Patents by Inventor Chikara Komuro

Chikara Komuro 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: 20160001012
    Abstract: Slightly above a rupture-intended line, a peripheral surface of a projection portion of a stopper cap is pushed in a direction from an outer side to an inner side (in an arrow direction). The stopper cap is pushed over on the principle of leverage in an oblique direction with, as a fulcrum P, the side (the back side) opposite in a circumferential direction to the side (the near side) at which a pushing force PW acts, so that an intermittent portion is ruptured due to bending of the flexible stopper cap. Then, a residual area remains at the syringe side, and a separation area is separated together with the stopper cap from the syringe to perform unsealing. Thus, a syringe label which allows for easy unsealing along the intermittent portion and with which an unsealed state is easily confirmed, and a drug solution-filled syringe using the label, are provided.
    Type: Application
    Filed: February 27, 2014
    Publication date: January 7, 2016
    Inventors: Masayuki Igarashi, Chikara Komuro, Keisuke Takeyama
  • Patent number: 6475525
    Abstract: The pharmaceutical preparation comprising colforsin dapropate hydrochloride and an alkali metal halide is the oral preparation with excellent storage stability.
    Type: Grant
    Filed: October 16, 2000
    Date of Patent: November 5, 2002
    Assignee: Nippon Kayaku Kabushiki Kaisha
    Inventors: Chikara Komuro, Tomio Yahiro, Hiroyuki Yoshida
  • Patent number: 5610315
    Abstract: This invention relates to a process for the preparation of a 6,7-diacyl-7-deacetylforskolin derivative represented by the general formula: ##STR1## wherein R.sup.1 and R.sup.2 each stands for an acyl group and R.sup.3 stands for an aliphatic group having 2 to 3 carbon atoms, which comprises eliminating the acyl group at position 1 in a 1,6,7-triacyl-7-deacetylforskolin derivative represented by the general formula: ##STR2## wherein R.sup.1, R.sup.2 and R.sup.3 are as defined above, by solvolysis. The compound of the formula (I) is expected as medicine.
    Type: Grant
    Filed: May 16, 1995
    Date of Patent: March 11, 1997
    Assignee: Nippon Kayaku Kabushiki Kaisha
    Inventors: Tochiro Tatee, Akira Shiozawa, Hirotaka Yamamoto, Yuh-ichiro Ichikawa, Aya Ishikawa, Chikara Komuro, Kazuhisa Narita
  • Patent number: 5302730
    Abstract: This invention relates to a process for the preparation of a 6,7-diacyl-7-deacetylforskolin derivative represented by the general formula: ##STR1## wherein R.sup.1 and R.sup.2 each stands for an acyl group and R.sup.3 stands for an aliphatic group having 2 to 3 carbon atoms, which comprises eliminating the acyl group at position 1 in a 1,6,7-triacyl-7-deacetylforskolin derivative represented by the general formula: ##STR2## wherein R.sup.1, R.sup.2 and R.sup.3 are as defined above, by solvolysis. The compound of the formula (I) is expected as medicine.
    Type: Grant
    Filed: June 4, 1993
    Date of Patent: April 12, 1994
    Inventors: Tochiro Tatee, Akira Shiozawa, Hirotaka Yamamoto, Yuh-ichiro Ichikawa, Aya Narita, Chikara Komuro, Kazuhisa Narita