HRP20120174T1 - Derivat policikličnog cinamida - Google Patents
Derivat policikličnog cinamida Download PDFInfo
- Publication number
- HRP20120174T1 HRP20120174T1 HR20120174T HRP20120174T HRP20120174T1 HR P20120174 T1 HRP20120174 T1 HR P20120174T1 HR 20120174 T HR20120174 T HR 20120174T HR P20120174 T HRP20120174 T HR P20120174T HR P20120174 T1 HRP20120174 T1 HR P20120174T1
- Authority
- HR
- Croatia
- Prior art keywords
- group
- methyl
- phenyl
- methoxy
- vinyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Neurosurgery (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US78051706P | 2006-03-09 | 2006-03-09 | |
| JP2006063562 | 2006-03-09 | ||
| US86170206P | 2006-11-30 | 2006-11-30 | |
| JP2006322728 | 2006-11-30 | ||
| PCT/JP2007/054532 WO2007102580A1 (fr) | 2006-03-09 | 2007-03-08 | Dérivé polycyclique de cinnamide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20120174T1 true HRP20120174T1 (hr) | 2012-03-31 |
Family
ID=38474999
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HR20120174T HRP20120174T1 (hr) | 2006-03-09 | 2007-03-08 | Derivat policikličnog cinamida |
Country Status (15)
| Country | Link |
|---|---|
| EP (1) | EP1992618B1 (fr) |
| KR (1) | KR101464651B1 (fr) |
| AR (1) | AR059955A1 (fr) |
| AU (1) | AU2007223158B2 (fr) |
| CA (1) | CA2643796A1 (fr) |
| CY (1) | CY1112767T1 (fr) |
| EA (1) | EA016464B1 (fr) |
| GE (1) | GEP20115139B (fr) |
| HN (1) | HN2008001374A (fr) |
| HR (1) | HRP20120174T1 (fr) |
| IL (1) | IL193770A (fr) |
| MA (1) | MA30268B1 (fr) |
| MX (1) | MX2008011221A (fr) |
| PL (1) | PL1992618T3 (fr) |
| WO (1) | WO2007102580A1 (fr) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0511504A (pt) | 2004-05-26 | 2008-01-22 | Eisai R&D Man Co Ltd | composto ou um sal farmaceuticamente aceitável do mesmo, e, agente preventivo ou terapêutico para uma doença resultante de beta-amilóides |
| ATE458729T1 (de) | 2004-10-26 | 2010-03-15 | Eisai R&D Man Co Ltd | Amorphe form einer zimtsäureamidverbindung |
| MY144960A (en) | 2005-11-24 | 2011-11-30 | Eisai R&D Man Co Ltd | Morpholine type cinnamide compound |
| TWI370130B (en) | 2005-11-24 | 2012-08-11 | Eisai R&D Man Co Ltd | Two cyclic cinnamide compound |
| TWI378091B (en) | 2006-03-09 | 2012-12-01 | Eisai R&D Man Co Ltd | Multi-cyclic cinnamide derivatives |
| US7737141B2 (en) | 2006-07-28 | 2010-06-15 | Eisai R&D Management Co., Ltd. | Prodrug of cinnamide compound |
| JP2010518080A (ja) * | 2007-02-08 | 2010-05-27 | メルク・シャープ・エンド・ドーム・コーポレイション | 治療薬 |
| US20080207900A1 (en) | 2007-02-28 | 2008-08-28 | Teiji Kimura | Two cyclic oxomorphorin derivatives |
| AU2008250436B2 (en) | 2007-05-11 | 2013-03-28 | F. Hoffmann-La Roche Ag | Hetarylanilines as modulators for amyloid beta |
| EP2152695A2 (fr) * | 2007-06-01 | 2010-02-17 | Schering Corporation | Modulateurs de sécrétase gamma |
| ES2529648T3 (es) * | 2007-08-31 | 2015-02-24 | Eisai R&D Management Co., Ltd. | Compuesto policíclico |
| US7935815B2 (en) * | 2007-08-31 | 2011-05-03 | Eisai R&D Management Co., Ltd. | Imidazoyl pyridine compounds and salts thereof |
| EP2217604A1 (fr) | 2007-11-05 | 2010-08-18 | Schering Corporation | Modulateurs de gamma-secrétase |
| WO2009076337A1 (fr) * | 2007-12-11 | 2009-06-18 | Schering Corporation | Modulateurs de la gamma sécrétase |
| RU2527177C2 (ru) | 2007-12-20 | 2014-08-27 | Энвиво Фармасьютикалз, Инк. | Четырехзамещенные бензолы |
