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公开(公告)号:US20240241195A1
公开(公告)日:2024-07-18
申请号:US18582293
申请日:2024-02-20
IPC分类号: G01R33/28 , A61K49/10 , C07C67/14 , C07C67/293 , C07C69/716 , C07F7/08 , G01R33/46 , G01R33/44
CPC分类号: G01R33/282 , A61K49/10 , C07C67/14 , C07C67/293 , C07C69/716 , C07F7/081 , C07F7/083 , G01R33/4608 , C07B2200/05 , G01R33/445
摘要: A method for preparing an NMR material, comprising generating parahydrogen in gas or liquid form at a first location; transporting the parahydrogen away from the first location; mixing a precursor compound including a metabolite component with a catalyst for hydrogenation; hydrogenating the precursor compound using the parahydrogen; transferring polarization in the precursor compound to a nuclear spin of the metabolite component; cleaving a side arm of the precursor compound in a chemical reaction, with the metabolite molecule being one of the products of the reaction; separating the metabolite molecule from the catalyst for hydrogenation and other products of the reaction; and generating metabolite molecules for use in an MRI scanner by extracting a sample of the metabolite molecule having at least 5% polarization.
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公开(公告)号:US20240228451A1
公开(公告)日:2024-07-11
申请号:US18556727
申请日:2022-04-21
申请人: Panafina, Inc.
IPC分类号: C07D305/12 , C07C51/347 , C07C51/487 , C07C67/14 , C07C67/31 , C07C67/313 , C07D309/30 , C07D309/32
CPC分类号: C07D305/12 , C07C51/347 , C07C51/487 , C07C67/14 , C07C67/31 , C07C67/313 , C07D309/30 , C07D309/32
摘要: Provided according to embodiments of the invention are methods of forming a lipstatin derivative, (S)-1-((2S,3S)-3-ethyl-4-oxooxetan-2-yl) tridecan-2-yl formyl-L-alaninate. Such methods include one or more reaction steps that include the Mitsunobu coupling of N-formyl L-alanine in the presence of di-t-butyl azodicarboxylate (DBAD) and triphenylphosphine. Compounds formed by a method of the invention, compositions that include a compound formed by a method of the invention, and methods of inhibiting lipase activity and/or treating pancreatitis using a compound formed by a method of the invention are also provided.
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公开(公告)号:US11940510B2
公开(公告)日:2024-03-26
申请号:US17995232
申请日:2021-03-31
IPC分类号: G01R33/28 , A61K49/10 , C07C67/14 , C07C67/293 , C07C69/716 , C07F7/08 , G01R33/46 , G01R33/44
CPC分类号: G01R33/282 , A61K49/10 , C07C67/14 , C07C67/293 , C07C69/716 , C07F7/081 , C07F7/083 , G01R33/4608 , C07B2200/05 , G01R33/445
摘要: A method for preparing an NMR material, comprising generating parahydrogen in gas or liquid form at a first location; transporting the parahydrogen away from the first location; mixing a precursor compound including a metabolite component with a catalyst for hydrogenation; hydrogenating the precursor compound using the parahydrogen; transferring polarization in the precursor compound to a nuclear spin of the metabolite component; cleaving a side arm of the precursor compound in a chemical reaction, with the metabolite molecule being one of the products of the reaction; separating the metabolite molecule from the catalyst for hydrogenation and other products of the reaction; and generating metabolite molecules for use in an MRI scanner by extracting a sample of the metabolite molecule having at least 5% polarization.
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公开(公告)号:US20240074958A1
公开(公告)日:2024-03-07
申请号:US18112411
申请日:2023-02-21
发明人: Douglas A. Klumpp , Rachel A. Klumpp , Zachary Liveris , Michael Stentzel , Robert M. Sobel , Smaro G. Kokkinidou
IPC分类号: A61K8/37 , A01N37/44 , A23L2/56 , A23L27/20 , A61Q9/02 , A61Q11/00 , A61Q19/00 , C07C67/14 , C07C227/08 , C07C229/28
CPC分类号: A61K8/37 , A01N37/44 , A23L2/56 , A23L27/203 , A61Q9/02 , A61Q11/00 , A61Q19/00 , C07C67/14 , C07C227/08 , C07C229/28 , A23V2002/00
摘要: A compound that includes a menthol glycinate. The menthol glycinate includes a menthol connected to a glycine or glycine derivative, via an ester linkage. The groups on the N atom are referred to as R1 and R2, and R1 and R2 are independently selected from the group consisting of: alkyl and R1 and R2 together with the N atom to which they are attached form a 4-8-member ring. R1 and R2 each contain at most 20 carbon atoms.
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公开(公告)号:US20220259137A1
公开(公告)日:2022-08-18
申请号:US17736541
申请日:2022-05-04
IPC分类号: C07C69/63 , C09K5/04 , C10M171/00 , C10M105/54 , C07C67/14 , C10M105/18 , C10M105/38
摘要: A compound of formula (I): wherein W is independently selected from the group consisting of H, F, Cl, Br, and I; X is independently selected from the group consisting of H, F, Cl, Br, and I; Y is independently selected from the group consisting of F, Cl, Br, and I; Z is independently selected from the group consisting of H, F, Cl, Br, and I; n is an integer from 1 to 8; and n′ is an integer from 1 to 12.
