MA44721B1 - Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer - Google Patents
Inhibiteurs de mcl1 macrocycliques pour le traitement du cancerInfo
- Publication number
- MA44721B1 MA44721B1 MA44721A MA44721A MA44721B1 MA 44721 B1 MA44721 B1 MA 44721B1 MA 44721 A MA44721 A MA 44721A MA 44721 A MA44721 A MA 44721A MA 44721 B1 MA44721 B1 MA 44721B1
- Authority
- MA
- Morocco
- Prior art keywords
- macrocyclic
- cancer treatment
- acid
- mcl1 inhibitors
- pentaazaheptacyclo
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D497/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D497/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D515/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D515/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains four or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
L'invention concerne un composé qui est l'acide 17-chloro-5,13,14,22-tétraméthyl-28-oxa-2,9-dithia-5,6,12,13,22-pentaazaheptacyclo[27.7.1.14,7.011,15.016,21.020,24.030,35]octatriaconta-1(37),4(38),6,11,14,16,18,20,23,29,31,33,35-tridécaène-23-carboxylique (formule 1), des énantiomères et des sels pharmaceutiquement acceptables correspondants. L'invention concerne également des compositions pharmaceutiques de l'acide 17-chloro-5,13,14,22-tétraméthyl-28-oxa-2,9-dithia-5,6,12,13,22-pentaazaheptacyclo[27.7.1.14,7.011,15.016,21.020,24.030,35]octatriaconta-1(37),4(38),6,11,14,16,18,20,23,29,31,33,35-tridécaène-23-carboxylique, et des énantiomères et des sels pharmaceutiquement acceptables correspondants, et des méthodes de traitement du cancer avec ces composés et ces compositions.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201662326156P | 2016-04-22 | 2016-04-22 | |
PCT/EP2017/059511 WO2017182625A1 (fr) | 2016-04-22 | 2017-04-21 | Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer |
Publications (2)
Publication Number | Publication Date |
---|---|
MA44721A MA44721A (fr) | 2019-02-27 |
MA44721B1 true MA44721B1 (fr) | 2020-05-29 |
Family
ID=58664658
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA44721A MA44721B1 (fr) | 2016-04-22 | 2017-04-21 | Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer |
Country Status (37)
Country | Link |
---|---|
US (4) | US9840518B2 (fr) |
EP (1) | EP3445767B1 (fr) |
JP (1) | JP6894449B2 (fr) |
KR (1) | KR102388208B1 (fr) |
CN (1) | CN109071566B (fr) |
AR (1) | AR108301A1 (fr) |
AU (1) | AU2017252222B2 (fr) |
BR (1) | BR112018070677B1 (fr) |
CA (1) | CA3020378A1 (fr) |
CL (1) | CL2018002410A1 (fr) |
CO (1) | CO2018008759A2 (fr) |
CR (1) | CR20180499A (fr) |
CY (1) | CY1123186T1 (fr) |
DK (1) | DK3445767T3 (fr) |
DO (1) | DOP2018000222A (fr) |
EA (1) | EA036551B1 (fr) |
ES (1) | ES2791319T3 (fr) |
HR (1) | HRP20200673T1 (fr) |
HU (1) | HUE049591T2 (fr) |
IL (1) | IL262237B (fr) |
LT (1) | LT3445767T (fr) |
MA (1) | MA44721B1 (fr) |
ME (1) | ME03729B (fr) |
MX (1) | MX2018012711A (fr) |
NI (1) | NI201800093A (fr) |
PE (1) | PE20181803A1 (fr) |
PH (1) | PH12018502227A1 (fr) |
PL (1) | PL3445767T3 (fr) |
PT (1) | PT3445767T (fr) |
RS (1) | RS60257B1 (fr) |
SG (1) | SG11201805838UA (fr) |
SI (1) | SI3445767T1 (fr) |
SV (1) | SV2018005742A (fr) |
TN (1) | TN2018000319A1 (fr) |
TW (1) | TWI742074B (fr) |
WO (1) | WO2017182625A1 (fr) |
ZA (1) | ZA201807766B (fr) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
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CA3013650A1 (fr) | 2016-02-04 | 2017-08-10 | The Johns Hopkins University | Rapadocins, inhibiteurs du transporteur equilibrant 1 des nucleosides et leurs utilisations |
