MA45189A - Nouveaux dérivés hétérocycliques utiles en tant qu'inhibiteurs de shp2 - Google Patents
Nouveaux dérivés hétérocycliques utiles en tant qu'inhibiteurs de shp2Info
- Publication number
- MA45189A MA45189A MA045189A MA45189A MA45189A MA 45189 A MA45189 A MA 45189A MA 045189 A MA045189 A MA 045189A MA 45189 A MA45189 A MA 45189A MA 45189 A MA45189 A MA 45189A
- Authority
- MA
- Morocco
- Prior art keywords
- derivatives useful
- heterocyclic derivatives
- new heterocyclic
- shp2 inhibitors
- shp2
- Prior art date
Links
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
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/537—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines spiro-condensed or forming part of bridged ring 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/538—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- 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
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero 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
- 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
- C07D471/10—Spiro-condensed 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
- C07D471/12—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
- C07D471/20—Spiro-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
- C07D498/10—Spiro-condensed systems
-
- 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Ophthalmology & Optometry (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2016085122 | 2016-06-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA45189A true MA45189A (fr) | 2019-04-10 |
Family
ID=60578379
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA045189A MA45189A (fr) | 2016-06-07 | 2017-06-07 | Nouveaux dérivés hétérocycliques utiles en tant qu'inhibiteurs de shp2 |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US10858359B2 (fr) |
| EP (2) | EP3464272B1 (fr) |
| JP (3) | JP6751203B2 (fr) |
| KR (5) | KR20210019607A (fr) |
| CN (3) | CN109311848B (fr) |
| AU (1) | AU2017276457B2 (fr) |
| CA (1) | CA3026784A1 (fr) |
| CY (1) | CY1125042T1 (fr) |
| DK (1) | DK3464272T3 (fr) |
| EA (3) | EA202092441A1 (fr) |
| ES (1) | ES2908801T3 (fr) |
| HR (1) | HRP20220251T1 (fr) |
| HU (1) | HUE057838T2 (fr) |
| LT (1) | LT3464272T (fr) |
| MA (1) | MA45189A (fr) |
| MX (3) | MX388576B (fr) |
| PH (1) | PH12018550202A1 (fr) |
| PL (1) | PL3464272T3 (fr) |
| PT (1) | PT3464272T (fr) |
| RS (1) | RS62987B1 (fr) |
| SG (2) | SG11201810983PA (fr) |
| SI (1) | SI3464272T1 (fr) |
| WO (1) | WO2017211303A1 (fr) |
Families Citing this family (157)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11466017B2 (en) | 2011-03-10 | 2022-10-11 | Board Of Regents, The University Of Texas System | Heterocyclic inhibitors of PTPN11 |
| JO3517B1 (ar) | 2014-01-17 | 2020-07-05 | Novartis Ag | ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2 |
| CN109475531B (zh) | 2016-05-31 | 2021-08-17 | 得克萨斯州立大学董事会 | Ptpn11的杂环抑制剂 |
| KR20210019607A (ko) * | 2016-06-07 | 2021-02-22 | 자코바이오 파마슈티칼스 컴퍼니 리미티드 | Shp2 억제제로서 유용한 신규한 헤테로환형 유도체 |
| KR102457146B1 (ko) | 2016-06-14 | 2022-10-19 | 노파르티스 아게 | Shp2의 활성을 억제하기 위한 화합물 및 조성물 |
| IL311645B2 (en) | 2016-07-12 | 2025-11-01 | Revolution Medicines Inc | 2,5- disubstituted 3-methyl pyrazines and 2,5,6-trisubstituted 3-methyl pyrazines asallosteric shp2 inhibitors |
| WO2018057884A1 (fr) | 2016-09-22 | 2018-03-29 | Relay Therapeutics, Inc. | Inhibiteurs de phosphatase shp2 et leurs procédés d'utilisation |
| TWI848901B (zh) | 2016-10-24 | 2024-07-21 | 美商傳達治療有限公司 | Shp2磷酸酶抑制劑及其使用方法 |
| KR20190110588A (ko) | 2017-01-23 | 2019-09-30 | 레볼루션 메디슨즈, 인크. | 알로스테릭 shp2 억제제로서의 피리딘 화합물 |
| SG11201906209SA (en) | 2017-01-23 | 2019-08-27 | Revolution Medicines Inc | Bicyclic compounds as allosteric shp2 inhibitors |
| NZ758458A (en) * | 2017-03-23 | 2022-07-29 | Jacobio Pharmaceuticals Co Ltd | Novel heterocyclic derivatives useful as shp2 inhibitors |
| EP3630770B1 (fr) | 2017-05-26 | 2024-08-28 | Relay Therapeutics, Inc. | Dérivés de pyrazolo[3,4-b]pyrazine en tant qu'inhibiteurs de la phosphatase shp2 |
| BR112020004246A2 (pt) | 2017-09-07 | 2020-09-01 | Revolution Medicines, Inc. | composições inibidoras de shp2 e métodos para o tratamento de câncer |
| US10435389B2 (en) | 2017-09-11 | 2019-10-08 | Krouzon Pharmaccuticals, Inc. | Octahydrocyclopenta[c]pyrrole allosteric inhibitors of SHP2 |
| EP3687997A1 (fr) | 2017-09-29 | 2020-08-05 | Relay Therapeutics, Inc. | Dérivés de pyrazolo[3,4-b]pyrazine utilisés en tant qu'inhibiteurs de la phosphatase shp2 |
| CA3078565A1 (fr) | 2017-10-12 | 2019-04-18 | Revolution Medicines, Inc. | Pyridine, pyrazine et composes de triazine utilises en tant qu'inhibiteurs allosteriques de shp2 |
| KR20200099530A (ko) | 2017-12-15 | 2020-08-24 | 레볼루션 메디슨즈, 인크. | 알로스테릭 shp2 억제제로서의 다환식 화합물 |
| AU2019222026B2 (en) | 2018-02-13 | 2022-05-12 | Shanghai Blueray Biopharma Co., Ltd. | Pyrimidine-fused cyclic compound, preparation method therefor and application thereof |
| BR112020017283A2 (pt) | 2018-03-02 | 2020-12-15 | Otsuka Pharmaceutical Co., Ltd | Compostos farmacêuticos |
| JP7265275B2 (ja) | 2018-03-21 | 2023-04-26 | スージョウ プーヘー バイオファーマ カンパニー リミテッド | Shp2阻害剤およびその使用 |
| WO2019183364A1 (fr) | 2018-03-21 | 2019-09-26 | Relay Therapeutics, Inc. | Inhibiteurs de la phosphatase pyrazolo[3,4-b]pyrazine shp2 et leurs procédés d'utilisation |
| EP4506035A3 (fr) * | 2018-03-21 | 2025-04-16 | Relay Therapeutics, Inc. | Inhibiteurs de la phosphatase shp2 et leurs procédés d'utilisation |
| JP2021521155A (ja) | 2018-04-10 | 2021-08-26 | レヴォリューション・メディスンズ,インコーポレイテッド | Shp2阻害剤組成物、癌を処置するための方法、およびshp変異を有する対象を特定するための方法 |
| JP7297871B2 (ja) | 2018-05-02 | 2023-06-26 | ナビール ファーマ,インコーポレイティド | Ptpn11の置換されたヘテロ環式インヒビター |
| CN110143949A (zh) * | 2018-05-09 | 2019-08-20 | 北京加科思新药研发有限公司 | 可用作shp2抑制剂的新型杂环衍生物 |
| MX2021000795A (es) | 2018-07-24 | 2021-04-12 | Taiho Pharmaceutical Co Ltd | Compuestos heterociclicos para inhibir la actividad de shp2. |
