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公开(公告)号:US20240335559A1
公开(公告)日:2024-10-10
申请号:US18579456
申请日:2022-07-15
发明人: Petr CIGLER , Klara GRANTZ SASKOVA , Vaclav VANEK , Zuzana HEJDANKOVA , Lenka LOUKOTOVA , Pavel SVEC , Anastasiia PRISS , Silvia PETREZSELYOVA
IPC分类号: A61K48/00 , A61K8/42 , A61K9/127 , A61K9/51 , C07C233/62 , C07C237/10 , C07D207/12 , C07D311/00 , C12N15/88
CPC分类号: A61K48/0033 , A61K8/42 , A61K9/1271 , A61K9/5123 , C07C233/62 , C07C237/10 , C07D207/12 , C07D311/00 , C12N15/88 , C07C2601/14
摘要: The present invention relates to a lipidoid of general formula I, wherein X is selected from —C(═O)NH—, —C(═O)O—, —C(═S)O—, —C(═O)S—, —C(═S)S—, —C(═O)NHNH—, —CH2—, —O—, —OC(═O)—, —S—, —SC(═O)—, —NH—, —NHNH—, —NHC(═O)—, —NHNHC(═O)—, —C═C—, —CH═CH—, a five-membered heterocycle containing at least 2 nitrogen atoms, —CH2C(═O)NH—, —CH2C(═S)O—, —CH2C(═S)S—, —CH2C(═O)NHNH—, —N═CH—, —CH═N—, —NH—N═CH—, and —CH═N—NH—; Y is alkylene C2-C10 chain; R1 is selected from alkyl C1-C46, alkenyl C2-C46, alkynyl C2-C46; Z is selected from H, —OH, —CH3, —CH2OH, —NH2, —C(═O)NH2, —CONH(CH2)2OH, —CON[(CH2)2OH]2, —CONHCH(CH2OH)2, —CONHCH2CH(—OH)CH2OH, —CONH(CH2)2C(═O)NH2, —CON[CH2C(═O)NH2]2, —CONH(CH2)2NHC(═O)NH2, —CONH(CH2)3—N+(CH3)2—(CH2)2—SO3—, —CONH(CH2)3—N+(CH3)2—(CH2)2—COO−, —COO(CH2)2—O—P(═O)(O—)—O(CH2)2—N+(CH3)3, —N+(CH3)2—(CH2)3—SO3—, —N+(CH3)2—(CH2)2—COO−, formula (II), and formula (III), wherein R2 is independently selected from hydrogen and —CH3; E is independently selected from O and S atoms; n is an integer within the range of from 1 to 5; and T is selected from —X—Y—N(R1)2, —C(═O)O(C1-C3 alkyl), —C(═O)OCH2CH2OH, formula (IV), formula (V), formula (VI), —C(═O)OH, —CONH(CH2)2OH, —CON[(CH2)2OH]2, —CONHCH(CH2OH)2, CONH(CH2)2C(═O)NH2, —CON[CH2C(═O)NH2]2, —CONHCH[C(═O)NH2]2, —CONH(CH2)2NHC(═O)NH2, —C(═O)NH2, —CONH(CH2)3—N+(CH3)2—(CH2)2—SO3—, —CONH(CH2)3—N+(CH3)2—(CH2)2—COO−, —NH2, —NHC(═O)CH3, —COO(CH2)2—O—P(═O)(O—)—O(CH2)2—N+(CH3)3, —OH, —O(C1-C3 alkyl), —NHC(═O)NH(CH3), —NHC(═S)N(CH3)2, —NHC(═S)NH(CH3), —NHC(═N—CN)NH2, —NHC(═N—CN)NH(CH3), —NHC(═N—CN)N(CH3)2, —NHC[═N—S(═O)2NH2]NH2, —N+(CH3)2—(CH2)3—SO3—, —N+(CH3)2—(CH2)2—COO−, wherein R2, E and n are as defined above; and/or if Z is —OH or —CH2OH, and T is —C(═O)OH, then Z together with T and three carbon atoms between them may form a cyclic lactone containing 4 to 5 carbon atoms; and pharmaceutically acceptable salts, addition salts and solvates thereof. This lipidoid is useful as a transfection agent. The invention further describes transfection reagents, transfection particles containing this lipidoid, and their use.
