MA49126A - Dérivés de phényle utilisés en tant que modulateurs des récepteurs des pge2 - Google Patents

Dérivés de phényle utilisés en tant que modulateurs des récepteurs des pge2

Info

Publication number
MA49126A
MA49126A MA049126A MA49126A MA49126A MA 49126 A MA49126 A MA 49126A MA 049126 A MA049126 A MA 049126A MA 49126 A MA49126 A MA 49126A MA 49126 A MA49126 A MA 49126A
Authority
MA
Morocco
Prior art keywords
modulators
derivatives used
phenyl derivatives
pge2 receptors
pge2
Prior art date
Application number
MA049126A
Other languages
English (en)
Other versions
MA49126B1 (fr
Inventor
Christoph Boss
Olivier Corminboeuf
Heinz Fretz
Isabelle Lyothier
Davide Pozzi
Sylvia Richard-Bildstein
Hervé Siendt
Thierry Sifferlen
Original Assignee
Idorsia Pharmaceuticals 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 Idorsia Pharmaceuticals Ltd filed Critical Idorsia Pharmaceuticals Ltd
Publication of MA49126A publication Critical patent/MA49126A/fr
Publication of MA49126B1 publication Critical patent/MA49126B1/fr

Links

Classifications

    • 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
    • C07D413/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • 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
    • 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
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)
MA49126A 2017-05-18 2018-05-17 Dérivés de phényle utilisés en tant que modulateurs des récepteurs des pge2 MA49126B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP2017062031 2017-05-18
PCT/EP2018/062862 WO2018210994A1 (fr) 2017-05-18 2018-05-17 Dérivés de phényle utilisés en tant que modulateurs des récepteurs des pge2

Publications (2)

Publication Number Publication Date
MA49126A true MA49126A (fr) 2020-03-25
MA49126B1 MA49126B1 (fr) 2021-10-29

Family

ID=62186480

Family Applications (1)

Application Number Title Priority Date Filing Date
MA49126A MA49126B1 (fr) 2017-05-18 2018-05-17 Dérivés de phényle utilisés en tant que modulateurs des récepteurs des pge2

Country Status (32)

Country Link
US (1) US11712438B2 (fr)
EP (1) EP3625222B1 (fr)
JP (1) JP7159214B2 (fr)
KR (1) KR102632028B1 (fr)
CN (1) CN110612296A (fr)
AR (1) AR111941A1 (fr)
AU (1) AU2018269666B2 (fr)
BR (1) BR112019024109A2 (fr)
CA (1) CA3060597A1 (fr)
CL (1) CL2019003275A1 (fr)
CO (1) CO2019010578A2 (fr)
CR (1) CR20190559A (fr)
CY (1) CY1124608T1 (fr)
DK (1) DK3625222T3 (fr)
EA (1) EA201992676A1 (fr)
ES (1) ES2893452T3 (fr)
HR (1) HRP20211533T1 (fr)
HU (1) HUE056080T2 (fr)
IL (1) IL270623B2 (fr)
LT (1) LT3625222T (fr)
MA (1) MA49126B1 (fr)
MX (1) MX2019013718A (fr)
PE (1) PE20191814A1 (fr)
PH (1) PH12019502563A1 (fr)
PL (1) PL3625222T3 (fr)
PT (1) PT3625222T (fr)
RS (1) RS62440B1 (fr)
SG (1) SG11201908729UA (fr)
SI (1) SI3625222T1 (fr)
TW (1) TWI765041B (fr)
UA (1) UA125123C2 (fr)
WO (1) WO2018210994A1 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CR20180323A (es) 2015-11-20 2018-08-06 Idorsia Pharmaceuticals Ltd Derivados de indol n-sustituídos como moduladores de los receptores de pge2
CA3063788A1 (fr) 2017-05-18 2018-11-22 Idorsia Pharmaceuticals Ltd Derives de pyrimidine
KR102612649B1 (ko) 2017-05-18 2023-12-11 이도르시아 파마슈티컬스 리미티드 Pge2 수용체 조절제로서의 벤조푸란 및 벤조티오페논 유도체
US11839613B2 (en) 2017-05-18 2023-12-12 Idorsia Pharmaceuticals Ltd Pyrimidine derivatives as PGE2 receptor modulators
WO2019136320A1 (fr) 2018-01-05 2019-07-11 Icahn School Of Medicine At Mount Sinai Procédé d'augmentation de la prolifération de cellules bêta pancréatiques, procédé de traitement et composition
EP3768267A4 (fr) 2018-03-20 2022-04-20 Icahn School of Medicine at Mount Sinai Composés inhibiteurs de kinase, compositions et procédés d'utilisation
EP3906028A4 (fr) * 2018-12-31 2022-10-12 Icahn School of Medicine at Mount Sinai Composés inhibiteurs de kinase, compositions et méthodes d'utilisation
KR20230107228A (ko) 2020-11-13 2023-07-14 오노 야꾸힝 고교 가부시키가이샤 Ep4 길항약과 면역 체크포인트 저해 물질의 병용에 의한 암 치료

