MA52421A - Composés pharmaceutiques - Google Patents

Composés pharmaceutiques

Info

Publication number
MA52421A
MA52421A MA052421A MA52421A MA52421A MA 52421 A MA52421 A MA 52421A MA 052421 A MA052421 A MA 052421A MA 52421 A MA52421 A MA 52421A MA 52421 A MA52421 A MA 52421A
Authority
MA
Morocco
Prior art keywords
pharmaceutical compounds
pharmaceutical
compounds
Prior art date
Application number
MA052421A
Other languages
English (en)
Inventor
Ildiko Maria Buck
Gianni Chessari
James Edward Harvey Day
Hideto Fujiwara
Christopher Charles Frederick Hamlett
Steven Douglas Hiscock
Rhian Sara Holvey
Steven Howard
Christopher Norbert Johnson
John Walter Liebeschuetz
Nicholas John Palmer
Denis Jeffrey David St
David Geoffrey Twigg
Andrew James Woodhead
Original Assignee
Otsuka Pharma Co Ltd
Taiho Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GBGB1803439.7A external-priority patent/GB201803439D0/en
Priority claimed from GBGB1814135.8A external-priority patent/GB201814135D0/en
Application filed by Otsuka Pharma Co Ltd, Taiho Pharmaceutical Co Ltd filed Critical Otsuka Pharma Co Ltd
Publication of MA52421A publication Critical patent/MA52421A/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
MA052421A 2018-03-02 2019-03-01 Composés pharmaceutiques MA52421A (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1803439.7A GB201803439D0 (en) 2018-03-02 2018-03-02 Pharmaceutical compounds
GBGB1814135.8A GB201814135D0 (en) 2018-08-30 2018-08-30 Pharmaceutical compounds

Publications (1)

Publication Number Publication Date
MA52421A true MA52421A (fr) 2021-01-06

Family

ID=65911230

Family Applications (1)

Application Number Title Priority Date Filing Date
MA052421A MA52421A (fr) 2018-03-02 2019-03-01 Composés pharmaceutiques

Country Status (17)

Country Link
US (1) US11466016B2 (fr)
EP (1) EP3759111A1 (fr)
JP (1) JP7326305B2 (fr)
KR (1) KR20200127005A (fr)
CN (1) CN111902415A (fr)
AU (1) AU2019226480B2 (fr)
BR (1) BR112020017283A2 (fr)
CA (1) CA3092011A1 (fr)
IL (1) IL276232B2 (fr)
MA (1) MA52421A (fr)
MX (1) MX2020008754A (fr)
NZ (1) NZ766835A (fr)
PH (1) PH12020551305A1 (fr)
SG (1) SG11202006778TA (fr)
TW (1) TW202000667A (fr)
WO (1) WO2019167000A1 (fr)
ZA (1) ZA202004729B (fr)

Families Citing this family (38)

