MA53722A - Modulateurs de la monoacylglycérol lipase - Google Patents
Modulateurs de la monoacylglycérol lipaseInfo
- Publication number
- MA53722A MA53722A MA053722A MA53722A MA53722A MA 53722 A MA53722 A MA 53722A MA 053722 A MA053722 A MA 053722A MA 53722 A MA53722 A MA 53722A MA 53722 A MA53722 A MA 53722A
- Authority
- MA
- Morocco
- Prior art keywords
- monoacylglycerol lipase
- modulators
- lipase modulators
- monoacylglycerol
- lipase
- Prior art date
Links
- 102000005398 Monoacylglycerol Lipase Human genes 0.000 title 1
- 108020002334 Monoacylglycerol lipase Proteins 0.000 title 1
Classifications
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/18—Bridged systems
-
- 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
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Epidemiology (AREA)
- Rheumatology (AREA)
- Ophthalmology & Optometry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862738684P | 2018-09-28 | 2018-09-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA53722A true MA53722A (fr) | 2022-03-30 |
Family
ID=68109429
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA053722A MA53722A (fr) | 2018-09-28 | 2019-09-27 | Modulateurs de la monoacylglycérol lipase |
Country Status (12)
| Country | Link |
|---|---|
| US (4) | US20200102311A1 (fr) |
| EP (1) | EP3856179A1 (fr) |
| JP (2) | JP7413368B2 (fr) |
| KR (1) | KR20210069079A (fr) |
| CN (1) | CN113164458B (fr) |
| AU (1) | AU2019349962A1 (fr) |
| BR (1) | BR112021005936A2 (fr) |
| CA (1) | CA3111309A1 (fr) |
| MA (1) | MA53722A (fr) |
| MX (1) | MX2021003661A (fr) |
| TW (1) | TW202035409A (fr) |
| WO (1) | WO2020065614A1 (fr) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113164459B (zh) | 2018-09-28 | 2024-09-03 | 詹森药业有限公司 | 单酰基甘油脂肪酶调节剂 |
| WO2020065614A1 (fr) | 2018-09-28 | 2020-04-02 | Janssen Pharmaceutica Nv | Modulateurs de la monoacylglycérol lipase |
| ES3037365T3 (en) | 2019-09-30 | 2025-10-01 | Janssen Pharmaceutica Nv | Radiolabelled mgl pet ligands |
| BR112022019077A2 (pt) * | 2020-03-26 | 2022-12-27 | Janssen Pharmaceutica Nv | Moduladores da monoacilglicerol lipase |
| CA3242372A1 (fr) | 2021-12-29 | 2023-07-06 | Psy Therapeutics, Inc. | Inhibition de la monoacylglycerol lipase (magl) |
| AU2022425324A1 (en) | 2021-12-30 | 2024-05-30 | Jiangsu Hansoh Pharmaceutical Group Co., Ltd. | Tricyclic derivative inhibitor, preparation method therefor, and application thereof |
Family Cites Families (71)
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|---|---|---|---|---|
| US4816463A (en) | 1986-04-01 | 1989-03-28 | Warner-Lambert Company | Substituted diimidazo [1,5-a: 4',5'-d]pyridines having antihypertensive activity |
| US4812462A (en) | 1986-04-01 | 1989-03-14 | Warner-Lambert Company | 4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylic acid analogs having antihypertensive activity |
| WO1992005784A1 (fr) | 1990-10-02 | 1992-04-16 | Warner-Lambert Company | Derives et analogues de 4,5,6,7-tetrahydro-1h-imidazo[4,5-c]pyridine utilises comme antagonistes des recepteurs de l'angiotensine ii |
