Patents by Inventor Yuka Kuno

Yuka Kuno 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: 10392345
    Abstract: Disclosed herein are a crystal comprising a compound, which has ?-opioid receptor antagonistic action, few side effects, and high safety, and having high purity and excellent physical properties (stability, solubility, etc.), and a method for producing the crystal. The crystal is a crystal of a salt comprising: a compound represented by a formula (I) [wherein R2 is a hydrogen atom or a halogen atom, and R1 is a group selected from the group consisting of and an acid selected from the group consisting of hydrochloric acid, hydrobromic acid, and oxalic acid, or a hydrate thereof.
    Type: Grant
    Filed: May 19, 2016
    Date of Patent: August 27, 2019
    Assignees: SANWA KAGAKU KENKYUSHO CO., LTD., UBE INDUSTRIES, LTD.
    Inventors: Ryo Iwamura, Yasunori Tsuzaki, Hiroyuki Setoguchi, Hiroto Akaza, Yasuhito Yamamoto, Akira Takama, Yuka Kuno
  • Publication number: 20180148409
    Abstract: Disclosed herein are a crystal comprising a compound, which has ?-opioid receptor antagonistic action, few side effects, and high safety, and having high purity and excellent physical properties (stability, solubility, etc.), and a method for producing the crystal. The crystal is a crystal of a salt comprising: a compound represented by a formula (I) [wherein R2 is a hydrogen atom or a halogen atom, and R1 is a group selected from the group consisting of and an acid selected from the group consisting of hydrochloric acid, hydrobromic acid, and oxalic acid, or a hydrate thereof.
    Type: Application
    Filed: May 19, 2016
    Publication date: May 31, 2018
    Inventors: Ryo Iwamura, Yasunori Tsuzaki, Hiroyuki Setoguchi, Hiroto Akaza, Yasuhito Yamamoto, Akira Takama, Yuka Kuno
  • Patent number: 9586905
    Abstract: A compound having a V2 receptor agonistic activity is provided. Providing a pharmaceutical composition which contains, as an active ingredient, a compound represented by general formula (I) described below: [R1 is formula described below: (A is a lower alkylene group which may be substituted with lower alkyl group; R6 is a hydrogen atom; R7 is a hydroxyl group, an aromatic heterocyclic group which may be substituted with lower alkyl group, carbamoyl group); R2 is a hydrogen atom or lower alkyl group; R3 is lower alkyl group which may be substituted with 1-3 fluorine atoms, or halogen atom; R4 is a five-membered aromatic monocyclic heterocyclic group, five-membered non-aromatic monocyclic heterocyclic group, (provided each heterocyclic groups contain at least one nitrogen atom and may be substituted with a lower alkyl group); and R5 is a lower alkyl group, halogen atom], or pharmacologically acceptable salt thereof.
    Type: Grant
    Filed: December 26, 2013
    Date of Patent: March 7, 2017
    Assignee: SANWA KAGAKU KENKYUSHO CO., LTD.
    Inventors: Katsunori Kitamoto, Nobuyoshi Kasugai, Hiroyo Kataoka, Yasushi Ohsawa, Yuka Kuno, Hiroki Fujieda, Keita Sakai, Hiroki Nagano, Naoki Takahashi, Toru Izuchi, Mitsuaki Takeuchi, Daisuke Kurumazuka, Toshiyuki Miyazawa, Satoko Harada, Izumi Gotoh, Yukiyasu Asano, Yurie Yamada, Morio Okabe
  • Publication number: 20150291533
    Abstract: A compound having a V2 receptor agonistic activity is provided. Providing a pharmaceutical composition which contains, as an active ingredient, a compound represented by general formula (I) described below: [R1 is formula described below: (A is a lower alkylene group which may be substituted with lower alkyl group; R6 is a hydrogen atom; R7 is a hydroxyl group, an aromatic heterocyclic group which may be substituted with lower alkyl group, carbamoyl group); R2 is a hydrogen atom or lower alkyl group; R3 is lower alkyl group which may be substituted with 1-3 fluorine atoms, or halogen atom; R4 is a five-membered aromatic monocyclic heterocyclic group, five-membered non-aromatic monocyclic heterocyclic group, (provided each heterocyclic groups contain at least one nitrogen atom and may be substituted with a lower alkyl group); and R5 is a lower alkyl group, halogen atom], or pharmacologically acceptable salt thereof.
    Type: Application
    Filed: December 26, 2013
    Publication date: October 15, 2015
    Inventors: Katsunori Kitamoto, Nobuyoshi Kasugai, Hiroyo Kataoka, Yasushi Ohsawa, Yuka Kuno, Hiroki Fujieda, Keita Sakai, Hiroki Nagano, Naoki Takahashi, Toru Izuchi, Mitsuaki Takeuchi, Daisuke Kurumazuka, Toshiyuki Miyazawa, Satoko Harada, Izumi Gotoh, Yukiyasu Asano, Yurie Yamada, Morio Okabe