| EP4356973A3 (fr) * | 2018-08-10 | 2024-06-26 | Navire Pharma, Inc. | Dérivés de 6-(4-amino-3-méthyl-2-oxa-8-azaspiro[4.5!décan-8-yl)-3-(2,3-dichlorophényl)-2-méthylpyrimidin-4(3h)-one et composés apparentés en tant qu'inhibiteurs de ptpn11 (shp2) |
| TWI827677B (zh) * | 2018-09-18 | 2024-01-01 | 美商尼坎醫療公司 | 作為src同源-2磷酸酶抑制劑之稠合三環衍生物 |
| US20210393623A1 (en) | 2018-09-26 | 2021-12-23 | Jacobio Pharmaceuticals Co., Ltd. | Novel Heterocyclic Derivatives Useful as SHP2 Inhibitors |
| CA3113379A1 (fr) * | 2018-09-29 | 2020-04-02 | Novartis Ag | Procede de fabrication d'un compose pour inhiber l'activite de shp2 |
| WO2020065452A1 (fr) * | 2018-09-29 | 2020-04-02 | Novartis Ag | Fabrication de composés et de compositions pour inhiber l'activité de shp2 |
| WO2020072656A1 (fr) | 2018-10-03 | 2020-04-09 | Gilead Sciences, Inc. | Dérivés d'imidozopyrimidine |
| CN113473990A (zh) | 2018-10-08 | 2021-10-01 | 锐新医药公司 | 用于治疗癌症的shp2抑制剂组合物 |
| TW202028183A (zh) * | 2018-10-10 | 2020-08-01 | 大陸商江蘇豪森藥業集團有限公司 | 含氮雜芳類衍生物調節劑、其製備方法和應用 |
| CN114341124B (zh) | 2018-10-17 | 2024-09-20 | Array生物制药公司 | 蛋白质酪氨酸磷酸酶抑制剂 |
| CN111138412B (zh) * | 2018-11-06 | 2023-09-15 | 上海奕拓医药科技有限责任公司 | 一种螺芳环化合物及其应用 |
| CN113272303B (zh) | 2018-11-30 | 2024-09-17 | 上海拓界生物医药科技有限公司 | 嘧啶并五元氮杂环类衍生物、其制备方法及其在医药上的应用 |
| MX2021002804A (es) | 2018-12-05 | 2021-07-15 | Mirati Therapeutics Inc | Terapias de combinacion. |
| US20230148450A9 (en) | 2019-03-01 | 2023-05-11 | Revolution Medicines, Inc. | Bicyclic heteroaryl compounds and uses thereof |
| WO2020180770A1 (fr) | 2019-03-01 | 2020-09-10 | Revolution Medicines, Inc. | Composés hétérocyclyle bicycliques et leurs utilisations |
| CN111647000B (zh) * | 2019-03-04 | 2021-10-12 | 勤浩医药(苏州)有限公司 | 吡嗪类衍生物及其在抑制shp2中的应用 |
| JP7734586B2 (ja) | 2019-03-07 | 2025-09-05 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | Shp2アンタゴニストとしてのカルボキサミド-ピリミジン誘導体 |
| PE20220141A1 (es) | 2019-04-02 | 2022-01-27 | Array Biopharma Inc | Inhibidores de la proteina tirosina fosfatasa |
| CA3127475A1 (fr) | 2019-04-08 | 2020-10-15 | Merck Patent Gmbh | Derives de pyrimidinone utilises en tant qu'antagonistes de shp2 |
| US11453681B2 (en) | 2019-05-23 | 2022-09-27 | Gilead Sciences, Inc. | Substituted eneoxindoles and uses thereof |
| CN114245807B (zh) | 2019-06-25 | 2025-05-02 | 吉利德科学公司 | Flt3l-fc融合蛋白和使用方法 |
| AU2020306124A1 (en) | 2019-06-28 | 2022-02-03 | Tuojie Biotech (Shanghai) Co., Ltd. | Pyrimidine five-membered nitrogen heterocyclic derivative, preparation method thereof and pharmaceutical use thereof |
| CN111704611B (zh) * | 2019-07-25 | 2022-01-14 | 上海凌达生物医药有限公司 | 一类芳基螺环类shp2抑制剂化合物、制备方法和用途 |
| EP3772513A1 (fr) * | 2019-08-09 | 2021-02-10 | C.N.C.C.S. S.c.a.r.l. Collezione Nazionale Dei Composti Chimici e Centro Screening | Inhibiteurs d'shp2 |
| GB201911928D0 (en) * | 2019-08-20 | 2019-10-02 | Otsuka Pharma Co Ltd | Pharmaceutical compounds |
| WO2021043077A1 (fr) * | 2019-09-06 | 2021-03-11 | 四川科伦博泰生物医药股份有限公司 | Composé de pyrazine substituée et procédé de préparation correspondant et son utilisation |
| EP4034539A1 (fr) | 2019-09-24 | 2022-08-03 | Relay Therapeutics, Inc. | Inhibiteurs de phosphatase shp2, procédés de production et d'utilisation associés |
| CN112724145A (zh) * | 2019-10-14 | 2021-04-30 | 杭州雷索药业有限公司 | 用于抑制shp2活性的吡嗪衍生物 |
| PH12022550835A1 (en) | 2019-10-18 | 2023-07-03 | Forty Seven Inc | Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia |
| MY209360A (en) | 2019-10-31 | 2025-07-03 | Forty Seven Llc | Anti-cd47 and anti-cd20 based treatment of blood cancer |
| CA3160142A1 (fr) | 2019-11-04 | 2021-05-14 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| US11739074B2 (en) | 2019-11-04 | 2023-08-29 | Revolution Medicines, Inc. | Ras inhibitors |
| CN120988055A (zh) | 2019-11-04 | 2025-11-21 | 锐新医药公司 | Ras抑制剂 |
| JP7812056B2 (ja) | 2019-11-08 | 2026-02-09 | レヴォリューション・メディスンズ,インコーポレイテッド | 二環式ヘテロアリール化合物及びその使用 |
| TWI778443B (zh) | 2019-11-12 | 2022-09-21 | 美商基利科學股份有限公司 | Mcl1抑制劑 |
| CN114980976A (zh) | 2019-11-27 | 2022-08-30 | 锐新医药公司 | 共价ras抑制剂及其用途 |
| CN117736207A (zh) | 2019-12-24 | 2024-03-22 | 卡尔那生物科学株式会社 | 二酰基甘油激酶调节化合物 |
| BR112022010086A2 (pt) | 2020-01-07 | 2022-09-06 | Revolution Medicines Inc | Dosagem do inibidor de shp2 e métodos de tratamento de câncer |
| CN113135910A (zh) * | 2020-01-19 | 2021-07-20 | 北京诺诚健华医药科技有限公司 | 嘧啶-4(3h)-酮类杂环化合物、其制备方法及其在医药学上的应用 |
| AU2021219668B2 (en) | 2020-02-14 | 2025-06-12 | Gilead Sciences, Inc. | Antibodies and fusion proteins that bind to CCR8 and uses thereof |
| CA3173358A1 (fr) | 2020-02-28 | 2021-09-02 | Novartis Ag | Combinaison pharmaceutique triple comprenant du dabrafenib, un inhibiteur d'erk et un inhibiteur de shp2 |
| WO2021218752A1 (fr) * | 2020-04-26 | 2021-11-04 | Betta Pharmaceuticals Co., Ltd | Inhibiteurs de shp2, compositions et utilisations de ceux-ci |
| CN115279749B (zh) * | 2020-04-30 | 2024-05-10 | 贝达药业股份有限公司 | Shp2抑制剂及其组合物和应用 |
| CA3181922A1 (fr) | 2020-05-01 | 2021-11-04 | Gilead Sciences, Inc. | Composes de 2,4-dioxopyrimidine inhibant cd73 |
| CN113754683A (zh) | 2020-06-05 | 2021-12-07 | 上海奕拓医药科技有限责任公司 | 同位素取代的螺芳环化合物及其应用 |
| TW202214253A (zh) | 2020-06-18 | 2022-04-16 | 美商銳新醫藥公司 | 延遲、預防及治療對ras抑制劑之後天抗性之方法 |
| WO2021259077A1 (fr) * | 2020-06-22 | 2021-12-30 | 四川科伦博泰生物医药股份有限公司 | Composé de pyrazine substitué, composition pharmaceutique le comprenant et utilisation associée |
| TW202216723A (zh) | 2020-07-08 | 2022-05-01 | 瑞士商諾華公司 | 用於抑制shp2活性的化合物及組成物之製造 |
| AU2021344830A1 (en) | 2020-09-03 | 2023-04-06 | Revolution Medicines, Inc. | Use of SOS1 inhibitors to treat malignancies with SHP2 mutations |
| MX2023003060A (es) | 2020-09-15 | 2023-04-05 | Revolution Medicines Inc | Derivados indolicos como inhibidores de ras en el tratamiento del cancer. |
| EP4267250A1 (fr) | 2020-12-22 | 2023-11-01 | Qilu Regor Therapeutics Inc. | Inhibiteurs de sos1 et utilisations associées |
| EP4039685A1 (fr) | 2021-02-08 | 2022-08-10 | Irbm S.P.A. | Inhibiteurs azabicycliques de shp2 |
| CA3213837A1 (fr) * | 2021-03-23 | 2022-09-29 | Shanghai Haiyan Pharmaceutical Technology Co., Ltd. | Derive de cetone substitue par un heterocycle, et composition et son utilisation medicinale |
