MA40225A - Composés dihydroisoquinolinone substitués - Google Patents

Composés dihydroisoquinolinone substitués

Info

Publication number
MA40225A
MA40225A MA040225A MA40225A MA40225A MA 40225 A MA40225 A MA 40225A MA 040225 A MA040225 A MA 040225A MA 40225 A MA40225 A MA 40225A MA 40225 A MA40225 A MA 40225A
Authority
MA
Morocco
Prior art keywords
compounds
salts
well
substituted
substituted dihydroisoquinolinone
Prior art date
Application number
MA040225A
Other languages
English (en)
Other versions
MA40225B1 (fr
Inventor
Michael Raymond Collins
Robert Steven Kania
Robert Arnold Kumpf
Pei-Pei Kung
Daniel Tyler Richter
Scott Channing Sutton
Martin James Wythes
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of MA40225A publication Critical patent/MA40225A/fr
Publication of MA40225B1 publication Critical patent/MA40225B1/fr

Links

Classifications

    • 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
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B59/00Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
    • C07B59/002Heterocyclic compounds
    • 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
    • C07D401/14Heterocyclic 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
    • 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
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms 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
    • C07D413/14Heterocyclic 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
    • 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

Abstract

La présente invention concerne des composés de formule générale (i) dans laquelle r1, r2, r3, r4, l, x et z sont tels que définis ici, ainsi que leurs sels pharmaceutiquement acceptables, des compositions pharmaceutiques comprenant ces composés et sels, ainsi que des procédés d'utiliser de tels composés, sels et compositions pour le traitement de la croissance cellulaire anormale, y compris le cancer.
MA40225A 2014-06-17 2015-06-05 Composés dihydroisoquinolinone substitués MA40225B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201462013410P 2014-06-17 2014-06-17
US201562156533P 2015-05-04 2015-05-04
EP15730290.2A EP3157915B1 (fr) 2014-06-17 2015-06-05 Composés dihydroisoquinolinone substitués
PCT/IB2015/054272 WO2015193765A1 (fr) 2014-06-17 2015-06-05 Composés dihydroisoquinolinone substitués

Publications (2)

Publication Number Publication Date
MA40225A true MA40225A (fr) 2019-02-27
MA40225B1 MA40225B1 (fr) 2019-05-31

Family

ID=53434412

Family Applications (1)

Application Number Title Priority Date Filing Date
MA40225A MA40225B1 (fr) 2014-06-17 2015-06-05 Composés dihydroisoquinolinone substitués

Country Status (40)

