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)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (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 (18)

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)
RU (1) RU2020130228A (fr)
SG (1) SG11202006778TA (fr)
TW (1) TW202000667A (fr)
WO (1) WO2019167000A1 (fr)
ZA (1) ZA202004729B (fr)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
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US11466017B2 (en) 2011-03-10 2022-10-11 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of PTPN11
EP3463343B1 (fr) 2016-05-31 2022-03-23 Board of Regents, The University of Texas System Inhibiteurs hétérocycliques de ptpn11
EP3464272B1 (fr) 2016-06-07 2021-12-08 Jacobio Pharmaceuticals Co., Ltd. Nouveaux dérivés hétérocycliques utiles en tant qu'inhibiteurs de shp2
US11529347B2 (en) 2016-09-22 2022-12-20 Relay Therapeutics, Inc. SHP2 phosphatase inhibitors and methods of use thereof
TW201819386A (zh) 2016-10-24 2018-06-01 美商傳達治療有限公司 Shp2磷酸酶抑制劑及其使用方法
AU2018239542C1 (en) 2017-03-23 2021-02-11 Jacobio Pharmaceuticals Co., Ltd. Novel heterocyclic derivatives useful as SHP2 inhibitors
US11591336B2 (en) 2017-05-26 2023-02-28 D. E. Shaw Research, Llc Substituted pyrazolo[3,4-b]pyrazines as SHP2 phosphatase inhibitors
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
NZ766835A (en) 2018-03-02 2023-09-29 Otsuka Pharma Co Ltd Pharmaceutical compounds
CN112166110B (zh) 2018-03-21 2023-08-11 传达治疗有限公司 Shp2磷酸酶抑制剂及其使用方法
IL278297B2 (en) 2018-05-02 2023-12-01 Navire Pharma Inc Transmutable heterocyclic PTPN11 inhibitors
MX2021000795A (es) * 2018-07-24 2021-04-12 Taiho Pharmaceutical Co Ltd Compuestos heterociclicos para inhibir la actividad de shp2.
BR112021002327A2 (pt) 2018-08-10 2021-05-04 Navire Pharma, Inc. derivados de 6-(4-amino-3-metil-2-oxa-8-azaespiro[4,5]decan-8-il)-3-(2,3-diclorofenil)-2-metilpirimidin-4(3h)-ona e compostos relacionados como inibidores de ptpn11(shp2) para o tratamento do câncer
CA3113233A1 (fr) 2018-09-18 2020-03-26 Nikang Therapeutics, Inc. Derives d'anneaux tricycliques fusionnes utilises en tant qu'inhibiteurs de la phosphatase src a homologie-2
WO2020072656A1 (fr) 2018-10-03 2020-04-09 Gilead Sciences, Inc. Dérivés d'imidozopyrimidine
TW202116773A (zh) * 2019-07-04 2021-05-01 英屬開曼群島商百濟神州有限公司 作為HPK1抑制劑之吡咯并[2,3-b]吡及其用途
US20220402916A1 (en) 2019-09-18 2022-12-22 Merck Sharp & Dohme Corp. Small molecule inhibitors of kras g12c mutant
AU2020354475A1 (en) 2019-09-24 2022-05-05 Relay Therapeutics, Inc. SHP2 phosphatase inhibitors and methods of making and using the same
CR20220230A (es) 2019-10-28 2022-06-15 Merck Sharp & Dohme Inhibidores de pequeñas moléculas de mutante g12c de kras
WO2021085653A1 (fr) 2019-10-31 2021-05-06 Taiho Pharmaceutical Co., Ltd. Dérivés de 4-aminobut-2-enamide et sels de ces derniers
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
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
US20230174518A1 (en) 2020-04-24 2023-06-08 Taiho Pharmaceutical Co., Ltd. Kras g12d protein inhibitors
IL299131A (en) 2020-06-18 2023-02-01 Revolution Medicines Inc Methods for delaying, preventing and treating acquired resistance to RAS inhibitors
EP4183395A1 (fr) 2020-07-15 2023-05-24 Taiho Pharmaceutical Co., Ltd. Combinaison contenant un composé pyrimidine destinée à être utilisée dans le traitement de tumeurs
WO2022060583A1 (fr) 2020-09-03 2022-03-24 Revolution Medicines, Inc. Utilisation d'inhibiteurs de sos1 pour traiter des malignités à mutations de shp2
US11690915B2 (en) 2020-09-15 2023-07-04 Revolution Medicines, Inc. Ras inhibitors
WO2022232320A1 (fr) * 2021-04-27 2022-11-03 Merck Sharp & Dohme Corp. Inhibiteurs à petites molécules de mutant de kras g12c
AR125782A1 (es) 2021-05-05 2023-08-16 Revolution Medicines Inc Inhibidores de ras
JP2024516450A (ja) 2021-05-05 2024-04-15 レボリューション メディシンズ インコーポレイテッド 共有結合性ras阻害剤及びその使用
WO2022235870A1 (fr) 2021-05-05 2022-11-10 Revolution Medicines, Inc. Inhibiteurs de ras pour le traitement du cancer