| EP4067358A1 (fr) | 2021-04-02 | 2022-10-05 | C.N.C.C.S. S.c.a.r.l. Collezione Nazionale Dei Composti Chimici e Centro Screening | Dérivés de (s)-1-(5-((pyridin-3-yl)thio)pyrazin-2-yl)-4'h,6'h-spiro[pipéridine-4,5'-pyrrolo[1,2-b]pyrazol]-4'-amine et composés similaires en tant qu'inhibiteurs de shp2 pour le traitement par ex. du cancer |
| TW202302145A (zh) | 2021-04-14 | 2023-01-16 | 美商基利科學股份有限公司 | CD47/SIRPα結合及NEDD8活化酶E1調節次單元之共抑制以用於治療癌症 |
| IL308193A (en) | 2021-05-05 | 2024-01-01 | Revolution Medicines Inc | RAS inhibitors |
| AU2022271244A1 (en) | 2021-05-05 | 2023-12-07 | Huyabio International, Llc | Shp2 inhibitor monotherapy and uses thereof |
| AU2022271243A1 (en) | 2021-05-05 | 2023-11-30 | Huyabio International, Llc | Combination therapies comprising shp2 inhibitors and pd-1 inhibitors |
| WO2022235866A1 (fr) | 2021-05-05 | 2022-11-10 | Revolution Medicines, Inc. | Inhibiteurs de ras covalents et leurs utilisations |
| TW202309053A (zh) | 2021-05-05 | 2023-03-01 | 美商銳新醫藥公司 | Ras抑制劑 |
| JP7656087B2 (ja) * | 2021-05-13 | 2025-04-02 | 中国科学院上海薬物研究所 | Shp2活性を阻害する複素環化合物、その製造方法および使用 |
| US20220389394A1 (en) | 2021-05-18 | 2022-12-08 | Gilead Sciences, Inc. | METHODS OF USING FLT3L-Fc FUSION PROTEINS |
| TW202313041A (zh) | 2021-06-09 | 2023-04-01 | 瑞士商諾華公司 | 包含達拉菲尼、曲美替尼和shp2抑制劑之三重藥物組合 |
| TW202317100A (zh) | 2021-06-23 | 2023-05-01 | 瑞士商諾華公司 | 包含kras g12c抑制劑的藥物組合及其用於治療癌症之用途 |
| KR20240005901A (ko) | 2021-06-23 | 2024-01-12 | 길리애드 사이언시즈, 인코포레이티드 | 디아실글리세롤 키나제 조절 화합물 |
| JP7654118B2 (ja) | 2021-06-23 | 2025-03-31 | ギリアード サイエンシーズ, インコーポレイテッド | ジアシルグリセロールキナーゼ調節化合物 |
| AU2022298639C1 (en) | 2021-06-23 | 2025-07-17 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| KR20240025616A (ko) | 2021-06-23 | 2024-02-27 | 길리애드 사이언시즈, 인코포레이티드 | 다이아실글리세롤 키나제 조절 화합물 |
| IL309984A (en) * | 2021-07-09 | 2024-03-01 | Kanaph Therapeutics Inc | Shp2 inhibitor and use thereof |
| CN117916242A (zh) * | 2021-07-09 | 2024-04-19 | 治纳辅医药科技有限公司 | Shp2抑制剂及其用途 |
| CN113461538A (zh) * | 2021-07-12 | 2021-10-01 | 无锡双启科技有限公司 | 一种2-氯-3-溴苯胺的制备方法 |
| JP2024532374A (ja) | 2021-09-01 | 2024-09-05 | ノバルティス アーゲー | Tead阻害剤を含む医薬品組み合わせ物及び癌の治療のためのその使用 |
| AR127308A1 (es) | 2021-10-08 | 2024-01-10 | Revolution Medicines Inc | Inhibidores ras |
| CN118139858A (zh) | 2021-10-28 | 2024-06-04 | 吉利德科学公司 | 吡地嗪-3(2h)-酮衍生物 |
| WO2023077030A1 (fr) | 2021-10-29 | 2023-05-04 | Gilead Sciences, Inc. | Composés cd73 |
| US20230220106A1 (en) | 2021-12-08 | 2023-07-13 | Dragonfly Therapeutics, Inc. | Antibodies targeting 5t4 and uses thereof |
| US20230203202A1 (en) | 2021-12-08 | 2023-06-29 | Dragonfly Therapeutics, Inc. | Proteins binding nkg2d, cd16 and 5t4 |
| EP4452414A2 (fr) | 2021-12-22 | 2024-10-30 | Gilead Sciences, Inc. | Agents de dégradation de doigt de zinc de la famille ikaros et utilisations associées |
| WO2023122615A1 (fr) | 2021-12-22 | 2023-06-29 | Gilead Sciences, Inc. | Agents de dégradation des doigts de zinc de la famille ikaros et leurs utilisations |
| WO2023122938A1 (fr) * | 2021-12-28 | 2023-07-06 | Js Innomed Holdings Ltd. | Composés hétérocycliques utilisés en tant qu'inhibiteurs de shp2, compositions comprenant le composé hétérocyclique, et leurs procédés d'utilisation |
| TW202340168A (zh) | 2022-01-28 | 2023-10-16 | 美商基利科學股份有限公司 | Parp7抑制劑 |
| CN119136806A (zh) | 2022-03-08 | 2024-12-13 | 锐新医药公司 | 用于治疗免疫难治性肺癌的方法 |
| WO2023169170A1 (fr) * | 2022-03-10 | 2023-09-14 | 捷思英达控股有限公司 | Composé hétérocyclique utilisé en tant qu'inhibiteur de shp2, composition comprenant un composé hétérocyclique, et procédé l'utilisant |
| ES2999273T3 (en) | 2022-03-17 | 2025-02-25 | Gilead Sciences Inc | Ikaros zinc finger family degraders and uses thereof |
| CN119031937A (zh) | 2022-03-24 | 2024-11-26 | 吉利德科学公司 | 用于治疗表达Trop-2的癌症的联合疗法 |
| TWI876305B (zh) | 2022-04-05 | 2025-03-11 | 美商基利科學股份有限公司 | 用於治療結腸直腸癌之組合療法 |
| KR20250004824A (ko) | 2022-04-21 | 2025-01-08 | 길리애드 사이언시즈, 인코포레이티드 | Kras g12d 조절 화합물 |
| WO2023230205A1 (fr) | 2022-05-25 | 2023-11-30 | Ikena Oncology, Inc. | Inhibiteurs de mek et leurs utilisations |
| JP2025521232A (ja) | 2022-06-10 | 2025-07-08 | レボリューション メディシンズ インコーポレイテッド | 大環状ras阻害剤 |
| IL317958A (en) | 2022-07-01 | 2025-02-01 | Gilead Sciences Inc | CD73 compounds |
| WO2024040131A1 (fr) | 2022-08-17 | 2024-02-22 | Treeline Biosciences, Inc. | Inhibiteurs de pyridopyrimidine kras |
| US20240091351A1 (en) | 2022-09-21 | 2024-03-21 | Gilead Sciences, Inc. | FOCAL IONIZING RADIATION AND CD47/SIRPa DISRUPTION ANTICANCER COMBINATION THERAPY |
| EP4345101A1 (fr) | 2022-09-29 | 2024-04-03 | Irbm S.P.A. | Dérivés d'azole utilisés en tant qu'inhibiteurs de shp2 |
| JP2025536369A (ja) | 2022-10-21 | 2025-11-05 | リーディングタック ファーマシューティカル(シャオシン)カンパニー,リミテッド | Kras g12d分解剤及びその製造方法並びに応用 |
| JP2025537482A (ja) | 2022-10-21 | 2025-11-18 | リーディングタック ファーマシューティカル(シャオシン)カンパニー,リミテッド | pan-KRAS分解剤及びその製造方法並びに応用 |
| CN115677660B (zh) * | 2022-10-27 | 2024-05-03 | 中国药科大学 | 苯基脲类化合物及其制备方法、用途和药物组合物 |
| US20240254118A1 (en) | 2022-12-22 | 2024-08-01 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
| JP2026503032A (ja) * | 2023-01-05 | 2026-01-27 | カナプ セラピューティクス インコーポレイテッド | Shp2阻害剤及びその使用 |
| EP4687905A1 (fr) | 2023-03-30 | 2026-02-11 | Revolution Medicines, Inc. | Compositions pour induire une hydrolyse de ras gtp et leurs utilisations |
| WO2024211663A1 (fr) | 2023-04-07 | 2024-10-10 | Revolution Medicines, Inc. | Composés macrocycliques condensés en tant qu'inhibiteurs de ras |
| EP4688790A1 (fr) | 2023-04-07 | 2026-02-11 | Revolution Medicines, Inc. | Composés macrocycliques condensés en tant qu'inhibiteurs de ras |
| EP4695260A1 (fr) | 2023-04-11 | 2026-02-18 | Gilead Sciences, Inc. | Composés modulateurs de kras |
| KR20250169290A (ko) | 2023-04-14 | 2025-12-02 | 레볼루션 메디슨즈, 인크. | Ras 억제제의 결정형, 이를 함유하는 조성물 및 이의 사용 방법 |
| KR20250172857A (ko) | 2023-04-14 | 2025-12-09 | 레볼루션 메디슨즈, 인크. | Ras 억제제의 결정형 |
| KR20250175331A (ko) | 2023-04-21 | 2025-12-16 | 길리애드 사이언시즈, 인코포레이티드 | Prmt5 억제제 및 이의 용도 |
| WO2024229406A1 (fr) | 2023-05-04 | 2024-11-07 | Revolution Medicines, Inc. | Polythérapie pour une maladie ou un trouble lié à ras |