Country Link
US (4) US9481666B2 (fr)
EP (2) EP3521285A1 (fr)
JP (1) JP6152495B1 (fr)
KR (1) KR101877187B1 (fr)
CN (1) CN107207464B (fr)
AP (1) AP2016009605A0 (fr)
AU (1) AU2015275826B2 (fr)
BR (1) BR112016029612B1 (fr)
CA (1) CA2894298C (fr)
CL (1) CL2016003246A1 (fr)
CR (2) CR20200484A (fr)
CU (1) CU24408B1 (fr)
CY (1) CY1121706T1 (fr)
DK (1) DK3157915T3 (fr)
EA (1) EA031892B1 (fr)
ES (1) ES2721031T3 (fr)
GE (1) GEP20186933B (fr)
HR (1) HRP20190604T1 (fr)
HU (1) HUE042964T2 (fr)
IL (1) IL248991B (fr)
LT (1) LT3157915T (fr)
MA (1) MA40225B1 (fr)
MD (1) MD4820C1 (fr)
ME (1) ME03419B (fr)
MX (1) MX2016016764A (fr)
MY (1) MY185765A (fr)
NZ (1) NZ726108A (fr)
PE (1) PE20161552A1 (fr)
PH (1) PH12016502378A1 (fr)
PL (1) PL3157915T3 (fr)
PT (1) PT3157915T (fr)
RS (1) RS58632B1 (fr)
SG (1) SG11201609386YA (fr)
SI (1) SI3157915T1 (fr)
SV (1) SV2016005333A (fr)
TN (1) TN2016000529A1 (fr)
TW (1) TWI561516B (fr)
UA (1) UA118380C2 (fr)
UY (1) UY36170A (fr)
WO (1) WO2015193765A1 (fr)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA111305C2 (uk) 2012-12-21 2016-04-11 Пфайзер Інк. Конденсовані лактами арилу та гетероарилу
MY185765A (en) 2014-06-17 2021-06-06 Pfizer Substituted dihydroisoquinolinone compounds
TW201708210A (zh) * 2015-06-30 2017-03-01 葛蘭素史克智慧財產(第二)有限公司 Zeste同源物2增強子之抑制劑
TW201718598A (zh) 2015-08-27 2017-06-01 美國禮來大藥廠 Ezh2抑制劑
AU2017260854B2 (en) 2016-05-05 2020-01-30 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of Zeste Homolog 2 inhibitors
US10266542B2 (en) 2017-03-15 2019-04-23 Mirati Therapeutics, Inc. EZH2 inhibitors
EP3655392A1 (fr) 2017-07-17 2020-05-27 Abbvie Deutschland GmbH & Co. KG Composés de quinoléine à substitution en positions 1, 2, 3 et 4 utilisés en tant que modulateurs de s1p
BR112020008325A2 (pt) * 2017-11-14 2020-10-20 Pfizer Inc. terapias de combinação com o inibidor de ezh2
KR102451529B1 (ko) 2018-01-31 2022-10-06 미라티 테라퓨틱스, 인크. Prc2 억제제
AU2019255310B2 (en) 2018-04-18 2022-11-24 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
US11919912B2 (en) 2018-05-21 2024-03-05 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
JP2021531340A (ja) 2018-07-09 2021-11-18 フォンダシヨン、アジール、デ、アブグルスFondation Asile Des Aveugles 眼障害を治療するためのprc2サブユニットの阻害
WO2020086857A1 (fr) * 2018-10-24 2020-04-30 Vanderbilt University Modulateurs et inhibiteurs de wdr5
KR20200101219A (ko) * 2019-02-19 2020-08-27 한미약품 주식회사 신규한 헤테로트리시클릭 유도체 화합물 및 이의 용도
WO2022018594A1 (fr) 2020-07-20 2022-01-27 Pfizer Inc. Synthèse de nouveaux intermédiaires pour 3,4-dihydroisoquinolinones substituées
WO2022122037A1 (fr) * 2020-12-11 2022-06-16 上海奕拓医药科技有限责任公司 Dérivé de dihydroisoquinolinone et son application
WO2023098880A1 (fr) * 2021-12-02 2023-06-08 上海翰森生物医药科技有限公司 Dérivé de cycle fusionné, son procédé de préparation et son application
WO2023111810A1 (fr) 2021-12-14 2023-06-22 Pfizer Inc. Polythérapies et leurs utilisations pour le traitement du cancer

