MA49128A - Dérivés de pyrimidine utilisés en tant que modulateurs des récepteurs des pge2 - Google Patents

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

Info

Publication number
MA49128A
MA49128A MA049128A MA49128A MA49128A MA 49128 A MA49128 A MA 49128A MA 049128 A MA049128 A MA 049128A MA 49128 A MA49128 A MA 49128A MA 49128 A MA49128 A MA 49128A
Authority
MA
Morocco
Prior art keywords
modulators
pyrimidine derivatives
derivatives used
pge2 receptors
pge2
Prior art date
Application number
MA049128A
Other languages
English (en)
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 MA49128A publication Critical patent/MA49128A/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic 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
    • A61K31/5355—Non-condensed oxazines and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic 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
    • C07D239/26—Heterocyclic 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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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 chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic 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
    • C07D405/02—Heterocyclic 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
    • C07D405/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic 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
    • C07D405/14—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic 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
    • C07D413/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
MA049128A 2017-05-18 2018-05-17 Dérivés de pyrimidine utilisés en tant que modulateurs des récepteurs des pge2 MA49128A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP2017061989 2017-05-18

Publications (1)

Publication Number Publication Date
MA49128A true MA49128A (fr) 2021-03-17

Family

ID=62196584

Family Applications (1)

Application Number Title Priority Date Filing Date
MA049128A MA49128A (fr) 2017-05-18 2018-05-17 Dérivés de pyrimidine utilisés en tant que modulateurs des récepteurs des pge2

Country Status (32)

Country Link
US (1) US11839613B2 (fr)
EP (1) EP3625228B1 (fr)
JP (1) JP7159215B2 (fr)
KR (1) KR102626982B1 (fr)
CN (1) CN110612299A (fr)
AR (1) AR111808A1 (fr)
AU (1) AU2018268311B2 (fr)
BR (1) BR112019024105A2 (fr)
CA (1) CA3060394A1 (fr)
CL (1) CL2019003274A1 (fr)
CO (1) CO2019010505A2 (fr)
CR (1) CR20190560A (fr)
CY (1) CY1124799T1 (fr)
DK (1) DK3625228T3 (fr)
EA (1) EA201992677A1 (fr)
ES (1) ES2887041T3 (fr)
HR (1) HRP20211380T1 (fr)
HU (1) HUE056382T2 (fr)
IL (1) IL270620B2 (fr)
LT (1) LT3625228T (fr)
MA (1) MA49128A (fr)
MX (1) MX2019013638A (fr)
PE (1) PE20191811A1 (fr)
PH (1) PH12019502564A1 (fr)
PL (1) PL3625228T3 (fr)
PT (1) PT3625228T (fr)
RS (1) RS62398B1 (fr)
SG (1) SG11201908097YA (fr)
SI (1) SI3625228T1 (fr)
TW (1) TW201900178A (fr)
UA (1) UA125124C2 (fr)
WO (1) WO2018210988A1 (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
TW201900179A (zh) 2017-05-18 2019-01-01 瑞士商愛杜西亞製藥有限公司 作為pge2受體調節劑之苯并呋喃及苯并噻吩衍生物
CA3063788A1 (fr) 2017-05-18 2018-11-22 Idorsia Pharmaceuticals Ltd Derives de pyrimidine
MA49126B1 (fr) 2017-05-18 2021-10-29 Idorsia Pharmaceuticals Ltd Dérivés de phényle utilisés en tant que modulateurs des récepteurs des pge2
WO2021060281A1 (fr) * 2019-09-24 2021-04-01 Ａｇｃ株式会社 Antagoniste double des récepteurs ep2/ep4 de la prostaglandine e2
KR20230107228A (ko) 2020-11-13 2023-07-14 오노 야꾸힝 고교 가부시키가이샤 Ep4 길항약과 면역 체크포인트 저해 물질의 병용에 의한 암 치료
CN113248354B (zh) * 2021-07-07 2022-04-22 山东国邦药业有限公司 一种氟氯苯乙酮的合成方法
CN114539193A (zh) * 2022-01-20 2022-05-27 海南普利制药股份有限公司 一种盐酸胺碘酮中间体的制备方法