Family Cites Families (88)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5948786A (en) 1996-04-12 1999-09-07 Sumitomo Pharmaceuticals Company, Limited Piperidinylpyrimidine derivatives
DE60038902D1 (de) 2000-03-24 2008-06-26 Asterand Uk Ltd Verwendung von prostanoid-ep4-rezeptor-antagonisten zur behandlung von kopfschmerzen und nachweisverfahren für solche antagonisten
HN2001000224A (es) 2000-10-19 2002-06-13 Pfizer Compuestos de imidazol condensado con arilo o heteroarilo como agentes anti - inflamatorios y analgesicos.
GB0031295D0 (en) 2000-12-21 2001-01-31 Glaxo Group Ltd Naphthalene derivatives
GB0031302D0 (en) 2000-12-21 2001-01-31 Glaxo Group Ltd Napthalene derivatives
GB0103269D0 (en) 2001-02-09 2001-03-28 Glaxo Group Ltd Napthalene derivatives
BR0309188A (pt) 2002-04-12 2005-02-09 Pfizer Compostos pirazolo como agentes antiinflamatórios e analgésicos
EP1494667A1 (fr) 2002-04-12 2005-01-12 Pfizer Japan Inc. Composes imidazole servant d'agents anti-inflammatoires et analgesiques
AU2003233297A1 (en) 2002-05-23 2003-12-12 Theratechnologies Inc Antagonistic peptides of prostaglandin e2 receptor subtype ep4
JP5015586B2 (ja) 2003-01-29 2012-08-29 アステランド ユーケイ リミテッド Ep4受容体アンタゴニスト
CA2536887C (fr) 2003-08-26 2012-03-06 Teijin Pharma Limited Derive de pyrrolopyrimidinone
EA009201B1 (ru) 2003-09-03 2007-12-28 Пфайзер Инк. Фенил - или пиридиламидные соединения в качестве антагонистов простагландина e2
US8084457B2 (en) 2003-09-15 2011-12-27 Lead Discovery Center Gmbh Pharmaceutically active 4,6-disubstituted aminopyrimidine derivatives as modulators of protein kinases
GB0324269D0 (en) 2003-10-16 2003-11-19 Pharmagene Lab Ltd EP4 receptor antagonists
CA2565660C (fr) 2004-05-04 2009-11-03 Pfizer Inc. Composes aryl- ou heteroarylamides ortho-substitues
CA2565813C (fr) 2004-05-04 2010-10-26 Pfizer Inc. Composes methylaryl- ou heteroarylamides substitues
GT200500284A (es) 2004-10-15 2006-03-27 Aventis Pharma Inc Pirimidinas como antagonistas del receptor de prostaglandina d2
EP1885722B1 (fr) 2005-05-19 2011-11-16 Merck Canada Inc. Derives de quinoleine a titre d'antagonistes de ep4
WO2006128129A2 (fr) 2005-05-26 2006-11-30 Synta Pharmaceuticals Corp. Traitement anticancereux
AR060403A1 (es) 2006-04-12 2008-06-11 Sanofi Aventis Compuestos de amino- pirimidina 2,6- sustituidos -4- monosustituidos como antagonistas del receptor de prostaglandina d2
WO2007121578A1 (fr) 2006-04-24 2007-11-01 Merck Frosst Canada Ltd. Dérivés d'indolamide comme antagonistes du récepteur ep4