| CA2705411A1 (fr) | 2007-12-21 | 2009-07-02 | F. Hoffmann-La Roche Ag | Derives heteroaryles en tant qu'antagonistes du recepteur a orexine |
| KR101244517B1 (ko) | 2008-01-11 | 2013-03-18 | 에프. 호프만-라 로슈 아게 | 아밀로이드 베타에 대한 조절제 |
| AU2009216851B2 (en) | 2008-02-22 | 2013-11-07 | F. Hoffmann-La Roche Ag | Modulators for amyloid beta |
| JP2012501336A (ja) * | 2008-08-27 | 2012-01-19 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | シンナミド化合物の製造法 |
| WO2010040661A1 (fr) | 2008-10-09 | 2010-04-15 | F. Hoffmann-La Roche Ag | Modulateurs pour l'amyloïde bêta |
| CA2742317A1 (fr) * | 2008-11-06 | 2010-05-14 | Schering Corporation | Modulateurs de secretase gamma |
| JP2012508180A (ja) * | 2008-11-06 | 2012-04-05 | シェーリング コーポレイション | γ−セクレターゼ調節剤 |
| AU2009312856A1 (en) | 2008-11-10 | 2010-05-14 | F. Hoffmann-La Roche Ag | Heterocyclic gamma secretase modulators |
| CA2742472A1 (fr) | 2008-11-13 | 2010-05-20 | Schering Corporation | Modulateurs de gamma secretase |
| CA2747744A1 (fr) | 2008-12-22 | 2010-07-01 | Theodros Asberom | Modulateurs de gamma secretase |
| TW201030002A (en) | 2009-01-16 | 2010-08-16 | Bristol Myers Squibb Co | Bicyclic compounds for the reduction of beta-amyloid production |
| JP2012121809A (ja) * | 2009-02-26 | 2012-06-28 | Eisai R & D Management Co Ltd | 多環式化合物の製造法およびその中間体 |
| JP2012051805A (ja) | 2009-02-26 | 2012-03-15 | Eisai R & D Management Co Ltd | テトラヒドロトリアゾロピリジン誘導体の製造方法 |
| EP2401277A1 (fr) | 2009-02-26 | 2012-01-04 | Eisai R&D Management Co., Ltd. | Sel de dérivé de tétrahydrotriazolopyridine et ses cristaux |
| JP2012051807A (ja) * | 2009-02-26 | 2012-03-15 | Eisai R & D Management Co Ltd | アリールイミダゾール化合物 |
| TW201035101A (en) * | 2009-02-26 | 2010-10-01 | Eisai R&D Man Co Ltd | Nitrogen-containing fused heterocyclic compound |
| US20120142672A1 (en) | 2009-07-13 | 2012-06-07 | Tatsuki Koike | Heterocyclic compound and use thereof |
| US8871760B2 (en) * | 2009-09-21 | 2014-10-28 | Roche Palo Alto Llc | [1,2,4]triazolo[3,4-C][1,4]oxazines as P2X7 modulators |
| AU2011206635B2 (en) * | 2010-01-15 | 2015-01-22 | Cellzome Limited | Novel substituted triazole derivatives as gamma secretase modulators |
| US8486967B2 (en) | 2010-02-17 | 2013-07-16 | Hoffmann-La Roche Inc. | Heteroaryl substituted piperidines |
| US8513230B2 (en) | 2010-03-05 | 2013-08-20 | Karyopharm Therapeutics, Inc. | Nuclear transport modulators and uses thereof |
| EP2611805A1 (fr) | 2010-09-02 | 2013-07-10 | Takeda Pharmaceutical Company Limited | Triazoles fusionnés pour le traitement ou la prophylaxie du trouble cognitif léger |
| JP2014012641A (ja) * | 2010-10-29 | 2014-01-23 | Dainippon Sumitomo Pharma Co Ltd | 新規ピリジン誘導体 |
| CN103402359B (zh) * | 2011-01-17 | 2016-08-24 | 卡尔约药物治疗公司 | 含烯烃核运输调节剂及其用途 |
| EP2736887B1 (fr) | 2011-07-29 | 2017-10-18 | Karyopharm Therapeutics, Inc. | Modulateurs de transport nucléaire contenant de l'hydrazide et leurs utilisations |
| EP2736883B1 (fr) | 2011-07-29 | 2019-09-04 | Karyopharm Therapeutics, Inc. | Modulateurs de transport nucléaire et leurs utilisations |
| WO2013055793A1 (fr) | 2011-10-12 | 2013-04-18 | University Of Pittsburg-Of The Commonwealth System Of Higher Education | Petites molécules ciblant la localisation et/ou le niveau nucléaire des récepteurs de l'androgène dans le cancer de la prostate |
| IN2014DN09434A (fr) | 2012-05-09 | 2015-07-17 | Karyopharm Therapeutics Inc | |
| CN104583208B (zh) | 2012-05-16 | 2016-09-28 | 杨森制药公司 | 可用于治疗(尤其是)阿尔茨海默病的取代的3,4-二氢-2H-吡啶并[1,2-a]吡嗪-1,6-二酮衍生物 |