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
AU3445100A (en) 2000-03-24 2001-10-08 Pharmagene Lab Ltd Use of prostanoid ep4 receptor antagonists for the treatment of headache and assays for such antagonists
HN2001000224A (es) 2000-10-19 2002-06-13 Pfizer Compuestos de imidazol condensado con arilo o heteroarilo como agentes anti - inflamatorios y analgesicos.
GB0031302D0 (en) 2000-12-21 2001-01-31 Glaxo Group Ltd Napthalene derivatives
GB0031295D0 (en) 2000-12-21 2001-01-31 Glaxo Group Ltd Naphthalene derivatives
GB0103269D0 (en) 2001-02-09 2001-03-28 Glaxo Group Ltd Napthalene derivatives
WO2003087061A1 (fr) 2002-04-12 2003-10-23 Pfizer Japan Inc. Composes de pyrazole en tant qu'agents anti-inflammatoires et analgesiques
BR0309305A (pt) 2002-04-12 2005-02-15 Pfizer Compostos de imidazol como agentes antiinflamatórios e analgésicos
BR0311247A (pt) 2002-05-23 2005-03-15 Theratechnologies Inc Peptìdeos antagonistas do receptor subtipo ep4 da prostaglandina e2
WO2004067524A1 (fr) 2003-01-29 2004-08-12 Pharmagene Laboratories Limited Antagonistes aux recepteurs ep4
EP1661896A4 (fr) 2003-08-26 2008-07-16 Teijin Pharma Ltd Derive de pyrrolopyrimidinethione
BRPI0414130B8 (pt) 2003-09-03 2021-05-25 Askat Inc compostos de fenilamida ou piridilamida, seu uso e composições farmacêuticas que os compreendem.
EP1678147B1 (fr) 2003-09-15 2012-08-08 Lead Discovery Center GmbH Derives d'aminopyrimidine a disubstitution 4,6 actifs sur le plan pharmaceutique en tant que modulateurs des proteine kinases
GB0324269D0 (en) 2003-10-16 2003-11-19 Pharmagene Lab Ltd EP4 receptor antagonists
CA2565813C (fr) 2004-05-04 2010-10-26 Pfizer Inc. Composes methylaryl- ou heteroarylamides substitues
JP4054369B2 (ja) 2004-05-04 2008-02-27 ファイザー株式会社 オルト置換アリールまたはヘテロアリールアミド化合物
HN2005000795A (es) 2004-10-15 2010-08-19 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
AU2007260529B2 (en) 2006-06-12 2012-04-19 Merck Canada Inc. Indoline amide derivatives as EP4 receptor ligands
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
PT2044056E (pt) 2006-07-14 2012-12-05 Novartis Ag Derivados de pirimidina como inibidores de alk-5
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
AU2008221194B2 (en) 2007-02-26 2013-06-27 Merck Canada Inc. Indole and indoline cyclopropyl amide derivatives as EP4 receptor antagonists
CN101641325A (zh) 2007-03-26 2010-02-03 安斯泰来制药株式会社 鸟氨酸衍生物
WO2008116304A1 (fr) 2007-03-26 2008-10-02 Merck Frosst Canada Ltd. Dérivés de naphtalène et quinoléine sulfonylurée comme antagonistes du récepteur ep4
EP2014657A1 (fr) * 2007-06-21 2009-01-14 Bayer Schering Pharma Aktiengesellschaft Diaminopyrimidine en tant que modulateurs du récepteur EP2
EP2460787A1 (fr) 2007-07-03 2012-06-06 Astellas Pharma Inc. Composés d'amide et leur utilidsation comme anagonistes de la PGE2.
NZ584454A (en) 2007-10-12 2011-09-30 Ingenium Pharmaceuticals Gmbh N-[6-phenyl-pyrimidin-4-yl]-amides and urea derivatives as inhibitors of protein kinases
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
