MA43032A - Inhibiteurs isoindolinone de l'interaction mdm2-p53 ayant une activité anticancéreuse - Google Patents

Inhibiteurs isoindolinone de l'interaction mdm2-p53 ayant une activité anticancéreuse

Info

Publication number
MA43032A
MA43032A MA043032A MA43032A MA43032A MA 43032 A MA43032 A MA 43032A MA 043032 A MA043032 A MA 043032A MA 43032 A MA43032 A MA 43032A MA 43032 A MA43032 A MA 43032A
Authority
MA
Morocco
Prior art keywords
mdm2
interaction
cancer activity
isoindolinone
inhibitors
Prior art date
Application number
MA043032A
Other languages
English (en)
Inventor
Ildiko Maria Buck
Celine Florence Cano
Gianni Chessari
Benjamin David Cons
Sarah Cully
Bernard Thomas Golding
Roger John Griffin
Ian Robert Hardcastle
Kim Louise Hirst
Rhian Sara Holvey
Steven Howard
Christopher Norbert Johnson
Arwel Lewis
Duncan Charles Miller
Dale Robert Mitchell
Martin Edward Mäntylä Noble
James Daniel Osborne
Joanne Peach
David Charles Rees
Denis Jeffrey David St
Emiliano Tamanini
David Wyn Watson
Benjamin Paul Whittaker
Original Assignee
Astex Therapeutics Ltd
Cancer Research Tech 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
Application filed by Astex Therapeutics Ltd, Cancer Research Tech Ltd filed Critical Astex Therapeutics Ltd
Publication of MA43032A publication Critical patent/MA43032A/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/4035Isoindoles, e.g. phthalimide
    • 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
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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 two hetero rings
    • C07D405/06Heterocyclic 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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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 two hetero rings
    • C07D405/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0803Compounds with Si-C or Si-Si linkages
    • C07F7/081Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/553Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
    • C07F9/572Five-membered rings
    • C07F9/5728Five-membered rings condensed with carbocyclic rings or carbocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05Isotopically modified compounds, e.g. labelled

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
MA043032A 2015-09-29 2016-09-29 Inhibiteurs isoindolinone de l'interaction mdm2-p53 ayant une activité anticancéreuse MA43032A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB1517217.4A GB201517217D0 (en) 2015-09-29 2015-09-29 Pharmaceutical compounds

Publications (1)

Publication Number Publication Date
MA43032A true MA43032A (fr) 2018-08-08

Family

ID=54544291

Family Applications (1)

Application Number Title Priority Date Filing Date
MA043032A MA43032A (fr) 2015-09-29 2016-09-29 Inhibiteurs isoindolinone de l'interaction mdm2-p53 ayant une activité anticancéreuse

Country Status (27)