| US20250042922A1 (en) | 2023-06-30 | 2025-02-06 | Gilead Sciences, Inc. | Kras modulating compounds |
| US20250066328A1 (en) | 2023-07-26 | 2025-02-27 | Gilead Sciences, Inc. | Parp7 inhibitors |
| AU2024297978A1 (en) | 2023-07-26 | 2026-02-05 | Gilead Sciences, Inc. | Parp7 inhibitors |
| WO2025034702A1 (fr) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Rmc-6291 destiné à être utilisé dans le traitement d'une maladie ou d'un trouble lié à une protéine ras |
| WO2025034919A1 (fr) | 2023-08-08 | 2025-02-13 | Quanta Therapeutics, Inc. | Polythérapies avec des modulateurs de kras |
| TW202521120A (zh) * | 2023-08-17 | 2025-06-01 | 大陸商北京加科思新藥研發有限公司 | 藥物組合物及其應用 |
| US20250109147A1 (en) | 2023-09-08 | 2025-04-03 | Gilead Sciences, Inc. | Kras g12d modulating compounds |
| US20250101042A1 (en) | 2023-09-08 | 2025-03-27 | Gilead Sciences, Inc. | Kras g12d modulating compounds |
| TW202528315A (zh) | 2023-09-21 | 2025-07-16 | 美商樹線生物科學公司 | 螺環二氫哌喃并吡啶KRas抑制劑 |
| US20250154171A1 (en) | 2023-10-12 | 2025-05-15 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025081291A1 (fr) * | 2023-10-16 | 2025-04-24 | Canwell Biotech Limited | Dérivés de benzo [c] [1, 2] oxaborol-1(3h)-ol utilisés comme inhibiteurs de shp2, compositions et méthodes associées |
| WO2025096589A1 (fr) | 2023-11-03 | 2025-05-08 | Gilead Sciences, Inc. | Inhibiteurs de prmt5 et leurs utilisations |
| WO2025106901A1 (fr) | 2023-11-17 | 2025-05-22 | Quanta Therapeutics, Inc. | Polythérapies anticancéreuses avec un modulateur de kras et un inhibiteur de la voie rtk-mapk |
| WO2025137640A1 (fr) | 2023-12-22 | 2025-06-26 | Gilead Sciences, Inc. | Inhibiteurs azaspiro de wrn |
| WO2025137507A1 (fr) | 2023-12-22 | 2025-06-26 | Regor Pharmaceuticals, Inc. | Inhibiteurs de sos1 et leurs utilisations |
| WO2025171296A1 (fr) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| WO2025240847A1 (fr) | 2024-05-17 | 2025-11-20 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| WO2025245127A1 (fr) | 2024-05-21 | 2025-11-27 | Treeline Biosciences, Inc. | Inhibiteurs de dihydropyranopyrimidine kras spirocycliques |
| WO2025245003A1 (fr) | 2024-05-21 | 2025-11-27 | Gilead Sciences, Inc. | Inhibiteurs de prmt5 et leurs utilisations |
| WO2025255438A1 (fr) | 2024-06-07 | 2025-12-11 | Revolution Medicines, Inc. | Procédés de traitement d'une maladie ou d'un trouble lié à la protéine ras |
| WO2025265060A1 (fr) | 2024-06-21 | 2025-12-26 | Revolution Medicines, Inc. | Compositions thérapeutiques et procédés de gestion d'effets liés au traitement |
| WO2026006747A1 (fr) | 2024-06-28 | 2026-01-02 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| WO2026015801A1 (fr) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Méthodes de traitement d'une maladie ou d'un trouble liés à ras |
| WO2026015825A1 (fr) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Utilisation d'un inhibiteur de ras pour traiter le cancer du pancréas |
| WO2026015790A1 (fr) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Méthodes de traitement d'une maladie ou d'un trouble lié à ras |
| WO2026015796A1 (fr) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Méthodes de traitement d'une maladie ou d'un trouble lié à ras |
Family Cites Families (174)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3377826B2 (ja) | 1993-05-06 | 2003-02-17 | ヘキスト・アクチェンゲゼルシャフト | 液晶組成物に使用するための新規化合物 |
| JP2002500618A (ja) | 1995-10-31 | 2002-01-08 | イーライ・リリー・アンド・カンパニー | 抗血栓性ジアミン |
| WO2000059884A1 (fr) | 1999-01-26 | 2000-10-12 | Dana-Farber Cancer Institute, Inc. | Composes pharmaceutiquement actifs et procedes d'utilisation |
| US7375125B2 (en) | 1999-08-04 | 2008-05-20 | Ore Pharmaceuticals, Inc. | Melanocortin-4 receptor binding compounds and methods of use thereof |
| EP1415987B1 (fr) | 2000-10-20 | 2007-02-28 | Eisai R&D Management Co., Ltd. | Composes heteroaromatiques azotes pour le traitement des maladies de cancer |
| EP1467736A2 (fr) | 2001-12-21 | 2004-10-20 | Bayer Pharmaceuticals Corporation | Polytherapies antiangiogeneses a base de derives de pyridazine ou pyridine |
| US6855709B2 (en) | 2002-02-22 | 2005-02-15 | Pharmacia & Upjohn Company | Pyridyl sulfone derivatives |
| DE10246657A1 (de) | 2002-10-07 | 2004-04-15 | Merck Patent Gmbh | Chirales Phenolderivat, dieses enthaltendes Flüssigkristallmedium, Verfahren zur Herstellung eines Flüssigkristallmediums und elektrooptische Flüssigkristallanzeige |
| CA2500492C (fr) | 2002-11-18 | 2010-03-16 | Solomon Ungashe | Arylsulfonamides |
| SE0203712D0 (sv) | 2002-12-13 | 2002-12-13 | Astrazeneca Ab | Novel compounds |
| AP2005003365A0 (en) | 2003-02-07 | 2005-09-30 | Janssen Pharmaceutica Nv | Hiv inhibiting 1, 2, 4-triazines. |
| WO2004071426A2 (fr) | 2003-02-11 | 2004-08-26 | Kemia Inc. | Composes destines au traitement d'une infection virale |
| GB2400101A (en) | 2003-03-28 | 2004-10-06 | Biofocus Discovery Ltd | Compounds capable of binding to the active site of protein kinases |
| WO2004099158A1 (fr) | 2003-04-30 | 2004-11-18 | Ricerca Biosciences, Llc. | N-oxydes monocycliques utilises comme antagonistes des proteines bcl-2 |
| WO2005004810A2 (fr) | 2003-07-02 | 2005-01-20 | Merck & Co., Inc. | Derives arylsulfonamide |
| CA2531510A1 (fr) | 2003-07-08 | 2005-01-20 | Astrazeneca Ab | Derives de spiro '1-azabicyclo '2.2.2!octan-3,5'-oxazolidin -2-one! possedant une affinite avec le recepteur d'acetylcholine nicotinique alpha7 |
| CA2540640A1 (fr) | 2003-09-30 | 2005-04-14 | Amgen Inc. | Ligands de recepteur vanilloide et leur utilisation dans certains traitements |
| GB0325956D0 (en) | 2003-11-06 | 2003-12-10 | Addex Pharmaceuticals Sa | Novel compounds |
| TW200528459A (en) | 2004-01-06 | 2005-09-01 | Achillion Pharmaceuticals Inc | Azabenzofuran substituted thioureas; inhibitors of viral replication |
| BRPI0506817A (pt) | 2004-01-12 | 2007-05-29 | Cytopia Res Pty Ltd | inibidores seletivos de quinase |
| US7435831B2 (en) | 2004-03-03 | 2008-10-14 | Chemocentryx, Inc. | Bicyclic and bridged nitrogen heterocycles |
| AU2005219438B2 (en) | 2004-03-03 | 2011-02-17 | Chemocentryx, Inc. | Bicyclic and bridged nitrogen heterocycles |