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公开(公告)号:US20240307382A1
公开(公告)日:2024-09-19
申请号:US18330185
申请日:2023-06-06
发明人: Kathleen Ann Martin , Carmela Sidrauski , Jennifer M. Frost , Marina Pliushchev , Yunsong Tong , Lawrence A. Black , Xiangdong Xu , Lei Shi , Qingwei Zhang , SeungWon Chung , Ramzi Farah Sweis , Michael J. Dart , John T. Randolph , Kathleen J. Murauski
IPC分类号: A61K31/4965 , A61K31/196 , A61K31/341 , A61K31/36 , A61K31/381 , A61K31/415 , A61K31/4196 , A61K31/42 , A61K31/421 , A61K31/422 , A61K31/4245 , A61K31/425 , A61K31/426 , A61K31/437 , A61K31/4427 , A61K31/472 , A61K31/4985 , A61K31/519 , A61K31/5355 , A61K45/06 , C07C233/62 , C07D217/26 , C07D231/14 , C07D237/20 , C07D241/20 , C07D249/10 , C07D261/18 , C07D263/34 , C07D275/03 , C07D277/56 , C07D285/06 , C07D307/68 , C07D317/46 , C07D333/38 , C07D401/04 , C07D413/04 , C07D471/04 , C07D487/04 , C07D495/04
CPC分类号: A61K31/4965 , A61K31/196 , A61K31/341 , A61K31/36 , A61K31/381 , A61K31/415 , A61K31/4196 , A61K31/42 , A61K31/421 , A61K31/422 , A61K31/4245 , A61K31/425 , A61K31/426 , A61K31/437 , A61K31/4427 , A61K31/472 , A61K31/4985 , A61K31/519 , A61K31/5355 , A61K45/06 , C07C233/62 , C07D217/26 , C07D231/14 , C07D237/20 , C07D241/20 , C07D249/10 , C07D261/18 , C07D263/34 , C07D275/03 , C07D277/56 , C07D285/06 , C07D307/68 , C07D317/46 , C07D333/38 , C07D401/04 , C07D413/04 , C07D471/04 , C07D487/04 , C07D495/04
摘要: Provided herein are compounds, compositions, and methods useful for modulating the integrated stress response (ISR) and for treating related diseases; disorders and conditions.
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公开(公告)号:US20210053908A1
公开(公告)日:2021-02-25
申请号:US16899376
申请日:2020-06-11
申请人: CORTEXYME, INC.
发明人: Andrei W. Konradi , Robert A. Galemmo, JR. , Stephen S. Dominy , Casey C. Lynch , Leslie J. Holsinger
IPC分类号: C07C233/62 , C07D213/82 , C07D239/34 , C07D239/36 , C07D413/12 , C07D257/04 , C07D261/12 , C07D213/70 , C07C317/28 , C07C233/78 , C07C235/10 , C07C235/50 , C07B59/00 , C07C237/42 , C07D401/12 , C07C381/00 , C07C323/42 , C07D213/65 , C07D213/68 , C07D239/38 , C07C247/18 , C07F5/02 , A61P31/04 , A61P25/00 , A61K31/165 , A61K31/167 , A61K31/41 , A61K31/42 , A61K31/44 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/4439 , A61K31/505 , A61K31/513 , A61K31/655 , A61K45/06 , C07C245/08 , C07C247/16 , C07C323/40 , C07D213/81
摘要: The present invention provides compounds according to Formula I as described herein, and their use for inhibiting the lysine gingipain protease (Kgp) from the bacterium Porphyromonas gingivalis. Also described are gingipain activity probe compounds and methods for assaying gingipain activity are also described, as well as methods for the treatment of disorders associated with P. gingivalis infection, including brain disorders such as Alzheimer's disease.
