JP2022017447A5 - - Google Patents

Download PDF

Info

Publication number
JP2022017447A5
JP2022017447A5 JP2021179107A JP2021179107A JP2022017447A5 JP 2022017447 A5 JP2022017447 A5 JP 2022017447A5 JP 2021179107 A JP2021179107 A JP 2021179107A JP 2021179107 A JP2021179107 A JP 2021179107A JP 2022017447 A5 JP2022017447 A5 JP 2022017447A5
Authority
JP
Japan
Prior art keywords
disease
stereoisomers
pharmaceutically acceptable
syndrome
acceptable salt
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2021179107A
Other languages
English (en)
Japanese (ja)
Other versions
JP7381543B2 (ja
JP2022017447A (ja
Filing date
Publication date
Priority claimed from PCT/US2017/016509 external-priority patent/WO2017136727A2/en
Application filed filed Critical
Publication of JP2022017447A publication Critical patent/JP2022017447A/ja
Publication of JP2022017447A5 publication Critical patent/JP2022017447A5/ja
Application granted granted Critical
Publication of JP7381543B2 publication Critical patent/JP7381543B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2021179107A 2016-02-05 2021-11-02 化合物、組成物及び方法 Active JP7381543B2 (ja)

Applications Claiming Priority (12)

Application Number Priority Date Filing Date Title
US201662292202P 2016-02-05 2016-02-05
US62/292,202 2016-02-05
US201662341019P 2016-05-24 2016-05-24
US62/341,019 2016-05-24
US201662363775P 2016-07-18 2016-07-18
US62/363,775 2016-07-18
US201662385217P 2016-09-08 2016-09-08
US62/385,217 2016-09-08
US201662417219P 2016-11-03 2016-11-03
US62/417,219 2016-11-03
PCT/US2017/016509 WO2017136727A2 (en) 2016-02-05 2017-02-03 Compounds, compositions and methods
JP2018541178A JP6974331B2 (ja) 2016-02-05 2017-02-03 化合物、組成物及び方法

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2018541178A Division JP6974331B2 (ja) 2016-02-05 2017-02-03 化合物、組成物及び方法

Publications (3)

Publication Number Publication Date
JP2022017447A JP2022017447A (ja) 2022-01-25
JP2022017447A5 true JP2022017447A5 (cg-RX-API-DMAC7.html) 2022-04-18
JP7381543B2 JP7381543B2 (ja) 2023-11-15

Family

ID=58054535

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2018541178A Active JP6974331B2 (ja) 2016-02-05 2017-02-03 化合物、組成物及び方法
JP2021179107A Active JP7381543B2 (ja) 2016-02-05 2021-11-02 化合物、組成物及び方法

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2018541178A Active JP6974331B2 (ja) 2016-02-05 2017-02-03 化合物、組成物及び方法

Country Status (23)

Country Link
US (7) US9815850B2 (cg-RX-API-DMAC7.html)
EP (1) EP3414239A2 (cg-RX-API-DMAC7.html)
JP (2) JP6974331B2 (cg-RX-API-DMAC7.html)
KR (1) KR102808827B1 (cg-RX-API-DMAC7.html)
CN (4) CN118994190A (cg-RX-API-DMAC7.html)
AU (1) AU2017213628B2 (cg-RX-API-DMAC7.html)
CA (1) CA3012832A1 (cg-RX-API-DMAC7.html)
CL (1) CL2018002081A1 (cg-RX-API-DMAC7.html)
CO (1) CO2018008707A2 (cg-RX-API-DMAC7.html)
CR (1) CR20180413A (cg-RX-API-DMAC7.html)
DO (1) DOP2018000175A (cg-RX-API-DMAC7.html)
EA (1) EA201891620A1 (cg-RX-API-DMAC7.html)
EC (1) ECSP18066138A (cg-RX-API-DMAC7.html)
IL (2) IL287136B2 (cg-RX-API-DMAC7.html)
MA (1) MA44007A (cg-RX-API-DMAC7.html)
MX (3) MX2018009448A (cg-RX-API-DMAC7.html)
MY (1) MY196648A (cg-RX-API-DMAC7.html)
PH (1) PH12018501583A1 (cg-RX-API-DMAC7.html)
SA (1) SA518392146B1 (cg-RX-API-DMAC7.html)
SG (2) SG10201913587WA (cg-RX-API-DMAC7.html)
TN (1) TN2018000276A1 (cg-RX-API-DMAC7.html)
TW (2) TWI781920B (cg-RX-API-DMAC7.html)
WO (1) WO2017136727A2 (cg-RX-API-DMAC7.html)