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3846412A (en) 1971-03-18 1974-11-05 Lepetit Spa Dihydro-2-amino-isoquinolines and their derivatives
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
GB9518953D0 (en) 1995-09-15 1995-11-15 Pfizer Ltd Pharmaceutical formulations
WO2000035298A1 (fr) 1996-11-27 2000-06-22 Wm. Wrigley Jr. Company Chewing-gum contenant des agents medicamenteux actifs
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
FR2889526B1 (fr) 2005-08-04 2012-02-17 Aventis Pharma Sa 7-aza-indazoles substitues, compositions les contenant, procede de fabrication et utilisation
US20070093515A1 (en) 2005-08-16 2007-04-26 Arrington Mark P Phosphodiesterase 10 inhibitors
WO2007075783A2 (fr) * 2005-12-22 2007-07-05 Wyeth Isoquinoline-1,3(2h,4h)-diones, 1-thioxo-1,4-dihydro-2h-isoquinoline-3-ones et 1,4-dihydro-3(2h)-isoquinolones et procedes d'utilisation correspondant
US20100113415A1 (en) 2008-05-29 2010-05-06 Rajapakse Hemaka A Epha4 rtk inhibitors for treatment of neurological and neurodegenerative disorders and cancer
CA2726508C (fr) * 2008-06-17 2016-06-07 Astrazeneca Ab Composes pyridines
US8440693B2 (en) * 2009-12-22 2013-05-14 Novartis Ag Substituted isoquinolinones and quinazolinones
US20110251216A1 (en) 2010-02-19 2011-10-13 The Regents Of The University Of Michigan Compositions and methods for inhibiting ezh2
US8846935B2 (en) 2010-05-07 2014-09-30 Glaxosmithkline Llc Indazoles
US8637509B2 (en) 2010-05-07 2014-01-28 Glaxosmithkline Llc Azaindazoles
EP2566327B1 (fr) 2010-05-07 2017-03-29 Glaxosmithkline LLC Indoles
US8895245B2 (en) 2010-09-10 2014-11-25 Epizyme, Inc. Inhibitors of human EZH2 and methods of use thereof
WO2012035078A1 (fr) 2010-09-16 2012-03-22 Novartis Ag Inhibiteurs de la 17α-hydroxylase/c17,20-lyase
US20130310379A1 (en) 2010-11-19 2013-11-21 Constellation Pharmaceuticals Modulators of methyl modifying enzymes, compositions and uses thereof
WO2012118812A2 (fr) 2011-02-28 2012-09-07 Epizyme, Inc. Composés hétéroaryles bicycliques substitués condensés en 6,5
TWI598336B (zh) * 2011-04-13 2017-09-11 雅酶股份有限公司 經取代之苯化合物
JO3438B1 (ar) 2011-04-13 2019-10-20 Epizyme Inc مركبات بنزين مستبدلة بأريل أو أريل غير متجانس
KR20140082742A (ko) 2011-09-30 2014-07-02 글락소스미스클라인 엘엘씨 암을 치료하는 방법
WO2013059944A1 (fr) * 2011-10-28 2013-05-02 British Columbia Cancer Agency Branch Régulateurs épigénétiques et utilisations associées
WO2013173441A2 (fr) 2012-05-16 2013-11-21 Glaxosmithkline Llc Inhibiteurs d'homologue d'activateur de zeste 2
CA2884848C (fr) 2012-09-28 2017-08-22 Pfizer Inc. Composes de benzamide et heterobenzamide
FR3000059A1 (fr) 2012-12-21 2014-06-27 Saint Gobain Placo Composition pour plaques de platre et produits obtenus
AU2013363768B2 (en) 2012-12-21 2016-02-04 F. Hoffmann-La Roche Ag Peptides as oxytocin agonists
UA111305C2 (uk) 2012-12-21 2016-04-11 Пфайзер Інк. Конденсовані лактами арилу та гетероарилу
NZ711896A (en) 2012-12-21 2018-04-27 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor
GEP201706757B (en) 2012-12-21 2017-10-25 Alios Biopharma Inc Substituted nucleosides, nucleotides and analogs thereof
FR3000065A1 (fr) 2012-12-21 2014-06-27 Univ Lille Ii Droit & Sante Composes bicycliques ayant une activite potentialisatrice de l'activite d'un antibiotique actif contre les mycobacteries-composition et produit pharmaceutiques comprenant de tels composes
PL2935222T3 (pl) 2012-12-21 2019-02-28 Epizyme Inc Inhibitory PRMT5 i ich zastosowania
MY191741A (en) 2012-12-21 2022-07-13 Gilead Sciences Inc Polycyclic-carbamoylpyridone compounds and their pharmaceutical use
US9233974B2 (en) 2012-12-21 2016-01-12 Gilead Sciences, Inc. Antiviral compounds
LT2934568T (lt) 2012-12-21 2018-02-12 Sanofi Dvigubi glp1/gip arba trigubi glp/gip/gliukagono agonistai
MY185765A (en) 2014-06-17 2021-06-06 Pfizer Substituted dihydroisoquinolinone compounds