Country Link
US (3) US10544132B2 (fr)
EP (2) EP3356350B1 (fr)
JP (2) JP7029387B2 (fr)
KR (1) KR20180081706A (fr)
CN (2) CN108290871B (fr)
AU (2) AU2016330030C1 (fr)
BR (1) BR112018005932B1 (fr)
CA (1) CA2999400A1 (fr)
DK (1) DK3356350T3 (fr)
ES (1) ES2934181T3 (fr)
FI (1) FI3356350T3 (fr)
GB (1) GB201517217D0 (fr)
HK (1) HK1250715A1 (fr)
HR (1) HRP20221487T1 (fr)
HU (1) HUE060638T2 (fr)
IL (1) IL258213B (fr)
LT (1) LT3356350T (fr)
MA (1) MA43032A (fr)
MX (1) MX2018004008A (fr)
PH (1) PH12018500610A1 (fr)
PL (1) PL3356350T3 (fr)
PT (1) PT3356350T (fr)
SA (1) SA518391218B1 (fr)
SG (1) SG10201912833XA (fr)
SI (1) SI3356350T1 (fr)
TW (1) TWI761315B (fr)
WO (1) WO2017055860A1 (fr)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0811643D0 (en) 2008-06-25 2008-07-30 Cancer Rec Tech Ltd New therapeutic agents
GB201517217D0 (en) 2015-09-29 2015-11-11 Astex Therapeutics Ltd And Cancer Res Technology Ltd Pharmaceutical compounds
GB201517216D0 (en) 2015-09-29 2015-11-11 Cancer Res Technology Ltd And Astex Therapeutics Ltd Pharmaceutical compounds
US10925880B2 (en) * 2016-09-23 2021-02-23 Bayer Pharma Aktiengesellschaft Combination of PI3K-inhibitors
GB201704965D0 (en) 2017-03-28 2017-05-10 Astex Therapeutics Ltd Pharmaceutical compounds
GB201704966D0 (en) 2017-03-28 2017-05-10 Astex Therapeutics Ltd Pharmaceutical compounds
CN107118183B (zh) * 2017-05-17 2021-02-02 成都化润药业有限公司 一种四氢-3-呋喃甲醇的合成方法
WO2019061324A1 (fr) 2017-09-29 2019-04-04 Curis Inc. Formes cristallines d'immunomodulateurs
WO2019073399A1 (fr) * 2017-10-11 2019-04-18 Aurigene Discovery Technologies Limited Formes cristallines de 1,2,4-oxadiazole à substitution en position 3
US11497735B2 (en) 2017-11-06 2022-11-15 Aurigene Discovery Technologies Limited Conjoint therapies for immunomodulation
CN111868088A (zh) * 2018-03-20 2020-10-30 诺华股份有限公司 药物组合
CN110194760B (zh) * 2019-05-27 2021-08-17 浙江农林大学暨阳学院 制备3-亚苄基-2-(7’-喹啉)-2,3-二氢-异吲哚-1-酮类化合物的方法
JP2022534650A (ja) * 2019-05-31 2022-08-03 海思科医▲薬▼有限公司 Btk阻害薬環誘導体、その調製方法及びその医薬品適用
GB201919219D0 (en) 2019-12-23 2020-02-05 Otsuka Pharma Co Ltd Cancer biomarkers
JP7508584B2 (ja) * 2020-04-29 2024-07-01 リレー セラピューティクス, インコーポレイテッド PI3Kα阻害剤およびそれらの使用
CN116194088A (zh) 2020-08-27 2023-05-30 大冢制药株式会社 使用mdm2拮抗剂治疗癌症的生物标志物
GB202103080D0 (en) 2021-03-04 2021-04-21 Otsuka Pharma Co Ltd Cancer biomarkers
CN118302427A (zh) * 2021-12-02 2024-07-05 上海翰森生物医药科技有限公司 稠环类衍生物调节剂、其制备方法和应用