Families Citing this family (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI638815B (zh) 2013-02-15 2018-10-21 英商葛蘭素史克智慧財產發展有限公司 作為激酶抑制劑之雜環醯胺類(一)
ES2930749T3 (es) 2015-07-02 2022-12-21 Hoffmann La Roche Lactamas bicíclicas como inhibidores de la proteína de interacción con el receptor 1 (RIP1) cinasa para tratar, por ejemplo, enfermedades inflamatorias
JP7112324B2 (ja) 2015-07-22 2022-08-03 エナンタ ファーマシューティカルズ インコーポレイテッド Rsv阻害剤としてのベンゾジアゼピン誘導体
US10961258B2 (en) 2015-12-21 2021-03-30 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as kinase inhibitors
CN108699077B (zh) 2016-01-15 2021-03-02 英安塔制药有限公司 作为rsv抑制剂的杂环化合物
MA44007A (fr) * 2016-02-05 2018-12-19 Denali Therapeutics Inc Inhibiteurs du récepteur interagissant avec protéine kinase 1
TWI759301B (zh) 2016-05-24 2022-04-01 美商安美基公司 聚乙二醇化卡非佐米化合物
US20170362206A1 (en) 2016-06-16 2017-12-21 Denali Therapeutics Inc. Compounds, compositions, and methods
JP7349359B2 (ja) 2016-10-17 2023-09-22 エフ. ホフマン-ラ ロシュ アーゲー 二環式ピリドンラクタム及びその使用方法。
JP6890179B2 (ja) * 2016-12-02 2021-06-18 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft 二環式アミド化合物及びその使用方法
US11072607B2 (en) * 2016-12-16 2021-07-27 Genentech, Inc. Inhibitors of RIP1 kinase and methods of use thereof
WO2018152413A1 (en) 2017-02-16 2018-08-23 Enanta Pharmaceuticals, Inc. Processes for the preparation of benzodiazepine derivatives
CA3052767A1 (en) 2017-02-27 2018-08-30 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as kinase inhibitors
WO2018226801A1 (en) 2017-06-07 2018-12-13 Enanta Pharmaceuticals, Inc. Aryldiazepine derivatives as rsv inhibitors
US11091501B2 (en) 2017-06-30 2021-08-17 Enanta Pharmaceuticals, Inc. Heterocyclic compounds as RSV inhibitors
US10851115B2 (en) 2017-06-30 2020-12-01 Enanta Pharmaceuticals, Inc. Heterocyclic compounds as RSV inhibitors
AU2018300043B2 (en) 2017-07-14 2021-04-01 F. Hoffmann-La Roche Ag Bicyclic ketone compounds and methods of use thereof
CN107759574B (zh) * 2017-08-29 2020-07-03 南京药石科技股份有限公司 一种5-氟-1h-吡唑-3-甲酸酯中间体及其合成方法
KR102645995B1 (ko) 2017-09-29 2024-03-11 이난타 파마슈티칼스, 인코포레이티드 Rsv 억제제로서의 병용 약학 제제
JP7362600B2 (ja) 2017-10-11 2023-10-17 エフ. ホフマン-ラ ロシュ アーゲー Rip1キナーゼ阻害剤として使用するための二環式化合物
MA50503A (fr) * 2017-10-31 2020-09-09 Hoffmann La Roche Sulfones et sulfoxydes bicycliques et procédés d'utilisation associés
US10647711B2 (en) 2017-11-13 2020-05-12 Enanta Pharmaceuticals, Inc. Azepin-2-one derivatives as RSV inhibitors
MX394621B (es) 2017-11-13 2025-03-24 Enanta Pharm Inc Procesos para la resolucion de los derivados de la benzodiazepina-2-ona y de la benzoazepin-2-ona
CN108129288B (zh) * 2017-12-27 2021-01-22 上海毕得医药科技股份有限公司 一种反式-3-羟基环丁基甲酸的合成方法
US10975094B2 (en) 2018-04-11 2021-04-13 Enanta Pharmaceuticals, Inc. Heterocyclic compounds as RSV inhibitors
EP3781571B1 (en) 2018-04-20 2024-01-17 F. Hoffmann-La Roche AG N-[4-oxo-2,3-dihydro-pyrido[3,2-b][1,4]oxazepin-3-yl]-5,6-dihydro-4h-pyrrolo[1,2-b]pyrazole-2-carboxamide derivatives and related compounds as rip1 kinase inhibitors for treating e.g. irritable bowel syndrome (ibs)
CN112384510B (zh) * 2018-05-03 2025-06-13 里格尔药品股份有限公司 Rip1抑制性化合物以及制备和使用其的方法
CN120535512A (zh) * 2018-05-03 2025-08-26 里格尔药品股份有限公司 Rip1抑制性化合物以及制备和使用其的方法
CA3104757A1 (en) * 2018-06-26 2020-01-02 Shanghai Institute Of Organic Chemistry, Chinese Academy Of Sciences Cell necrosis inhibitor, preparation method therefor and use thereof
WO2020044206A1 (en) 2018-08-29 2020-03-05 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as kinase inhibitors for use in the treatment cancer
KR102812440B1 (ko) * 2018-09-10 2025-05-26 가껭세이야꾸가부시기가이샤 신규한 헤테로방향족 아미드 유도체 및 이를 함유하는 약제
CN111138448B (zh) 2018-11-02 2022-08-02 中国科学院上海药物研究所 抑制rip1激酶的杂环酰胺及其用途
WO2020088194A1 (zh) 2018-11-02 2020-05-07 中国科学院上海药物研究所 抑制rip1激酶的杂环酰胺及其用途
EP3670667A1 (en) * 2018-12-19 2020-06-24 Paris Sciences et Lettres - Quartier Latin Identification of cognate pairs of ligands and receptors
TW202043229A (zh) 2019-01-11 2020-12-01 瑞士商赫孚孟拉羅股份公司 雙環酮化合物及其使用方法
SG11202108064XA (en) * 2019-01-25 2021-08-30 Beijing Scitech Mq Pharmaceuticals Ltd Acylamino bridged heterocyclic compound, and composition and application thereof
BR112021018335A2 (pt) 2019-03-18 2021-11-23 Enanta Pharm Inc Derivados de benzodiazepina como inibidores de rsv
US11179400B2 (en) 2019-04-09 2021-11-23 Enanta Pharmaceuticals, Inc. Heterocyclic compounds as RSV inhibitors
AU2020285269B2 (en) * 2019-05-31 2022-11-17 Medshine Discovery Inc. Bicyclic compound as RIP-1 kinase inhibitor and application thereof
CN110172068A (zh) * 2019-06-05 2019-08-27 河南龙湖生物技术有限公司 具有抗肿瘤活性的苯并噻唑类化合物及其制备方法和应用
US12365695B2 (en) * 2019-08-09 2025-07-22 Bisichem Co., Ltd. Fused ring heteroaryl compounds as RIPK1 inhibitors
WO2021046515A1 (en) 2019-09-06 2021-03-11 Board Of Regents, The University Of Texas System Inhibitors of receptor interacting protein kinase i for the treatment of disease
CN115279763B (zh) * 2019-09-06 2025-01-28 里格尔药品股份有限公司 Rip1抑制化合物以及制备和使用所述化合物的方法
JP7493586B2 (ja) 2019-09-06 2024-05-31 ライジェル ファーマシューティカルズ, インコーポレイテッド Rip1阻害化合物ならびにそれを作製および使用するための方法
