Patents by Inventor Adam Mazur

Adam Mazur has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Patent number: 7462597
    Abstract: Isolated corticotropin releasing factor derivatives, and nucleic acids encoding the same, are effective for treating corticotropin releasing factor 2 receptor modulated disorders such as muscular dystrophy.
    Type: Grant
    Filed: May 4, 2005
    Date of Patent: December 9, 2008
    Assignee: The Procter & Gamble Company
    Inventors: Robert Joseph Isfort, Wieslaw Adam Mazur
  • Patent number: 7192923
    Abstract: Isolated corticotropin releasing factor derivatives, and nucleic acids encoding the same, are effective for treating corticotropin releasing factor 2 receptor modulated disorders such as muscular dystrophy.
    Type: Grant
    Filed: December 11, 2002
    Date of Patent: March 20, 2007
    Assignee: The Procter & Gamble Company
    Inventors: Robert Joseph Isfort, Wieslaw Adam Mazur
  • Patent number: 7192924
    Abstract: Isolated corticotropin releasing factor derivatives, and nucleic acids encoding the same, are effective for treating corticotropin releasing factor 2 receptor modulated disorders such as muscular dystrophy.
    Type: Grant
    Filed: December 11, 2002
    Date of Patent: March 20, 2007
    Assignee: The Procter & Gamble Company
    Inventors: Robert Joseph Isfort, Wieslaw Adam Mazur
  • Patent number: 7132539
    Abstract: The present invention relates to compounds which comprise a nitrogen-containing ring scaffold substituted by an R1 alkyl units selected from the group consisting of C1–C12 linear or branched alkyl, C3–C8 cyclic alkyl, C2–C12 linear or branched alkenyl, or haloalkyl, for example, the 2-keto-3-alkylpiperazines having the formula: wherein R is selected from the group consisting of phenyl, 3-fluorophenyl, 4-fluorophenyl, 3,5-difluorophenyl, and 4-chlorophenyl; R1 is selected from the group consisting of methyl, ethyl, propyl, iso-propyl, butyl, iso-butyl, sec-butyl, tert-butyl, cyclopropyl, cyclopropylmethyl, cyclopentyl, cyclopentylmethyl, cyclohexyl, cyclohexylmethyl, benzyl, allyl, 1-methylallyl, 2-methylallyl, but-2-enyl, and propargyll; R7a is selected from the group consisting of hydrogen, —CO2H, —CONH2, —CONHCH3, and —CON(CH3)2; R8 is benzyl, substituted benzyl, or naphthalen-2-ylmethyl.
    Type: Grant
    Filed: October 20, 2003
    Date of Patent: November 7, 2006
    Assignee: The Procter & Gamble Company
    Inventors: Frank Hallock Ebetino, Xinrong Tian, Wieslaw Adam Mazur, Anny-Odile Colson
  • Patent number: 7087759
    Abstract: Disclosed are MC-3/MC-4 receptor ligands, the ligands having the following formula: wherein A is a conformationally restricted ring system selected from the group consisting of: a) non-aromatic carbocyclic rings; b) aromatic carbocyclic rings; c) non-aromatic heterocyclic rings; d) aromatic heterocyclic rings; wherein said rings comprises from 5 to 8 atoms; and W is a unit which preferable comprises D-1-fluorophenyalanine, Y comprises a heteroatom, and Z comprises an aromatic carbocyclic ring. Also disclosed are pharmaceutical compositions comprising the ligands of the invention as well as methods of treating diseases mediated through MC-3/MC-4 receptors.
    Type: Grant
    Filed: May 28, 2004
    Date of Patent: August 8, 2006
    Assignee: The Procter & Gamble Company
    Inventors: Wieslaw Adam Mazur, Xinrong Tian, Xiufeng Eric Hu, Frank Hallock Ebetino
  • Publication number: 20060128613
    Abstract: Disclosed are MC-4 and/or MC-3 receptor ligands, the ligands having a structure according to Formula (I): wherein R2, R4, R4?, R5, R6, R6?, R7, R8, R8?, R9, R9?, R10, Ar, Z1, Z2, Z3, X, B, D, p, q, r and s are as described in the specification and claims, and optical isomers, diastereomers or enantiomers thereof; pharmaceutically-acceptable salts, hydrates, and biohydrolyzable esters, amides or imides thereof. Also disclosed are pharmaceutical compositions comprising the ligands of Formula (I), as well as methods of treating diseases mediate by the MC-4/MC-3 receptors, as described in the Detailed Descriptions section of the specification.
    Type: Application
    Filed: March 12, 2003
    Publication date: June 15, 2006
    Inventors: Frank Ebetino, Adam Mazur, Jeffrey Hayes, Feng Wang, Mark Solinsky, Anny-Odile Colson, Qishen Lin
  • Patent number: 6936585
    Abstract: Isolated corticotropin releasing factor derivatives, and nucleic acids encoding the same, are effective for treating corticotropin releasing factor 2 receptor modulated disorders such as muscular dystrophy.