| EP2687528A1 (fr) * | 2012-07-17 | 2014-01-22 | Ares Trading S.A. | Dérivés de triazole fusionnés comme modulateurs de gamma-sécrétase |
| AU2013366668B2 (en) | 2012-12-20 | 2017-07-20 | Janssen Pharmaceutica Nv | Novel tricyclic 3,4-dihydro-2H-pyrido[1,2-alpha]pyrazine -1,6-dione derivatives as gamma secretase modulators |
| AU2014206834B2 (en) | 2013-01-17 | 2017-06-22 | Janssen Pharmaceutica Nv | Novel substituted pyrido-piperazinone derivatives as gamma secretase modulators |
| WO2014144772A1 (fr) | 2013-03-15 | 2014-09-18 | Karyopharm Therapeutics Inc. | Procédés de promotion de la cicatrisation d'une plaie à l'aide d'inhibiteurs de crm1 |
| CN110386919B (zh) | 2013-06-21 | 2023-07-14 | 卡尔约药物治疗公司 | 核转运调节剂及其用途 |
| US20160257657A1 (en) | 2013-09-20 | 2016-09-08 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Small molecule inhibitors of the nuclear translocation of androgen receptor for the treatment of castration-resistant prostate cancer |
| EP3046561B1 (fr) | 2013-09-20 | 2023-02-22 | University of Pittsburgh - Of the Commonwealth System of Higher Education | Composés destinés au traitement du cancer de la prostate |
| US10562897B2 (en) | 2014-01-16 | 2020-02-18 | Janssen Pharmaceutica Nv | Substituted 3,4-dihydro-2H-pyrido[1,2-a]pyrazine-1,6-diones as gamma secretase modulators |
| CN111484483B (zh) | 2014-08-15 | 2023-05-26 | 卡尔约药物治疗公司 | 赛灵克斯的多晶型物 |
| EP3397634A1 (fr) | 2015-12-31 | 2018-11-07 | Karyopharm Therapeutics, Inc. | Modulateurs de transport nucléaire et leurs utilisations |
| US10526295B2 (en) | 2015-12-31 | 2020-01-07 | Karyopharm Therapeutics Inc. | Nuclear transport modulators and uses thereof |
| PL3419979T3 (pl) * | 2016-02-23 | 2020-06-29 | Pfizer Inc. | Związki 6,7-dihydro-5h-pirazolo[5,1-b][1,3]oksazyno-2- karboksyamidowe |
| US10980806B2 (en) | 2016-03-24 | 2021-04-20 | University of Pittsburgh—of the Commonwealth System of Higher Education | Small molecule inhibitors of the nuclear translocation of androgen receptor for the treatment of castration-resistant prostate cancer |
| US11602530B2 (en) | 2016-11-28 | 2023-03-14 | Biogen Ma Inc. | CRM1 inhibitors for treating epilepsy |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE288898T1 (de) * | 2000-12-04 | 2005-02-15 | Hoffmann La Roche | Phenylethenyl- oder phenylethinylderivate als glutamatrezeptorantagonisten |
| JP2006518738A (ja) * | 2003-02-12 | 2006-08-17 | トランス テック ファーマ,インコーポレイテッド | 治療薬としての置換アゾール誘導体 |
| US20050187277A1 (en) * | 2004-02-12 | 2005-08-25 | Mjalli Adnan M. | Substituted azole derivatives, compositions, and methods of use |
| BRPI0511504A (pt) * | 2004-05-26 | 2008-01-22 | Eisai R&D Man Co Ltd | composto ou um sal farmaceuticamente aceitável do mesmo, e, agente preventivo ou terapêutico para uma doença resultante de beta-amilóides |
-
2007
- 2007-03-08 PL PL07738023T patent/PL1992618T3/pl unknown
- 2007-03-08 GE GEAP200710893A patent/GEP20115139B/en unknown
- 2007-03-08 EP EP07738023A patent/EP1992618B1/fr active Active
- 2007-03-08 AR ARP070100958A patent/AR059955A1/es not_active Application Discontinuation
- 2007-03-08 HR HR20120174T patent/HRP20120174T1/hr unknown
- 2007-03-08 KR KR1020087023309A patent/KR101464651B1/ko not_active Expired - Fee Related
- 2007-03-08 WO PCT/JP2007/054532 patent/WO2007102580A1/fr not_active Ceased
- 2007-03-08 EA EA200870336A patent/EA016464B1/ru not_active IP Right Cessation