US12448375B2 (en) 2019-09-11 2025-10-21 Ohio State Innovation Foundation Kinase inhibitors for the treatment of neurodegenerative diseases
IL291665B2 (en) 2019-09-27 2025-07-01 Univ Texas Inhibitors of receptor interacting protein kinase i for the treatment of disease
US11505558B1 (en) 2019-10-04 2022-11-22 Enanta Pharmaceuticals, Inc. Antiviral heterocyclic compounds
MX2022003984A (es) 2019-10-04 2022-07-27 Enanta Pharm Inc Compuestos heterociclicos antivirales.
CA3156594A1 (en) 2019-11-07 2021-05-14 Yan Chen Heterocyclic rip1 inhibitory compounds
EP4065565A4 (en) * 2019-11-26 2023-12-06 Board of Regents, The University of Texas System Inhibitors of receptor interacting protein kinase i for the treatment of disease
UY39032A (es) 2020-01-24 2021-07-30 Enanta Pharm Inc Compuestos heterocíclicos como agentes antivirales
IL295975A (en) * 2020-02-28 2022-10-01 Univ Texas Inhibitors of receptor interacting protein kinase i for the treatment of disease
AR121717A1 (es) * 2020-04-02 2022-06-29 Rigel Pharmaceuticals Inc Inhibidores de rip1k
CA3173330A1 (en) * 2020-04-17 2021-10-21 Genzyme Corporation Eclitasertib for use in treating conditions involving systemichyperinflammatory response
TW202214617A (zh) 2020-06-02 2022-04-16 法商賽諾菲公司 作為ripk1抑制劑之異㗁唑啶及其用途
TWI824259B (zh) * 2020-07-01 2023-12-01 美商雷傑製藥公司 Rip1k抑制劑
US11534439B2 (en) 2020-07-07 2022-12-27 Enanta Pharmaceuticals, Inc. Dihydroquinoxaline and dihydropyridopyrazine derivatives as RSV inhibitors
WO2022086840A1 (en) 2020-10-19 2022-04-28 Enanta Pharmaceuticals, Inc. Heterocyclic compounds as anti-viral agents
CA3202764A1 (en) 2020-11-23 2022-05-27 Enanta Pharmaceuticals, Inc. Novel spiropyrrolidine derived antiviral agents
CN114716427B (zh) * 2021-01-07 2024-04-26 成都贝诺科成生物科技有限公司 一种作为rip抑制剂的化合物及其制备方法和用途
WO2022171110A1 (en) * 2021-02-10 2022-08-18 Zai Lab (Us) Llc Fused tricyclic compounds as rip1-kinase inhibitors and uses thereof
WO2022171111A1 (en) * 2021-02-10 2022-08-18 Zai Lab (Us) Llc Heteroaryl-fused bicyclic compound as rip1-kinase inhibitors and uses thereof
WO2022182861A1 (en) 2021-02-26 2022-09-01 Enanta Pharmaceuticals, Inc. Antiviral heterocyclic compounds
AR125587A1 (es) 2021-03-11 2023-08-02 Rigel Pharmaceuticals Inc Inhibidores heterocíclicos de la quinasa de rip1
JP7651929B2 (ja) 2021-04-19 2025-03-27 住友ゴム工業株式会社 ゴム組成物及びタイヤ
US11970502B2 (en) 2021-05-04 2024-04-30 Enanta Pharmaceuticals, Inc. Macrocyclic antiviral agents
CN114989156B (zh) * 2021-05-19 2024-07-05 成都贝诺科成生物科技有限公司 一种受体相互作用蛋白抑制剂及其制备方法和用途
CN117460722A (zh) 2021-08-10 2024-01-26 艾伯维公司 烟酰胺ripk1抑制剂
WO2023043284A1 (en) * 2021-09-17 2023-03-23 Bisichem Co., Ltd. Fused heterocyclic rings as ripk1 inhibitors
AU2022388696A1 (en) 2021-11-11 2024-06-27 Genzyme Corporation Isoxazolidines as ripk1 inhibitors and use thereof
WO2023086350A1 (en) 2021-11-12 2023-05-19 Enanta Pharmaceuticals, Inc. Alkyne-containing antiviral agents
WO2023086352A1 (en) 2021-11-12 2023-05-19 Enanta Pharmaceuticals, Inc. Novel spiropyrrolidine derived antiviral agents
US11919910B2 (en) 2021-11-12 2024-03-05 Enanta Pharmaceuticals, Inc. Spiropyrrolidine derived antiviral agents
US11993600B2 (en) 2021-12-08 2024-05-28 Enanta Pharmaceuticals, Inc. Saturated spirocyclics as antiviral agents
KR20230100646A (ko) 2021-12-24 2023-07-05 제일약품주식회사 Ripk1 저해제로서의 신규한 화합물 및 이를 포함하는 약학적 조성물
EP4209213A1 (en) 2022-01-05 2023-07-12 Universität zu Köln Signalling-pathway inhibitor combinations for use in the treatment of cancer diseases
WO2023137007A1 (en) * 2022-01-11 2023-07-20 Enanta Pharmaceuticals, Inc. Processes for the preparation of 4,6,7-trifluoro-1h-indole-2-carboxylic acid
IL314082A (en) 2022-01-12 2024-09-01 Denali Therapeutics Inc Crystal forms of (S)-5-benzyl-N-(5-methyl-4-oxo-2,3,4,5-tetrahydropyrido[3,2-b][1,4]oxazapin-3-yl)- H4- 1,2,4-triazole-3-carboxamide
CN116640156B (zh) * 2022-02-22 2025-10-24 上海齐鲁制药研究中心有限公司 Ripk1抑制剂
EP4495119A4 (en) 2022-03-16 2025-06-25 Jiangsu Hengrui Pharmaceuticals Co., Ltd. FUSED HETEROCYCLIC COMPOUND, PREPARATION METHOD AND MEDICAL USE THEREOF
US12145942B2 (en) 2022-04-05 2024-11-19 Enanta Pharmaceuticals, Inc. Spiropyrrolidine derived antiviral agents
AR129003A1 (es) 2022-04-07 2024-07-03 Enanta Pharm Inc Compuestos heterocíclicos antivirales
WO2023211997A1 (en) 2022-04-27 2023-11-02 Enanta Pharmaceuticals, Inc. Antiviral compounds
WO2024170776A1 (en) 2023-02-17 2024-08-22 Universität Zu Köln Triple kinase inhibition for the treatment of type i interferon response associated disorders
WO2025037940A1 (en) * 2023-08-16 2025-02-20 Bisichem Co., Ltd. Pyrazole-1-carboxamides as rip1 kinase inhibitors
WO2025045253A1 (zh) * 2023-08-31 2025-03-06 杭州百诚医药科技股份有限公司 苯并氮杂䓬酮类衍生物及其用途
CN118084889B (zh) * 2024-01-16 2024-09-27 宁夏医科大学 吲哚3-芳基-5-甲酰胺类衍生物及用途
CN117849327A (zh) * 2024-03-06 2024-04-09 军科正源(北京)药物研究有限责任公司 用于检测苏金单抗抗药性抗体的方法
EP4652998A1 (en) 2024-05-21 2025-11-26 Technische Universität München Treatment of receptor-interacting protein kinase 1- mediated disease with eclitasertib