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公开(公告)号:US10730826B2
公开(公告)日:2020-08-04
申请号:US16353786
申请日:2019-03-14
申请人: CORTEXYME, INC.
发明人: Andrei W. Konradi , Robert A. Galemmo, Jr. , Stephen S. Dominy , Casey C. Lynch , Leslie J. Holsinger
IPC分类号: C07C233/62 , C07D213/82 , C07D239/34 , C07D239/36 , C07D413/12 , C07D257/04 , C07D261/12 , C07D213/70 , C07C317/28 , C07C233/78 , C07C235/10 , C07C235/50 , C07B59/00 , C07C237/42 , C07D401/12 , C07C381/00 , C07C323/42 , C07D213/65 , C07D213/68 , C07D239/38 , C07C247/18 , C07F5/02 , A61P31/04 , A61P25/00 , A61K31/165 , A61K31/167 , A61K31/41 , A61K31/42 , A61K31/44 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/4439 , A61K31/505 , A61K31/513 , A61K31/655 , A61K45/06 , C07C245/08 , C07C247/16 , C07C323/40 , C07D213/81
摘要: The present invention provides compounds according to Formula I as described herein, and their use for inhibiting the lysine gingipain protease (Kgp) from the bacterium Porphyromonas gingivalis. Also described are gingipain activity probe compounds and methods for assaying gingipain activity are also described, as well as methods for the treatment of disorders associated with P. gingivalis infection, including brain disorders such as Alzheimer's disease.
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公开(公告)号:US10676470B2
公开(公告)日:2020-06-09
申请号:US16399821
申请日:2019-04-30
申请人: Cortexyme, Inc.
IPC分类号: C07C233/62 , C07C233/78 , C07C247/16 , C07D417/12 , C07D277/64 , C07D409/12 , C07D213/50 , C07C247/18 , C07D277/24 , C07D213/53 , C07D277/28
摘要: The present invention relates generally to therapeutics targeting the bacterium Porphyromonas gingivalis, including its protease Lysine gingipain (Kgp), and their use for the treatment of disorders associated with P. gingivalis infection, including brain disorders such as Alzheimer's disease. In certain embodiments, the invention provides compounds according to Formula I, as described herein, and pharmaceutically acceptable salts thereof.
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公开(公告)号:US10434180B2
公开(公告)日:2019-10-08
申请号:US15214331
申请日:2016-07-19
发明人: Delphine Bregeon , Patrick Dennler , Christian Belmant , Laurent Gauthier , François Romagne , Eliane Fischer , Roger Schibli
IPC分类号: A61K31/5517 , C07K16/00 , C07K16/30 , C07K19/00 , C07C217/08 , C07C223/02 , C07C229/26 , C07C233/62 , C07C247/04 , C07D225/08 , C07D257/08 , C07D277/06 , C07F9/50 , C12N9/10 , C12P21/00 , G01N33/68 , A61K47/48 , A61K47/68
摘要: The present application relates to methods for the enzymatic functionalization of immunoglobulins, in particular with drugs. Also disclosed herein are linking reagents, functionalized antibodies, pharmaceutical compositions, and method of treating disease and/or conditions.
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公开(公告)号:US10132799B2
公开(公告)日:2018-11-20
申请号:US14414432
申请日:2013-07-10
发明人: Christian Belmant , Delphine Bregeon , Patrick Dennler , Eliane Fischer , François Romagne , Roger Schibli , Laurent Gauthier
IPC分类号: A61K47/48 , C07K16/00 , C07K16/30 , C07K19/00 , A61K31/5517 , C07C217/08 , C07C223/02 , C07C229/26 , C07C233/62 , C07C247/04 , C07C323/12 , C07C323/60 , C07D225/08 , C07D257/08 , C07D277/06 , C07F9/50 , C12N9/10 , C12P21/00 , G01N33/68 , G01N33/532 , G01N33/50 , A61K47/68
摘要: Provided is a method for the functionalization of immunoglobulins through the use of transglutaminase, including methods for screening functionalized antibodies for characteristics of interest, antibody compositions comprising a plurality of functionalized antibodies, and functionalized antibodies with rodent constant regions.