| AU2005223610B2 (en) * | 2004-03-23 | 2008-05-29 | Banyu Pharmaceutical Co., Ltd. | Substituted quinazoline or pyridopyrimidine derivative |
| JP4865702B2 (ja) | 2004-05-03 | 2012-02-01 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | サイトカイン阻害剤 |
| NZ551603A (en) | 2004-06-24 | 2010-11-26 | Incyte Corp | N-substituted piperidines and their use as pharmaceuticals |
| US20070043057A1 (en) | 2005-02-09 | 2007-02-22 | Threshold Pharmaceuticals, Inc. | Lonidamine analogs |
| CA2577588C (fr) | 2004-10-29 | 2013-09-10 | Tibotec Pharmaceuticals Ltd. | Derives de pyrimidine bicycliques inhibant le vih |
| WO2006063010A2 (fr) | 2004-12-08 | 2006-06-15 | Nuada, Llc | Composes et procedes d'utilisation |
| GB0428082D0 (en) | 2004-12-22 | 2005-01-26 | Welcome Trust The Ltd | Therapeutic compounds |
| EP2135863A1 (fr) | 2004-12-23 | 2009-12-23 | Mallinckrodt, Inc. | Dérivés de pyrazine fluorescents et leurs procédés d'utilisation dans l'évaluation de la fonction rénale |
| US7622583B2 (en) | 2005-01-14 | 2009-11-24 | Chemocentryx, Inc. | Heteroaryl sulfonamides and CCR2 |
| CN101384183B (zh) | 2005-02-04 | 2012-07-04 | 西诺米克斯公司 | 包含连接有杂芳基部分的化合物及其作为用于食物组合物的新型鲜味调节剂、促味剂和味觉增强剂的应用 |
| WO2006087305A1 (fr) | 2005-02-16 | 2006-08-24 | Neurosearch A/S | Derives aryle diazabicycliques et utilisation medicale |
| WO2007046867A2 (fr) | 2005-05-19 | 2007-04-26 | Xenon Pharmaceuticals Inc. | Derives de piperidine et leurs utilisations comme agents therapeutiques |
| CA2609388C (fr) | 2005-05-30 | 2013-08-06 | Banyu Pharmaceutical Co., Ltd. | Nouveau derive de piperidine |
| JP2007013804A (ja) | 2005-07-01 | 2007-01-18 | Mitsubishi Electric Corp | 属性指定通信方法および通信装置 |
| CA2606004A1 (fr) * | 2005-08-02 | 2007-02-08 | Neurogen Corporation | Dipiperazinyl cetones et analogues apparentes |
| CA2625189A1 (fr) | 2005-10-19 | 2007-04-26 | Gruenenthal Gmbh | Nouveaux ligands du recepteur vanilloide et leur utilisation dans la production de medicaments |
| WO2007057742A2 (fr) | 2005-11-18 | 2007-05-24 | Pfizer Products Inc. | Nouveaux derives de piperazinone |
| CA2636314A1 (fr) | 2005-11-29 | 2007-06-07 | Toray Industries, Inc. | Derive d'arylmethylene uree et utilisation de celui-ci |
| AU2006328551A1 (en) | 2005-12-21 | 2007-06-28 | Janssen Pharmaceutica N.V. | Substituted pyrazinone derivatives as alpha2c-adrenoreceptor antagonists |
| WO2007084728A2 (fr) | 2006-01-19 | 2007-07-26 | Abbott Laboratories | 2-imino-benzimidazoles |
| NZ569329A (en) | 2006-01-30 | 2011-09-30 | Transtech Pharma Inc | Substituted imidazole derivatives and their use as PTPase inhibitors |
| CA2645137A1 (fr) | 2006-03-07 | 2007-09-13 | James F. Blake | Derives heterobicycliques de pyrazole et methodes d'utilisation |
| DE602007007206D1 (de) | 2006-04-20 | 2010-07-29 | Janssen Pharmaceutica Nv | Substituierte pyrazinonderivate zur verwendung als arzneimittel |
| MX2008014921A (es) | 2006-05-22 | 2008-12-09 | Janssen Pharmaceutica Nv | Derivados de piracinona sustituidos para uso como un medicamento. |
| AR063707A1 (es) | 2006-09-11 | 2009-02-11 | Cgi Pharmaceuticals Inc | Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmacéuticas que las comprenden. |
| US7838523B2 (en) | 2006-09-11 | 2010-11-23 | Cgi Pharmaceuticals, Inc. | Certain substituted amides, method of making, and method of use thereof |
| ATE467622T1 (de) | 2006-10-04 | 2010-05-15 | Hoffmann La Roche | Pyrazin-2-carboxamid-derivate als cb2- rezeptormodulatoren |
| DE102007018150A1 (de) | 2007-04-16 | 2008-10-23 | Grünenthal GmbH | VR1-Rezeptor-Liganden und µ-Opioid-Rezeptor-Liganden zur Behandlung von Schmerz |
| JP2010518083A (ja) | 2007-02-12 | 2010-05-27 | メルク・シャープ・エンド・ドーム・コーポレイション | ピペリジン誘導体 |
| WO2008104077A1 (fr) | 2007-02-28 | 2008-09-04 | Methylgene Inc. | Inhibiteurs à petite molécule de protéines arginine méthyltransférases (prmt) |
| AU2008221263B2 (en) | 2007-03-01 | 2012-02-23 | Novartis Ag | Pim kinase inhibitors and methods of their use |
| US8313729B2 (en) | 2007-03-01 | 2012-11-20 | Medibeacon, LLC | Integrated photoactive small molecules and uses thereof |
| WO2008112674A1 (fr) | 2007-03-12 | 2008-09-18 | Irm Llc | Composés et compositions comme inhibiteurs de l'activité du récepteur cannabinoïde 1 |
| CA2698753A1 (fr) | 2007-09-06 | 2009-03-12 | Array Biopharma Inc. | Pyrazolo-pyridines en tant qu'inhibiteurs de tyrosine kinase |
| WO2009036066A1 (fr) | 2007-09-10 | 2009-03-19 | Curis, Inc. | Inhibiteurs du récepteur du facteur de croissance endothélial vasculaire (vegfr) contenant une fraction de liaison au zinc |
| ES2499018T3 (es) | 2007-09-20 | 2014-09-26 | Irm Llc | Compuestos y composiciones como moduladores de la actividad de GPR119 |
| EP2386558B1 (fr) | 2007-10-18 | 2014-10-01 | Boehringer Ingelheim International GmbH | Antagonistes du CGRP |
| US20100216816A1 (en) | 2007-10-24 | 2010-08-26 | Barrow James C | Pyrazinyl amide-t type calcium channel antagonists |
| US20110027264A1 (en) | 2008-02-29 | 2011-02-03 | Xianhai Huang | Gamma secretase modulators for the treatment of alzheimer's disease |
| ATE531372T1 (de) | 2008-04-07 | 2011-11-15 | Amgen Inc | Gem-disubstituierte und spirocyclische aminopyridine/pyrimidine als zellcyclus- inhibitoren |
| AR071619A1 (es) | 2008-05-07 | 2010-06-30 | Galapagos Nv | Compuestos de pirazina fusionados utiles para el tratamiento de enfermedades degenerativas e inflamatorias y composiciones farmaceuticas que los contienen. |
| EP2328586A2 (fr) | 2008-05-20 | 2011-06-08 | Cephalon, Inc. | Dérivés pyridazinone substitués comme ligands des récepteurs de l'histamine-3 (h3) |
| KR20110026481A (ko) | 2008-06-20 | 2011-03-15 | 메타볼렉스, 인코포레이티드 | 아릴 gpr119 작동약 및 이의 용도 |
| PE20110419A1 (es) | 2008-08-22 | 2011-07-13 | Novartis Ag | Compuestos de pirrolo-pirimidina como inhibidores de cdk |
| JP5731978B2 (ja) | 2008-09-26 | 2015-06-10 | インテリカイン, エルエルシー | 複素環キナーゼ阻害剤 |
| JP2012512255A (ja) | 2008-12-17 | 2012-05-31 | アムジエン・インコーポレーテツド | ホスホジエステラーゼ10阻害剤としてのアミノピリジンおよびカルボキシピリジン化合物 |
| CA2744935A1 (fr) | 2008-12-19 | 2010-06-24 | Boehringer Ingelheim International Gmbh | Nouveaux composes |