JP5183628B2 (ja) 2006-06-12 2013-04-17 メルク カナダ インコーポレイテッド Ep4受容体リガンドとしてのインドリンアミド誘導体
US20080280891A1 (en) 2006-06-27 2008-11-13 Locus Pharmaceuticals, Inc. Anti-cancer agents and uses thereof
WO2008008059A1 (fr) 2006-07-12 2008-01-17 Locus Pharmaceuticals, Inc. Agents anti-cancer et leurs utilisations
AU2007271964B2 (en) 2006-07-14 2012-01-19 Novartis Ag Pyrimidine derivatives as ALK-5 inhibitors
JP5259592B2 (ja) 2006-08-11 2013-08-07 メルク カナダ インコーポレイテッド Ep4受容体リガンドとしてのチオフェンカルボキサミド誘導体
WO2008039882A1 (fr) 2006-09-30 2008-04-03 Sanofi-Aventis U.S. Llc Combinaison de niacine et d'un antagoniste du récepteur de prostaglandine d2
ES2400293T3 (es) 2007-02-26 2013-04-08 Merck Canada Inc. Derivados de indol e indolina ciclopropilamida como antagonistas de receptores EP4
WO2008123207A1 (fr) 2007-03-26 2008-10-16 Astellas Pharma Inc. Dérivé de l'ornithine
CN101636385B (zh) 2007-03-26 2012-09-05 默克弗罗斯特加拿大有限公司 作为ep4受体拮抗剂的萘和喹啉磺酰脲衍生物
EP2014657A1 (fr) * 2007-06-21 2009-01-14 Bayer Schering Pharma Aktiengesellschaft Diaminopyrimidine en tant que modulateurs du récepteur EP2
US20110028463A1 (en) 2007-07-03 2011-02-03 Astellas Pharma Inc. Amide compounds
ATE510827T1 (de) 2007-10-12 2011-06-15 Ingenium Pharmaceuticals Gmbh Inhibitoren von proteinkinasen
CA2714743C (fr) 2008-02-19 2017-01-17 Janssen Pharmaceutica N.V. Aryl-hydroxyethylamino-pyrimidines et triazines en tant que modulateurs d'amide d'acide gras hydrolase
ES2518919T3 (es) 2008-05-14 2014-11-05 Astellas Pharma Inc. Derivados del ácido 4-(Indol-7-ilcarbonilaminometil)ciclohexanocarboxílico como antagonistas del receptor EP4 útiles para el tratamiento de la insuficiencia renal crónica o la nefropatía diabética
US20130225528A1 (en) 2008-05-21 2013-08-29 Ariad Pharmaceuticals, Inc. Phosphorus Derivatives as Kinase Inhibitors
CA2733247C (fr) 2008-08-14 2018-04-03 Beta Pharma Canada Inc. Derives d'amides heterocycliques en tant qu'antagonistes du recepteur ep4
CN102164942B (zh) 2008-09-19 2017-02-15 生物科技研究有限公司 三萜系化合物及其使用的方法
CN102224154A (zh) 2008-09-25 2011-10-19 默克弗罗斯特加拿大有限公司 作为EP4受体拮抗剂的β-咔啉磺酰脲衍生物
WO2011022348A1 (fr) 2009-08-18 2011-02-24 Janssen Pharmaceutica Nv Modulateurs d'éthylène diamine d'une amide hydrolase d'acide gras
JP2013511544A (ja) 2009-11-23 2013-04-04 レクシコン ファーマシューティカルズ インコーポレイテッド 過敏性腸症候群を治療するための方法及びアッセイ
KR20130031296A (ko) 2010-05-21 2013-03-28 케밀리아 에이비 신규한 피리미딘 유도체
CN103097358B (zh) 2010-09-21 2015-04-08 卫材R&D管理有限公司 药物组合物
NZ609887A (en) 2010-09-29 2015-01-30 Nb Health Lab Co Ltd Antibody against human prostaglandin e2 receptor ep4