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公开(公告)号:US20180134677A1
公开(公告)日:2018-05-17
申请号:US15870276
申请日:2018-01-12
发明人: Fajun Nan , Min Li , Zhaobing Gao , Yangming Zhang , Haining Hu , Haiyan Xu , Huanan Liu , Xiaoping Pi
IPC分类号: C07D307/24 , A61K31/167 , C07C237/22 , C07C237/04 , C07C235/74 , C07C235/16 , C07C233/62 , C07C333/08 , C07C231/02 , C07C275/64 , C07C273/18 , C07C271/28 , C07C269/06 , C07C269/04 , A61K31/341 , A61K31/277 , A61K31/27 , A61K31/17 , C07C237/48
CPC分类号: C07D307/24 , A61K31/167 , A61K31/17 , A61K31/27 , A61K31/277 , A61K31/341 , C07C231/02 , C07C233/62 , C07C235/16 , C07C235/74 , C07C237/04 , C07C237/22 , C07C237/48 , C07C269/04 , C07C269/06 , C07C271/28 , C07C273/18 , C07C275/64 , C07C333/08 , C07C2601/02 , C07C2601/14
摘要: The present invention provides a compound represented by general formula I or a pharmaceutical acceptable salt thereof, the preparation method therefor and the use thereof in preparing a medicine for treating a neurological disease, such as epilepsy, convulsion, neuropathic pain, acute ischemic stroke, and a neurodegenerative disease. The compound according to present invention has a better absorption in brain tissue when compared with RTG. In addition, the compound provided by present invention has not only a greatly enhanced efficacy, but also a neurotoxicity greatly lower than that of RTG, and thus possesses a wider safety window.
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公开(公告)号:US20180099977A1
公开(公告)日:2018-04-12
申请号:US15786134
申请日:2017-10-17
申请人: The Broad Institute, Inc. , The General Hospital Corporation d/b/a Massachusetts General Hospital , Massachusetts Institute of Technology
发明人: Edward Holson , Florence Fevrier Wagner , Michel Weiwer , Li-Huei Tsai , Stephen J. Haggarty , Yan-Ling Zhang
IPC分类号: C07D491/107 , C07D401/12 , A61K31/445 , A61K31/437 , A61K31/167 , A61K31/402 , A61K31/403 , A61K31/4035 , A61K31/352 , C07D491/08 , C07D487/10 , C07D487/04 , C07D407/12 , C07D311/04 , C07D295/185 , C07D237/04 , C07D231/04 , C07C233/42 , A61K31/5377 , A61K31/519 , A61K31/501 , A61K31/50 , A61K31/4965 , A61K31/496 , A61K31/4545 , A61K31/4535 , A61K31/4439 , A61K31/4433 , A61K31/4418 , A61K31/439 , A61K31/4178 , A61K31/415 , A61K31/397 , A61K31/381 , A61K31/351 , C07D471/04 , C07D205/04 , C07D209/44 , C07D209/52 , C07D211/34 , C07D211/62 , C07D295/195 , C07C237/24 , C07D333/24 , C07D241/12 , C07D213/56 , C07D205/06 , C07C237/20 , C07C235/82 , C07C233/62 , C07C233/56 , C07C233/43 , C07C211/52 , C07C281/06 , C07C275/40 , C07C275/30 , C07C271/28 , C07D213/40 , C07D211/22 , C07D493/08 , C07D409/12 , C07D405/12 , C07D333/20 , C07D311/82 , C07D309/08 , C07D403/12
摘要: The present invention relates to compounds of formula (I): or a pharmaceutically acceptable salt, hydrate, solvate, or prodrug thereof, wherein U, J, V, X, R2a, R2b, R2c, R5 and t are as described herein. The present invention relates generally to inhibitors of histone deacetylase and to methods of making and using them. These compounds are useful for promoting cognitive function and enhancing learning and memory formation. In addition, these compounds are useful for treating, alleviating, and/or preventing various conditions, including for example, neurological disorders, memory and cognitive function disorders/impairments, extinction learning disorders, fungal diseases and infections, inflammatory diseases, hematological diseases, and neoplastic diseases in humans and animals.
