Patents by Inventor Yuko Asamitsu
Yuko Asamitsu 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).
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Publication number: 20230365589Abstract: The present invention provides an amine derivative having a DYRK-inhibiting activity and represented by formula (1): wherein A1, A2, L1, L2, X, Z, R1 and R4 are as defined in the description, or a pharmaceutically acceptable salt thereof.Type: ApplicationFiled: September 17, 2021Publication date: November 16, 2023Applicants: Sumitomo Pharma Co., Ltd., CARNA BIOSCIENCES, INC.Inventors: Shingo TOJO, Daisuke URABE, Hitoshi WATANABE, Wataru KAWAHATA, Hideki MORIYAMA, Yuko ASAMITSU
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Publication number: 20230138851Abstract: The present invention provides a compound that has an inhibitory effect on DYRK and that is represented by general formula (I): wherein Q, R1, R2 and R3 are as defined in the description.Type: ApplicationFiled: January 28, 2021Publication date: May 4, 2023Applicant: CARNA BIOSCIENCES, INC.Inventors: Ayako SAWA, Wataru KAWAHATA, Yuko ASAMITSU, Masaaki SAWA, Yasuhiro IWATA, Hideki MORIYAMA, Shingo TOJO, Daisuke URABE
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Patent number: 10538521Abstract: The present invention provides a novel 2,4,6-substituted pyrimidine derivative, which is a compound represented by formula (I) (in the formula, ring A is a 6-membered heteroaryl group having at least one N atom optionally substituted with R1, R2, and R3; Z is an optionally substituted alkoxy group, an optionally substituted amino group, an optionally substituted heterocycloalkyl group, or an optionally substituted heteroaryl group; and R1, R2, and R3 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, an optionally substituted alkyl group, an optionally substituted cycloalkyl group, an optionally substituted alkoxy group, an optionally substituted cycloalkyloxy group, an optionally substituted heterocycloalkyloxy group, an optionally substituted phenoxy group, an optionally substituted amino group, a nitro group, and a hydroxy group) or a pharmaceutically acceptable salt thereof.Type: GrantFiled: October 25, 2017Date of Patent: January 21, 2020Assignees: CARNA BIOSCIENCES, INC., THE KITASATO INSTITUTEInventors: Masaaki Sawa, Yuko Asamitsu, Yuko Uno, Satoshi Omura, Kazuhiko Otoguro, Masato Iwatsuki, Aki Ishiyama, Rei Hokari
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Publication number: 20190345154Abstract: The present invention provides a novel 2,4,6-substituted pyrimidine derivative, which is a compound represented by formula (I) (in the formula, ring A is a 6-membered heteroaryl group having at least one N atom optionally substituted with R1, R2, and R3; Z is an optionally substituted alkoxy group, an optionally substituted amino group, an optionally substituted heterocycloalkyl group, or an optionally substituted heteroaryl group; and R1, R2, and R3 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, an optionally substituted alkyl group, an optionally substituted cycloalkyl group, an optionally substituted alkoxy group, an optionally substituted cycloalkyloxy group, an optionally substituted heterocycloalkyloxy group, an optionally substituted phenoxy group, an optionally substituted amino group, a nitro group, and a hydroxy group) or a pharmaceutically acceptable salt thereof.Type: ApplicationFiled: October 25, 2017Publication date: November 14, 2019Applicants: CARNA BIOSCIENCES, INC., THE KITASATO INSTITUTEInventors: Masaaki SAWA, Yuko ASAMITSU, Yuko UNO, Satoshi OMURA, Kazuhiko OTOGURO, Masato IWATSUKI, Aki ISHIYAMA, Rei HOKARI
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Patent number: 9656995Abstract: The purpose of the present invention is to provide a novel triazine derivative of the formula (I): wherein R1 represents a substituted or unsubstituted lower alkyl group, R2 represents a hydrogen atom or a substituted or unsubstituted lower alkyl group, A represents a nitrogen atom or C—R3, R3 represents a hydrogen atom, a cyano group, a substituted or unsubstituted acyl group, a substituted or unsubstituted sulfonyl group, or a substituted or unsubstituted carbamoyl group, and R4 represents a substituted or unsubstituted lower alkyl group, or a substituted or unsubstituted cycloalkyl group, or a pharmaceutically acceptable salt thereof.Type: GrantFiled: July 15, 2014Date of Patent: May 23, 2017Assignee: CARNA BIOSCIENCES, INC.Inventors: Wataru Kawahata, Tokiko Asami, Masaaki Sawa, Yuko Asamitsu, Takayuki Irie, Takahiro Miyake, Takao Kiyoi
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Publication number: 20160168122Abstract: The purpose of the present invention is to provide a novel triazine derivative of the formula (I): wherein R1 represents a substituted or unsubstituted lower alkyl group, R2 represents a hydrogen atom or a substituted or unsubstituted lower alkyl group, A represents a nitrogen atom or C—R3, R3 represents a hydrogen atom, a cyano group, a substituted or unsubstituted acyl group, a substituted or unsubstituted sulfonyl group, or a substituted or unsubstituted carbamoyl group, and R4 represents a substituted or unsubstituted lower alkyl group, or a substituted or unsubstituted cycloalkyl group, or a pharmaceutically acceptable salt thereof.Type: ApplicationFiled: July 15, 2014Publication date: June 16, 2016Inventors: Wataru KAWAHATA, Tokiko ASAMI, Masaaki SAWA, Yuko ASAMITSU, Takayuki IRIE, Takahiro MIYAKE, Takao KIYOI
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Publication number: 20150011751Abstract: To provide a novel triazine derivative represented by the following formula (I): A triazine derivative represented by the following formula (I): wherein R1 represents a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic ring, a substituted or unsubstituted heterocyclic fused ring, or a substituted or unsubstituted alkynyl group, R2 represents a hydrogen atom, a halogen atom, a substituted or unsubstituted lower alkyl group, or a substituted or unsubstituted alkoxy group, R3 represents a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic ring, or a substituted or unsubstituted heterocyclic fused ring, R4 represents a hydrogen atom, a substituted or unsubstituted lower alkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted amino group, or a halogen atom, and R5 represents a hydrogen atom, a substituted or unsubstituted lower alkyl group, or R1 and R5 may be combined to form a saturated or unsaturateType: ApplicationFiled: March 7, 2013Publication date: January 8, 2015Inventors: Wataru Kawahata, Tokiko Asami, Masaaki Sawa, Yuko Asamitsu, Takayuki Irie, Takahiro Miyake, Takao Kiyoi