Patents by Inventor Naoshi Nakagawa

Naoshi Nakagawa 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: 7358400
    Abstract: A method of industrially advantageously producing a cyclopropane monoacetal derivative represented by the formula (III) conveniently and also in a fewer steps by reacting a halogenated unsaturated carbonyl compound represented by the formula (II) with an alcoholate. wherein each symbol is as defined in the specification.
    Type: Grant
    Filed: March 25, 2005
    Date of Patent: April 15, 2008
    Assignees: Kuraray Co., Ltd., Daiichi Pharmaceutical Co., Ltd.
    Inventors: Kenichi Koyakumaru, Shingo Ueyama, Katsuji Ujita, Tatsuhiko Hayashibara, Naoshi Nakagawa, Toshifumi Akiba, Tatsuru Saito
  • Publication number: 20070220262
    Abstract: An input assisting apparatus assists an input from a user. An input receiving unit receives the input from the user. An input-verification-data creating unit creates input verification data based on contents of the input received by the input receiving unit.
    Type: Application
    Filed: September 18, 2006
    Publication date: September 20, 2007
    Applicant: FUJITSU LIMITED
    Inventors: Shigenari Suzuki, Kazufumi Nara, Kaoru Ota, Kazunori Nomura, Naoshi Nakagawa
  • Publication number: 20070197490
    Abstract: The present invention relates to a method of producing a mixture of 5?-pregnane derivatives represented by the formula (II) and the formula (III), which is characterized by reacting a pregnane derivative represented by the formula (I) with a metal selected from alkali metals and alkaline earth metals in the presence of a proton donor and an amine and/or ammonia. According to the present invention, a method capable of producing 5?-pregnane derivatives useful as synthetic intermediates for squalamine, in a high yield from easily available raw materials, can be provided: wherein R1 is a hydroxyl-protecting group, and R2, R11 and R12 are each independently a hydrogen atom or a hydroxyl-protecting group.
    Type: Application
    Filed: March 31, 2005
    Publication date: August 23, 2007
    Applicant: Kuraray Co., Ltd.
    Inventors: Kenichi Koyakumaru, Takashi Sugioka, Shigeo Ohzono, Naoshi Nakagawa
  • Publication number: 20070191643
    Abstract: A method of industrially advantageously producing a cyclopropane monoacetal derivative represented by the formula (III) conveniently and also in a fewer steps by reacting a halogenated unsaturated carbonyl compound represented by the formula (II) with an alcoholate. wherein each symbol is as defined in the specification.
    Type: Application
    Filed: March 25, 2005
    Publication date: August 16, 2007
    Applicants: Kuraray Co,, Ltd., Daiichi Pharmaceutical Co., Ltd.
    Inventors: Kenichi Koyakumaru, Shingo Ueyama, Katsuji Ujita, Tatsuhiko Hayashibara, Naoshi Nakagawa, Toshifumi Akiba, Tatsuru Saito
  • Publication number: 20070149494
    Abstract: The present invention relates to a method of producing 5?-pregnane derivatives represented by the formula (II), which is characterized by reacting a pregnane derivative represented by the formula (I) with a metal selected from alkali metals and alkaline earth metals in the presence of a proton donor and an amine and/or ammonia. According to the present invention, a method capable of producing 5?-pregnane derivatives useful as synthetic intermediates for squalamine, in a high yield from easily available raw materials, can be provided: wherein R1 is a hydroxyl-protecting group, and R2, R11 and R12 are each independently a hydrogen atom or a hydroxyl-protecting group and R3 and R4 are each hydrogen atoms in combination form a bond.
    Type: Application
    Filed: March 31, 2005
    Publication date: June 28, 2007
    Applicant: KURARAY CO., LTD.
    Inventors: Takashi Sugioka, Shigeo Ohzono, Kenichi Koyakumaru, Naoshi Nakagawa
  • Patent number: 6288165
    Abstract: A process for producing vinyl acetate polymers comprises, after polymerization of at least one monomer comprising vinyl acetate, adding a conjugated polyene having a boiling point of at least 20° C. Saponified products of the vinyl acetate polymers obtained by this process can give molded articles causing little coloring and generation of gel-like agglomerates.
    Type: Grant
    Filed: December 5, 1997
    Date of Patent: September 11, 2001
    Assignee: Kuraray Co., Ltd.