| WO2010074244A1 (fr) | 2008-12-25 | 2010-07-01 | 大正製薬株式会社 | Dérivé d'isoquinoléine |
| KR20110119707A (ko) | 2009-01-22 | 2011-11-02 | 유니진 래보러토리즈 인코포레이티드 | 비만 치료 |
| WO2010086613A1 (fr) | 2009-01-30 | 2010-08-05 | Betagenon Ab | Composés utiles en tant qu'inhibiteurs tel que ampk |
| AU2010222289B2 (en) | 2009-03-13 | 2013-07-11 | Advinus Therapeutics Private Limited | Substituted fused pyrimidine compounds |
| CN102596923B (zh) | 2009-07-08 | 2015-04-29 | 波罗的海生物公司 | 1,2,4-噻唑烷-3-酮衍生物及其在癌症治疗中的用途 |
| CA2771190C (fr) | 2009-08-17 | 2020-01-21 | Memorial Sloan-Kettering Cancer Center | Composes de liaison a une proteine de choc thermique, compositions et procedes pour les fabriquer et les utiliser |
| EP2473500A2 (fr) | 2009-09-01 | 2012-07-11 | Pfizer Inc. | Dérivés de benzimidazole |
| KR20120092629A (ko) | 2009-10-09 | 2012-08-21 | 아이알엠 엘엘씨 | Gpr119 활성의 조절제로서의 화합물 및 조성물 |
| US8759377B2 (en) | 2009-11-23 | 2014-06-24 | Vanderbilt University | Substituted dioxopiperidines and dioxopyrrolidines as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
| ES2438509T3 (es) | 2009-12-14 | 2014-01-17 | Merck Patent Gmbh | Inhibidores de la esfingosina quinasa |
| CN104341401B (zh) | 2009-12-18 | 2017-02-15 | 北京凯因科技股份有限公司 | C型肝炎病毒复制的新型抑制剂 |
| US8431575B2 (en) | 2010-02-18 | 2013-04-30 | Transtech Pharma, Inc. | Phenyl-heteroaryl derivatives and methods of use thereof |
| JP5918214B2 (ja) | 2010-04-13 | 2016-05-18 | ノバルティス アーゲー | がんを治療するためのサイクリン依存性キナーゼ4またはサイクリン依存性キナーゼ(cdk4/6)阻害剤およびmtor阻害剤を含む組合せ |
| WO2011135276A1 (fr) | 2010-04-29 | 2011-11-03 | The University Of Edinburgh | (8-aza-bicyclo[3.2.1]oct-8-yl)-[5-(1h-pyrazol-4-yl]-méthanones 3,3-disubstituées en tant qu'inhibiteurs de 11-(bêta)-hsd1 |
| WO2011146401A1 (fr) | 2010-05-17 | 2011-11-24 | Intermune, Inc. | Nouveaux inhibiteurs de la réplication du virus de l'hépatite c |
| MX351368B (es) | 2010-05-26 | 2017-10-12 | Sunovion Pharmaceuticals Inc | Compuestos heteroarilo y metodos para utilizarlos. |
| EA025611B1 (ru) | 2010-07-29 | 2017-01-30 | Райджел Фармасьютикалз, Инк. | Активирующие ampk гетероциклические соединения и способы их использования |
| JP2013230986A (ja) | 2010-08-25 | 2013-11-14 | Kyorin Pharmaceutical Co Ltd | 新規ヒダントイン誘導体及びそれらを有効成分とする医薬 |
| CN102432598A (zh) | 2010-09-29 | 2012-05-02 | 江苏恒瑞医药股份有限公司 | 三环化合物、其制备方法及其在医药上的应用 |
| US20140066431A1 (en) * | 2010-11-15 | 2014-03-06 | Exelixis, Inc. | Benzoxazepines as Inhibitors of PI3K/mTOR and Methods of Their Use and Manufacture |
| GB201020161D0 (en) | 2010-11-26 | 2011-01-12 | Almac Discovery Ltd | Pharmaceutical compounds |
| JP5937102B2 (ja) | 2010-12-14 | 2016-06-22 | エレクトロフォレティクス リミテッド | カゼインキナーゼ1デルタ(ck1デルタ)阻害剤 |
| US8987271B2 (en) | 2010-12-22 | 2015-03-24 | Eutropics Pharmaceuticals, Inc. | 2,2′-biphenazine compounds and methods useful for treating disease |
| US20120184572A1 (en) | 2011-01-13 | 2012-07-19 | Metabolex, Inc. | Aryl gpr119 agonists and uses thereof |
| JP2014515029A (ja) | 2011-04-29 | 2014-06-26 | アイカーン・スクール・オブ・メディシン・アト・マウント・シナイ | キナーゼ阻害剤 |
| US9586928B2 (en) | 2011-05-16 | 2017-03-07 | The Scripps Research Institute | Modulators of the nuclear hormone receptor ROR |
| US20120316182A1 (en) * | 2011-06-10 | 2012-12-13 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
| EP2554544A1 (fr) | 2011-08-01 | 2013-02-06 | Almirall, S.A. | Dérivés de pyridin-2(1h)-one en tant qu'inhibiteurs de JAK |
| WO2013039851A1 (fr) | 2011-09-12 | 2013-03-21 | Mallinckrodt Llc | Agents optiques permettant d'obtenir des images de métalloprotéases matricielles et de les visualiser |
| MX365923B (es) | 2011-12-12 | 2019-06-20 | Celgene Int Ii Sarl | Derivados de acido carboxilico que comprenden cuatro ciclos, que actuan como moduladores del receptor del peptido 1 similar al glucagon (glp-1) para terapia de enfermedades como la diabetes. |
| EP2817388B1 (fr) | 2012-02-22 | 2020-03-25 | Merck Patent GmbH | Milieu cristallin liquide |
| GB201204985D0 (en) | 2012-03-21 | 2012-05-02 | Genentech Inc | Compounds |
| US8889730B2 (en) | 2012-04-10 | 2014-11-18 | Pfizer Inc. | Indole and indazole compounds that activate AMPK |
| RU2632899C2 (ru) | 2012-04-25 | 2017-10-11 | Раквалиа Фарма Инк. | Амидопроизводные как блокаторы ttx-s |
| BR112014027133A2 (pt) | 2012-05-09 | 2017-06-27 | Basf Se | compostos, composição agrícola ou veterinária, método para o controle das pragas de invertebrados, material de propagação dos vegetais e método para o tratamento ou proteção de um animal. |
| WO2014000178A1 (fr) | 2012-06-27 | 2014-01-03 | Merck Sharp & Dohme Corp. | Dérivés de sulfamide et leurs méthodes d'utilisation permettant d'améliorer la pharmacocinétique d'un médicament |
| US9434725B2 (en) | 2012-06-27 | 2016-09-06 | F. Hoffmann-La Roche Ag | 5-azaindazole compounds and methods of use |
| EP3584246A1 (fr) | 2012-08-16 | 2019-12-25 | The Scripps Research Institute | Nouveaux ligands kappa opioïdes |
| JOP20130273B1 (ar) | 2012-09-11 | 2021-08-17 | Genzyme Corp | مثبطات انزيم (سينثاز) غلوكوسيل سيراميد |
| AU2013341115B2 (en) * | 2012-11-09 | 2016-07-14 | Glaxosmithkline Llc | Novel compounds as diacylglycerol acyltransferase inhibitors |
| CN108434149B (zh) | 2013-03-15 | 2021-05-28 | G1治疗公司 | 针对Rb阳性异常细胞增殖的HSPC节制性治疗 |
| RU2015141592A (ru) | 2013-03-15 | 2017-04-21 | Ф. Хоффманн-Ля Рош Аг | АРИЛ-СУЛЬФАМИДЫ И СУЛЬФАМАТЫ В КАЧЕСТВЕ МОДУЛЯТОРОВ RORc |
| WO2014184014A1 (fr) | 2013-05-15 | 2014-11-20 | Basf Se | Composés de n-(1,2,5-oxadiazol-3-yl)carboxamide et leur utilisation en tant qu'herbicides |
| WO2014184074A1 (fr) | 2013-05-15 | 2014-11-20 | Basf Se | Composés de n-(tétrazol-5-yl)- et n-(triazol-5-yl)hétarylcarboxamide substitués et leur utilisation en tant qu'herbicides |
| GB201309508D0 (en) | 2013-05-28 | 2013-07-10 | Redx Pharma Ltd | Compounds |
| WO2014201172A1 (fr) | 2013-06-11 | 2014-12-18 | Receptos, Inc. | Nouveaux modulateurs du récepteur glp-1 |
| AU2014284279A1 (en) | 2013-07-03 | 2016-02-18 | Beth Israel Deaconess Medical Center, Inc. | SHP2 inhibitors and methods of treating autoimmune and/or glomerulonephritis-associated diseases using SHP2 inhibitors |