| AU2003244632A1 (en) | 2002-07-25 | 2004-02-25 | Pharmacia Italia S.P.A. | Bicyclo-pyrazoles active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them |
| AU2003244649A1 (en) | 2002-07-25 | 2004-02-23 | Pharmacia Italia Spa | Bicyclo-pyrazoles active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them |
| GB0312609D0 (en) | 2003-06-02 | 2003-07-09 | Astrazeneca Ab | Novel compounds |
| FR2857363B1 (fr) | 2003-07-10 | 2007-09-07 | Aventis Pharma Sa | 4,5,6,7-tetrahydro-1h-pyrazolo[3,4-c] pyridines substituees compositions les contenant et utilisation |
| AR045037A1 (es) | 2003-07-10 | 2005-10-12 | Aventis Pharma Sa | Tetrahidro-1h-pirazolo [3,4-c] piridinas sustituidas, composiciones que las contienen y su utilizacion. |
| WO2006023750A2 (fr) | 2004-08-23 | 2006-03-02 | Merck & Co., Inc. | Derives de triazole accoles inhibiteurs de la dipeptidyl peptidase-iv utilises dans le traitement ou la prevention du diabete |
| EP1844003A4 (fr) | 2005-01-27 | 2010-09-22 | Astrazeneca Ab | Nouveaux composes biaromatiques, inhibiteurs du recepteur p2x7 |
| US7402596B2 (en) | 2005-03-24 | 2008-07-22 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
| WO2006110516A1 (fr) | 2005-04-11 | 2006-10-19 | Abbott Laboratories | Antagonistes de l'acylhydrazide p2x7 et leurs utilisations |
| US7943617B2 (en) | 2006-11-27 | 2011-05-17 | Bristol-Myers Squibb Company | Heterobicyclic compounds useful as kinase inhibitors |
| FR2915197B1 (fr) | 2007-04-18 | 2009-06-12 | Sanofi Aventis Sa | Derives de triazolopyridine-carboxamides, leur preparation et leur application therapeutique. |
| KR20100023040A (ko) | 2007-06-21 | 2010-03-03 | 쉐링 코포레이션 | 폴리사이클릭 구아닌 유도체 및 이의 용도 |
| BRPI0812594A2 (pt) | 2007-08-10 | 2015-06-23 | Lundbeck & Co As H | Composto ou sal ou hidrato do mesmo, composição farmacêutica, métodos para modulação da atividade de um receptor p2x7, para tratamento de uma condição responsiva á modulação do receptor p2x7 em um paciente, para inibição de morte de células gangliônicas retinais em um paciente, para determinação da presença ou ausência de receptor p2x7 em uma amostra, preparação farmacêutica acondicionada, e, uso de um composto ou sal ou hidrato do mesmo. |
| FR2921342B1 (fr) | 2007-09-20 | 2010-03-12 | Airbus France | Carenage aerodynamique arriere inferieur pour dispositif d'accrochage d'un moteur d'aeronef |
| EP2090576A1 (fr) | 2008-02-01 | 2009-08-19 | Merz Pharma GmbH & Co.KGaA | 6-halo-pyrazolo[1,5-a]pyridines, leur procédé de préparation et leur utilisation en tant que modulateurs des récepteurs metabotropiques du glutamate (mGluR) |
| CA2722035C (fr) | 2008-04-22 | 2016-10-11 | Janssen Pharmaceutica Nv | Antagonistes de p2x7 substitues par une quinoline ou isoquinoline |
| WO2010060854A1 (fr) | 2008-11-25 | 2010-06-03 | Nerviano Medical Sciences S.R.L. | Dérivés bicycliques de pyrazole et d'isoxazole en tant qu'agents antitumoraux et antineurodégénératifs |
| WO2010066629A2 (fr) | 2008-12-09 | 2010-06-17 | F. Hoffmann-La Roche Ag | Nouvelles azaindoles |
| JP5654001B2 (ja) | 2009-04-29 | 2015-01-14 | グラクソ グループ リミテッドGlaxo Group Limited | P2X7調節因子としての5,6,7,8−テトラヒドロ[1,2,4]トリアゾロ[4,3−a]ピラジン誘導体 |
