carl M. Mendel, Timothy B. Seaton, Steve P. Weinstein
  • Patent number: 6376552
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for treating gallstones, particularly gallstones associated with weight loss or associated with gall bladder disease related to obesity.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: April 23, 2002
    Assignee: Knoll Pharmaceutical Company
    Inventors: Carl M. Mendel, Timothy B. Seaton, Steve P. Weinstein
  • Patent number: 6372798
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for treating hyperactivity disorders, such as attention deficit hyperactivity disorder and hyperkinetic disorder.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: April 16, 2002
    Assignee: Knoll Pharmaceutical Company
    Inventors: Carl M. Mendel, Timothy B. Seaton, Steve P. Weinstein
  • Patent number: 6372797
    Abstract: A compound of formula I or a pharmaceutically acceptable salt thereof in which R1 and R2 are independently H or methyl (for example N,N-dimethyl-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutyl amine hydrochloride optionally in the form of its monohydrate) is used for treating menstrual function and infertility.
    Type: Grant
    Filed: March 17, 2000
    Date of Patent: April 16, 2002
    Assignee: Knoll Pharmaceutical Company
    Inventors: Carl M. Mendel, Timothy B. Seaton, Steve P. Weinstein