Family Cites Families (173)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6204261B1 (en) 1995-12-20 2001-03-20 Vertex Pharmaceuticals Incorporated Inhibitors of interleukin-1β Converting enzyme inhibitors
US4477464A (en) 1983-02-10 1984-10-16 Ciba-Geigy Corporation Hetero-benzazepine derivatives and their pharmaceutical use
EP0187037A3 (en) 1984-12-21 1988-03-23 Takeda Chemical Industries, Ltd. Piperidine derivatives, their production and use
JPH035933Y2 (cg-RX-API-DMAC7.html) 1987-08-04 1991-02-15
EP0322779A3 (en) 1987-12-29 1991-05-08 Yoshitomi Pharmaceutical Industries, Ltd. Benzolactam compounds and pharmaceutical uses thereof
JPH0256318A (ja) 1988-08-19 1990-02-26 Fujio Asai 丸棒材の繰出しケース
JPH0295996A (ja) 1988-10-03 1990-04-06 Honda Motor Co Ltd 鞍乗型車両
JPH0334977A (ja) 1989-06-29 1991-02-14 Yoshitomi Pharmaceut Ind Ltd イミダゾリルベンゾラクタム化合物
AU641769B2 (en) 1990-06-18 1993-09-30 Merck & Co., Inc. Inhibitors of HIV reverse transcriptase
EP0481614A1 (en) 1990-10-01 1992-04-22 Merck & Co. Inc. Substituted pyridopyrimidinones and related heterocycles as angiotensin II antagonists
US5206234A (en) 1990-10-22 1993-04-27 Merck & Co., Inc. Benzolactam analogs as antagonists of cck
US5206235A (en) 1991-03-20 1993-04-27 Merck & Co., Inc. Benzo-fused lactams that promote the release of growth hormone
US5457196A (en) 1991-09-27 1995-10-10 Merrell Dow Pharmaceuticals Inc. 2-substituted indane-2-carboxyalkyl derivatives useful as inhibitors of enkephalinase and ACE
DE69220744T2 (de) 1991-09-27 1997-11-13 Merrell Pharma Inc 2-Substituierte Indan-2-Mercaptoacetylamid-Verbindungen mit Enkephalinase und ACE-Hemmwirkung
JP3358069B2 (ja) 1991-12-24 2002-12-16 武田薬品工業株式会社 三環性複素環類、その製造法及び剤
US5484917A (en) 1993-06-16 1996-01-16 Pfizer Inc. Substituted tetrahydrobenzazepinones
AU4282993A (en) 1992-07-01 1994-01-31 Pfizer Inc. Benzothiazepine and benzoxazepine derivatives as cholecystokinin receptor antagonists
NZ254656A (en) 1992-08-24 1995-12-21 Merrell Dow Pharma Tricyclic benzazepine derivatives; preparation and pharmaceutical compositions
US5420271A (en) 1992-08-24 1995-05-30 Merrell Dow Pharmaceuticals, Inc. 2-substituted indane-2-mercaptoacetylamide tricyclic derivatives useful as inhibitors of enkephalinase
US5283241A (en) 1992-08-28 1994-02-01 Merck & Co., Inc. Benzo-fused lactams promote release of growth hormone
DE59309867D1 (de) 1992-09-03 1999-12-16 Boehringer Ingelheim Pharma Neue aminosäurederivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende pharmazeutische zusammensetzungen
US5583130A (en) 1992-09-25 1996-12-10 Merck & Co., Inc. Benzo-fused lactams promote release of growth hormone
US5317017A (en) 1992-09-30 1994-05-31 Merck & Co., Inc. N-biphenyl-3-amido substituted benzolactams stimulate growth hormone release
US5374721A (en) 1992-10-14 1994-12-20 Merck & Co., Inc. Benzo-fused lactams promote release of growth hormone
DE69332946T2 (de) 1992-10-16 2004-05-19 Suprex Corp. Automatisierte extrakion mittels eines superkritischen fluidum
GB2272439A (en) 1992-11-13 1994-05-18 Merck & Co Inc Benzo-fused lactams that inhibit the release of growth hormone
US5284841A (en) 1993-02-04 1994-02-08 Merck & Co., Inc. Benzo-fused lactams promote release of growth hormone
GB9307833D0 (en) 1993-04-15 1993-06-02 Glaxo Inc Modulators of cholecystokinin and gastrin
KR960702444A (ko) 1993-05-13 1996-04-27 고야 마사시 3-아미노아제핀 화합물 및 그 의약 용도(3-aminoazepine compound and pharmaceutical use thereof)
US5430144A (en) 1993-07-26 1995-07-04 Merck & Co., Inc. Benzo-fused lactams promote release of growth hormone
ES2081747B1 (es) 1993-09-07 1997-01-16 Esteve Labor Dr Amidas derivadas de tienopirroles, su preparacion y su aplicacion como medicamentos.
US5606054A (en) 1993-12-14 1997-02-25 Merck & Co., Inc. Heterocyclic-fused lactams promote release of growth hormone
JPH09511223A (ja) 1994-04-14 1997-11-11 グラクソ、ウェルカム、インコーポレーテッド Cckまたはガストリンを調節する5−ヘテロシクロ−1,5−ベンゾジアゼピン
WO1995030687A1 (de) 1994-05-07 1995-11-16 Boehringer Ingelheim Kg Neurokinin (tachykinin)-antagonisten
IL114955A (en) 1994-08-17 1999-12-22 Novo Nordisk As N-substituted naphthofused lactams and pharmaceutical compositions containing them
GB9420763D0 (en) 1994-10-14 1994-11-30 Glaxo Inc Acetamide derivatives
GB9420748D0 (en) 1994-10-14 1994-11-30 Glaxo Inc 1,5 benzodiazepine derivatives
GB9420747D0 (en) 1994-10-14 1994-11-30 Glaxo Inc 1,5 benzodiazepine derivatives
BR9510403A (pt) 1994-11-17 1997-12-23 Ciba Geigy Ag Monômeros reticuláveis e composição bem como polímeros reticulados
US5587375A (en) 1995-02-17 1996-12-24 Bristol-Myers Squibb Company Azepinone compounds useful in the inhibition of ACE and NEP
US5691331A (en) 1995-06-07 1997-11-25 Merck & Co., Inc. N-(2,4-Dioxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3yl) -3- amides
WO1996040656A1 (en) 1995-06-07 1996-12-19 Merck & Co., Inc. Novel n-(2,4-dioxo-2,3,4,5-tetrahydro-1h-1,5-benzodiazepin-3yl)-3-amides
US5726171A (en) 1995-06-07 1998-03-10 Merck & Co Inc N-(1-alkyl-5-phenyl-2,3,4,5-tetrahydro-1H-benzo B! 1,4!diazepin-3yl)-acetamides
US5700797A (en) 1995-06-07 1997-12-23 Merck & Co, Inc. N-(2,4-dioxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3-yl)-3-amides