| GB0907515D0 (en) | 2009-04-30 | 2009-06-10 | Glaxo Group Ltd | Compounds |
| 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 |
| WO2011050202A1 (fr) | 2009-10-23 | 2011-04-28 | Janssen Pharmaceutica Nv | Composés hétérocycliques condensés en tant que modulateurs de récepteur d'orexine |
| WO2011103715A1 (fr) | 2010-02-25 | 2011-09-01 | Merck Sharp & Dohme Corp. | Antagonistes de canal task |
| MX342161B (es) | 2010-04-02 | 2016-09-19 | Euroscreen Sa | Compuestos antagonistas selectivos de receptor nk-3 novedosos, composicion farmaceutica y metodos para utilizarse en trastornos transmitidos por receptores nk-3. |
| US20110252717A1 (en) | 2010-04-16 | 2011-10-20 | Graf Fernandez Rodrigo | Foldable structures for a construction |
| EP2619204A4 (fr) | 2010-09-21 | 2014-08-27 | Merck Sharp & Dohme | Triazolopyrazinones comme antagonistes des récepteurs p2x7 |
| KR20130140020A (ko) | 2010-10-22 | 2013-12-23 | 얀센 파마슈티카 엔.브이. | 모노아실글리세롤 리파아제 억제제로서의 아미노-피롤리딘-아제티딘 다이아미드 |
| KR20130142137A (ko) | 2010-10-22 | 2013-12-27 | 얀센 파마슈티카 엔.브이. | 모노아실글리세롤 리파아제 억제제로서의 피페리딘-4-일-아제티딘 다이아미드 |
| US9586962B2 (en) | 2011-04-20 | 2017-03-07 | Janssen Pharmaceutica Nv | Disubstituted octahydropyrrolo [3,4-C] pyrroles as orexin receptor modulators |
| ES2699226T3 (es) * | 2011-10-14 | 2019-02-08 | Bristol Myers Squibb Co | Compuestos de tetrahidroisoquinolina sustituidos como inhibidores del factor XIa |
| US9273947B2 (en) | 2012-02-07 | 2016-03-01 | Lg Innotek Co., Ltd. | Sensing magnet apparatus for motor |
| US9056874B2 (en) | 2012-05-04 | 2015-06-16 | Novartis Ag | Complement pathway modulators and uses thereof |
| SG11201408284VA (en) | 2012-05-22 | 2015-02-27 | Xenon Pharmaceuticals Inc | N-substituted benzamides and their use in the treatment of pain |
| US8859774B2 (en) | 2012-05-25 | 2014-10-14 | Corcept Therapeutics, Inc. | Heteroaryl-ketone fused azadecalin glucocorticoid receptor modulators |
| JO3459B1 (ar) | 2012-09-09 | 2020-07-05 | H Lundbeck As | تركيبات صيدلانية لعلاج مرض الزهايمر |
| AU2013331380B2 (en) | 2012-10-15 | 2018-03-22 | Epizyme, Inc. | Substituted benzene compounds |
| TWI606045B (zh) | 2012-10-16 | 2017-11-21 | 健生藥品公司 | RORγt之亞甲基聯結的喹啉基調節劑 |
| AU2013337824B2 (en) | 2012-11-01 | 2018-03-08 | Incyte Holdings Corporation | Tricyclic fused thiophene derivatives as JAK inhibitors |
| US9796729B2 (en) | 2012-11-23 | 2017-10-24 | Glaxosmithkline Llc | Compounds as diacylglycerol acyltransferase inhibitors |
| KR102212923B1 (ko) | 2012-12-21 | 2021-02-04 | 플렉시콘 인코퍼레이티드 | 키나제 조절을 위한 화합물 및 방법, 및 그에 대한 적응증 |
| US9233974B2 (en) | 2012-12-21 | 2016-01-12 | Gilead Sciences, Inc. | Antiviral compounds |
| KR20150100814A (ko) | 2012-12-21 | 2015-09-02 | 콴티셀 파마슈티컬스, 인크. | 히스톤 데메틸라제 억제제 |
| US9561228B2 (en) | 2013-02-08 | 2017-02-07 | Celgene Avilomics Research, Inc. | ERK inhibitors and uses thereof |
| NZ710640A (en) | 2013-03-06 | 2019-03-29 | Janssen Pharmaceutica Nv | Benzoimidazol-2-yl pyrimidine modulators of the histamine h4 receptor |