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US11466017B2 (en) 2011-03-10 2022-10-11 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of PTPN11
JP7044375B2 (ja) 2016-05-31 2022-03-30 ボード オブ リージェンツ,ザ ユニバーシティ オブ テキサス システム Ptpn11の複素環式阻害剤
CN112250670B (zh) 2016-06-07 2021-06-08 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
US11529347B2 (en) 2016-09-22 2022-12-20 Relay Therapeutics, Inc. SHP2 phosphatase inhibitors and methods of use thereof
WO2018081091A1 (fr) 2016-10-24 2018-05-03 Relay Therapeutics, Inc. Dérivés de pyrazolo [3,4-b] pyrazine en tant qu'inhibiteurs de la phosphatase shp2
SG11201908820VA (en) 2017-03-23 2019-10-30 Jacobio Pharmaceuticals Co Ltd Novel heterocyclic derivatives useful as shp2 inhibitors
EP3630770A1 (fr) 2017-05-26 2020-04-08 Relay Therapeutics, Inc. Dérivés de pyrazolo[3,4-b]pyrazine en tant qu'inhibiteurs de la phosphatase 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
CN111902415A (zh) 2018-03-02 2020-11-06 大冢制药株式会社 药学化合物
CA3094690A1 (fr) 2018-03-21 2019-09-26 Relay Therapeutics, Inc. Inhibiteurs de la phosphatase shp2 et leurs procedes d'utilisation
EP3787627A4 (fr) 2018-05-02 2021-12-01 Navire Pharma, Inc. Inhibiteurs hétérocycliques substitués de ptpn11
MX2021000795A (es) * 2018-07-24 2021-04-12 Taiho Pharmaceutical Co Ltd Compuestos heterociclicos para inhibir la actividad de shp2.
CA3109181A1 (fr) 2018-08-10 2020-02-13 Navire Pharma, Inc. Derives de 6-(4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl)-3-(2,3-dichlorophenyl)-2-methylpyrimidin-4(3h)-one et composes apparentes en tant qu'inhibiteurs de ptpn11 (shp2) p our le traitement du cancer
EP3853234A1 (fr) 2018-09-18 2021-07-28 Nikang Therapeutics, Inc. Dérivés d'anneaux tricycliques fusionnés utilisés en tant qu'inhibiteurs de la phosphatase src à homologie-2
WO2020072656A1 (fr) 2018-10-03 2020-04-09 Gilead Sciences, Inc. Dérivés d'imidozopyrimidine
AU2020299892A1 (en) * 2019-07-04 2022-01-27 Beigene, Ltd. Pyrrolo [2, 3-b] pyrazines as HPK1 inhibitor and the use thereof
US20220402916A1 (en) 2019-09-18 2022-12-22 Merck Sharp & Dohme Corp. Small molecule inhibitors of kras g12c mutant
BR112022005349A2 (pt) 2019-09-24 2022-06-14 Relay Therapeutics Inc Inibidores de shp2 fosfatase e métodos de produção e uso dos mesmos
AU2020372881A1 (en) 2019-10-28 2022-06-09 Merck Sharp & Dohme Llc Small molecule inhibitors of KRAS G12C mutant
US20230023023A1 (en) 2019-10-31 2023-01-26 Taiho Pharmaceutical Co., Ltd. 4-aminobut-2-enamide derivatives and salts thereof
BR112022008858A2 (pt) 2019-11-08 2022-09-06 Revolution Medicines Inc Composto, composição farmacêutica e métodos para inibir sos1 em um sujeito, para inibir a interação de sos1 e uma proteína, para tratar ou prevenir uma doença e para tratar ou prevenir câncer
WO2021106231A1 (fr) 2019-11-29 2021-06-03 Taiho Pharmaceutical Co., Ltd. Composé ayant une activité inhibitrice contre la mutation kras g12d
US20230174518A1 (en) 2020-04-24 2023-06-08 Taiho Pharmaceutical Co., Ltd. Kras g12d protein inhibitors
US20230181536A1 (en) 2020-04-24 2023-06-15 Taiho Pharmaceutical Co., Ltd. Anticancer combination therapy with n-(1-acryloyl-azetidin-3-yl)-2-((1h-indazol-3-yl)amino)methyl)-1h-imidazole-5-carboxamide inhibitor of kras-g12c
KR20230042600A (ko) 2020-06-18 2023-03-28 레볼루션 메디슨즈, 인크. Ras 억제제에 대한 획득된 저항성을 지연, 예방, 및 치료하는 방법
WO2022014640A1 (fr) 2020-07-15 2022-01-20 大鵬薬品工業株式会社 Combinaison contenant un composé pyrimidine destinée à être utilisée dans le traitement de tumeurs
KR20230081726A (ko) 2020-09-03 2023-06-07 레볼루션 메디슨즈, 인크. Shp2 돌연변이가 있는 악성 종양을 치료하기 위한 sos1 억제제의 용도
JP2023541916A (ja) 2020-09-15 2023-10-04 レボリューション メディシンズ インコーポレイテッド がんの治療における、ras阻害剤としてのインドール誘導体
EP4329750A1 (fr) * 2021-04-27 2024-03-06 Merck Sharp & Dohme LLC Inhibiteurs à petites molécules de mutant de kras g12c
CN117500811A (zh) 2021-05-05 2024-02-02 锐新医药公司 共价ras抑制剂及其用途
PE20240089A1 (es) 2021-05-05 2024-01-16 Revolution Medicines Inc Inhibidores de ras para el tratamiento del cancer
EP4334321A1 (fr) 2021-05-05 2024-03-13 Revolution Medicines, Inc. Inhibiteurs de ras
CN115340545A (zh) * 2021-05-14 2022-11-15 浙江海正药业股份有限公司 双环杂芳基类衍生物及其制备方法和用途
CN117769554A (zh) 2021-05-28 2024-03-26 大鹏药品工业株式会社 Kras突变蛋白的小分子抑制剂
AR127308A1 (es) 2021-10-08 2024-01-10 Revolution Medicines Inc Inhibidores ras
WO2023168036A1 (fr) 2022-03-04 2023-09-07 Eli Lilly And Company Procédé de traitement comprenant des inhibiteurs de kras g12c et des inhibiteurs de shp2
WO2023172940A1 (fr) 2022-03-08 2023-09-14 Revolution Medicines, Inc. Méthodes de traitement du cancer du poumon réfractaire immunitaire
WO2023240263A1 (fr) 2022-06-10 2023-12-14 Revolution Medicines, Inc. Inhibiteurs de ras macrocycliques