EP0761680A3 (en) 1995-09-12 1999-05-06 Ono Pharmaceutical Co., Ltd. Tetrazole compounds having Interleukin-1beta converting enzyme inhibitory activity
HU222745B1 (hu) 1995-09-15 2003-09-29 Sanofi-Synthelabo Kinolin-2(1H)-on-származékok mint szerotonin antagonisták, elżállításuk és alkalmazásuk
US6136834A (en) 1995-12-27 2000-10-24 Ono Pharmaceutical Co., Ltd. Tetrazole compounds and pharmaceutical agents containing such derivative
US5747235A (en) 1996-01-26 1998-05-05 Eastman Kodak Company Silver halide light sensitive emulsion layer having enhanced photographic sensitivity
JPH09295996A (ja) 1996-03-06 1997-11-18 Takeda Chem Ind Ltd システインプロテアーゼ阻害化合物
NZ329847A (en) 1996-06-29 1999-01-28 Samjin Pharm Co Ltd Piperazine derivatives and process for the preparation thereof
DE19638020A1 (de) 1996-09-18 1998-03-19 Solvay Pharm Gmbh Die gastrointestinale Durchblutung fördernde Arzneimittel
CA2274250A1 (en) 1996-12-06 1998-06-11 Vertex Pharmaceuticals Incorporated Inhibitors of interleukin-1.beta. converting enzyme
JPH10251295A (ja) 1997-03-07 1998-09-22 Ono Pharmaceut Co Ltd テトラゾール誘導体
EP0994894A1 (en) 1997-08-11 2000-04-26 Cor Therapeutics, Inc. SELECTIVE FACTOR Xa INHIBITORS
US6211174B1 (en) 1997-10-31 2001-04-03 Merck & Co., Inc. Naphtho-fused lactams promote release of growth hormone
FR2781483A1 (fr) 1998-07-21 2000-01-28 Hoechst Marion Roussel Inc Derives de thioazepinone, procede de preparation et intermediaires de ce procede, application a titre de medicament et compositions pharmaceutiques les renfermant
DE19858253A1 (de) 1998-12-17 2000-06-21 Aventis Pharma Gmbh Verwendung von Inhibitoren des KQt1-Kanals zur Herstellung eines Medikaments zur Behandlung von Krankheiten, die durch Helminthen und Ektoparasiten hervorgerufen werden
JP2000256318A (ja) 1999-03-02 2000-09-19 Toa Eiyo Ltd 縮合複素環誘導体、その製造法およびそれを含有する医薬品
FR2803594B1 (fr) 2000-01-11 2002-07-19 Centre Nat Rech Scient Oligomeres de mimes contraints non peptidiques de dipeptides ou de tripeptides, et leurs utilisations
WO2001074784A1 (en) 2000-04-03 2001-10-11 Dupont Pharmaceuticals Company CYCLIC LACTAMS AS INHIBITORS OF A-β PROTEIN PRODUCTION
IL151576A0 (en) 2000-04-03 2003-04-10 Bristol Myers Squibb Pharma Co Cyclic lactams as inhibitors of a-beta protein production
WO2001079261A1 (en) 2000-04-14 2001-10-25 Corvas International, Inc. Tetrahydro-azepinone derivatives as thrombin inhibitors
ES2347133T3 (es) 2000-04-24 2010-10-26 Vertex Pharmaceuticals Incorporated Procedimiento e intermedios para preparar acetales de acido aspartico sustituidos.
GB0012671D0 (en) 2000-05-24 2000-07-19 Merck Sharp & Dohme Therapeutic agents
IL147629A0 (en) 2000-06-01 2002-08-14 Bristol Myers Squibb Pharma Co LACTAMS SUBSTITUTED BY CYCLIC SUCCINATES AS INHIBITORS OF Aβ PROTEIN PRODUCTION
AUPQ969800A0 (en) 2000-08-28 2000-09-21 Fujisawa Pharmaceutical Co., Ltd. Pyrazolopyridine compound and pharmaceutical use thereof
EP1351946A2 (en) 2000-09-01 2003-10-15 Icos Corporation Materials and methods to potentiate cancer treatment
GB0021831D0 (en) 2000-09-06 2000-10-18 Astrazeneca Ab Chemical compounds
JP4558314B2 (ja) 2001-07-20 2010-10-06 ベーリンガー インゲルハイム (カナダ) リミテッド ウイルスポリメラーゼインヒビター
EP2335700A1 (en) 2001-07-25 2011-06-22 Boehringer Ingelheim (Canada) Ltd. Hepatitis C virus polymerase inhibitors with a heterobicylic structure
US7294457B2 (en) 2001-08-07 2007-11-13 Boehringer Ingelheim (Canada) Ltd. Direct binding assay for identifying inhibitors of HCV polymerase
WO2003031376A1 (en) 2001-10-12 2003-04-17 Aventis Pharmaceuticals Inc. Solid phase synthesis of substituted 1,5-benzodiazepine-2-one and 1,5-benzothiazepine-2-one
US7057046B2 (en) * 2002-05-20 2006-06-06 Bristol-Myers Squibb Company Lactam glycogen phosphorylase inhibitors and method of use
CA2489560A1 (en) 2002-06-27 2004-01-08 Schering Aktiengesellschaft Substituted quinoline ccr5 receptor antagonists
US7098235B2 (en) 2002-11-14 2006-08-29 Bristol-Myers Squibb Co. Triglyceride and triglyceride-like prodrugs of glycogen phosphorylase inhibiting compounds
AU2003299612A1 (en) 2002-12-13 2004-07-09 Cytokinetics Compounds, compositions and methods
CA2518830A1 (en) 2003-03-14 2004-09-30 Merck & Co., Inc. Carboxamide spirohydantoin cgrp receptor antagonists
EP1633348B1 (en) 2003-05-02 2008-10-08 Elan Pharmaceuticals, Inc. 4- BROMO - 5 - (2- CHLORO - BENZOYLAMINO) - 1H - PYRAZOLE - 3 - CARBOXYLIC ACID AMIDE DERIVATIVES AND RELATED COMPOUNDS AS BRADYKININ B sb 1 /sb RECEPTOR ANTAGONISTS FOR THE TREATMENT OF INFLAMMATORY DISEASES
JP2005035933A (ja) 2003-07-15 2005-02-10 Takeda Chem Ind Ltd 含窒素縮合複素環化合物の製造方法
EP2384753B1 (en) 2003-08-29 2016-01-06 The Brigham and Women's Hospital, Inc. Hydantoin derivatives as inhibitors of cellular necrosis
KR20060130027A (ko) 2003-10-10 2006-12-18 버텍스 파마슈티칼스 인코포레이티드 세린 프로테아제, 특히 hcv ns3-ns4a 프로테아제의억제제
WO2005056577A2 (en) 2003-12-05 2005-06-23 The Regents Of The University Of California Peptide inhibitors of hiv
US20070010428A1 (en) 2004-09-03 2007-01-11 Mcmurray John S Inhibitors of signal transduction and activator of transcription 3
US7390798B2 (en) 2004-09-13 2008-06-24 Merck & Co., Inc. Carboxamide spirolactam CGRP receptor antagonists