| NO335177B1 (no) | 2013-03-06 | 2014-10-13 | Cambi Technology As | Fremgangsmåte og anordning for termisk biologisk nedbryting og avvanning av biomasse |
| GEP201706780B (en) | 2013-03-14 | 2017-11-27 | Boehringer Ingelheim Int | Substituted 2-aza-bicyclo [2.2.1]heptane-3-carboxylic acid (benzyl-cyano-methyl)-amides inhibitors of cathepsin c |
| TWI644671B (zh) | 2013-03-14 | 2018-12-21 | 比利時商健生藥品公司 | P2x7調節劑 |
| JO3383B1 (ar) | 2013-03-14 | 2019-03-13 | Lilly Co Eli | مثبطات cdc7 |
| WO2014140076A1 (fr) | 2013-03-14 | 2014-09-18 | Glaxosmithkline Intellectual Property (No.2) Limited | Dérivés 2,3-disubstitués de 1-acyl-4-amino-1,2,3,4-tétrahydroquinoléine et leur utilisation comme inhibiteurs de bromodomaines |
| WO2014152537A1 (fr) | 2013-03-14 | 2014-09-25 | Janssen Pharmaceutica Nv | Modulateurs de p2x7 |
| TWI627174B (zh) | 2013-03-14 | 2018-06-21 | 比利時商健生藥品公司 | P2x7調控劑 |
| JP6294953B2 (ja) | 2013-03-14 | 2018-03-14 | ヤンセン ファーマシューティカ エヌ.ベー. | P2x7調節物質 |
| HUE039473T2 (hu) | 2013-03-14 | 2019-01-28 | Curadev Pharma Private Ltd | Kinurenin útvonal inhibitorok |
| US9242969B2 (en) | 2013-03-14 | 2016-01-26 | Novartis Ag | Biaryl amide compounds as kinase inhibitors |
| RU2667509C2 (ru) | 2013-03-14 | 2018-09-21 | Ньюлинк Джинетикс Корпорейшин | Трициклические соединения в качестве ингибиторов иммуносупрессии, опосредуемой метаболизированием триптофана |
| CA2907814C (fr) | 2013-03-29 | 2021-07-13 | Euroscreen Sa | Nouvelles n-acyl-(3-substitues)-(8-methyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazines utilisees en tant qu'antagonistes selectifs des recepteurs nk-3, composition pharmaceutique, methodes d'utilisation dans le traitement de troubles medies par les recepteurs nk-3 |
| JP2016531127A (ja) | 2013-08-22 | 2016-10-06 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | アルキニルアルコール及び使用方法 |
| WO2016040789A1 (fr) | 2014-09-11 | 2016-03-17 | Janssen Pharmaceutica Nv | 2-azabicycles substitués et leur utilisation comme modulateurs de récepteurs de l'orexine |
| EA201790600A1 (ru) | 2014-09-12 | 2017-07-31 | Янссен Фармацевтика Нв | Модулирующие p2x7 n-ацил-триазолопиразины |
| JP6592510B2 (ja) | 2014-09-12 | 2019-10-16 | ヤンセン ファーマシューティカ エヌ.ベー. | P2x7調節因子 |
| EP3279191B1 (fr) * | 2015-03-30 | 2020-09-02 | Takeda Pharmaceutical Company Limited | Composé hétérocyclique |
| US10385057B2 (en) | 2015-11-20 | 2019-08-20 | Lundbeck La Jolla Research Center, Inc. | Pyrazole compounds and methods of making and using same |
| MX2019008690A (es) * | 2017-01-23 | 2019-09-18 | Pfizer | Compuestos espiro heterociclicos como inhibidores de magl. |
| CN113164459B (zh) | 2018-09-28 | 2024-09-03 | 詹森药业有限公司 | 单酰基甘油脂肪酶调节剂 |
| WO2020065614A1 (fr) | 2018-09-28 | 2020-04-02 | Janssen Pharmaceutica Nv | Modulateurs de la monoacylglycérol lipase |
| WO2020211798A1 (fr) | 2019-04-16 | 2020-10-22 | 上海翰森生物医药科技有限公司 | Inhibiteur contenant un dérivé d'anneau bicyclique, et son procédé de préparation et ses utilisations |
| ES3037365T3 (en) | 2019-09-30 | 2025-10-01 | Janssen Pharmaceutica Nv | Radiolabelled mgl pet ligands |