| CN104341386A (zh) * | 2013-07-23 | 2015-02-11 | 中国科学院上海药物研究所 | 一类芳基杂环小分子化合物、其衍生物及其制备方法和用途 |
| EP3029031A4 (fr) | 2013-07-30 | 2017-01-11 | Takeda Pharmaceutical Company Limited | Composé hétérocyclique |
| EP3027625B1 (fr) | 2013-07-31 | 2018-05-30 | Merck Sharp & Dohme Corp. | Derives spiro-fusionnes de piperidine utiles dans le traitement, entre autres, de l'hypertension et de l' insuffisance cardiaque aiguë ou chronique |
| US20150087673A1 (en) | 2013-09-26 | 2015-03-26 | Rigel Pharmaceuticals, Inc. | Methods for using and biomarkers for ampk-activating compounds |
| CA2926571C (fr) | 2013-10-08 | 2022-05-17 | Qing-bin LU | Composes anticancereux non a base de platine destines a etre utilises dans la chimiotherapie-cible |
| EP3060550B1 (fr) | 2013-10-21 | 2019-05-15 | Merck Patent GmbH | Composés hétéroaryle servant d'inhibiteurs de la btk et leurs utilisations |
| US10131841B2 (en) | 2013-12-16 | 2018-11-20 | Merck Patent Gmbh | Liquid-crystalline medium |
| WO2015091420A1 (fr) | 2013-12-19 | 2015-06-25 | Bayer Pharma Aktiengesellschaft | Utilisation de dérivés de bipipéridinyle substitués comme antagonistes des alpha-2c-adrénorécepteurs |
| EP3094627B1 (fr) | 2014-01-17 | 2018-08-22 | Novartis AG | Dérivés de 1-pyridazin-/triazin-3-yl-piper(-azine)/idine/pyrolidine et compositions les contenant pour l'inhibition de l'activité de shp2 |
| CN105899493B (zh) | 2014-01-17 | 2019-03-29 | 诺华股份有限公司 | 用于抑制shp2活性的1-(三嗪-3-基/哒嗪-3-基)-哌(-嗪)啶衍生物及其组合物 |
| JO3517B1 (ar) * | 2014-01-17 | 2020-07-05 | Novartis Ag | ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2 |
| WO2015123437A1 (fr) | 2014-02-13 | 2015-08-20 | Incyte Corporation | Cyclopropylamines en tant qu'inhibiteurs de lsd1 |
| MA39337B1 (fr) | 2014-02-14 | 2019-11-29 | Takeda Pharmaceuticals Co | Modulateurs de pyrazines de gpr6 |
| US10000469B2 (en) | 2014-03-25 | 2018-06-19 | Duke University | Heat shock protein 70 (hsp-70) receptor ligands |
| CN106132963B (zh) | 2014-04-07 | 2019-08-06 | 荷兰转化研究中心有限责任公司 | (5,6-二氢)嘧啶并[4,5-e]吲嗪 |
| EP3145912A1 (fr) | 2014-05-23 | 2017-03-29 | F. Hoffmann-La Roche AG | Dérivés de benzène sulfonamide et leur utilisation comme modulateurs de rorc |
| CN105294655B (zh) | 2014-07-26 | 2019-03-15 | 广东东阳光药业有限公司 | Cdk类小分子抑制剂的化合物及其用途 |
| WO2016022644A1 (fr) | 2014-08-06 | 2016-02-11 | Merck Sharp & Dohme Corp. | Antagonistes hétérocycliques des récepteurs cgrp |
| WO2016022645A1 (fr) | 2014-08-06 | 2016-02-11 | Merck Sharp & Dohme Corp. | Antagonistes hétérocycliques du récepteur du cgrp |
| EP2985334B1 (fr) | 2014-08-15 | 2018-06-20 | Merck Patent GmbH | Milieu liquide cristallin |
| CN112125901A (zh) * | 2014-09-05 | 2020-12-25 | 赛尔基因昆蒂赛尔研究公司 | 赖氨酸特异性脱甲基酶-1的抑制剂 |
| WO2016040449A1 (fr) | 2014-09-10 | 2016-03-17 | Raze Therapeutics, Inc. | Inhibiteurs de la 3-phosphoglycérate déshydrogénase) et leurs utilisations |
| TWI788655B (zh) | 2015-02-27 | 2023-01-01 | 美商林伯士拉克許米公司 | 酪胺酸蛋白質激酶2(tyk2)抑制劑及其用途 |
| JP6726677B2 (ja) | 2015-03-11 | 2020-07-22 | チア タイ ティエンチン ファーマシューティカル グループ カンパニー リミテッドChia Tai Tianqing Pharmaceutical Group Co., Ltd. | 抗がん剤としての置換2−h−ピラゾール誘導体 |
| JP2018509448A (ja) | 2015-03-25 | 2018-04-05 | ノバルティス アーゲー | 組合せ医薬 |
| TWI703150B (zh) | 2015-06-04 | 2020-09-01 | 美商庫拉腫瘤技術股份有限公司 | 用於抑制menin及mll蛋白之交互作用的方法及組合物 |
| EP3302057A4 (fr) | 2015-06-04 | 2018-11-21 | Kura Oncology, Inc. | Méthodes et compositions d'inhibition de l'interaction de la ménine avec les protéines mll |
| WO2016203405A1 (fr) * | 2015-06-19 | 2016-12-22 | Novartis Ag | Composés et compositions pour inhiber l'activité de shp2 |
| US10287266B2 (en) | 2015-06-19 | 2019-05-14 | Novartis Ag | Compounds and compositions for inhibiting the activity of SHP2 |
| WO2016203404A1 (fr) | 2015-06-19 | 2016-12-22 | Novartis Ag | Composés et compositions pour inhiber l'activité de shp2 |
| RU2604047C1 (ru) | 2015-07-10 | 2016-12-10 | Фортис Аксис, Закрытое Акционерное Общество | Массажёр для воздействия на мышцы спины трех отделов позвоночника |
| BR112018005208B1 (pt) | 2015-09-17 | 2023-12-12 | Marvin J. Miller | Compostos heterocíclicos que contêm benzilamina e composições úteis contra infecção micobacteriana |
| CN108779117B (zh) | 2015-12-27 | 2021-08-31 | 重庆复创医药研究有限公司 | 一类激酶抑制剂 |
| WO2017156397A1 (fr) | 2016-03-11 | 2017-09-14 | Board Of Regents, The University Of Texas Sysytem | Inhibiteurs hétérocycliques de ptpn11 |
| WO2017162215A1 (fr) | 2016-03-25 | 2017-09-28 | 正大天晴药业集团股份有限公司 | Inhibiteur de cdk pyrrolopyrimidine substituée, composition pharmaceutique le comprenant et son utilisation |
| CN107286150B (zh) | 2016-04-11 | 2020-07-07 | 中国科学院上海有机化学研究所 | N-杂环类化合物、其中间体、制备方法、药物组合物和应用 |
| CN109475531B (zh) | 2016-05-31 | 2021-08-17 | 得克萨斯州立大学董事会 | Ptpn11的杂环抑制剂 |
| KR20210019607A (ko) * | 2016-06-07 | 2021-02-22 | 자코바이오 파마슈티칼스 컴퍼니 리미티드 | Shp2 억제제로서 유용한 신규한 헤테로환형 유도체 |
| KR102457146B1 (ko) * | 2016-06-14 | 2022-10-19 | 노파르티스 아게 | Shp2의 활성을 억제하기 위한 화합물 및 조성물 |
| IL311645B2 (en) | 2016-07-12 | 2025-11-01 | Revolution Medicines Inc | 2,5- disubstituted 3-methyl pyrazines and 2,5,6-trisubstituted 3-methyl pyrazines asallosteric shp2 inhibitors |
| EP3290412A1 (fr) | 2016-08-31 | 2018-03-07 | Università degli Studi di Siena | Inhibiteurs des nucléocapsides du vih-1 |
| WO2018057884A1 (fr) | 2016-09-22 | 2018-03-29 | Relay Therapeutics, Inc. | Inhibiteurs de phosphatase shp2 et leurs procédés d'utilisation |
| WO2018089433A1 (fr) | 2016-11-08 | 2018-05-17 | Navitor Pharmaceuticals, Inc. | Inhibiteurs de mtorc phényle et leurs utilisations |
| JP2020503352A (ja) | 2017-01-03 | 2020-01-30 | ヴィーブ ヘルスケア ユーケー(ナンバー5)リミテッド | ヒト免疫不全ウイルス複製の阻害剤としてのピリジン−3−イル酢酸誘導体 |
| CA3048340A1 (fr) * | 2017-01-10 | 2018-07-19 | Novartis Ag | Combinaison pharmaceutique comprenant un inhibiteur d'alk et un inhibiteur de shp2 |
| US20190350885A1 (en) * | 2017-01-25 | 2019-11-21 | Indiana University Research And Technology Corporation | Prophylaxis treatment for acute myeloid leukemia |
| NZ758458A (en) * | 2017-03-23 | 2022-07-29 | Jacobio Pharmaceuticals Co Ltd | Novel heterocyclic derivatives useful as shp2 inhibitors |
