Patents by Inventor Yusuke Kono
Yusuke Kono 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: 20240102925Abstract: A moisture content measurement method that calculates moisture content of dehydrated sludge using a calibration curve for calculating the moisture content of the dehydrated sludge, the calibration curve being obtained by performing multivariate regression analysis after first-order differential processing or an offset correction is performed on absorbance for reflected light or reflectance for infrared rays from dehydrated sludge, the absorbance or the reflectance being obtained by measuring the dehydrated sludge using an infrared measurement apparatus provided with a light-receiving unit that can receive at least infrared rays reflected from a target object to be measured and a light source that has a plurality of infrared LEDs that can emit infrared rays having respectively different wavelengths or a light source having an infrared-region tungsten lamp or halogen lamp.Type: ApplicationFiled: November 30, 2021Publication date: March 28, 2024Inventors: Yasuko KOBAYASHI, Jun TANAKA, Takuya KAMBAYASHI, Yusuke KAGA, Shunsuke KONO, Kotaro KITAMURA, Makiko UDAGAWA, Hiroki MIYAKAWA
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Patent number: 11914444Abstract: An in-vehicle electronic system comprises a core ECU (Electronic Control Unit) mounted in a vehicle and a plurality of slave ECUs that is capable of communicating with the core ECU through an in-vehicle communication network, wherein the core ECU is configured to manage a current time while a main power source of the vehicle is in an off state and manage an activation time of each of the plurality of slave ECUs in a sleep state with a management table while the main power source is in an off state, wherein the core ECU is configured to send an activation signal to each slave ECU through the in-vehicle communication network when the current time becomes the activation time of each of the plurality of slave ECUs while the main power source is in an off state.Type: GrantFiled: February 24, 2022Date of Patent: February 27, 2024Assignee: HONDA MOTOR CO., LTD.Inventors: Tomoya Tokunaga, Yusuke Yoshimura, Satoshi Kono
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Publication number: 20230161238Abstract: An illumination apparatus includes a light source, an optical member, and an integrator. The optical member is rotatable around a rotation axis AR. A planar shape of the optical member is annular around the rotation axis AR. A first surface of the optical member is provided with a recessed and protruding portion. Multiple recessed and protruding structure units are consecutively formed on the optical member . Adjacent recessed and protruding structure units are in a mirror symmetry relation, and the recessed and protruding portions of the adjacent recessed and protruding structure units are smoothly connected together. Recessed portions and protruding portions of the recessed and protruding portion of each recessed and protruding structure unit are smoothly connected together. An area occupied by the recessed and protruding portion of each recessed and protruding structure unit is larger in size than incident light from the light surface.Type: ApplicationFiled: February 17, 2021Publication date: May 25, 2023Applicant: SONY GROUP CORPORATIONInventors: Toshifumi YASUI, Yusuke KONO
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Patent number: 11098078Abstract: The present invention has an object of providing a peptide synthesis method using a carrier capable of reversibly repeating the dissolved state and the insolubilized state, wherein the problem of an amino acid active species existing in the reaction system in de-protection reaction can be easily solved. The present invention provides a peptide synthesis method comprising the following steps: a step of condensing an N-Fmoc protected amino acid with a peptide having a C-terminal protected with a carrier which is crystallized according to a change of a composition of a dissolving solvent, in the presence of a condensing agent, to obtain an N-Fmoc-C-carrier protected peptide, a step of adding an alkylamine having 1 to 14 carbon atoms or hydroxyl amine to the reaction system, a step of de-protecting the N-terminal, and a step of changing the composition of the solvent dissolving the C-carrier protected peptide, to crystallize and separate the peptide.Type: GrantFiled: March 2, 2016Date of Patent: August 24, 2021Assignee: JITSUBO Co., Ltd.Inventors: Yusuke Kono, Hideaki Suzuki, Susumu Muto
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Patent number: 10654891Abstract: The purpose of the present invention is to provide a cross-linked peptide containing a novel non-peptide cross-linked structure, and a method for synthesizing the same. A cross-linked peptide having a novel non-peptide cross-linked structure, a useful intermediate for synthesizing the cross-linked peptide, and a method for synthesizing the novel cross-linked peptide and the intermediate are provided. The cross-linked peptide is characterized by having an —NR— bond in the cross-linked structure. By using the method for synthesizing the cross-linked peptide, a cross-link can be freely designed and an change can be freely made to a cross-link.Type: GrantFiled: May 17, 2016Date of Patent: May 19, 2020Assignee: Jitsubo Co., Ltd.Inventors: Yusuke Kono, Shuji Fujita, Hideaki Suzuki, Mari Okumoto, Takashi Nakae, Kazuhiro Chiba