    Inventors: Takeshi Moritani, Kaoru Ikeda, Akimasa Aoyama, Takaharu Kawahara, Yukihiro Ohara, Naoshi Nakagawa, Toshinori Tsugaru
  • Patent number: 6007712
    Abstract: A waste water treatment apparatus which is compact, and excellent in durability, has a high treatment performance and can stably operate for a long time is provided. In a waste water treatment apparatus at least comprising a waste water treatment tank in which a carrier particle immobilizing a microbe is charged and decomposing and eliminating an organic matter and/or an inorganic matter contained in a waste water, and a membrane module for filtrating a water to be treated which flows out from said treatment tank, a non-permeating water not passing thorough the membrane module is returned and circulated to said treatment tank. In a waste water treatment apparatus at least comprising a waste water treatment tank in which a carrier particle immobilizing a microbe is charged and decomposing and eliminating an organic matter and/or an inorganic matter contained in a waste water, a carrier immobilizing a microbe is an acetalized polyvinyl alcohol hydrogel.
    Type: Grant
    Filed: February 25, 1998
    Date of Patent: December 28, 1999
    Assignee: Kuraray Co., Ltd.
    Inventors: Eiji Tanaka, Tamio Higashi, Takanori Kitamura, Takeshi Matsuda, Hiroaki Fujii, Naoshi Nakagawa, Shinji Komori, Tadao Shiotani, Masanobu Abe
  • Patent number: 5744547
    Abstract: A process for producing vinyl acetate polymers comprises, after polymerization of at least one monomer comprising vinyl acetate, adding a conjugated polyene having a boiling point of at least 20.degree. C. Saponified products of the vinyl acetate polymers obtained by this process can give molded articles causing little coloring and generation of gel-like agglomerates.
    Type: Grant
    Filed: June 25, 1996
    Date of Patent: April 28, 1998
    Assignee: Kuraray Co., Ltd.
    Inventors: Takeshi Moritani, Kaoru Ikeda, Akimasa Aoyama, deceased, Takaharu Kawahara, Yukihiro Ohara, Naoshi Nakagawa, Toshinori Tsugaru
  • Patent number: 5587486
    Abstract: 1-amino-2-cyclohexene compounds represented by the following formula (I): ##STR1## wherein the substituents are as defined in the specification, a process for preparing the compounds and their use as intermediates in the production of medicinal and agricultural agents is disclosed.
    Type: Grant
    Filed: June 30, 1995
    Date of Patent: December 24, 1996
    Assignee: Kuraray Co., Ltd.
    Inventors: Naoshi Nakagawa, Tadashi Hatanaka, Tatsuhiko Hayashibara, Manzo Shiono
  • Patent number: 5494906
    Abstract: Vitamin D.sub.2 analogs in which a cyclopentane ring is introduced onto the 25-carbon of the side chain of 1.alpha.,25-dihydroxyvitamin D.sub.2 and its 24-epimer. The compounds are characterized by a marked intestinal calcium transport activity while exhibiting much lower activity than 1.alpha.,25-dihydroxyvitamin D.sub.3 in their ability to mobilize calcium from bone. Because of their preferential calcemic activity, these compounds would be useful for the treatment of diseases where bone formation is desired, such as osteoporosis.
    Type: Grant
    Filed: May 5, 1995
    Date of Patent: February 27, 1996
    Assignee: Wisconsin Alumni Research Foundation
    Inventors: Hector F. DeLuca, Naoshi Nakagawa
  • Patent number: 5478955
    Abstract: The invention is drawn to cholesterol derivatives in which a cyclopentane ring has been introduced onto the 25-carbon of the side chain and to 24-epimers of these compounds. The compounds are useful intermediates in the production of 26,27-dimethylene-1.alpha.,25-dihydroxyvitamin D.sub.2 and 26,27-dimethylene-24-epi-1.alpha.,25-dihydroxyvitamin D.sub.2. These vitamin D derivatives are useful for the treatment of diseases such as osteoporosis.