ATE411323T1 (de) * 2004-10-13 2008-10-15 Merck & Co Inc Cgrp-rezeptorantagonisten
DE602005027870D1 (de) * 2004-10-14 2011-06-16 Merck Sharp & Dohme Cgrp-rezeptorantagonisten
WO2006059164A2 (en) 2004-12-02 2006-06-08 Prosidion Limited Pyrrolopyridine-2-carboxylic acid amides
US7875627B2 (en) 2004-12-07 2011-01-25 Abbott Laboratories Thienopyridyl compounds that inhibit vanilloid receptor subtype 1 (VR1) and uses thereof
US20060217362A1 (en) 2004-12-29 2006-09-28 Tung Jay S Novel compounds useful for bradykinin B1 receptor antagonism
WO2006079077A2 (en) 2005-01-20 2006-07-27 Acadia Pharmaceuticals Inc. Use of diltiazem or analogs thereof as modulators of ghrelin receptor
US20060281763A1 (en) 2005-03-25 2006-12-14 Axon Jonathan R Carboxamide inhibitors of TGFbeta
CA2603049A1 (en) 2005-04-01 2006-10-05 Warner-Lambert Company Llc Tetrahydro-pyridoazepin-8-ones and related compounds for the treatment of schizophrenia
WO2006113432A2 (en) 2005-04-14 2006-10-26 Smithkline Beecham Corporation Compounds, compositions and methods
JO2787B1 (en) 2005-04-27 2014-03-15 امجين إنك, Alternative amide derivatives and methods of use
JP4551962B2 (ja) 2005-09-23 2010-09-29 コーリー ファーマシューティカル グループ,インコーポレイテッド 1H−イミダゾ[4,5−c]ピリジンおよびその類似体のための方法
WO2007067416A2 (en) 2005-12-05 2007-06-14 Affinium Pharmaceuticals, Inc. Heterocyclylacrylamide compounds as fabi inhibitors and antibacterial agents
US8324262B2 (en) 2005-12-20 2012-12-04 The Brigham And Women's Hospital, Inc. Tricyclic necrostatin compounds
GB0605689D0 (en) 2006-03-21 2006-05-03 Novartis Ag Organic compounds
JP2009531445A (ja) 2006-03-29 2009-09-03 アレイ バイオファーマ、インコーポレイテッド p38インヒビターおよびその使用方法
JP2009543762A (ja) 2006-06-09 2009-12-10 メルク エンド カムパニー インコーポレーテッド ナトリウムチャネル遮断薬としてのベンゾアゼピノン
JP5468899B2 (ja) 2006-07-20 2014-04-09 アフィニウム ファーマシューティカルズ, インク. Fabiインヒビターとしてのアクリルアミド誘導体
ES2343481T3 (es) 2006-07-21 2010-08-02 Vertex Pharmaceuticals, Inc. Antagonistas del receptor cgrp.
JP5616063B2 (ja) 2006-10-04 2014-10-29 ヤンセン・アールアンドデイ・アイルランド Hcv阻害剤として有用なカルボキシアミド4−[(4−ピリジル)アミノ]ピリミジン
CA2675511A1 (en) * 2006-10-10 2008-04-17 Amgen Inc. N-aryl pyrazole compounds for use against diabetes
EP1939187A1 (en) * 2006-12-20 2008-07-02 Sanofi-Aventis Substituted heteroaryl pyridopyrimidone derivatives
WO2008080056A2 (en) 2006-12-21 2008-07-03 Sloan-Kettering Institute For Cancer Research Pyridazinones and furan-containing compounds
CA2677331A1 (en) 2007-02-28 2008-09-04 Merck & Co., Inc. Substituted benzodiazepinones, benzoxazepinones and benzothiazepinones as sodium channel blockers
WO2008135525A2 (en) 2007-05-02 2008-11-13 Boehringer Ingelheim International Gmbh Substituted azetidines, manufacturing and use thereof as medicaments
WO2008156580A1 (en) 2007-06-13 2008-12-24 Merck & Co., Inc. Triazole derivatives for treating alzheimer's disease and related conditions
JP2010535167A (ja) 2007-08-03 2010-11-18 サノフィ−アベンティス カスパーゼイメージングプローブ
WO2009085256A1 (en) 2007-12-27 2009-07-09 Panacos Pharmaceuticals, Inc. Anti-hiv compounds
EP2085399A1 (en) * 2008-01-29 2009-08-05 Sanofi-Aventis substituted arylamide oxazepinopyrimidone derivatives
EP2090578A1 (en) * 2008-01-29 2009-08-19 Sanofi-Aventis Substituted arylamide diazepinopyrimidone derivatives for the treatment of neurodegenerative diseases caused by abnormal activity of GSK3-beta
JP4708443B2 (ja) 2008-01-31 2011-06-22 トヨタ自動車株式会社 作動制御マップおよび白線認識装置
US8796260B2 (en) 2008-02-19 2014-08-05 Merck Sharp & Dohme Corp. Imidazobenzazepine CGRP receptor antagonists
EP2262783A2 (en) 2008-02-21 2010-12-22 Sanofi-Aventis Covalently binding imaging probes
EP2288383A1 (en) 2008-05-14 2011-03-02 Amgen, Inc Combinations vegf(r) inhibitors and hepatocyte growth factor (c-met) inhibitors for the treatment of cancer
US7884074B2 (en) 2008-05-15 2011-02-08 Ikaria Development Subsidiary Two, LLC Compounds and methods for prevention and/or treatment of inflammation using the same
KR20110048491A (ko) 2008-07-28 2011-05-11 에자이 알앤드디 매니지먼트 가부시키가이샤 스피로아미노디하이드로티아진 유도체들
UY32049A (es) 2008-08-14 2010-03-26 Takeda Pharmaceutical Inhibidores de cmet
DE102008037790A1 (de) 2008-08-14 2010-02-18 Merck Patent Gmbh Bicyclische Triazolderivate
US8088890B2 (en) 2008-09-26 2012-01-03 Fibrex Medical Research & Development Gmbh Peptides and peptidomimetic compounds, the manufacturing thereof as well as their use for preparing a therapeutically and/or preventively active pharmaceutical composition
US8293897B2 (en) 2008-10-14 2012-10-23 Ning Xi Compounds comprising a spiro-ring and methods of use
JP2012512248A (ja) 2008-12-17 2012-05-31 メルク・シャープ・エンド・ドーム・コーポレイション Cgrp受容体アンタゴニストとしてのイミダゾリノン誘導体
WO2010083725A1 (zh) 2009-01-20 2010-07-29 山东轩竹医药科技有限公司 含有取代的含氮稠杂环的头孢菌素衍生物
US8624063B2 (en) 2009-06-30 2014-01-07 Wisconsin Alumni Research Foundation Non-lactone carbocyclic and heterocyclic antagonists and agonists of bacterial quorum sensing
KR20120104180A (ko) 2009-09-16 2012-09-20 사일린 파마슈티칼스, 인크 신규한 트리시클릭 단백질 키나제 조절제
JP2013509442A (ja) 2009-10-29 2013-03-14 サートリス ファーマシューティカルズ, インコーポレイテッド サーチュイン調節因子としての二環式ピリジンおよび類似体
US8481541B2 (en) 2010-03-22 2013-07-09 Hoffmann-La Roche Inc. Pyrrolopyrazine kinase inhibitors
US20130137642A1 (en) 2010-04-23 2013-05-30 Demetrios Vavvas Methods and compositions for preserving photoreceptor and retinal pigment epithelial cells