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Patent number: 10633418Abstract: The purpose of the present invention is to provide a cross-linked peptide containing a novel non-peptide cross-linked structure, and a method for synthesizing the same. A cross-linked peptide having a novel non-peptide cross-linked structure, a useful intermediate for synthesizing the cross-linked peptide, and a method for synthesizing the novel cross-linked peptide and the intermediate are provided. The cross-linked peptide is characterized by having an —NR— bond in the cross-linked structure. By using the method for synthesizing the cross-linked peptide, a cross-link can be freely designed and an change can be freely made to a cross-link.Type: GrantFiled: May 17, 2016Date of Patent: April 28, 2020Assignee: JITSUBO CO., LTD.Inventors: Yusuke Kono, Shuji Fujita, Hideaki Suzuki, Mari Okumoto, Takashi Nakae, Kazuhiro Chiba
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Publication number: 20180282679Abstract: Provided is a cell culture apparatus capable of constructing cultured cells under an environment closer to that in a living body. The cell culture apparatus includes: a culture substrate (11) having a culture surface (11a) on which cells S are cultured; and a drive unit (12) configured to allow opening and closing of the culture substrate (11) between a closed form and an open form. The closed form is a form in which the culture substrate (11) forms a flow path having an internal volume with the culture surface (11) being an internal surface of the flow path. The open form is a form in which the culture surface (11a) of the culture substrate (11) is opened outward more than the culture surface (11a) of the culture substrate (11) in the closed form.Type: ApplicationFiled: July 26, 2016Publication date: October 4, 2018Applicant: The Ritsumeikan TrustInventors: Satoshi KONISHI, Takuya FUJITA, Koji HATTORI, Yusuke KONO
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Publication number: 20180215782Abstract: The present invention has an object of providing a peptide synthesis method using a carrier capable of reversibly repeating the dissolved state and the insolubilized state, wherein the problem of an amino acid active species existing in the reaction system in de-protection reaction can be easily solved. The present invention provides a peptide synthesis method comprising the following steps: a step of condensing an N-Fmoc protected amino acid with a peptide having a C-terminal protected with a carrier which is crystallized according to a change of a composition of a dissolving solvent, in the presence of a condensing agent, to obtain an N-Fmoc-C-carrier protected peptide, a step of adding an alkylamine having 1 to 14 carbon atoms or hydroxyl amine to the reaction system, a step of de-protecting the N-terminal, and a step of changing the composition of the solvent dissolving the C-carrier protected peptide, to crystallize and separate the peptide.Type: ApplicationFiled: March 2, 2016Publication date: August 2, 2018Inventors: Yusuke KONO, Hideaki SUZUKI, Susumu MUTO
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Publication number: 20160333050Abstract: The purpose of the present invention is to provide a cross-linked peptide containing a novel non-peptide cross-linked structure, and a method for synthesizing the same. A cross-linked peptide having a novel non-peptide cross-linked structure, a useful intermediate for synthesizing the cross-linked peptide, and a method for synthesizing the novel cross-linked peptide and the intermediate are provided. The cross-linked peptide is characterized by having an —NR— bond in the cross-linked structure. By using the method for synthesizing the cross-linked peptide, a cross-link can be freely designed and an change can be freely made to a cross-link.Type: ApplicationFiled: May 17, 2016Publication date: November 17, 2016Inventors: Yusuke KONO, Shuji FUJITA, Hideaki SUZUKI, Mari OKUMOTO, Takashi NAKAE, Kazuhiro CHIBA
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Publication number: 20160333052Abstract: The purpose of the present invention is to provide a cross-linked peptide containing a novel non-peptide cross-linked structure, and a method for synthesizing the same. A cross-linked peptide having a novel non-peptide cross-linked structure, a useful intermediate for synthesizing the cross-linked peptide, and a method for synthesizing the novel cross-linked peptide and the intermediate are provided. The cross-linked peptide is characterized by having an —NR— bond in the cross-linked structure. By using the method for synthesizing the cross-linked peptide, a cross-link can be freely designed and an change can be freely made to a cross-link.Type: ApplicationFiled: May 17, 2016Publication date: November 17, 2016Inventors: Yusuke KONO, Shuji Fujita, Hideaki Suzuki, Mari Okumoto, Takashi Nakae, Kazuhiro Chiba