    Type: Grant
    Filed: December 11, 2002
    Date of Patent: August 30, 2005
    Assignee: The Procter & Gamble Company
    Inventors: Robert Joseph Isfort, Wieslaw Adam Mazur
  • Patent number: 6911447
    Abstract: Disclosed are MC-3/MC-4 receptor ligands, the ligands having the following formula: wherein A is a conformationally restricted ring system selected from the group consisting of: a) non-aromatic carbocyclic rings; b) aromatic carbocyclic rings; c) non-aromatic heterocyclic rings; d) aromatic heterocyclic rings; wherein said rings comprises from 5 to 8 atoms; and W is a unit which preferable comprises D-1-fluorophenyalanine, Y comprises a heteroatom, and Z comprises an aromatic carbocyclic ring. Also disclosed are pharmaceutical compositions comprising the ligands of the invention as well as methods of treating diseases mediated through MC-3/MC-4 receptors.
    Type: Grant
    Filed: April 12, 2002
    Date of Patent: June 28, 2005
    Assignee: The Procter & Gamble Company
    Inventors: Wieslaw Adam Mazur, Xinrong Tian, Xiufeng Eric Hu, Frank Hallock Ebetino
  • Publication number: 20040224985
    Abstract: Disclosed are MC-3/MC-4 receptor ligands, the ligands having the following formula: 1
    Type: Application
    Filed: May 28, 2004
    Publication date: November 11, 2004
    Applicant: The Procter & Gamble Company
    Inventors: Wieslaw Adam Mazur, Xinrong Tian, Xiufeng Eric Hu, Frank Hallock Ebetino
  • Publication number: 20030148958
    Abstract: Isolated corticotropin releasing factor derivatives, and nucleic acids encoding the same, are effective for treating corticotropin releasing factor 2 receptor modulated disorders such as muscular dystrophy.
    Type: Application
    Filed: December 11, 2002
    Publication date: August 7, 2003
    Applicant: The Procter & Gamble Company
    Inventors: Robert Joseph Isfort, Wieslaw Adam Mazur
  • Publication number: 20030148957
    Abstract: Isolated corticotropin releasing factor derivatives, and nucleic acids encoding the same, are effective for treating corticotropin releasing factor 2 receptor modulated disorders such as muscular dystrophy.
    Type: Application
    Filed: December 11, 2002
    Publication date: August 7, 2003
    Applicant: The Procter & Gamble Company
    Inventors: Robert Joseph Isfort, Wieslaw Adam Mazur
  • Publication number: 20030148956
    Abstract: Isolated corticotropin releasing factor derivatives, and nucleic acids encoding the same, are effective for treating corticotropin releasing factor 2 receptor modulated disorders such as muscular dystrophy.
    Type: Application
    Filed: December 11, 2002
    Publication date: August 7, 2003
    Applicant: The Procter & Gamble Company
    Inventors: Robert Joseph Isfort, Wieslaw Adam Mazur
  • Publication number: 20030109556
    Abstract: Disclosed are MC-3/MC-4 receptor ligands, the ligands having the following formula: 1
    Type: Application
    Filed: April 12, 2002
    Publication date: June 12, 2003
    Applicant: The Procter & Gamble Company
    Inventors: Wieslaw Adam Mazur, Xinrong Tian, Xiufeng Eric Hu, Frank Hallock Ebetino
  • Patent number: 4906789
    Abstract: A process for the production of bisphenol A from phenol and acetone, comprises introducing a substantially anhydrous reaction mixture of phenol, acetone, and recycled solution of bisphenol A and reaction by-products in phenol into a reaction zone containing a cation-exchange resin catalyst, such catalyst being a mixture of resin having a macroporous structure and resin having a microporous structure in a ratio of 0.05:1 to 0.5:1 by weight, the mol ratio of phenol to acetone being 5:1 to 30:1, and the concentration of bisphenol A being 12 to 20% by weight. The temperature of the reaction zone is maintained between 60 degrees and 95 degrees C. The resulting reacted reaction mixture is withdrawn from the reaction zone, the concentration of bisphenol A being 21 to 35% by weight and the amount of reaction by-products being 12 to 24% by weight. Such withdrawn reaction mixture is treated to recover bisphenol A product and to provide the recycled solution of bisphenol A and reaction by-products in phenol.
    Type: Grant
    Filed: September 28, 1988
    Date of Patent: March 6, 1990
    Assignees: Instytut Ciezkiej Syntezy Organicznej "Blachownia", Zaklady Chemiczne "Blachownia"
    Inventors: Edward Grzywa, Maciej Kiedik, Jo Kolt, Adam Mazur, Jerzy Marszycki, Eugeniusz Zajac, Anna Rzodeczko, Jerzy Czyz, Kazimierz Terelak, Zbigniew Swiderski, Teodor Bek