Family Cites Families (74)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH374071A (de) 1959-04-30 1963-12-31 Geigy Ag J R Verfahren zur Herstellung von neuen Isoindolinderivaten
US3466298A (en) 1967-03-14 1969-09-09 American Home Prod Process for the preparation of 2-(2-aminoethyl)isoindolines
US3763178A (en) 1968-09-05 1973-10-02 American Home Prod Imidazolinyl phenyl carbonyl acid addition salts and related compounds
GB1325065A (en) 1970-02-12 1973-08-01 American Home Prod Imidazoline derivatives
AR203991A1 (es) 1972-03-16 1975-11-12 Rhone Poulenc Sa Procedimiento para preparar derivados de(hidroxi-2-amino-3-propoxi)-3-isoindolinona-1
FR2217000B1 (fr) 1973-02-08 1976-04-09 Rhone Poulenc Ind
GB1601701A (en) 1977-07-22 1981-11-04 Delmar Chem Production of heterocyclic benzamide compounds
US4200759A (en) 1978-07-20 1980-04-29 Delmar Chemicals, Limited Preparation of imidazo[2,1-a]isoindole compounds
US4244966A (en) 1979-09-24 1981-01-13 American Home Products Corporation 1,3-Dihydro-3-(2-hydroxy-, 2-bromo- or 2-chloroethyl)-2H-isoindol-1-one derivatives
US4312809A (en) 1980-10-31 1982-01-26 E. R. Squibb & Sons, Inc. Lactam derivatives of mercaptoacylamino acids
US4331600A (en) 1980-10-31 1982-05-25 Usv Pharmaceutical Corporation Intermediates for the synthesis of phthalimidines
FR2533563A1 (fr) 1982-09-23 1984-03-30 Adir Nouveaux derives de la sulfonyluree, leurs procedes de preparation et les compositions pharmaceutiques les renfermant
US4666828A (en) 1984-08-15 1987-05-19 The General Hospital Corporation Test for Huntington's disease
US4683202A (en) 1985-03-28 1987-07-28 Cetus Corporation Process for amplifying nucleic acid sequences
US4801531A (en) 1985-04-17 1989-01-31 Biotechnology Research Partners, Ltd. Apo AI/CIII genomic polymorphisms predictive of atherosclerosis
US5272057A (en) 1988-10-14 1993-12-21 Georgetown University Method of detecting a predisposition to cancer by the use of restriction fragment length polymorphism of the gene for human poly (ADP-ribose) polymerase
US5192659A (en) 1989-08-25 1993-03-09 Genetype Ag Intron sequence analysis method for detection of adjacent and remote locus alleles as haplotypes
HU212435B (en) 1990-06-07 1996-06-28 Sandoz Ag Herbicidal compositions containing substituted phthalides and heterocyclic phthalides as active ingredient and process for preparation of their active ingredients.
CA2262403C (fr) 1995-07-31 2011-09-20 Urocor, Inc. Biomarqueurs et cibles de diagnostic, de pronostic et de traitement du cancer de la prostate
US6218529B1 (en) 1995-07-31 2001-04-17 Urocor, Inc. Biomarkers and targets for diagnosis, prognosis and management of prostate, breast and bladder cancer
TW448172B (en) 1996-03-08 2001-08-01 Pharmacia & Upjohn Co Llc Novel hydroxamic acid derivatives useful for the treatment of diseases related to connective tissue degradation
DE19807423A1 (de) 1998-02-21 1999-08-26 Hoechst Marion Roussel De Gmbh Subustituierte Isoindolone, ihre Herstellung und ihre Verwendung in Arzneimitteln