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
WO2022250170A1 (fr) 2021-05-28 2022-12-01 Taiho Pharmaceutical Co., Ltd. Petites molécules inhibitrices de protéines mutées par kras
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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WO2005099688A2 (fr) 2004-04-07 2005-10-27 Takeda Pharmaceutical Company Limited Composes cycliques
RU2394825C2 (ru) 2004-11-22 2010-07-20 Вертекс Фармасьютикалз Инкорпорейтед Пирролопиразины, пригодные в качестве ингибиторов киназы аврора а
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
CN105899491B (zh) 2014-01-17 2019-04-02 诺华股份有限公司 用于抑制shp2活性的1-哒嗪-/三嗪-3-基-哌(-嗪)/啶/吡咯烷衍生物及其组合物
JO3517B1 (ar) 2014-01-17 2020-07-05 Novartis Ag ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2
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
US10287266B2 (en) 2015-06-19 2019-05-14 Novartis Ag Compounds and compositions for inhibiting the activity of 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
WO2016203404A1 (fr) * 2015-06-19 2016-12-22 Novartis Ag Composés et compositions pour inhiber l'activité de shp2
CN107709327A (zh) 2015-06-22 2018-02-16 小野药品工业株式会社 Brk抑制性化合物
WO2017156397A1 (fr) 2016-03-11 2017-09-14 Board Of Regents, The University Of Texas Sysytem Inhibiteurs hétérocycliques de ptpn11
EP3463343B1 (fr) * 2016-05-31 2022-03-23 Board of Regents, The University of Texas System Inhibiteurs hétérocycliques de ptpn11
EP3464272B1 (fr) 2016-06-07 2021-12-08 Jacobio Pharmaceuticals Co., Ltd. Nouveaux dérivés hétérocycliques utiles en tant qu'inhibiteurs de shp2
WO2017216706A1 (fr) 2016-06-14 2017-12-21 Novartis Ag Composés et compositions pour l'inhibition de l'activité de shp2
US11529347B2 (en) 2016-09-22 2022-12-20 Relay Therapeutics, Inc. SHP2 phosphatase inhibitors and methods of use thereof
TW201819386A (zh) 2016-10-24 2018-06-01 美商傳達治療有限公司 Shp2磷酸酶抑制劑及其使用方法
ES2964956T3 (es) 2017-01-10 2024-04-10 Novartis Ag Combinación farmacéutica que comprende un inhibidor de ALK y un inhibidor de SHP2
GB201706327D0 (en) 2017-04-20 2017-06-07 Otsuka Pharma Co Ltd A pharmaceutical compound
US11591336B2 (en) 2017-05-26 2023-02-28 D. E. Shaw Research, Llc Substituted pyrazolo[3,4-b]pyrazines as SHP2 phosphatase inhibitors
CA3074690A1 (fr) 2017-09-07 2019-03-14 Revolution Medicines, Inc. Compositions d'inhibiteur de la shp2 et methodes de traitement du cancer
KR20200099530A (ko) 2017-12-15 2020-08-24 레볼루션 메디슨즈, 인크. 알로스테릭 shp2 억제제로서의 다환식 화합물
EP3755699A1 (fr) 2018-02-21 2020-12-30 Relay Therapeutics, Inc. Inhibiteurs de la protéine shp2 phosphatase et leurs procédés d'utilisation
NZ766835A (en) 2018-03-02 2023-09-29 Otsuka Pharma Co Ltd Pharmaceutical compounds
CN112368272B (zh) 2018-03-21 2023-04-21 苏州浦合医药科技有限公司 Shp2抑制剂及其用途
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
IL278297B2 (en) 2018-05-02 2023-12-01 Navire Pharma Inc Transmutable heterocyclic PTPN11 inhibitors
MX2021000795A (es) 2018-07-24 2021-04-12 Taiho Pharmaceutical Co Ltd Compuestos heterociclicos para inhibir la actividad de shp2.
EP3856345A1 (fr) 2018-09-29 2021-08-04 Novartis AG Procédé de fabrication d'un composé pour inhiber l'activité de shp2
CA3112322A1 (fr) 2018-09-29 2020-04-02 Novartis Ag Fabrication de composes et de compositions pour inhiber l'activite de shp2
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
PH12020551305A1 (en) 2021-10-25
TW202000667A (zh) 2020-01-01
AU2019226480A1 (en) 2020-08-27
US11466016B2 (en) 2022-10-11
RU2020130228A (ru) 2022-04-04
CA3092011A1 (fr) 2019-09-06
KR20200127005A (ko) 2020-11-09
WO2019167000A1 (fr) 2019-09-06
IL276232B1 (en) 2023-12-01
JP7326305B2 (ja) 2023-08-15
MX2020008754A (es) 2020-12-07
EP3759111A1 (fr) 2021-01-06
IL276232B2 (en) 2024-04-01
AU2019226480B2 (en) 2022-12-15
JP2021514962A (ja) 2021-06-17
IL276232A (en) 2020-09-30
US20210107908A1 (en) 2021-04-15
BR112020017283A2 (pt) 2020-12-15
ZA202004729B (en) 2024-02-28
CN111902415A (zh) 2020-11-06
SG11202006778TA (en) 2020-08-28
NZ766835A (en) 2023-09-29

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