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公开(公告)号:US09890172B2
公开(公告)日:2018-02-13
申请号:US15147201
申请日:2016-05-05
IPC分类号: A61K31/4035 , C07D295/195 , C07D209/52 , C07D471/04 , A61K31/403 , C07D491/107 , C07D401/12 , C07D403/12 , C07D309/08 , C07D311/82 , C07D333/20 , C07D405/12 , C07D409/12 , C07D493/08 , C07D211/22 , C07D213/40 , C07C271/28 , C07C275/30 , C07C275/40 , C07C281/06 , C07C211/52 , C07C233/43 , C07C233/56 , C07C233/62 , C07C235/82 , C07C237/20 , C07D205/06 , C07D213/56 , C07D241/12 , C07D333/24 , C07C237/24 , C07D205/04 , C07D209/44 , C07D211/34 , C07D211/62 , A61K31/167 , A61K31/402 , A61K31/437 , A61K31/445 , A61K31/351 , A61K31/352 , A61K31/381 , A61K31/397 , A61K31/415 , A61K31/4178 , A61K31/439 , A61K31/4418 , A61K31/4433 , A61K31/4439 , A61K31/4535 , A61K31/4545 , A61K31/496 , A61K31/4965 , A61K31/50 , A61K31/501 , A61K31/519 , A61K31/5377 , C07C233/42 , C07D231/04 , C07D237/04 , C07D295/185 , C07D311/04 , C07D407/12 , C07D487/04 , C07D487/10 , C07D491/08
CPC分类号: C07D491/107 , A61K31/167 , A61K31/351 , A61K31/352 , A61K31/381 , A61K31/397 , A61K31/402 , A61K31/403 , A61K31/4035 , A61K31/415 , A61K31/4178 , A61K31/437 , A61K31/439 , A61K31/4418 , A61K31/4433 , A61K31/4439 , A61K31/445 , A61K31/4535 , A61K31/4545 , A61K31/496 , A61K31/4965 , A61K31/50 , A61K31/501 , A61K31/519 , A61K31/5377 , C07C211/52 , C07C233/42 , C07C233/43 , C07C233/56 , C07C233/62 , C07C235/82 , C07C237/20 , C07C237/24 , C07C271/28 , C07C275/30 , C07C275/40 , C07C281/06 , C07C2601/02 , C07C2601/08 , C07C2601/10 , C07C2601/14 , C07C2601/16 , C07C2602/08 , C07C2602/50 , C07D205/04 , C07D205/06 , C07D209/44 , C07D209/52 , C07D211/22 , C07D211/34 , C07D211/62 , C07D213/40 , C07D213/56 , C07D231/04 , C07D237/04 , C07D241/12 , C07D295/185 , C07D295/195 , C07D309/08 , C07D311/04 , C07D311/82 , C07D333/20 , C07D333/24 , C07D401/12 , C07D403/12 , C07D405/12 , C07D407/12 , C07D409/12 , C07D471/04 , C07D487/04 , C07D487/10 , C07D491/08 , C07D493/08
摘要: The present invention relates to compounds of formula (I): or a pharmaceutically acceptable salt, hydrate, solvate, or prodrug thereof, wherein U, J, V, X, R2a, R2b, R2c, R5 and t are as described herein. The present invention relates generally to inhibitors of histone deacetylase and to methods of making and using them. These compounds are useful for promoting cognitive function and enhancing learning and memory formation. In addition, these compounds are useful for treating, alleviating, and/or preventing various conditions, including for example, neurological disorders, memory and cognitive function disorders/impairments, extinction learning disorders, fungal diseases and infections, inflammatory diseases, hematological diseases, and neoplastic diseases in humans and animals.
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