| US12428423B2 (en) | 2017-04-01 | 2025-09-30 | Shengke Pharmaceuticals (Jiangsu) Ltd. | 1H-imidazo[4,5-h]quinazoline compound as protein kinase inhibitor |
| JP2020526557A (ja) | 2017-07-12 | 2020-08-31 | ヴァンダービルト ユニバーシティー | ムスカリン性アセチルコリン受容体m4のアンタゴニスト |
| CA3078565A1 (fr) | 2017-10-12 | 2019-04-18 | Revolution Medicines, Inc. | Pyridine, pyrazine et composes de triazine utilises en tant qu'inhibiteurs allosteriques de shp2 |
| CN118063442A (zh) | 2017-10-20 | 2024-05-24 | 范德比尔特大学 | 毒蕈碱性乙酰胆碱受体m4的拮抗剂 |
| CA3080941A1 (fr) | 2017-12-22 | 2019-06-27 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de nek et procedes d'utilisation |
| SG11202006832YA (en) | 2018-01-29 | 2020-08-28 | Merck Patent Gmbh | Gcn2 inhibitors and uses thereof |
| KR20200116481A (ko) | 2018-01-29 | 2020-10-12 | 메르크 파텐트 게엠베하 | Gcn2 억제제 및 이의 용도 |
| WO2019152454A1 (fr) | 2018-01-30 | 2019-08-08 | Research Development Foundation | Inhibiteurs de shp2 et méthodes d'utilisation associées |
| EA202091889A1 (ru) | 2018-02-08 | 2020-10-29 | Энио Фарма | Конденсированные производные тиофена и их применение |
| BR112020017283A2 (pt) | 2018-03-02 | 2020-12-15 | Otsuka Pharmaceutical Co., Ltd | Compostos farmacêuticos |
| JP7462951B2 (ja) | 2018-03-21 | 2024-04-08 | リャオ,シビン | Jak阻害剤 |
-
2017
- 2017-06-07 KR KR1020217004404A patent/KR20210019607A/ko not_active Ceased
- 2017-06-07 EP EP17809742.4A patent/EP3464272B1/fr active Active
- 2017-06-07 CA CA3026784A patent/CA3026784A1/fr active Pending
- 2017-06-07 CN CN201780035294.3A patent/CN109311848B/zh active Active
- 2017-06-07 CN CN202011246514.7A patent/CN112250670B/zh active Active
- 2017-06-07 SG SG11201810983PA patent/SG11201810983PA/en unknown
- 2017-06-07 SI SI201731100T patent/SI3464272T1/sl unknown
- 2017-06-07 PL PL17809742T patent/PL3464272T3/pl unknown
- 2017-06-07 KR KR1020237022188A patent/KR20230109185A/ko not_active Ceased
- 2017-06-07 KR KR1020217037106A patent/KR20210141778A/ko not_active Ceased
- 2017-06-07 HU HUE17809742A patent/HUE057838T2/hu unknown
- 2017-06-07 KR KR1020197000391A patent/KR102218333B1/ko not_active Expired - Fee Related
- 2017-06-07 MX MX2018015297A patent/MX388576B/es unknown
- 2017-06-07 RS RS20220205A patent/RS62987B1/sr unknown
- 2017-06-07 EA EA202092441A patent/EA202092441A1/ru unknown
- 2017-06-07 MA MA045189A patent/MA45189A/fr unknown
- 2017-06-07 PT PT178097424T patent/PT3464272T/pt unknown
- 2017-06-07 US US16/307,827 patent/US10858359B2/en active Active
- 2017-06-07 ES ES17809742T patent/ES2908801T3/es active Active
- 2017-06-07 LT LTEPPCT/CN2017/087471T patent/LT3464272T/lt unknown
- 2017-06-07 JP JP2019517133A patent/JP6751203B2/ja active Active
- 2017-06-07 EP EP21212393.9A patent/EP4108659A1/fr not_active Withdrawn
- 2017-06-07 WO PCT/CN2017/087471 patent/WO2017211303A1/fr not_active Ceased
- 2017-06-07 HR HRP20220251TT patent/HRP20220251T1/hr unknown
- 2017-06-07 CN CN202210183947.5A patent/CN114539273A/zh active Pending
- 2017-06-07 EA EA202092442A patent/EA202092442A3/ru unknown
- 2017-06-07 SG SG10202110874TA patent/SG10202110874TA/en unknown
- 2017-06-07 KR KR1020227029335A patent/KR20220124275A/ko not_active Ceased
- 2017-06-07 EA EA201990001A patent/EA201990001A1/ru unknown
- 2017-06-07 AU AU2017276457A patent/AU2017276457B2/en not_active Ceased
- 2017-06-07 DK DK17809742.4T patent/DK3464272T3/da active
-
2018
- 2018-12-07 MX MX2021015074A patent/MX2021015074A/es unknown
- 2018-12-07 PH PH12018550202A patent/PH12018550202A1/en unknown
- 2018-12-07 MX MX2021015073A patent/MX2021015073A/es unknown
-
2020
- 2020-08-13 JP JP2020136588A patent/JP2020189868A/ja active Pending
-
2022
- 2022-03-02 CY CY20221100180T patent/CY1125042T1/el unknown
- 2022-08-03 JP JP2022123777A patent/JP2022153616A/ja active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA49013A (fr) | Nouveaux dérivés hétérocycliques utiles en tant qu'inhibiteurs de shp2 | |
| MA45189A (fr) | Nouveaux dérivés hétérocycliques utiles en tant qu'inhibiteurs de shp2 | |
| MA47125A (fr) | Dérivés de pyrazole en tant qu'inhibiteurs de malt1 | |
| MA47123A (fr) | Dérivés de benzooxazole en tant qu'mmunomodulateurs | |
| EP3416964A4 (fr) | Dérivés de carboxamide utiles en tant qu'inhibiteurs de rsk | |
| MA46981A (fr) | Dérivés de benzimidazole en tant qu'inhibiteurs de bromodomaine | |
| MA40774A (fr) | Dérivés de diaryle-urée en tant qu'inhibiteurs de kinase p38 | |
| MA51878A (fr) | Composés d'aminothiazole en tant qu'inhibiteurs de c-kit | |
| MA45153A (fr) | Dérivés de carbonucléosides substitués utiles en tant qu'agents anticancéreux | |
| MA46339A (fr) | Dérivés de cyanopyrrolidine ayant une activité en tant qu'inhibiteurs de l'usp 30 | |
| MA43169A (fr) | Composés hétérocycliques utilisés en tant qu'inhibiteurs de pi3k-gamma | |
| MA42659A (fr) | Dérivés hétéroaryle utilisés en tant qu'inhibiteurs de parp | |
| MA53150A (fr) | Composés de benzimidazole en tant qu'inhibiteurs de c-kit | |
| MA45244A (fr) | Pyridines substituées utilisées en tant qu'inhibiteurs de dnmt1 | |
| ME03776B (fr) | Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase | |
| MA55194A (fr) | Composés hétérocycliques en tant qu'immunomodulateurs | |
| MA41140A (fr) | Dérivés de 2,4-dioxo-quinazoline-6-sulfonamide en tant qu'inhibiteurs de la parg | |
| MA47086A (fr) | Dérivés de dihydropyrimidine-carboxamide bicycliques utilisés en tant qu'inhibiteurs de rho-kinase | |
| MA54567A (fr) | Pyridine et composés de pyridimine en tant qu'inhibiteurs de pi3k-gamma | |
| MA44498A (fr) | Dérivés d'indoline substituée utilisés en tant qu'inhibiteurs de la réplication du virus de la dengue | |
| MA42592A (fr) | Utilisation de dérivés de 2-(pyrazolopyridin-3-yl) pyrimidine en tant qu'inhibiteurs de jak | |
| EP2970119A4 (fr) | Nouveaux dérivés d'indole utiles en tant qu'agents antidiabétiques | |
| MA44502A (fr) | Dérivés d'indole substitués utilisés en tant qu'inhibiteurs de réplication du virus de la dengue | |
| MA46878A (fr) | Composés de benzodiazolium en tant qu'inhibiteurs d'enac | |
| MA41341A (fr) | Dérivés indole utilisés en tant qu'inhibiteurs de la réplication du virus de la dengue |