US11066416B2 (en) | 2016-02-04 | 2021-07-20 | The Johns Hopkins University | Rapafucin derivative compounds and methods of use thereof |
CN108697729B (zh) | 2016-02-04 | 2023-05-09 | 约翰霍普金斯大学 | 新型GLUT抑制剂rapaglutin及其用途 |
ES2791319T3 (es) | 2016-04-22 | 2020-11-03 | Astrazeneca Ab | Inhibidores de MCL1 macrocíclicos para tratar el cáncer |
JP7013389B2 (ja) | 2016-05-19 | 2022-01-31 | バイエル アクチェンゲゼルシャフト | 大環状インドール誘導体 |
TW201904976A (zh) * | 2017-03-31 | 2019-02-01 | 瑞典商阿斯特捷利康公司 | Mcl-1抑制劑及其使用方法 |
TWI781996B (zh) * | 2017-03-31 | 2022-11-01 | 瑞典商阿斯特捷利康公司 | 合成mcl-1抑制劑之方法 |
BR112020003163A2 (pt) * | 2017-08-15 | 2020-09-15 | AbbVie Deutschland GmbH & Co. KG | inibidores macrocíclicos de mcl-1 e métodos de uso |
UY37843A (es) | 2017-08-15 | 2019-03-29 | Abbvie Inc | Inhibidores de mcl-1 macrocíclicos y métodos de uso |
EP3710447A1 (fr) * | 2017-11-17 | 2020-09-23 | Bayer Aktiengesellschaft | Dérivés d'indole macrocycliques annelés aryle |
WO2019096909A1 (fr) * | 2017-11-17 | 2019-05-23 | The Broad Institute, Inc. | Dérivés d'indole macrocycliques substitués par du fluor utilisés en tant qu'inhibiteurs de mcl-1, destinés à être utilisés dans le traitement du cancer |
EP3710450A1 (fr) * | 2017-11-17 | 2020-09-23 | Bayer Aktiengesellschaft | Dérivés d'indole macrocycliques substitués par du chlore |
EP3710448A1 (fr) * | 2017-11-17 | 2020-09-23 | Bayer Aktiengesellschaft | Dérivés d'indole substitués par du chlore macrocyclique |
CN111757884B (zh) * | 2017-11-17 | 2023-12-19 | 拜耳股份公司 | 取代的大环吲哚衍生物 |
WO2019096911A1 (fr) | 2017-11-17 | 2019-05-23 | The Broad Institute, Inc. | Dérivés d'indole macrocycliques |
TW202014184A (zh) | 2018-04-30 | 2020-04-16 | 瑞典商阿斯特捷利康公司 | 用於治療癌症之組合 |
TW202014423A (zh) | 2018-09-30 | 2020-04-16 | 大陸商江蘇恆瑞醫藥股份有限公司 | 吲哚類大環衍生物、其製備方法及其在醫藥上的應用 |
TWI810397B (zh) | 2018-11-14 | 2023-08-01 | 瑞典商阿斯特捷利康公司 | 治療癌症之方法 |
CN111205309B (zh) * | 2018-11-21 | 2023-04-07 | 江苏恒瑞医药股份有限公司 | 吲哚类大环衍生物、其制备方法及其在医药上的应用 |
US11691989B2 (en) | 2018-11-22 | 2023-07-04 | Ascentage Pharma (Suzhou) Co., Ltd. | Macrocyclic indoles as Mcl-1 inhibitors |
CN112204036B (zh) * | 2019-01-23 | 2022-12-27 | 苏州亚盛药业有限公司 | 作为mcl-1抑制剂的大环稠合的吡唑 |
KR20210153051A (ko) * | 2019-03-08 | 2021-12-16 | 제노 매니지먼트, 인크. | 매크로사이클릭 화합물 |
WO2020221272A1 (fr) * | 2019-04-30 | 2020-11-05 | 江苏恒瑞医药股份有限公司 | Dérivé macrocyclique d'indole, son procédé de préparation et son utilisation en médecine |
US20230092679A1 (en) | 2019-05-20 | 2023-03-23 | Novartis Ag | Mcl-1 inhibitor antibody-drug conjugates and methods of use |
ES2975083T3 (es) * | 2019-06-21 | 2024-07-03 | Janssen Pharmaceutica Nv | Inhibidores macrocíclicos de MCL-1 |
CN114096546A (zh) | 2019-07-09 | 2022-02-25 | 詹森药业有限公司 | 用作mcl-1抑制剂的大环螺环衍生物 |
US20220372014A1 (en) * | 2019-10-01 | 2022-11-24 | The Johns Hopkins University | Neuroprotective compounds and methods of use thereof |
WO2021092053A1 (fr) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Composés macrocycliques inhibiteurs de mcl-1 destinés à être utilisées dans la gestion clinique d'états pathologiques provoqués ou induits par des cellules sénescentes ainsi que dans le traitement du cancer |
WO2021092061A1 (fr) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Polythérapie pour le traitement de maladies associées à la sénescence |
KR20220103985A (ko) | 2019-11-21 | 2022-07-25 | 얀센 파마슈티카 엔.브이. | Mcl-1 억제제로서의 거대환식 술포닐 유도체 |