    Type: Grant
    Filed: November 10, 1994
    Date of Patent: December 26, 1995
    Assignee: Wisconsin Alumni Research Foundation
    Inventors: Hector F. DeLuca, Naoshi Nakagawa
  • Patent number: 5457217
    Abstract: Vitamin D.sub.2 analogs in which a cyclopentane ring is introduced into the side chain of 1.alpha.,25-dihydroxyvitamin D.sub.2. The compounds are characterized by a marked intestinal calcium transport activity while exhibiting much lower activity than 1.alpha.,25-dihydroxyvitamin D.sub.3 in their ability to mobilize calcium from bone. Because of their preferential calcemic activity, these compounds would be useful for the treatment of diseases where bone formation is desired, such as osteoporosis.
    Type: Grant
    Filed: December 9, 1994
    Date of Patent: October 10, 1995
    Assignee: Wisconsin Alumni Research Foundation
    Inventors: Hector F. DeLuca, Naoshi Nakagawa
  • Patent number: 5430873
    Abstract: During a software designing operation, a designer accesses a level prescribing unit through an interaction managing control unit. The level prescribing unit provides the guidance to specification information and design parts, etc. at a desired design level. If the designer selects and inputs specification information or design parts, the design editor corresponding to the design specification information in a design editor unit is activated, so that the designer is guided and aided through a display to produce a desired software. At this time, the information about the state of the editing operation "completed" or "not completed" is stored with the directory. The designed document satisfying a specific condition, for example, a document determined to be "design completed", is stored as a data base by a design data base storing unit.
    Type: Grant
    Filed: September 14, 1992
    Date of Patent: July 4, 1995
    Assignee: Fujitsu Limited
    Inventors: Hiroaki Abe, Itaru Fukao, Harumi Taneda, Yuji Kubota, Yasuhiko Arima, Naoshi Nakagawa, Takeo Konno, Yoshinori Arihara, Yuriko Suzuki
  • Patent number: 5397775
    Abstract: Vitamin D.sub.2 analogs in which a cyclopentane ring is introduced onto the 25-carbon of the side chain of 1.alpha.,25-dihydroxyvitamin D.sub.2 and its 24-epimer. The compounds are characterized by a marked intestinal calcium transport activity while exhibiting much lower activity than 1.alpha.,25-dihydroxyvitamin D.sub.3 in their ability to mobilize calcium from bone. Because of their preferential calcemic activity, these compounds would be useful for the treatment of diseases where bone formation is desired, such as osteoporosis.
    Type: Grant
    Filed: June 2, 1993
    Date of Patent: March 14, 1995
    Assignee: Wisconsin Alumni Research Foundation
    Inventors: Hector F. De Luca, Naoshi Nakagawa
  • Patent number: 5373004
    Abstract: Vitamin D.sub.2 analogs in which a cyclopentane ring is introduced into the side chain of 1.alpha.,25-dihydroxyvitamin D.sub.2 The compounds are characterized by a marked intestinal calcium transport activity while exhibiting much lower activity than 1.alpha.,25-dihydroxyvitamin D.sub.3 in their ability to mobilize calcium from bone. Because of their preferential calcemic activity, these compounds would be useful for the treatment of diseases where bone formation is desired, such as osteoporosis.
    Type: Grant
    Filed: November 24, 1993
    Date of Patent: December 13, 1994
    Assignee: Wisconsin Alumni Research Foundation
    Inventors: Hector F. DeLuca, Naoshi Nakagawa
  • Patent number: 5359055
    Abstract: There are provided pregnane derivatives represented by formula ##STR1## wherein A.sup.1 represents a hydrogen atom or a hydroxyl group, A.sup.2 represents a substituent such as a hydroxyl group when A.sup.1 represents a hydrogen atom, or A.sup.2 represents a hydrogen atom when A.sup.1 represents a hydroxyl group, or A.sup.1 and A.sup.2 are combined together to form an oxo group; D.sup.1 represents a substituent such as a hydroxyl group, and D.sup.2 represents a hydrogen atom, or D.sup.1 and D.sup.2 are combined together to form an epoxy group or a single bond; D.sup.3, D.sup.5 and D.sup.7 each represents a hydrogen atom, D.sup.4 represents a hydroxyl group, and D.sup.6 represents a substituent such as a hydroxyl group, or D.sup.3 and D.sup.4 may be combined together to form an epoxy group or a single bond, or D.sup.4 and D.sup.5 may be combined together to form a single bond, or D.sup.5 and D.sup.6 may be combined together to form an epoxy group or a single bond, or D.sup.6 and D.sup.