WO2011142381A1 (ja) 2010-05-11 2011-11-17 Fujita Takashi ベンゾ若しくはピリドイミダゾール誘導体
WO2011149963A1 (en) 2010-05-24 2011-12-01 Vanderbilt University Substituted-6-methylnicotinamides as mglur5 positive allosteric modulators
US9029501B2 (en) 2010-11-02 2015-05-12 Rigel Pharmaceuticals, Inc. Method for making macrocycles
US9938269B2 (en) 2011-06-30 2018-04-10 Abbvie Inc. Inhibitor compounds of phosphodiesterase type 10A
TWI622583B (zh) 2011-07-01 2018-05-01 基利科學股份有限公司 作為離子通道調節劑之稠合雜環化合物
WO2013012918A1 (en) 2011-07-19 2013-01-24 Infinity Pharmaceuticals Inc. Heterocyclic compounds and uses thereof
WO2013013826A1 (en) 2011-07-27 2013-01-31 Friedrich-Alexander-Universität Erlangen-Nürnberg Necroptosis inhibitors for the treatment of inflammatory diseases of the gastrointestinal tract
JO3148B1 (ar) 2011-07-27 2017-09-20 Lilly Co Eli مركب مثبط لإشارات مسار notch
WO2013059791A2 (en) 2011-10-21 2013-04-25 Massachusetts Eye And Ear Infirmary Methods and compositions for promoting axon regeneration and nerve function
US9062075B2 (en) 2011-12-02 2015-06-23 Aurigene Discovery Technologies Limited Tetrahydropyridine derivatives as FabI inhibitors
SG11201402409UA (en) 2011-12-02 2014-10-30 Aurigene Discovery Tech Ltd Substituted pyridine derivatives as fabi inhibitors
JP2015518504A (ja) 2012-04-03 2015-07-02 スリーエム イノベイティブ プロパティズ カンパニー 光塩基発生剤を含む架橋性組成物
WO2013189241A1 (zh) 2012-06-20 2013-12-27 上海恒瑞医药有限公司 嘧啶二胺类衍生物、其制备方法及其在医药上的应用
TWI520962B (zh) 2012-06-29 2016-02-11 As the c-Met tyrosine kinase inhibitors novel fused pyridine derivatives
BR112015000649A2 (pt) 2012-07-13 2017-06-27 Hoffmann La Roche compostos, composição farmacêutica, uso de um composto, método para tratar ou melhorar câncer e invenção
US9394263B2 (en) 2012-08-09 2016-07-19 F. Hoffmann-La Roche Ag Substituted hetero-azepinones
CN103664904A (zh) 2012-09-07 2014-03-26 李振 一种γ-分泌酶抑制剂及其用途
WO2014072930A2 (en) 2012-11-09 2014-05-15 Aurigene Discovery Technologies Limited Fused pyridine derivatives as antibacterial agents
TWI638815B (zh) * 2013-02-15 2018-10-21 英商葛蘭素史克智慧財產發展有限公司 作為激酶抑制劑之雜環醯胺類(一)
WO2014144547A2 (en) 2013-03-15 2014-09-18 The Regents Of The University Of California Amide derivatives of lactam based n-acylethanolamine acid amidase (naaa) inhibitors
FR3003860B1 (fr) 2013-03-29 2015-11-27 Oreal Composes derives d'iridoides proteges ou non, composition les comprenant, utilisation comme colorant des fibres keratiniques et dispositifs
US20160051629A1 (en) 2013-04-15 2016-02-25 Yeda Research And Development Co. Ltd. Inhibition of rip kinases for treating lysosomal storage diseases
WO2015027137A1 (en) 2013-08-23 2015-02-26 University Of Tennessee Research Foundation Improved synthesis of capuramycin and its analogues
WO2015103583A1 (en) 2014-01-06 2015-07-09 President And Fellows Of Harvard College Monobactams and methods of their synthesis and use
WO2015104677A1 (en) 2014-01-10 2015-07-16 Piramal Enterprises Limited Heterocyclic compounds as ezh2 inhibitors
WO2015184257A2 (en) 2014-05-30 2015-12-03 Icahn School Of Medicine At Mount Sinai Small molecule transcription modulators of bromodomains
US9616047B2 (en) 2014-06-30 2017-04-11 Regents Of University Of Minnesota Inhibitors of beta-catenin in treatment of colorectal cancer
WO2016023918A1 (en) 2014-08-13 2016-02-18 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Prevention of tumour metastasis by inhibition of necroptosis
BR112017003546A2 (pt) 2014-08-21 2017-12-05 Glaxosmithkline Ip Dev Ltd amidas heterocíclicas como inibidores de rip1 quinase como medicamentos
CN107108512B (zh) 2014-10-10 2021-05-04 基因泰克公司 治疗性化合物及其用途
EP3017825A1 (en) 2014-11-06 2016-05-11 Ludwig-Maximilians-Universität München An inhibitor of the RIPK1-dependent necrosis pathway and a pharmaceutical composition comprising the same
EP3224237B1 (en) 2014-12-24 2024-09-11 National Institute Of Biological Sciences, Beijing Necrosis inhibitors
CN107108492B (zh) 2014-12-24 2021-03-19 北京生命科学研究所 细胞坏死抑制剂
WO2016113668A1 (en) 2015-01-13 2016-07-21 Novartis Ag Pyrrolidine derivatives as angiotensin ii type 2 antagonists
JP2018505199A (ja) 2015-02-13 2018-02-22 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited (S)−5−ベンジル−N−(5−メチル−4−オキソ−2,3,4,5テトラヒドロベンゾ[b][1,4]オキサゼピン−3−イル)−4H−1,2,4−トリアゾール−3−カルボキサミドの結晶形
TWI609687B (zh) 2015-04-14 2018-01-01 美國禮來大藥廠 平滑肌肉瘤之標靶性治療
ES2930749T3 (es) * 2015-07-02 2022-12-21 Hoffmann La Roche Lactamas bicíclicas como inhibidores de la proteína de interacción con el receptor 1 (RIP1) cinasa para tratar, por ejemplo, enfermedades inflamatorias
WO2017022962A1 (ko) 2015-07-07 2017-02-09 가톨릭대학교 산학협력단 Ripk 억제제를 유효성분으로 포함하는 면역질환의 예방 또는 치료용 조성물
CN108431004B (zh) 2015-10-23 2021-02-12 武田药品工业株式会社 杂环化合物
US10961258B2 (en) 2015-12-21 2021-03-30 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as kinase inhibitors
CN107043378A (zh) 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种吡咯并[3,2-d]嘧啶类化合物的制备方法及其中间体
CN107043377A (zh) 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种tlr7激动剂的三氟乙酸盐、晶型b及其制备方法、药物组合物和用途
MA44007A (fr) 2016-02-05 2018-12-19 Denali Therapeutics Inc Inhibiteurs du récepteur interagissant avec protéine kinase 1