DE60024631T2 (de) 1999-07-26 2006-06-14 Banyu Pharma Co Ltd Biaryl-harnstoff-derivate
WO2001032928A2 (fr) 1999-11-05 2001-05-10 Phase-1 Molecular Toxicology Methodes permettant de determiner une hypersensibilite a un agent
DE10134482A1 (de) 2001-07-16 2003-01-30 Bayer Ag Substituierte Isoindole und ihre Verwendung
JP4477351B2 (ja) 2001-12-18 2010-06-09 エフ.ホフマン−ラ ロシュ アーゲー シス−2,4,5−トリフェニル−イミダゾリン類及び腫瘍の処理へのそれらの使用
FR2840302B1 (fr) 2002-06-03 2004-07-16 Aventis Pharma Sa Derives d'isoindolones, procede de preparation et intermediaire de ce procede a titre de medicaments et compositions pharmaceutiques les renfermant
US7521451B2 (en) 2002-11-26 2009-04-21 Maruishi Pharmaceutical Co., Ltd. Isoindoline derivative
JP2004217591A (ja) 2003-01-16 2004-08-05 Dai Ichi Seiyaku Co Ltd シス選択的フルオロシクロプロパン誘導体の製造方法
US7320992B2 (en) 2003-08-25 2008-01-22 Amgen Inc. Substituted 2,3-dihydro-1h-isoindol-1-one derivatives and methods of use
JP2005255660A (ja) 2004-03-10 2005-09-22 Katsuhiko Tomooka 多官能基を有するラクタム類とその製法
JPWO2005095341A1 (ja) 2004-03-30 2007-08-16 協和醗酵工業株式会社 含窒素複素環化合物
TW200613272A (en) 2004-08-13 2006-05-01 Astrazeneca Ab Isoindolone compounds and their use as metabotropic glutamate receptor potentiators
GB0419481D0 (en) 2004-09-02 2004-10-06 Cancer Rec Tech Ltd Isoindolin-1-one derivatives
CA2752738C (fr) 2005-02-22 2014-05-27 The Regents Of The University Of Michigan Inhibiteurs de mdm2, sous forme de petites molecules et utilisations de ces derniers
US7705021B2 (en) 2005-05-02 2010-04-27 Fox Chase Cancer Center Isoindolone compounds, compositions containing the same, and methods of use thereof for the treatment of viral infections related to the etiology of cancer
WO2007021309A1 (fr) 2005-08-12 2007-02-22 Astrazeneca Ab Isoindolones substitués et leur utilisation comme potentiateurs métabotropiques du récepteur glutamate
US7727978B2 (en) 2006-08-24 2010-06-01 Bristol-Myers Squibb Company Cyclic 11-beta hydroxysteroid dehydrogenase type I inhibitors
EP2108642A1 (fr) * 2006-10-17 2009-10-14 Kyowa Hakko Kirin Co., Ltd. Inhibiteurs de jak
GB0706072D0 (en) 2007-03-28 2007-05-09 Sterix Ltd Compound
MX2009013169A (es) 2007-06-03 2010-04-30 Univ Vanderbilt Moduladores alostericos positivos del mglur5 benzamida y metodos de elaboracion y uso de los mismos.
US20090156735A1 (en) * 2007-12-14 2009-06-18 General Electric Company Composition, article, and associated method
GB0811643D0 (en) 2008-06-25 2008-07-30 Cancer Rec Tech Ltd New therapeutic agents
DE102008031517A1 (de) 2008-07-03 2010-01-07 Merck Patent Gmbh Pyrrolopyridinyl-pyrimidin-2-yl-amin-derivate
EP2340021B1 (fr) 2008-09-18 2012-11-07 F. Hoffmann-La Roche AG Pyrrolidine-2-carboxamides substitués
US8354444B2 (en) 2008-09-18 2013-01-15 Hoffmann-La Roche Inc. Substituted pyrrolidine-2-carboxamides
FR2944282B1 (fr) * 2009-04-09 2013-05-03 Sanofi Aventis Derives de quinazolinedione, leur preparation et leurs diverses applications therapeutiques
CA2780547C (fr) 2009-11-12 2015-02-03 The Regents Of The University Of Michigan Antagonistes, de type spiro-oxindole, de l'oncoproteine mdm2