Also Published As

Publication number Publication date
AU2015275826A1 (en) 2016-11-24
US20150361067A1 (en) 2015-12-17
SI3157915T1 (sl) 2019-05-31
CY1121706T1 (el) 2020-07-31
MA40225B1 (fr) 2019-05-31
CU24408B1 (es) 2019-05-03
PL3157915T3 (pl) 2019-07-31
CL2016003246A1 (es) 2017-07-14
KR20170016493A (ko) 2017-02-13
CN107207464B (zh) 2019-10-22
MD4820B1 (ro) 2022-08-31
MD4820C1 (ro) 2023-03-31
BR112016029612A2 (pt) 2017-08-22
CR20200484A (es) 2021-04-26
ME03419B (fr) 2020-01-20
MD20160136A2 (ro) 2017-05-31
HUE042964T2 (hu) 2019-07-29
CU20160180A7 (es) 2017-03-03
CA2894298C (fr) 2017-04-18
WO2015193765A1 (fr) 2015-12-23
TN2016000529A1 (en) 2018-04-04
SV2016005333A (es) 2017-03-06
EP3157915B1 (fr) 2019-02-27
GEP20186933B (en) 2018-12-10
EP3521285A1 (fr) 2019-08-07
UY36170A (es) 2016-01-29
EA031892B1 (ru) 2019-03-29
US20190040047A1 (en) 2019-02-07
UA118380C2 (uk) 2019-01-10
KR101877187B1 (ko) 2018-07-10
HRP20190604T1 (hr) 2019-05-31
TW201609697A (zh) 2016-03-16
CR20160574A (es) 2017-02-23
CN107207464A (zh) 2017-09-26
US9481666B2 (en) 2016-11-01
ES2721031T3 (es) 2019-07-26
PH12016502378A1 (en) 2017-02-20
IL248991B (en) 2020-02-27
CA2894298A1 (fr) 2015-12-17
TWI561516B (en) 2016-12-11
MY185765A (en) 2021-06-06
MX2016016764A (es) 2017-04-25
US20170298048A1 (en) 2017-10-19
PE20161552A1 (es) 2017-01-11
EA201692114A1 (ru) 2017-06-30
SG11201609386YA (en) 2017-01-27
AP2016009605A0 (en) 2016-12-31
AU2015275826B2 (en) 2019-05-16
DK3157915T3 (en) 2019-04-23
RS58632B1 (sr) 2019-05-31
IL248991A0 (en) 2017-01-31
US10570121B2 (en) 2020-02-25
US20160376254A1 (en) 2016-12-29
PT3157915T (pt) 2019-05-16
EP3157915A1 (fr) 2017-04-26
LT3157915T (lt) 2019-04-25
JP2017519013A (ja) 2017-07-13
NZ726108A (en) 2020-06-26
BR112016029612B1 (pt) 2021-01-19
JP6152495B1 (ja) 2017-06-21

Similar Documents

Publication Publication Date Title
MA40225A (fr) Composés dihydroisoquinolinone substitués
MA45920A (fr) Inhibiteurs de pyridopyrimidinone cdk2/4/6
MA40111A1 (fr) Dérivés du tétrahydronaphtalène inhibant la protéine mcl-1
MA44721B1 (fr) Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer
MA42410B1 (fr) Oxystérols et leurs méthodes d'utilisation
MA47079B1 (fr) Composés amino-triazolopyidines et leur utilisation pour traiter le cancer
MX2021013075A (es) Oxisteroles y metodos de uso de los mismos.
MA38175A1 (fr) Lactames fusionnés à un aryle et hétéroaryle
MA39898B1 (fr) Composés 4-amino-imidazoquinoline
MA41134A (fr) Composés substitués de 5-amino-6h-thiazolo[4,5-d]pyrimidine-2,7-dione pour le traitement et la prophylaxie des infections virales
MA39995B1 (fr) Composés destinés à traiter l'amyotrophie spinale
MA37400B1 (fr) Composés hétérocyclyle en tant qu'inhibiteurs de mek
MA40123A1 (fr) Pyrimidines utilisées en tant qu'inhibiteurs du facteur xia
MA39777A (fr) Composes organiques de la famille des monobactams pour le traitement d'infections bactériennes
MA33745B1 (fr) Piperidines substituees qui accroissent l'activite de p53, et utilisation de ces composes
MA40955A (fr) 2-amino-6-(difluorométhyl)-5,5-difluoro-6-phényl-3,4,5,6-tétrahydropyridines comme inhibiteurs de bace1
MA44674B1 (fr) Inhibiteurs de bromodomaine
MA37762B1 (fr) Composés n-aryltriazole utilisés comme antagonistes de lpar
EP4316591A3 (fr) Oxystérols et leurs procédés d'utilisation
MA37764A1 (fr) Composés n-alkyltriazole utilisés comme antagonistes de lpar
MA35749B1 (fr) Dérivés nucléosidiques 4'-azido, 3'-fluoro substitués en tant qu'inhibiteurs de la réplication de l'arn du vhc
MA45598B1 (fr) Stéroles 24-hydroxylés substitués en position 11 pour le traitement des maladies liées au récepteur nmda
TN2016000188A1 (fr) Derives de purines 2,6-substitues et leur utilisation dans le traitement de troubles proliferatifs.
MA38315B1 (fr) Composés tétracycliques substitués par un hétérocycle et procédés pour les utiliser pour le traitement de maladies virales
MA39315A1 (fr) Dérivés de pyridazine à utiliser dans la prévention ou le traitement d'un trouble ataxique