Patents by Inventor Yuichiro Amano

Yuichiro Amano 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: 11972246
    Abstract: An information processing apparatus includes a processor that: receives, from a user terminal, a request for first update regarding a first vehicle, notifies the user terminal that the first update is to be performed at a shop, when the first update is update of hardware, and notifies the user terminal that the first update is to be performed through wireless communication, when the first update is update of software.
    Type: Grant
    Filed: April 14, 2022
    Date of Patent: April 30, 2024
    Assignee: TOYOTA JIDOSHA KABUSHIKI KAISHA
    Inventors: Yuta Tone, Yukinori II, Tadayuki Tanaka, Naoki Ishizuka, Yuichiro Yano, Nariaki Amano, Yusuke Maeda, Kei Yazaki, Yu Hamada
  • Patent number: 11179384
    Abstract: The present invention is directed to methods for the treatment of non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steato-hepatitis (NASH) with a phosphodiesterase 4 (PDE4) inhibitor.
    Type: Grant
    Filed: August 25, 2017
    Date of Patent: November 23, 2021
    Assignee: TAKEDA GMBH
    Inventors: Guido Hanauer, Hiroshi Nagabukuro, Yuichiro Amano
  • Publication number: 20210283122
    Abstract: The present invention is directed to methods for the treatment of non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steato-hepatitis (NASH) with a phosphodiesterase 4 (PDE4) inhibitor.
    Type: Application
    Filed: August 25, 2017
    Publication date: September 16, 2021
    Inventors: Guido HANAUER, Hiroshi NAGABUKURO, Yuichiro AMANO
  • Patent number: 10252997
    Abstract: The present invention relates to a compound which may be useful as an agent for the prophylaxis or treatment of cancer, hepatitis, hepatic fibrosis, fatty liver and the like.
    Type: Grant
    Filed: March 30, 2016
    Date of Patent: April 9, 2019
    Assignee: Takeda Pharmaceutical Company Limited
    Inventors: Ryo Mizojiri, Moriteru Asano, Daisuke Tomita, Hiroshi Banno, Michiko Tawada, Noriyuki Nii, Krista E. Gipson, Hironobu Maezaki, Shuntarou Tsuchiya, Mayumi Imai, Yuichiro Amano
  • Publication number: 20180079723
    Abstract: The present invention relates to a compound which may be useful as an agent for the prophylaxis or treatment of cancer, hepatitis, hepatic fibrosis, fatty liver and the like.
    Type: Application
    Filed: March 30, 2016
    Publication date: March 22, 2018
    Applicant: Takeda Pharmaceutical Company Limited
    Inventors: Ryo Mizojiri, Moriteru ASANO, Daisuke TOMITA, Hiroshi BANNO, Michiko TAWADA, Noriyuki NII, Krista E. GIPSON, Hironobu MAEZAKI, Shuntaro TSUCHIYA, Mayumi IMAI, Yuichiro AMANO
  • Patent number: 7553867
    Abstract: The present invention provides a compound represented by the formula (I): [wherein R is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, p is 0, 1 or 2, and when p is 2, each R may be the same or different, R1 is a hydrogen atom or an optionally substituted hydrocarbon group, R2 is an optionally substituted aromatic group, Ring A is an optionally substituted monocyclic aromatic ring or optionally substituted bicyclic aromatic fused ring, X1 is an oxygen atom or a sulfur atom, X2 is a bond, an oxygen atom or —S(O)n— (wherein n is 0, 1 or 2), Y is a bond, an oxygen atom, —S(O)m—, —C(?O)—N(R3)— or —N(R3)—C(?O)— (R3 is a hydrogen atom, an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, and m is 0, 1 or 2), M1, M2 and M3 may be the same or different and are each independently a bond or an optionally substituted divalent aliphatic hydrocarbon group, and M4 is an optionally substituted divalent aliphatic hydrocarbon group] or a
    Type: Grant
    Filed: September 4, 2003
    Date of Patent: June 30, 2009
    Assignee: Takeda Pharmaceutical Company Limited
    Inventors: Kazumasa Hamamura, Shigekazu Sasaki, Yuichiro Amano, Junichi Sakamoto, Kohji Fukatsu
  • Publication number: 20090082333
    Abstract: A preventive/remedy for xanthoma which contains a compound having an inhibitory effect on squalene synthase, its prodrug or its salt.
    Type: Application
    Filed: April 21, 2006
    Publication date: March 26, 2009
    Applicants: NATIONAL UNIVERSITY CORPORATION KOBE UNIVERSITY, TAKEDA PHARMACEUTICAL COMPANY LIMITED
    Inventors: Masashi Shiomi, Takashi Ito, Ryuichi Tozawa, Yuichiro Amano
  • Publication number: 20080058310
    Abstract: A novel high-density lipoprotein(HDL)-cholesterol level elevating agent containing a compound which has a squalene synthase inhibitory activity.
    Type: Application
    Filed: June 7, 2007
    Publication date: March 6, 2008
    Applicant: Takeda Pharmaceutical Company Limited
    Inventors: Tomoyuki Nishimoto, Ryuichi Tozawa, Masakuni Kori, Yuichiro Amano
  • Publication number: 20060242716
    Abstract: The present invention provides a non-human mammal, or a part of its living body, which stably retains a DNA encoding a heterologous PPAR? in an expressible state, and has one or more different genetic modifications resulting in a pathological condition identical or similar to a disease associated with the regulation of PPAR? activity or a foreign DNA under the control of a promoter having PPRE, as well as a method of screening for agonists/antagonists for the heterologous PPAR? using the animal.
    Type: Application
    Filed: July 14, 2003
    Publication date: October 26, 2006
    Inventors: Yuichiro Amano, Yasuo Sugiyama, Mayumi Nishida, Shigehisa Taketomi
  • Publication number: 20060100261
    Abstract: The present invention provides a compound represented by the formula (I): [wherein R is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, p is 0, 1 or 2, and when p is 2, each R may be the same or different, R1 is a hydrogen atom or an optionally substituted hydrocarbon group, R2 is an optionally substituted aromatic group, Ring A is an optionally substituted monocyclic aromatic ring or optionally substituted bicyclic aromatic fused ring, X1 is an oxygen atom or a sulfur atom, X2 is a bond, an oxygen atom or —S(O)n— (wherein n is 0, 1 or 2), Y is a bond, an oxygen atom, —S(O)m—, —C(?O)—N(R3)— or —N(R3)—C(?O)— (R3 is a hydrogen atom, an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, and m is 0, 1 or 2), M1, M2 and M3 may be the same or different and are each independently a bond or an optionally substituted divalent aliphatic hydrocarbon group, and M4 is an optionally substituted divalent aliphatic hydrocarbon group] or
    Type: Application
    Filed: September 4, 2003
    Publication date: May 11, 2006
    Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED INTELLECTUAL PROPERTY DEPARTMENT
    Inventors: Kazumasa Hamamura, Shigekazu Sasaki, Yuichiro Amano, Junichi Sakamoto, Kohji Fukatsu
  • Publication number: 20040063750
    Abstract: A novel high-density lipoprotein (HDL)-cholesterol level elevating agent containing a compound which has a squalene synthase inhibitory activity.
    Type: Application
    Filed: May 6, 2003
    Publication date: April 1, 2004
    Inventors: Tomoyuki Nishimoto, Ryuichi Tozawa, Masakuni Kori, Yuichiro Amano