WO2012066065A1 (fr) 2010-11-17 2012-05-24 Novartis Ag Composés phényl-hétéroaryl amine et leurs utilisations
WO2012066070A1 (fr) 2010-11-17 2012-05-24 Novartis Ag Composés 3-(aminoaryl)-pyridine
ES2545110T3 (es) 2010-12-10 2015-09-08 Rottapharm Biotech S.R.L. Derivados de piridinamida como antagonistas del receptor EP4
WO2012103071A2 (fr) 2011-01-25 2012-08-02 Eisai R&D Management Co., Ltd. Composés et compositions
DK2688883T3 (en) 2011-03-24 2016-09-05 Noviga Res Ab pyrimidine
EP2702043A1 (fr) 2011-04-29 2014-03-05 Exelixis, Inc. Inhibiteurs de la forme inductible de la 6-phosphofructose-2-kinase
US9518044B2 (en) 2011-06-20 2016-12-13 Emory University Prostaglandin receptor EP2 antagonists, derivatives, compositions, and uses related thereto
AU2011372747B2 (en) 2011-07-04 2016-12-22 Rottapharm Biotech S.R.L. Cyclic amine derivatives as EP4 receptor antagonists
EP2554662A1 (fr) 2011-08-05 2013-02-06 M Maria Pia Cosma Procédés pour le traitement de maladies rétiniennes dégénératives
US20150004175A1 (en) 2011-12-13 2015-01-01 Yale University Compositions and Methods for Reducing CTL Exhaustion
WO2013163190A1 (fr) * 2012-04-24 2013-10-31 Vertex Pharmaceutical Incorporated Inhibiteurs d'adn pk
AR091429A1 (es) 2012-06-29 2015-02-04 Lilly Co Eli Compuestos de fenoxietil piperidina
TWI572597B (zh) 2012-06-29 2017-03-01 美國禮來大藥廠 二甲基-苯甲酸化合物
EP2711364A1 (fr) 2012-09-21 2014-03-26 Chemilia AB 4-(Indolyl ou benzimidazolyl)amino-2-(2-(indol-3-yl)éthyl)aminopyrimidines utiles pour le traitement du cancer
CA2888338C (fr) 2012-11-27 2021-07-20 Thomas Helledays Stiftelse For Medicinsk Forskning Inhibiteurs mth1 pour le traitement du cancer
UA115576C2 (uk) 2012-12-06 2017-11-27 Байєр Фарма Акцієнгезелльшафт Похідні бензимідазолу як антагоністи ер4
EP2765128A1 (fr) 2013-02-07 2014-08-13 Almirall, S.A. Benzamides substitués présentant une activité vis-à-vis de récepteurs EP4
TW201443004A (zh) 2013-02-15 2014-11-16 Lilly Co Eli 苯氧基乙氧基化合物
TWI636046B (zh) 2013-05-17 2018-09-21 美國禮來大藥廠 苯氧基乙基二氫-1h-異喹啉化合物
BR112015030095B1 (pt) 2013-05-30 2023-02-28 Idorsia Pharmaceuticals Ltd Moduladores do receptor de cxcr7
MY168609A (en) 2013-06-12 2018-11-14 Kaken Pharma Co Ltd 4-alkynyl imidazole derivative and medicine comprising same as active ingredient
BR112016004194A8 (pt) 2013-09-04 2020-02-11 Bristol Myers Squibb Co compostos úteis como imunomoduladores
HUE038169T2 (hu) 2013-09-06 2018-09-28 Aurigene Discovery Tech Ltd 1,2,4-Oxadiazol származékok mint immunomodulátorok