US20230021562A1 (en) | 2019-11-21 | 2023-01-26 | Janssen Pharmaceutica Nv | Macrocylic indole derivatives mcl-1 inhibitors |
MX2022007474A (es) * | 2019-12-18 | 2022-08-04 | Zeno Man Inc | Compuestos macrociclicos. |
CN115151551B (zh) | 2020-02-21 | 2024-10-25 | 詹森药业有限公司 | 作为mcl-1抑制剂的大环吲哚衍生物 |
CN115335384B (zh) * | 2020-03-30 | 2024-10-22 | 江苏恒瑞医药股份有限公司 | 一种吲哚类大环衍生物的结晶形式及其制备方法 |
CA3178283A1 (fr) * | 2020-05-29 | 2021-12-02 | Frederik Jan Rita Rombouts | Derives macrocycliques de 7-pyrazol-5-yl-indole utilises en tant qu'inhibiteurs de mcl-1 |
CA3180903A1 (fr) | 2020-06-19 | 2021-12-23 | Frederik Jan Rita Rombouts | Derives de 7-(pyrazol-5-yl)-indole a liaison n en tant qu'inhibiteurs de mcl-1 |
AU2021294273A1 (en) | 2020-06-19 | 2023-02-23 | Janssen Pharmaceutica Nv | N-linked macrocyclic 4-(pyrazol-5-yl)-indole derivatives as inhibitors of MCL-1 |
JP2023532592A (ja) | 2020-07-08 | 2023-07-28 | ヤンセン ファーマシューティカ エヌ.ベー. | Mcl-1の阻害剤としての大環状エーテル含有インドール誘導体 |
WO2022032284A1 (fr) * | 2020-08-07 | 2022-02-10 | Zeno Management, Inc. | Composés macrocycliques |
WO2022115451A1 (fr) | 2020-11-24 | 2022-06-02 | Novartis Ag | Conjugués anticorps-médicament inhibiteurs de mcl-1 et procédés d'utilisation |
EP4008324A1 (fr) | 2020-12-07 | 2022-06-08 | Cellestia Biotech AG | Combinaisons comprenant un inhibiteur d'une protéine anti-apoptotique, telle que bcl-2, bcl-xl, bclw ou mcl-1, et un inhibiteur de voie de signalisation notch pour le traitement du cancer |
KR20230121807A (ko) | 2020-12-17 | 2023-08-21 | 얀센 파마슈티카 엔.브이. | Mcl-1의 억제제로서의 분지형 매크로사이클릭 4-(피라졸-5-일)-인돌유도체 |
KR20230145079A (ko) | 2021-02-12 | 2023-10-17 | 얀센 파마슈티카 엔브이 | 암의 치료를 위한 mcl-1 억제제로서의 마크로사이클릭1,3-브릿지된 6-클로로-7-피라졸-4-일-1h-인돌-2-카르복실레이트 및 6-클로로-7-피리미딘-5-일-1h-인돌-2-카르복실레이트 유도체 |
WO2022251247A1 (fr) * | 2021-05-28 | 2022-12-01 | Zeno Management, Inc. | Composés macrocycliques |
EP4351564A1 (fr) | 2021-06-11 | 2024-04-17 | Gilead Sciences, Inc. | Inhibiteurs de mcl-1 en combinaison avec des agents anticancéreux |
KR20240019330A (ko) | 2021-06-11 | 2024-02-14 | 길리애드 사이언시즈, 인코포레이티드 | Mcl-1 저해제와 항체 약물 접합체의 조합 |
CN115490708A (zh) * | 2021-06-18 | 2022-12-20 | 苏州亚盛药业有限公司 | 磺酰胺类大环衍生物及其制备方法和用途 |
WO2023057484A1 (fr) | 2021-10-06 | 2023-04-13 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Procédés de prédiction et d'amélioration de l'efficacité d'une thérapie par inhibiteur de mcl-1 |
WO2023225359A1 (fr) | 2022-05-20 | 2023-11-23 | Novartis Ag | Conjugués anticorps-médicament de composés anti-cancéreux et procédés d'utilisation |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008131000A2 (fr) * | 2007-04-16 | 2008-10-30 | Abbott Laboratories | Inhibiteurs mcl-1 indole 7-substitués |
PL2134685T3 (pl) | 2007-04-16 | 2016-02-29 | Abbvie Inc | Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1 |
AU2009330245C1 (en) * | 2008-12-22 | 2013-09-26 | Merck Sharp & Dohme Corp. | Novel antibacterial agents for the treatment of gram positive infections |
BR112012017756A2 (pt) * | 2009-12-23 | 2016-04-19 | Ironwood Pharmaceuticals Inc | moduladores crth2 |
PT2710018T (pt) * | 2011-05-19 | 2022-03-01 | Fundacion Del Sector Publico Estatal Centro Nac De Investigaciones Oncologicas Carlos Iii F S P Cnio | Compostos macrocíclicos como inibidores de proteína quinases |
US10093640B2 (en) | 2012-09-21 | 2018-10-09 | Vanderbilt University | Substituted benzofuran, benzothiophene and indole MCL-1 inhibitors |