| BR112022019077A2 (pt) | 2020-03-26 | 2022-12-27 | Janssen Pharmaceutica Nv | Moduladores da monoacilglicerol lipase |
-
2019
- 2019-09-27 WO PCT/IB2019/058241 patent/WO2020065614A1/fr not_active Ceased
- 2019-09-27 CA CA3111309A patent/CA3111309A1/fr active Pending
- 2019-09-27 JP JP2021517338A patent/JP7413368B2/ja active Active
- 2019-09-27 CN CN201980078966.8A patent/CN113164458B/zh active Active
- 2019-09-27 TW TW108135034A patent/TW202035409A/zh unknown
- 2019-09-27 MX MX2021003661A patent/MX2021003661A/es unknown
- 2019-09-27 AU AU2019349962A patent/AU2019349962A1/en not_active Abandoned
- 2019-09-27 KR KR1020217012861A patent/KR20210069079A/ko active Pending
- 2019-09-27 EP EP19780428.9A patent/EP3856179A1/fr active Pending
- 2019-09-27 US US16/586,263 patent/US20200102311A1/en not_active Abandoned
- 2019-09-27 BR BR112021005936-9A patent/BR112021005936A2/pt unknown
- 2019-09-27 MA MA053722A patent/MA53722A/fr unknown
-
2020
- 2020-12-23 US US17/132,406 patent/US11597728B2/en active Active
-
2023
- 2023-01-27 US US18/160,647 patent/US11993601B2/en active Active
- 2023-12-27 JP JP2023220520A patent/JP2024038151A/ja active Pending
-
2024
- 2024-05-24 US US18/673,909 patent/US20240327410A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CA3111309A1 (fr) | 2020-04-02 |
| EP3856179A1 (fr) | 2021-08-04 |
| AU2019349962A1 (en) | 2021-03-18 |
| CN113164458A (zh) | 2021-07-23 |
| US20240327410A1 (en) | 2024-10-03 |
| US20220315583A1 (en) | 2022-10-06 |
| CN113164458B (zh) | 2024-09-13 |
| JP7413368B2 (ja) | 2024-01-15 |
| TW202035409A (zh) | 2020-10-01 |
| JP2022502440A (ja) | 2022-01-11 |
| MX2021003661A (es) | 2021-08-19 |
| US20200102311A1 (en) | 2020-04-02 |
| US11597728B2 (en) | 2023-03-07 |
| BR112021005936A2 (pt) | 2021-06-29 |
| US11993601B2 (en) | 2024-05-28 |
| KR20210069079A (ko) | 2021-06-10 |
| US20230242531A1 (en) | 2023-08-03 |
| JP2024038151A (ja) | 2024-03-19 |
| WO2020065614A1 (fr) | 2020-04-02 |
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| MA53722A (fr) | Modulateurs de la monoacylglycérol lipase | |
| IL281492A (en) | Modulators of pnpla3 expression | |
| MA54386A (fr) | Modulateurs de trex1 | |
| IL283967A (en) | Modulators of hsd17b13 expression | |
| EP3675849A4 (fr) | Modulateurs de tétrahydrocannabinol | |
| EP3601569A4 (fr) | Modulateurs de l'expression de pcsk9 | |
| DK3749669T3 (da) | Ahr-modulatorer | |
| MA53924A (fr) | Modulateurs de l'expression d'apol1 | |
| HUE058145T2 (hu) | Deformálható érzékelõ | |
| MA54825A (fr) | Modulateurs de gpr35 | |
| EP3821026A4 (fr) | Enzymes variantes de phosphopentomutase modifiées | |
| EP3758704A4 (fr) | Modulateurs de l'expression d'irf4 | |
| EP4192957A4 (fr) | Modulateurs de trpml | |
| EP4025957C0 (fr) | Modulateur électro-optique | |
| EP4035739A4 (fr) | Hydrogel | |
| EP3777974C0 (fr) | Applicateur de lumière | |
| EP3958804A4 (fr) | Applicateur de lentille | |
| EP3779540A4 (fr) | Modulateur optique | |
| EP3954003A4 (fr) | Épissure de contact | |
| EP4022049A4 (fr) | Variants de lipase modifiés | |
| EP3994774C0 (fr) | Système optique | |
| EP3810137A4 (fr) | Formulations de nitroimidazole |