Patents by Inventor Hirohide Noguchi

Hirohide Noguchi 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).

  • Publication number: 20040266814
    Abstract: This invention provides a compound of the formula (I): 1
    Type: Application
    Filed: April 20, 2004
    Publication date: December 30, 2004
    Applicant: Pfizer Inc
    Inventors: Hirohide Noguchi, Chikara Uchida
  • Publication number: 20040127514
    Abstract: This invention provides a compound of the formula (I): 1
    Type: Application
    Filed: September 17, 2003
    Publication date: July 1, 2004
    Applicant: Pfizer Inc
    Inventors: Yasuhiro Katsu, Kana Kon-I, Mikio Morita, Hirohide Noguchi, Chikara Uchida
  • Publication number: 20040122043
    Abstract: This invention provides a compound of the formula (I): 1
    Type: Application
    Filed: September 17, 2003
    Publication date: June 24, 2004
    Applicant: Pfizer Inc
    Inventors: Satoru Iguchi, Yasuhiro Katsu, Kana Kon-I, Hirohide Noguchi, Chikara Uchida
  • Publication number: 20040034226
    Abstract: This invention provides a compound of the formula (I): 1
    Type: Application
    Filed: July 10, 2003
    Publication date: February 19, 2004
    Inventors: Chikara Uchida, Hirohide Noguchi, Alan Stobie, Geoffrey Gymer, David Fenwick
  • Patent number: 6624162
    Abstract: This invention provides a compound of the formula (I): or the pharmaceutically acceptable salts thereof wherein R1 is hydrogen, halo or alkyl; R2 and R3 are independently hydrogen, alkyl, alkenyl, alkynyl, aminoalkyl or hydroxyalkyl; or R2 and R3 taken together with the nitrogen atom to which they are attached may form hetrocyclic; R4 is hydrogen, halo, acyl, amino, amido, aryl, arylalkyl, or heteroaryl; R5 is hydrogen, halo, alkyl alkenyl, alkynyl, acyl, amino, amido, aryl, arylalkyl, or heteroaryl; R6 is hydrogen, alkyl or alkoxyalkyl; X is NR9 wherein R9 is hydrogen or alkyl; and Y is (CR7R8)n wherein n is an integer from 0 to 5. These compounds have 5-HT4 receptor binding activity, and thus are useful for the treatment of gastroesophageal reflux disease, non-ulcer dyspepsia, Functional dyspepsia, irritable bowel syndrome or the like in mammalian, especially humans. This invention also provides a pharmaceutical composition comprising the above compound.
    Type: Grant
    Filed: September 20, 2002
    Date of Patent: September 23, 2003
    Assignee: Pfizer Inc.
    Inventors: Chikara Uchida, Hirohide Noguchi, Alan Stobie, Geoffrey Gymer, David Fenwick
  • Publication number: 20030109549
    Abstract: A compound of the formula: 1
    Type: Application
    Filed: October 30, 2002
    Publication date: June 12, 2003
    Inventors: Fumitaka Ito, Hirohide Noguchi, Hiroshi Kondo
  • Publication number: 20030092699
    Abstract: This invention provides a compound of the formula (I): 1
    Type: Application
    Filed: September 20, 2002
    Publication date: May 15, 2003
    Inventors: Chikara Uchida, Hirohide Noguchi, Alan Stobie, Geoffrey Gymer, David Fenwick
  • Patent number: 6423725
    Abstract: A compound of the formula: or the pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4 and R5 are defined above are useful as ORL1-receptor agonists, and useful as analgesics or the like in mammalian subjects.
    Type: Grant
    Filed: March 6, 2000
    Date of Patent: July 23, 2002
    Assignee: Pfizer INC
    Inventors: Fumitaka Ito, Hirohide Noguchi, Yoriko Ohashi, Hiroshi Kondo, Tatsuya Yamagishi
  • Publication number: 20020049212
    Abstract: A compound of the formula: 1
    Type: Application
    Filed: January 3, 2001
    Publication date: April 25, 2002
    Inventors: Fumitaka Ito, Hirohide Noguchi, Yoriko Ohashi, Hirohisa Shimokawa
  • Patent number: 6172067
    Abstract: A compound of the formula: or a pharmaceutically acceptable salt thereof, wherein R is unsubstituted, mono-, di- or tri-substituted (C3-C11)cycloalkyl or (C3-C11)cycloalkenyl or the like, A is unsubstituted (C1-C7)alkyl or (C2-C5 )alkenyl, or unsubstituted, mono-, di- or tri-substituted aryl, or aromatic-heterocyclic or the like, Y is hydrogen, halo, amino or mercapto, or unsubstituted, mono-, di- or tri- substituted (C1-C10)alkyl-M—, (C3-C7)cycloalkyl-M—, (C2-C6)alkenyl-M—, (C1-C4)alkyl-NH-((C1-C4)alkyl)-M—, di(C1-C4)alkyl-N-((C1-C4)alkyl)-M—, aryl-M—, aromatic or non-aromatic heterocyclic-M—, aryl-(C1-C5)alkyl-M— or aromatic non-aromatic heterocyclic-(C1-C5)alkyl-M—, wherein M is a covalent bond O, S, NH or the like, or the like; Z1, Z2, Z3 and Z4 are hydrogen or the like, has ORL1-receptor agonist activity, and are useful as analgesics or the like in mammalian subjects.
    Type: Grant
    Filed: August 5, 1999
    Date of Patent: January 9, 2001
    Assignee: Pfizer Inc.
    Inventors: Fumitaka Ito, Hirohide Noguchi, Hiroshi Kondo