US10005728B2 (en) | 2013-08-28 | 2018-06-26 | Vanderbilt University | Substituted indole Mcl-1 inhibitors |
PT3105236T (pt) * | 2014-02-12 | 2017-12-22 | Viiv Healthcare Uk (No 5) Ltd | Macrociclos de benzotiazole como inibidores da replicação do vírus da imunodeficiência humana |
CN106456602B (zh) | 2014-03-27 | 2020-11-24 | 范德比尔特大学 | 取代的吲哚mcl-1抑制剂 |
JP6605493B2 (ja) * | 2014-04-11 | 2019-11-13 | バイエル ファーマ アクチエンゲゼルシャフト | 新規大環状化合物 |
US9949965B2 (en) | 2014-10-17 | 2018-04-24 | Vanderbilt University | Tricyclic indole Mcl-1 inhibitors and uses thereof |
ES2791319T3 (es) | 2016-04-22 | 2020-11-03 | Astrazeneca Ab | Inhibidores de MCL1 macrocíclicos para tratar el cáncer |
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2017
- 2017-04-21 ES ES17720720T patent/ES2791319T3/es active Active
- 2017-04-21 AR ARP170101026A patent/AR108301A1/es unknown
- 2017-04-21 BR BR112018070677-9A patent/BR112018070677B1/pt active IP Right Grant
- 2017-04-21 WO PCT/EP2017/059511 patent/WO2017182625A1/fr active Application Filing
- 2017-04-21 PL PL17720720T patent/PL3445767T3/pl unknown
- 2017-04-21 ME MEP-2020-99A patent/ME03729B/fr unknown
- 2017-04-21 CA CA3020378A patent/CA3020378A1/fr active Pending
- 2017-04-21 PE PE2018001558A patent/PE20181803A1/es unknown
- 2017-04-21 EA EA201892300A patent/EA036551B1/ru not_active IP Right Cessation
- 2017-04-21 MA MA44721A patent/MA44721B1/fr unknown
- 2017-04-21 EP EP17720720.6A patent/EP3445767B1/fr active Active
- 2017-04-21 DK DK17720720.6T patent/DK3445767T3/da active
- 2017-04-21 CN CN201780022366.0A patent/CN109071566B/zh active Active
- 2017-04-21 TW TW106113380A patent/TWI742074B/zh active
- 2017-04-21 SI SI201730246T patent/SI3445767T1/sl unknown
- 2017-04-21 HU HUE17720720A patent/HUE049591T2/hu unknown
- 2017-04-21 CO CONC2018/0008759A patent/CO2018008759A2/es unknown
- 2017-04-21 LT LTEP17720720.6T patent/LT3445767T/lt unknown
- 2017-04-21 AU AU2017252222A patent/AU2017252222B2/en active Active
- 2017-04-21 PT PT177207206T patent/PT3445767T/pt unknown
- 2017-04-21 TN TNP/2018/000319A patent/TN2018000319A1/en unknown
- 2017-04-21 RS RS20200549A patent/RS60257B1/sr unknown
- 2017-04-21 KR KR1020187033540A patent/KR102388208B1/ko active IP Right Grant
- 2017-04-21 US US15/493,210 patent/US9840518B2/en active Active
- 2017-04-21 SG SG11201805838UA patent/SG11201805838UA/en unknown
- 2017-04-21 MX MX2018012711A patent/MX2018012711A/es unknown
- 2017-04-21 CR CR20180499A patent/CR20180499A/es unknown
- 2017-04-21 JP JP2018553226A patent/JP6894449B2/ja active Active
- 2017-10-23 US US15/790,660 patent/US10196404B2/en active Active
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2018
- 2018-08-23 CL CL2018002410A patent/CL2018002410A1/es unknown
- 2018-09-12 SV SV2018005742A patent/SV2018005742A/es unknown
- 2018-09-25 NI NI201800093A patent/NI201800093A/es unknown
- 2018-10-05 DO DO2018000222A patent/DOP2018000222A/es unknown
- 2018-10-09 IL IL262237A patent/IL262237B/en unknown
- 2018-10-18 PH PH12018502227A patent/PH12018502227A1/en unknown
- 2018-11-19 ZA ZA2018/07766A patent/ZA201807766B/en unknown
- 2018-12-18 US US16/223,538 patent/US10889594B2/en active Active
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2020
- 2020-04-28 HR HRP20200673TT patent/HRP20200673T1/hr unknown
- 2020-05-14 CY CY20201100443T patent/CY1123186T1/el unknown
- 2020-12-04 US US17/111,896 patent/US11472816B2/en active Active
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