Patents by Inventor Naoko Hattori

Naoko Hattori 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: 11173174
    Abstract: [Problem] To provide, in place of injected agents (such as Vidaza® and Dacogen®) clinically used as therapeutic drugs for high-risk myelodysplastic syndromes, a medicine as a therapeutic drug or a prophylactic drug for various advanced solid tumors, said medicine having high stability with respect to cytidine deaminase which is a hydrolytic metabolic enzyme, being absorbed into the body even by oral administration, and having an effect of being integrated into a nucleic acid biosynthetic route and inhibiting DNA methyltransferases, i.e., DNMTs. [Solution] The aforementioned problem is solved by a novel compound represented by formula (I). (In the formula, R is a hydroxyl group or a hydrogen atom, and R1 and R2 are each a benzyl group that may have a substituent.
    Type: Grant
    Filed: April 24, 2018
    Date of Patent: November 16, 2021
    Assignee: Ohara Pharmaceutical Co., Ltd.
    Inventors: Sako Magoichi, Toshikazu Ushijima, Naoko Hattori
  • Publication number: 20200061093
    Abstract: [Problem] To provide, in place of injected agents (such as Vidaza® and Dacogen®) clinically used as therapeutic drugs for high-risk myelodysplastic syndromes, a medicine as a therapeutic drug or a prophylactic drug for various advanced solid tumors, said medicine having high stability with respect to cytidine deaminase which is a hydrolytic metabolic enzyme, being absorbed into the body even by oral administration, and having an effect of being integrated into a nucleic acid biosynthetic route and inhibiting DNA methyltransferases, i.e., DNMTs. [Solution] The aforementioned problem is solved by a novel compound represented by formula (I). (In the formula, R is a hydroxyl group or a hydrogen atom, and R1 and R2 are each a benzyl group that may have a substituent.
    Type: Application
    Filed: April 24, 2018
    Publication date: February 27, 2020
    Inventors: SAKO MAGOICHI, TOSHIKAZU USHIJ1MA, NAOKO HATTORI
  • Patent number: 8428883
    Abstract: A method for evaluation of a multi-component medicine by judging the degree of difference of the multi-component medicine to be evaluated from a group of multi-component medicines selected as a reference group by using a Mahalanobis distance obtained by combining the 3D-HPLC fingerprint data of a multi-component medicine with fingerprint data of 3D-HPLC of other multi-component medicines of the same kind forming a reference group, allocating variable axes in the MT method to the number of multi-component medicine and the elution time or detection wavelength of the fingerprint data, obtaining a unit space from the signal strength, and obtaining the Mahalanobis distance of the multi-component medicine from the unit space.
    Type: Grant
    Filed: June 6, 2005
    Date of Patent: April 23, 2013
    Assignee: Tsumura & Co.
    Inventors: Kouya Yano, Naoko Hattori
  • Publication number: 20080140375
    Abstract: A method for evaluation of a multi-component medicine comprising judging the degree of difference of the multi-component medicine to be evaluated from a group of multi-component medicines selected as a reference group by using a Mahalanobis distance obtained by a process comprising the following steps (1) to (8), (1) a step of obtaining fingerprint data of three-dimensional high performance liquid chromatography of the multi-component medicine to be evaluated, (2) a step of combining the fingerprint data obtained in (1) with fingerprint data of three-dimensional high performance liquid chromatography of other multi-component medicines of the same kind forming a reference group, (3) a step of allocating variable axes in the MT method to the number of multi-component medicine and either the elution time or detection wavelength of the fingerprint data of (2) above and regarding a signal strength as a characteristic amount in the MT method, (4) a step of obtaining a unit space from the characteristic amount of
    Type: Application
    Filed: June 6, 2005
    Publication date: June 12, 2008
    Applicant: Tsumura & Co.
    Inventors: Kouya Yano, Naoko Hattori
  • Publication number: 20060134659
    Abstract: It is an object of the present invention to provide a demethylation method that, from among multiple methylated regions present in the genome DNA of a living cell, can demethylate a specified methylated region only without influencing the other methylated regions, and to achieve the object, a target methylated region present in either a sense or antisense DNA chain in genome DNA of a living cell is demethylated, by artificially generating in the living cell the following (a) RNA comprising a base sequence equivalent to the base sequence of a region comprising all or part of the target methylated region in the DNA chain where the target methylated region is present, or (b) RNA comprising a base sequence equivalent to the base sequence of a region comprising a region neighboring the target methylated region in the DNA chain where the target methylated region is present.
    Type: Application
    Filed: September 6, 2005
    Publication date: June 22, 2006
    Applicant: TOUDAI TLO, Ltd.
    Inventors: Kunio Shiota, Satoshi Tanaka, Jun Ohgane, Takuya Imamura, Naka Hattori, Koichiro Nishino, Soshi Yamamoto, Naoko Hattori
  • Patent number: 6329502
    Abstract: &bgr;-Amino-&agr;-hydroxycarboxylic acid derivatives represented by the following formula and salts thereof which are useful as human immunodeficiency virus (HIV) protease inhibitors: The compounds are effective for treating a patient suffering from AIDS and AIDS related diseases.
    Type: Grant
    Filed: January 25, 1995
    Date of Patent: December 11, 2001
    Assignee: Japan Energy Corporation
    Inventors: Tsutomu Mimoto, Naoko Hattori, Makoto Shintani, Yuuichi Nagano, Yoshiaki Kiso
  • Patent number: 6313094
    Abstract: &bgr;-Amino-&agr;-hydroxycarboxylic acid derivatives represented by the following formula and salts thereof which are useful as human immunodeficiency virus (HIV) protease inhibitors: The compounds are effective for treating a patient suffering from AIDS and AIDS related diseases.
    Type: Grant
    Filed: May 20, 1994
    Date of Patent: November 6, 2001
    Assignee: Japan Energy Corporation
    Inventors: Tsutomu Mimoto, Naoko Hattori, Makoto Shintani, Yuuichi Nagano, Yoshiaki Kiso