WO2015044900A1 (fr) 2013-09-27 2015-04-02 Aurigene Discovery Technologies Limited Composés immunomodulateurs thérapeutiques
SG11201602962PA (en) 2013-10-17 2016-05-30 Vertex Pharma Co-crystals of (s)-n-methyl-8-(1-((2'-methyl-[4,5'-bipyrimidin]-6-yl)amino)propan-2-yl)quinoline-4-carboxamide and deuterated derivatives thereof as dna-pk inhibitors
LT3057959T (lt) * 2013-10-17 2018-06-11 Vertex Pharmaceuticals Incorporated Dnr-pk inhibitoriai
US9776964B2 (en) 2013-12-17 2017-10-03 Eli Lilly And Company Phenoxyethyl cyclic amine derivatives and their activity as EP4 receptor modulators
WO2015094912A1 (fr) 2013-12-17 2015-06-25 Eli Lilly And Company Composés d'acide diméthylbenzoïque
TW201607943A (zh) 2013-12-19 2016-03-01 拜耳製藥公司 作為ep4配體之新穎苯并咪唑衍生物
TW201623277A (zh) 2014-03-26 2016-07-01 安斯泰來製藥股份有限公司 醯胺化合物
WO2015167825A1 (fr) 2014-04-29 2015-11-05 Emory University Antagonistes du récepteur ep2 des prostaglandines, dérivés, compositions et utilisations associés
CN106572993B (zh) 2014-05-23 2019-07-16 卫材R&D管理有限公司 Ep4拮抗剂在制备治疗癌症的药物中的应用
WO2015187089A1 (fr) 2014-06-04 2015-12-10 Thomas Helledays Stiftelse För Medicinsk Forskning Inhibiteurs de mth1 destinés au traitement des états inflammatoires et auto-immuns
MA40240B1 (fr) 2014-06-19 2019-03-29 Ariad Pharma Inc Composés hétéroaryle d'inhibition de la kinase
WO2016021742A1 (fr) 2014-08-07 2016-02-11 Takeda Pharmaceutical Company Limited Composés hétérocycliques utilisés en tant qu'antagonistes des récepteurs ccr4
JP6269862B2 (ja) 2015-01-09 2018-01-31 小野薬品工業株式会社 三環性スピロ化合物
DK3325490T3 (da) 2015-07-23 2020-02-03 Takeda Pharmaceuticals Co 1-substituerede 1,2,3,4-tetrahydro-1,7-naphthyridin-8-aminderivater og deres anvendelse som ep4-receptorantagonister
BR112018007664B1 (pt) 2015-10-16 2023-12-19 Eisai R&D Management Co., Ltd Compostos antagonistas de ep4, composição compreendendo o composto e uso dos mesmos para tratar câncer
CR20180323A (es) 2015-11-20 2018-08-06 Idorsia Pharmaceuticals Ltd Derivados de indol n-sustituídos como moduladores de los receptores de pge2
US11124805B2 (en) 2016-07-13 2021-09-21 Vertex Pharmaceuticals Incorporated Methods, compositions and kits for increasing genome editing efficiency
EP3625224B1 (fr) 2017-05-18 2021-08-04 Idorsia Pharmaceuticals Ltd Dérivés d'indole n-substitués
KR102612649B1 (ko) 2017-05-18 2023-12-11 이도르시아 파마슈티컬스 리미티드 Pge2 수용체 조절제로서의 벤조푸란 및 벤조티오페논 유도체
CA3063788A1 (fr) 2017-05-18 2018-11-22 Idorsia Pharmaceuticals Ltd Derives de pyrimidine
US11839613B2 (en) 2017-05-18 2023-12-12 Idorsia Pharmaceuticals Ltd Pyrimidine derivatives as PGE2 receptor modulators