- 2007-03-08 MX MX2008011221A patent/MX2008011221A/es active IP Right Grant
- 2007-03-08 CA CA002643796A patent/CA2643796A1/fr not_active Abandoned
- 2007-03-08 AU AU2007223158A patent/AU2007223158B2/en not_active Ceased
-
2008
- 2008-08-28 IL IL193770A patent/IL193770A/en not_active IP Right Cessation
- 2008-09-05 HN HN2008001374A patent/HN2008001374A/es unknown
- 2008-09-08 MA MA31220A patent/MA30268B1/fr unknown
-
2012
- 2012-02-16 CY CY20121100165T patent/CY1112767T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GEP20115139B (en) | 2011-01-10 |
| EA016464B1 (ru) | 2012-05-30 |
| HK1122027A1 (en) | 2009-05-08 |
| CA2643796A1 (fr) | 2007-09-13 |
| HK1128085A1 (en) | 2009-10-16 |
| EP1992618B1 (fr) | 2012-01-18 |
| IL193770A0 (en) | 2009-05-04 |
| PL1992618T3 (pl) | 2012-06-29 |
| CY1112767T1 (el) | 2016-02-10 |
| KR20080108481A (ko) | 2008-12-15 |
| IL193770A (en) | 2012-10-31 |
| KR101464651B1 (ko) | 2014-11-24 |
| WO2007102580A1 (fr) | 2007-09-13 |
| MX2008011221A (es) | 2008-09-11 |
| EP1992618A4 (fr) | 2010-11-10 |
| AU2007223158B2 (en) | 2012-04-12 |
| AR059955A1 (es) | 2008-05-14 |
| HN2008001374A (es) | 2011-03-15 |
| EA200870336A1 (ru) | 2009-02-27 |
| AU2007223158A1 (en) | 2007-09-13 |
| MA30268B1 (fr) | 2009-03-02 |
| EP1992618A1 (fr) | 2008-11-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2019203444B2 (en) | Bicyclic lactams and methods of use thereof | |
| AU2019240299B2 (en) | SHP2 phosphatase inhibitors and methods of use thereof | |
| JP6382867B2 (ja) | Trkaキナーゼ阻害剤としてのピロリジニル尿素およびピロリジニルチオ尿素化合物 | |
| AU2011240808B2 (en) | 5, 7-substituted-imidazo [1, 2-c] pyrimidines as inhibitors of JAK kinases | |
| JP2022533120A5 (fr) | ||
| CN114945571B (zh) | 环状化合物及其使用方法 | |
| ES2550201T3 (es) | Moduladores de la PDE10 | |
| JP6785384B2 (ja) | 新規なヘテロ環化合物、その製造方法およびこれを含む薬学的組成物 | |
| CA2694401A1 (fr) | Compose polycyclique | |
| JP2011516512A5 (ja) | 新規な置換スピロ[シクロアルキル−1,3'−インドール]−2'(1'H)−オン誘導体およびp38マイトジェン活性化タンパク質キナーゼ阻害剤としてのそれらの使用 | |
| JP2019504821A (ja) | ユビキチン特異的プロテアーゼ1阻害剤としてのプリノン | |
| BG107899A (bg) | Б...нзимидазолови и пиридилимидазолови производни ка'о лиганди на gaba р...-...п'ори | |
| HUE032770T2 (en) | Novel nk-3 receptor selective antagonist compounds, pharmaceutical composition and methods for use in nk-3 receptors mediated disorders | |
| RU2005117383A (ru) | Производные фенилаланина в качестве ингибиторов дипептидилпептидазы для лечения или профилактики диабета | |
| CA2521929A1 (fr) | Derives bicycliques, leur preparation, compositions pharmaceutiques les contenant et leur usage therapeutique | |
| IL295076B2 (en) | Piperidinone derivatives as MDM2 inhibitors for cancer treatment | |
| HRP20160649T1 (hr) | Novi derivati tienopirimidina, postupci za njihovo pripremanje i njihova terapeutska uporaba | |
| HRP20250272T1 (hr) | Derivati benzimidazola i njihova uporaba | |
| RU2020114670A (ru) | Бициклические соединения для применения в качестве ингибиторов rip1 киназы | |
| JP2024512740A (ja) | 例えばがんの処置のためのSHP2阻害剤としての(S)-1-(5-((ピリジン-3-イル)チオ)ピラジン-2-イル)-4’H,6’H-スピロ[ピペリジン-4,5’-ピロロ[1,2-b]ピラゾール]-4’-アミン誘導体及び同様の化合物 | |
| JP2025081381A5 (fr) | ||
| US12180226B2 (en) | Spirotricycle RIPK1 inhibitors and methods of uses thereof | |
| CA3243942A1 (fr) | Nouveaux composés bicycliques en tant qu'inhibiteurs de rad51 | |
| TH2101006978A (th) | สารยับยั้งการกินตัวเองของเซลล์ชนิดเฮเทอโรแอริลอะมิโนไพริดีนเอไมด์และวิธีการใช้สารนั้น | |
| NZ737297B2 (en) | Bicyclic lactams and methods of use thereof |