    Type: Grant
    Filed: November 27, 1991
    Date of Patent: October 25, 1994
    Assignee: Kuraray Co., Ltd.
    Inventors: Jiro Tsuji, Takashi Takahashi, Masao Tsuji, Naoshi Nakagawa, Tetsuo Takigawa
  • Patent number: 5218109
    Abstract: Steroid compounds of the following general formulas (I), (II) and (III) are provided: ##STR1## In the above formulas, R.sup.1 and R.sup.2 each is a hydrogen atom or a hydroxyl-protecting group, R is a group of the formula --CH.sub.2 --X (in which X is a substituent such as a hydroxyl group), a carboxyl group or a protected carboxyl group, A.sup.1 is an aryl group, a lower alkyl group or an aralkyl group, and Z.sup.1, Z.sup.2, Z.sup.3 and Z.sup.4 each is a hydrogen atom, a hydroxyl group or a protected hydroxyl group.The above steroid compounds are useful as intermediates for the synthesis of vitamin D.sub.3 derivatives having a hydroxyl group at the 1.alpha.-position.
    Type: Grant
    Filed: March 5, 1990
    Date of Patent: June 8, 1993
    Assignee: Kuraray Co., Ltd.
    Inventors: Jiro Tsuji, Takashi Takahashi, Masao Tsuji, Naoshi Nakagawa, Tetsuo Takigawa
  • Patent number: 5194431
    Abstract: Vitamin D.sub.2 analogs in which a cyclopropane ring is introduced onto the 24-carbon of the side chain of 1.alpha.,25-dihydroxyvitamin D.sub.2 and 1.alpha.-hydroxyvitamin D.sub.2. The compounds are characterized by a marked intestinal calcium transport activity while exhibiting much lower activity than 1.alpha.,25-dihydroxy-vitamin D.sub.3 in their ability to mobilize calcium from bone. Because of their preferential calcemic activity, these compounds would be useful for the treatment of diseases where bone formation is desirbed, such as osteoporosis.
    Type: Grant
    Filed: July 8, 1992
    Date of Patent: March 16, 1993
    Assignee: Wisconsin Alumni Research Foundation
    Inventors: Hector F. DeLuca, Naoshi Nakagawa
  • Patent number: 5112998
    Abstract: There are provided pregnane derivatives represented by formula ##STR1## wherein A.sup.1 represents a hydrogen atom or a hydroxyl group, A.sup.2 represents a substituent such as a hydroxyl group when A.sup.1 represents a hydrogen atom, or A.sup.2 represents a hydrogen atom when A.sup.1 represents a hydroxyl group, or A.sup.1 and A.sup.2 are combined together to form an oxo group; D.sup.1 represents a substitutent such as a hydroxyl group, and D.sup.2 represents a hydrogen atom, or D.sup.1 and D.sup.2 are combined together to form an epoxy group or a single bond; D.sup.3, D.sup.5 and D.sup.7 each represents a hydrogen atom, D.sup.4 represents a hydroxyl group, and D.sup.6 represents a substitutent such as a hydroxyl group, or D.sup.3 and D.sup.4 may be combined together to form an epoxy group or a single bond, or D.sup.4 and D.sup.5 may be combined together to form a single bond, or D.sup.5 and D.sup.6 may be combined together to form an epoxy group or a single bond, or D.sup.6 and D.sup.
    Type: Grant
    Filed: June 15, 1990
    Date of Patent: May 12, 1992
    Assignee: Kuraray Co., Ltd.
    Inventors: Jiro Tsuji, Takashi Takahashi, Masao Tsuji, Naoshi Nakagawa, Tetsuo Takigawa
  • Patent number: 4792615
    Abstract: A method of producing .alpha.-dihydropolyprenyl monophosphates from .alpha.-dihydropolyprenols through .alpha.-dihydropolyprenyl dichlorophosphates in good yield and with ease is provided. A method of producing .alpha.-dihydropolyprenyl dichlorophosphates which are intermediate compounds useful for the first-mentioned method is also provided.
    Type: Grant
    Filed: December 22, 1986
    Date of Patent: December 20, 1988
    Inventors: Naoshi Nakagawa, Tetsuo Takigawa, Akira Kageyu, Michiya Shimamura, Masafumi Okada, Masao Mizuno