US8440693B2 (en) 2009-12-22 2013-05-14 Novartis Ag Substituted isoquinolinones and quinazolinones
JO2998B1 (ar) 2010-06-04 2016-09-05 Amgen Inc مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان
SG193002A1 (en) 2011-03-10 2013-09-30 Daiichi Sankyo Co Ltd Dispiropyrrolidine derivative
EP2721007B1 (fr) 2011-06-20 2015-04-29 Novartis AG Composés de cyclohexyl-isoquinolinone
WO2012175520A1 (fr) 2011-06-20 2012-12-27 Novartis Ag Dérivés d'isoquinolinone substitués par un hydroxy
JO3357B1 (ar) 2012-01-26 2019-03-13 Novartis Ag مركبات إيميدازوبيروليدينون
KR101401705B1 (ko) 2012-01-31 2014-06-27 울산대학교 산학협력단 로듐 촉매를 이용한 이소인돌린 유도체의 합성방법
US9365512B2 (en) 2012-02-13 2016-06-14 AbbVie Deutschland GmbH & Co. KG Isoindoline derivatives, pharmaceutical compositions containing them, and their use in therapy
EP2838898B1 (fr) * 2012-04-20 2017-01-18 Advinus Therapeutics Limited Composés hétéro-bicycliques substitués, compositions et leurs applications médicinales
RS60122B1 (sr) 2012-10-30 2020-05-29 Mei Pharma Inc Kombinovane terapije za lečenje hemorezistentnih kancera
BR112015031542A2 (pt) 2013-07-03 2017-07-25 Hoffmann La Roche métodos de previsão de reação de pacientes com câncer, método de tratamento de câncer, kit de previsão da reação ao tratamento e processos, métodos e usos inovadores
EP3094746A1 (fr) 2014-01-14 2016-11-23 Daiichi Sankyo Company, Limited Signatures géniques associées à la sensibilité aux inhibiteurs de mdm2
AU2015247646B2 (en) 2014-04-17 2019-06-06 The Regents Of The University Of Michigan MDM2 inhibitors and therapeutic methods using the same
EP3204514A1 (fr) 2014-10-09 2017-08-16 Daiichi Sankyo Co., Ltd. Algorithmes pour prédicteur basé sur des signatures géniques prédisant la sensibilité aux inhibiteurs de mdm2
EP3206697A2 (fr) 2014-10-17 2017-08-23 Biomirna Holdings Ltd. Produits diagnostiques et thérapeutiques pour le cancer du poumon avec mir-660
GB201517216D0 (en) 2015-09-29 2015-11-11 Cancer Res Technology Ltd And Astex Therapeutics Ltd Pharmaceutical compounds
GB201517217D0 (en) * 2015-09-29 2015-11-11 Astex Therapeutics Ltd And Cancer Res Technology Ltd Pharmaceutical compounds
MA47013A (fr) 2015-10-21 2018-08-29 Otsuka Pharma Co Ltd Composés benzolactames utilisés en tant qu'inhibiteurs de protéine kinase
TWI734715B (zh) 2015-11-19 2021-08-01 美商卡默森屈有限公司 趨化因子受體調節劑
GB201704966D0 (en) 2017-03-28 2017-05-10 Astex Therapeutics Ltd Pharmaceutical compounds
GB201704965D0 (en) 2017-03-28 2017-05-10 Astex Therapeutics Ltd Pharmaceutical compounds
US11339448B2 (en) 2018-07-27 2022-05-24 Ottawa Hospital Research Institute Treatment of acute myeloid leukemia
WO2020169073A1 (fr) 2019-02-24 2020-08-27 Ascentage Pharma (Suzhou) Co., Ltd. Méthodes de traitement et biomarqueurs pour des inhibiteurs de mdm2
GB201919219D0 (en) 2019-12-23 2020-02-05 Otsuka Pharma Co Ltd Cancer biomarkers
CN116194088A (zh) 2020-08-27 2023-05-30 大冢制药株式会社 使用mdm2拮抗剂治疗癌症的生物标志物
GB202103080D0 (en) 2021-03-04 2021-04-21 Otsuka Pharma Co Ltd Cancer biomarkers