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Patent number: 9376467Abstract: The purpose of the present invention is to provide a cross-linked peptide containing a novel non-peptide cross-linked structure, and a method for synthesizing the same. A cross-linked peptide having a novel non-peptide cross-linked structure, a useful intermediate for synthesizing the cross-linked peptide, and a method for synthesizing the novel cross-linked peptide and the intermediate are provided. The cross-linked peptide is characterized by having an —NR— bond in the cross-linked structure. By using the method for synthesizing the cross-linked peptide, a cross-link can be freely designed and an change can be freely made to a cross-link.Type: GrantFiled: February 28, 2012Date of Patent: June 28, 2016Assignee: JITSUBO CO., LTD.Inventors: Yusuke Kono, Shuji Fujita, Hideaki Suzuki, Mari Okumoto, Takashi Nakae, Kazuhiro Chiba
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Patent number: 9365615Abstract: The purpose of the present invention is to provide a cross-linked peptide containing a novel non-peptide cross-linked structure, and a method for synthesizing the same. A cross-linked peptide having a novel non-peptide cross-linked structure, a useful intermediate for synthesizing the cross-linked peptide, and a method for synthesizing the novel cross-linked peptide and the intermediate are provided. The cross-linked peptide is characterized by having an —NR— bond in the cross-linked structure. By using the method for synthesizing the cross-linked peptide, a cross-link can be freely designed and an change can be freely made to a cross-link.Type: GrantFiled: September 9, 2013Date of Patent: June 14, 2016Assignee: JITSUBO CO., LTD.Inventors: Yusuke Kono, Shuji Fujita, Hideaki Suzuki, Mari Okumoto, Takashi Nakae, Kazuhiro Chiba
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Patent number: 9284348Abstract: Disclosed are a carrier for use for separation purpose and a method for separation of a compound which enable a chemical reaction to be performed in a liquid phase, enable a compound of interest to be separated from the liquid phase after the completion of the reaction readily, enable the separated compound to be evaluated by structural analysis or the like while the compound being bound to the carrier, and enable the compound to be separated from the carrier readily. A carrier for separation which has a reaction site capable of reacting with other compound on a benzene ring, and a long-chain group having a specified carbon atom(s) at each of the ortho-position and the para-position of the reaction site through an oxygen atom.Type: GrantFiled: December 20, 2013Date of Patent: March 15, 2016Assignee: JITSUBO Co., Ltd.Inventors: Kazuhiro Chiba, Shokaku Kim, Yusuke Kono
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Publication number: 20150073121Abstract: The purpose of the present invention is to provide a cross-linked peptide containing a novel non-peptide cross-linked structure, and a method for synthesizing the same. A cross-linked peptide having a novel non-peptide cross-linked structure, a useful intermediate for synthesizing the cross-linked peptide, and a method for synthesizing the novel cross-linked peptide and the intermediate are provided. The cross-linked peptide is characterized by having an —NR— bond in the cross-linked structure. By using the method for synthesizing the cross-linked peptide, a cross-link can be freely designed and an change can be freely made to a cross-link.Type: ApplicationFiled: September 9, 2013Publication date: March 12, 2015Applicant: JITSUBO Co., Ltd.Inventors: Yusuke Kono, Shuji Fujita, Hideaki Suzuki, Mari Okumoto, Takashi Nakae, Kazuhiro Chiba
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Publication number: 20140107319Abstract: Disclosed are a carrier for use for separation purpose and a method for separation of a compound which enable a chemical reaction to be performed in a liquid phase, enable a compound of interest to be separated from the liquid phase after the completion of the reaction readily, enable the separated compound to be evaluated by structural analysis or the like while the compound being bound to the carrier, and enable the compound to be separated from the carrier readily. A carrier for separation which has a reaction site capable of reacting with other compound on a benzene ring, and a long-chain group having a specified carbon atom(s) at each of the ortho-position and the para-position of the reaction site through an oxygen atom.Type: ApplicationFiled: December 20, 2013Publication date: April 17, 2014Applicants: JITSUBO Co., Ltd., National University Corporation, Tokyo University of Agriculture and TechnologyInventors: Kazuhiro Chiba, Shokaku Kim, Yusuke Kono