Also Published As

Publication number Publication date
CN110612296A (zh) 2019-12-24
SI3625222T1 (sl) 2021-11-30
MA49126B1 (fr) 2021-10-29
CL2019003275A1 (es) 2020-05-04
IL270623B (en) 2022-11-01
WO2018210994A1 (fr) 2018-11-22
US20200179383A1 (en) 2020-06-11
JP7159214B2 (ja) 2022-10-24
CO2019010578A2 (es) 2019-10-09
HRP20211533T1 (hr) 2022-01-07
KR20200010352A (ko) 2020-01-30
RS62440B1 (sr) 2021-11-30
PT3625222T (pt) 2021-10-07
PL3625222T3 (pl) 2021-12-27
TWI765041B (zh) 2022-05-21
IL270623A (fr) 2019-12-31
EP3625222A1 (fr) 2020-03-25
AU2018269666B2 (en) 2022-02-03
ES2893452T3 (es) 2022-02-09
BR112019024109A2 (pt) 2020-06-02
MX2019013718A (es) 2020-01-30
AR111941A1 (es) 2019-09-04
IL270623B2 (en) 2023-03-01
HUE056080T2 (hu) 2022-01-28
AU2018269666A1 (en) 2020-01-16
CA3060597A1 (fr) 2018-11-22
PH12019502563A1 (en) 2020-07-20
EP3625222B1 (fr) 2021-07-21
EA201992676A1 (ru) 2020-05-06
PE20191814A1 (es) 2019-12-27
CR20190559A (es) 2020-02-10
US11712438B2 (en) 2023-08-01
LT3625222T (lt) 2021-11-10
UA125123C2 (uk) 2022-01-12
TW201900175A (zh) 2019-01-01
DK3625222T3 (da) 2021-10-25
SG11201908729UA (en) 2019-10-30
CY1124608T1 (el) 2022-07-22
JP2020520356A (ja) 2020-07-09
KR102632028B1 (ko) 2024-01-31

Similar Documents

Publication Publication Date Title
MA49126A (fr) Dérivés de phényle utilisés en tant que modulateurs des récepteurs des pge2
MA49128A (fr) Dérivés de pyrimidine utilisés en tant que modulateurs des récepteurs des pge2
MA54169A (fr) Tolyles substitués utilisés en tant que fongicides
DK3774791T3 (da) Heterocykliske forbindelser som immunmodulatorer
MA47123A (fr) Dérivés de benzooxazole en tant qu'mmunomodulateurs
MA43512A (fr) Composés hétérocycliques utiles en tant que modulateurs du tnf alpha
MA43169A (fr) Composés hétérocycliques utilisés en tant qu'inhibiteurs de pi3k-gamma
MA51438A (fr) Composés hétérocycliques utilisés en tant qu'inhibiteurs de lsd1
DK3433234T3 (da) Allosteriske modulatorer af nicotinacetylcholinreceptorer
MA43251A (fr) Utilisation de dérivés d'indole n-substitués comme modulateurs des récepteurs des pge2
MA44498A (fr) Dérivés d'indoline substituée utilisés en tant qu'inhibiteurs de la réplication du virus de la dengue
MA42659A (fr) Dérivés hétéroaryle utilisés en tant qu'inhibiteurs de parp
DK3294713T3 (da) Substituerede tetrahydroquinolinonforbindelser som ror-gamma-modulatorer
MA51429A (fr) Dérivés amino-fluoropipéridines utilisés en tant qu'inhibiteur de kinase
DK3532486T3 (da) Antistof-forbundne cykliske peptidtyrosin-tyrosinforbindelser som modulatorer af neuropeptid-y- receptorer
MA47370A (fr) Dérivés bis-hétéroaryliques en tant que modulateurs de l'agrégation des protéines
MA44502A (fr) Dérivés d'indole substitués utilisés en tant qu'inhibiteurs de réplication du virus de la dengue
MA48987A (fr) Dérivés d'indoline substitués utilisés en tant qu'inhibiteurs de réplication du virus de la dengue
MA41341A (fr) Dérivés indole utilisés en tant qu'inhibiteurs de la réplication du virus de la dengue
MA42810A (fr) Dérivés d'indole monosubstitués ou disubstitués utilisés en tant qu'inhibiteurs de la réplication du virus de la dengue
MA48943A (fr) Dérivés d'indoline substitués utilisés en tant qu'inhibiteurs de réplication du virus de la dengue
CL2020000139A1 (es) Moduladores de lxr que contienen amina o (tio)amida.
MA51133A (fr) Dérivés de pyrrole utilisés en tant qu'inhibiteurs d'acc
MA49374A (fr) Composés hétéroaromatiques utilisés en tant qu'inhibiteurs de vanine
MA50439A (fr) Nouveaux dérivés de pyrazolo-pyrrolo-pyrimidine-dione utilisés en tant qu'inhibiteurs de p2x3