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EP1732541A4 (fr) 2004-04-07 2008-03-05 Takeda Pharmaceutical Composes cycliques
EP2316835A1 (fr) 2004-11-22 2011-05-04 Vertex Pharmceuticals Incorporated Pyrrolopyrazines et pyrazolopyrazines utilisable comme inhibiteurs de proteines-kinases
CN102311447B (zh) 2010-07-07 2013-11-27 中国科学院广州生物医药与健康研究院 杂环并嘧啶酮类dpp-iv抑制剂
WO2013063214A1 (fr) 2011-10-27 2013-05-02 Merck Sharp & Dohme Corp. Nouveaux composés qui sont des inhibiteurs d'erk
JO3517B1 (ar) 2014-01-17 2020-07-05 Novartis Ag ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2
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
EP3094629B1 (fr) 2014-01-17 2018-08-22 Novartis AG Dérivés de 1-(triazin-3-yl/pyridazin-3-yl)-piper(-azine)idine et compositions les contenant pour l'inhibition de l'activité de shp2
EP3310779B1 (fr) * 2015-06-19 2019-05-08 Novartis AG Composés et compositions pour l'inhibition de l'activité de shp2
ES2805232T3 (es) 2015-06-19 2021-02-11 Novartis Ag Compuestos y composiciones para inhibir la actividad de SHP2
JP6878316B2 (ja) 2015-06-19 2021-05-26 ノバルティス アーゲー Shp2の活性を阻害するための化合物および組成物
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WO2017156397A1 (fr) 2016-03-11 2017-09-14 Board Of Regents, The University Of Texas Sysytem Inhibiteurs hétérocycliques de ptpn11
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CN112250670B (zh) 2016-06-07 2021-06-08 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
PL3468972T3 (pl) 2016-06-14 2020-11-16 Novartis Ag Związki i kompozycje do hamowania aktywności shp2
US11529347B2 (en) 2016-09-22 2022-12-20 Relay Therapeutics, Inc. SHP2 phosphatase inhibitors and methods of use thereof
WO2018081091A1 (fr) 2016-10-24 2018-05-03 Relay Therapeutics, Inc. Dérivés de pyrazolo [3,4-b] pyrazine en tant qu'inhibiteurs de la phosphatase shp2
KR102571130B1 (ko) 2017-01-10 2023-08-28 노파르티스 아게 Alk 저해제 및 shp2 저해제를 포함하는 약제학적 조합
GB201706327D0 (en) 2017-04-20 2017-06-07 Otsuka Pharma Co Ltd A pharmaceutical compound
EP3630770A1 (fr) 2017-05-26 2020-04-08 Relay Therapeutics, Inc. Dérivés de pyrazolo[3,4-b]pyrazine en tant qu'inhibiteurs de la phosphatase shp2
KR20200051684A (ko) 2017-09-07 2020-05-13 레볼루션 메디슨즈, 인크. 암 치료를 위한 shp2 억제제 조성물 및 방법
MX2020006273A (es) 2017-12-15 2020-09-14 Revolution Medicines Inc Compuestos policiclicos como inhibidores alostericos de shp2.
WO2019165073A1 (fr) 2018-02-21 2019-08-29 Relay Therapeutics, Inc. Inhibiteurs de la protéine shp2 phosphatase et leurs procédés d'utilisation
CN111902415A (zh) 2018-03-02 2020-11-06 大冢制药株式会社 药学化合物
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
EP3768680A1 (fr) 2018-03-21 2021-01-27 Relay Therapeutics, Inc. Inhibiteurs de la phosphatase pyrazolo[3,4-b]pyrazine shp2 et leurs procédés d'utilisation
EP3787627A4 (fr) 2018-05-02 2021-12-01 Navire Pharma, Inc. Inhibiteurs hétérocycliques substitués de ptpn11
MX2021000795A (es) 2018-07-24 2021-04-12 Taiho Pharmaceutical Co Ltd Compuestos heterociclicos para inhibir la actividad de shp2.
IL305106A (en) 2018-09-29 2023-10-01 Novartis Ag A process for producing a compound to inhibit the activity of SHP2
CN112867718A (zh) 2018-09-29 2021-05-28 诺华股份有限公司 用于抑制shp2活性的化合物和组合物的制造
GB201911928D0 (en) 2019-08-20 2019-10-02 Otsuka Pharma Co Ltd Pharmaceutical compounds
WO2021149817A1 (fr) 2020-01-24 2021-07-29 Taiho Pharmaceutical Co., Ltd. Amélioration de l'activité anti-tumorale de la pyrimidinone inhibitrice de shp2 en association avec de nouveaux médicaments anti-cancéreux contre le cancer

Also Published As

Publication number Publication date
JP7326305B2 (ja) 2023-08-15
US11466016B2 (en) 2022-10-11
BR112020017283A2 (pt) 2020-12-15
JP2021514962A (ja) 2021-06-17
EP3759111A1 (fr) 2021-01-06
CN111902415A (zh) 2020-11-06
IL276232B2 (en) 2024-04-01
RU2020130228A (ru) 2022-04-04
ZA202004729B (en) 2024-02-28
TW202000667A (zh) 2020-01-01
MX2020008754A (es) 2020-12-07
AU2019226480A1 (en) 2020-08-27
IL276232A (en) 2020-09-30
WO2019167000A1 (fr) 2019-09-06
IL276232B1 (en) 2023-12-01
KR20200127005A (ko) 2020-11-09
AU2019226480B2 (en) 2022-12-15
SG11202006778TA (en) 2020-08-28
NZ766835A (en) 2023-09-29
PH12020551305A1 (en) 2021-10-25
CA3092011A1 (fr) 2019-09-06
US20210107908A1 (en) 2021-04-15

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