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Patent number: 8633298Abstract: A carrier for use for separation purpose and a method for separation of a compound enable a chemical reaction to be performed in a liquid phase, a compound of interest to be separated from the liquid phase after the completion of the reaction readily, the separated compound to be evaluated by structural analysis or the like while the compound is being bound to the carrier, and the compound to be separated from the carrier readily. A carrier for separation is also provided which has a reaction site capable of reacting with other compound(s) on a benzene ring, and a long-chain group having a specified carbon atom(s) at each of the ortho-position and the para-position of the reaction site through an oxygen atom.Type: GrantFiled: September 20, 2006Date of Patent: January 21, 2014Assignee: Jitsubo Co., Ltd.Inventors: Kazuhiro Chiba, Shokaku Kim, Yusuke Kono
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Publication number: 20130345393Abstract: The purpose of the present invention is to provide a cross-linked peptide containing a novel non-peptide cross-linked structure, and a method for synthesizing the same. A cross-linked peptide having a novel non-peptide cross-linked structure, a useful intermediate for synthesizing the cross-linked peptide, and a method for synthesizing the novel cross-linked peptide and the intermediate are provided. The cross-linked peptide is characterized by having an —NR— bond in the cross-linked structure. By using the method for synthesizing the cross-linked peptide, a cross-link can be freely designed and an change can be freely made to a cross-link.Type: ApplicationFiled: February 28, 2012Publication date: December 26, 2013Applicant: JITSUBO Co., Ltd.Inventors: Yusuke Kono, Shuji Fujita, Hideaki Suzuki, Mari Okumoto, Takashi Nakae, Kazuhiro Chiba
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Patent number: 8344103Abstract: A solvent system which comprises two or more single organic solvents or two or more mixed organic solvents, characterized in that the state of the solvent system can be reversibly changed, with changing temperature conditions, from one state which is a homogeneously compatibilized mixed solvent system in which the two or more single or more mixed organic solvents constituting the solvent system have been homogeneously compatibilized and mixed to the other state which is a separated solvent system made up of two or more separated phases respectively consisting mainly of the two or more single or mixed organic solvents constituting solvent system, and that when the solvent system is the homogeneously mixed solvent system, a chemical component which is soluble in only one of the single or mixed organic solvents can be evenly dissolved in the system; and a process for producing a compound with the solvent system.Type: GrantFiled: November 3, 2006Date of Patent: January 1, 2013Assignee: Japan Science and Technology AgencyInventors: Kazuhiro Chiba, Yusuke Kono
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Patent number: 8293948Abstract: A reagent for organic synthesis with which a chemical reaction can be conducted in a liquid phase and unnecessary compound(s) can be easily separated at low cost from the liquid phase after completion of the reaction. The reagent for organic synthesis reversibly changes from a liquid-phase state to a solid-phase state with changes in solution composition and/or solution temperature, and is for use in organic synthesis reactions. This reagent for organic syntheses facilitates process development. With the reagent, research on and development of, e.g., medicines through, e.g., compound library synthesis, etc. can be accelerated. It can hence contribute to technical innovations in the biochemical industry and chemical industry.Type: GrantFiled: January 9, 2012Date of Patent: October 23, 2012Assignee: Jitsubo Co., Ltd.Inventors: Kazuhiro Chiba, Shokaku Kim, Yusuke Kono
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Publication number: 20120108788Abstract: A reagent for organic synthesis with which a chemical reaction can be conducted in a liquid phase and unnecessary compound(s) can be easily separated at low cost from the liquid phase after completion of the reaction. The reagent for organic synthesis reversibly changes from a liquid-phase state to a solid-phase state with changes in solution composition and/or solution temperature, and is for use in organic synthesis reactions. This reagent for organic syntheses facilitates process development. With the reagent, research on and development of, e.g., medicines through, e.g., compound library synthesis, etc. can be accelerated. It can hence contribute to technical innovations in the biochemical industry and chemical industry.Type: ApplicationFiled: January 9, 2012Publication date: May 3, 2012Applicant: JITSUBO Co., Ltd.Inventors: Kazuhiro Chiba, Shokaku Kim, Yusuke Kono