Also Published As

Publication number Publication date
EP3356350B1 (fr) 2022-11-16
PL3356350T3 (pl) 2023-01-23
GB201517217D0 (en) 2015-11-11
HK1250715A1 (zh) 2019-01-11
JP2022070998A (ja) 2022-05-13
EP3356350A1 (fr) 2018-08-08
US10981898B2 (en) 2021-04-20
AU2021202962A1 (en) 2021-06-03
JP7029387B2 (ja) 2022-03-03
CN108290871B (zh) 2022-08-23
EP4151633A1 (fr) 2023-03-22
BR112018005932A2 (pt) 2018-10-09
NZ740737A (en) 2021-10-29
US20190016708A1 (en) 2019-01-17
AU2016330030B2 (en) 2021-02-18
BR112018005932B1 (pt) 2023-11-28
LT3356350T (lt) 2023-01-10
ES2934181T3 (es) 2023-02-17
SI3356350T1 (sl) 2023-03-31
US20200079761A1 (en) 2020-03-12
AU2016330030A1 (en) 2018-04-12
AU2021202962B2 (en) 2023-01-12
HUE060638T2 (hu) 2023-04-28
AU2016330030C1 (en) 2022-03-10
CA2999400A1 (fr) 2017-04-06
IL258213A (en) 2018-05-31
WO2017055860A1 (fr) 2017-04-06
KR20180081706A (ko) 2018-07-17
DK3356350T3 (da) 2022-12-19
US20210276984A1 (en) 2021-09-09
PT3356350T (pt) 2022-12-27
MX2018004008A (es) 2018-11-09
CN115572252A (zh) 2023-01-06
SG10201912833XA (en) 2020-02-27
FI3356350T3 (fi) 2023-01-13
US10544132B2 (en) 2020-01-28
US20200247789A2 (en) 2020-08-06
PH12018500610A1 (en) 2018-09-24
HRP20221487T1 (hr) 2023-02-03
CN108290871A (zh) 2018-07-17
US12071429B2 (en) 2024-08-27
TW201722914A (zh) 2017-07-01
AU2021202962C1 (en) 2023-08-10
JP2018534253A (ja) 2018-11-22
IL258213B (en) 2021-10-31
TWI761315B (zh) 2022-04-21
SA518391218B1 (ar) 2022-12-22

Similar Documents

Publication Publication Date Title
MA43032A (fr) Inhibiteurs isoindolinone de l'interaction mdm2-p53 ayant une activité anticancéreuse
MA43031A (fr) Inhibiteurs d'isoindolinone de l'interaction mdm2-p53 ayant une activité anticancéreuse
IL283267B (en) Inhibitors of menin–mll interaction
IL259560A (en) Inhibitors of the menin-mll interaction
PL3512850T3 (pl) Inhibitory interakcji menina-mll
MA42924A (fr) Variants optimisés d'anticorps anti-vegf
MA46228A (fr) Inhibiteurs bicycliques fusionnés de l'interaction ménine-mll
DK3240773T3 (da) Picolinamidforbindelser med fungicid aktivitet
DK3145420T3 (da) Intraoperativ fremgangsmåde til tracking
DK3377484T3 (da) Fremgangsmåder til behandling af multipel sklerose under anvendelse af pyrimidin- og pyridinforbindelser med btk- inhiberende aktivitet
FR3025517B1 (fr) Ligands potentialisants de la bioactivite des gonadotrophines
CL2016000616A1 (es) Compuestos heterocíclicos de n-acilimino.
DK3253749T3 (da) Forbindelser med antitumoraktivitet
FR3030715B1 (fr) Etui d'allumeur
DK3484852T3 (da) Benzo-n-hydroxyamidforbindelser med antitumor-aktivitet
FR3033711B3 (fr) Structure d'assemblage pour piste-jouet
DK3335729T3 (da) Etanercept-sammensætning med forbedret stabilitet
ITUB20152292A1 (it) Accorgimenti per incastonare pietre e solitari.
ITUB201558643U1 (it) Struttura di portaugello.
GB201510017D0 (en) Activity assay
TH1501007139A (th) สารประกอบ 3,4-ไดไฮโดรไอโซควิโนลิน-2(1h)-อิล
TH1401006042A (th) rTMS ที่ฮาร์มอนิกของสัญญาณทางชีวภาพ
TH144620B (th) โครงสร้างของที่กันเเดด
TH144615B (th) โครงสร้างของที่บังเเดด
TH1501006763B (th) โครงสร้างเซคชั่นด้านหลังของตัวถังยานพาหนะ