Similar Documents

Publication Publication Date Title
JP2022017447A5 (cg-RX-API-DMAC7.html)
JP2024166311A (ja) 化合物、組成物、及び、方法
JP2022530985A (ja) 炎症性疾患または望ましくない免疫応答に関連する疾患の治療におけるイタコン酸誘導体およびその使用
JP2024086819A (ja) 化合物、組成物、及び、方法
JP2019508407A5 (cg-RX-API-DMAC7.html)
CN1675177A (zh) 莫达非尼多晶型
JP2020511461A5 (cg-RX-API-DMAC7.html)
JP5063600B2 (ja) ピリダジノ[4,5−b]インドール誘導体の新規な結晶形
JP6101789B2 (ja) Alx受容体アゴニストとしてのフッ素化架橋スピロ[2.4]ヘプタン誘導体
JP2024161449A (ja) ヤヌスキナーゼ阻害剤の結晶形
JP2024500101A (ja) 化合物の固体形態
JP2021073256A5 (cg-RX-API-DMAC7.html)
US20200113910A1 (en) Triazinetrione derivatives and their use as modulators of neurotrophin receptor and receptor tyrosine kinases
JP2013520488A (ja) ペルフェナジン−gabaのトリメシラート塩の結晶性形態物及びその製法方法
US6294540B1 (en) Carbocyclic nucleoside hemisulfate and its use in treating viral infections
JP6775009B2 (ja) 3−ビシクロ[3.2.0]ヘプ−3−エン−6オンエンの鏡像異性体の分離
JP6330038B2 (ja) Alx受容体アゴニストとしてのピペラジン置換架橋スピロ[2.4]ヘプタン誘導体
CN120731207A (zh) 6-烷氧基吡唑并嘧啶化合物及其药学用途
JPWO2021130492A5 (cg-RX-API-DMAC7.html)
AU2024226032A1 (en) Substituted pyrazolopyrimidine compounds and medical use thereof
JP6407268B2 (ja) Alx受容体アゴニストとしてのジフルオロエチル−オキサゾール置換架橋スピロ[2.4]ヘプタン誘導体
WO2013147216A1 (ja) (2-ヘテロアリールアミノ)コハク酸誘導体
JP2009520000A (ja) カンナビノイドcb1受容体モジュレーターとしての4,5−ジヒドロ−(1h)−ピラゾール誘導体
EP2899193B1 (en) Crystalline form of abacavir that is essentially free of solvent
JP7638880B2 (ja) P300/cbp hat阻害剤及びその使用方法