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公开(公告)号:US20210403410A1
公开(公告)日:2021-12-30
申请号:US17318581
申请日:2021-05-12
发明人: Thomas Millar , Burkhardt Schuett
IPC分类号: C07C69/533 , A61K31/23 , A61K31/231 , C07C69/587 , A61K9/00 , A61K9/06 , A61K9/08 , A61K9/107 , A61K31/232 , A61K47/14 , A61K47/38 , C07C67/14 , C07C69/26 , C07C69/58 , C07C69/22
摘要: Disclosed herein is an ophthalmic formulation comprising a compound of formula (I) wherein le is a linear or branched C9-C33 alkyl or a linear or branched C9-C33 alkenyl with 1 to 4 double bonds; R2 is a linear or branched C9-C19 alkyl or a linear or branched C9-C19 alkenyl with 1 to 4 double bonds; and an ophthalmologically acceptable carrier.
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公开(公告)号:US20210130722A1
公开(公告)日:2021-05-06
申请号:US17094457
申请日:2020-11-10
申请人: Polnox Corporation
发明人: Ashok L. Cholli , Murat Tonga
IPC分类号: C10L10/04 , C10M129/72 , C07C69/604 , C23F11/12 , C07C67/08 , C07C67/14 , C10M169/04 , C10L1/198 , C10L1/19 , C11D3/00 , A23D7/00 , A23D9/00 , C11C3/00
摘要: Disclosed are multifunctional compounds represented by structural formula (I): methods of producing compounds represented by structural formula (I) and their use in inhibiting corrosion in corrodible material.
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公开(公告)号:US20210130271A1
公开(公告)日:2021-05-06
申请号:US17123365
申请日:2020-12-16
发明人: Thomas CHEN , Daniel LEVIN , Satish PUPPALI
IPC分类号: C07C29/92 , A61K31/045 , C07C201/16 , C07C201/12 , C07C67/14 , C07C29/88 , C07C29/86 , A61K31/4188 , A61K45/06 , A61N5/10 , C07C29/78
摘要: The present invention provides a process for purifying a monoterpene or sesquiterpene having a purity greater than about 98.5% (w/w). The process comprises the steps of derivatizing the monoterpene (or sesquiterpene) to produce a monoterpene (or sesquiterpene) derivative, separating the monoterpene (or sesquiterpene) derivative, and releasing the monoterpene (or sesquiterpene) from the derivative. Also encompassed by the scope of the present invention is a pharmaceutical composition comprising a monoterpene (or sesquiterpene) having a purity greater than about 98.5% (w/w). The purified monoterpene can be used to treat a disease such as cancer. The present monoterpene (or sesquiterpene) may be administered alone, or may be co-administered with radiation or other therapeutic agents, such as chemotherapeutic agents.
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公开(公告)号:US20210093531A1
公开(公告)日:2021-04-01
申请号:US17037180
申请日:2020-09-29
发明人: Douglas A. Klumpp , Rachel A. Klumpp , Zachary Liveris , Michael Stentzel , Robert M. Sobel , Smaro G. Kokkinidou
IPC分类号: A61K8/37 , A01N37/44 , A61Q9/02 , A61Q19/00 , C07C67/14 , C07C227/08 , A61Q11/00 , C07C229/28 , A23L27/20 , A23L2/56
摘要: A compound that includes a menthol glycinate. The menthol glycinate includes a menthol connected to a glycine or glycine derivative, via an ester linkage. The groups on the N atom are referred to as R1 and R2, and R1 and R2 are independently selected from the group consisting of: H, alkyl and R1 and R2 together with the N atom to which they are attached form a 4-8-member ring. R1 and R2 each contain at most 20 carbon atoms.
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公开(公告)号:US10899691B2
公开(公告)日:2021-01-26
申请号:US16575587
申请日:2019-09-19
发明人: Thomas Chen , Daniel Levin , Satish Puppalli
IPC分类号: C07C29/92 , C07C67/14 , C07C201/12 , A61K31/045 , C07C29/78 , C07C29/88 , C07C201/16 , A61K31/4188 , A61K45/06 , A61N5/10 , C07C29/86
摘要: The present invention provides a process for purifying a monoterpene or sesquiterpene having a purity greater than about 98.5% (w/w). The process comprises the steps of derivatizing the monoterpene (or sesquiterpene) to produce a monoterpene (or sesquiterpene) derivative, separating the monoterpene (or sesquiterpene) derivative, and releasing the monoterpene (or sesquiterpene) from the derivative. Also encompassed by the scope of the present invention is a pharmaceutical composition comprising a monoterpene (or sesquiterpene) having a purity greater than about 98.5% (w/w). The purified monoterpene can be used to treat a disease such as cancer. The present monoterpene (or sesquiterpene) may be administered alone, or may be co-administered with radiation or other therapeutic agents, such as chemotherapeutic agents.
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