SI2565191T1 (sl) 2008-05-14 2014-12-31 Astellas Pharma Inc. Derivati 4-(indol-7-ilkarbonilaminometil)cikloheksan karboksilne kisline kot EP4 receptorski antagonisti, uporabni za zdravljenje kronične ledvične odpovedi ali diabetične nefropatije
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
WO2010032123A1 (fr) 2008-09-19 2010-03-25 Biotechnology Research Corporation Limited Composés triterpénoïdes et procédés pour les utiliser
US8685999B2 (en) 2008-09-25 2014-04-01 Merck Sharp & Dohme Corp. Beta carboline sulphonylurea derivatives as EP4 receptor antagonists
US8906914B2 (en) * 2009-08-18 2014-12-09 Janssen Pharmaceutica Nv Ethylene diamine modulators of fatty acid hydrolase
AU2010321905A1 (en) 2009-11-23 2012-05-24 Lexicon Pharmaceuticals, Inc. Methods and assays for the treatment of irritable bowel syndrome
CA2798578C (fr) 2010-05-21 2015-12-29 Chemilia Ab Nouveaux derives de pyrimidine
MX2013003162A (es) 2010-09-21 2013-05-06 Eisai R&D Man Co Ltd Composicion farmaceutica.
AU2011309028B2 (en) 2010-09-29 2016-03-17 Nb Health Laboratory Co. Ltd. Antibody against human prostaglandin E2 receptor EP4
CA2816679A1 (fr) 2010-11-17 2012-05-24 Novartis Ag Composes 3-(aminoaryl)-pyridine
WO2012066065A1 (fr) 2010-11-17 2012-05-24 Novartis Ag Composés phényl-hétéroaryl amine et leurs utilisations
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
RU2013147417A (ru) 2011-03-24 2015-04-27 Кемилиа Аб Новые производные пиримидина
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
ES2559513T3 (es) 2011-07-04 2016-02-12 Rottapharm Biotech S.R.L. Derivados de amina cíclica como antagonistas del receptor EP4
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
EP2841428B1 (fr) * 2012-04-24 2018-08-22 Vertex Pharmaceuticals Incorporated Inhibiteurs d'adn pk
TWI572597B (zh) 2012-06-29 2017-03-01 美國禮來大藥廠 二甲基－苯甲酸化合物
JO3296B1 (ar) 2012-06-29 2018-09-16 Lilly Co Eli مركبات فينوكسي إيثيل بيبريدين
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
MY173564A (en) 2013-05-30 2020-02-04 Idorsia Pharmaceuticals Ltd Cxcr7 receptor modulators
AU2014279113B2 (en) 2013-06-12 2018-04-12 Kaken Pharmaceutical Co., Ltd. 4-alkynyl imidazole derivative and medicine comprising same as active ingredient
CN105705489B (zh) 2013-09-04 2019-04-26 百时美施贵宝公司 用作免疫调节剂的化合物
AU2014316682B2 (en) 2013-09-06 2018-11-22 Aurigene Discovery Technologies Limited 1,2,4-oxadiazole derivatives as immunomodulators
WO2015044900A1 (fr) 2013-09-27 2015-04-02 Aurigene Discovery Technologies Limited Composés immunomodulateurs thérapeutiques
RU2675270C2 (ru) 2013-10-17 2018-12-18 Вертекс Фармасьютикалз Инкорпорейтед Сокристаллы и содержащие их фармацевтические композиции
BR112016008423B1 (pt) * 2013-10-17 2022-02-22 Vertex Pharmaceuticals Incorporated Composto, composição farmacêutica compreendendo o mesmo e seu uso
CN105793242B (zh) 2013-12-17 2018-02-16 伊莱利利公司 苯氧基乙基环状胺衍生物及其作为ep4受体调节剂的活性
EA028675B1 (ru) 2013-12-17 2017-12-29 Эли Лилли Энд Компани Соединения диметилбензойной кислоты
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
CN110354266A (zh) 2014-05-23 2019-10-22 卫材 R&D 管理有限公司 用于治疗癌症的组合疗法
EP3151833A4 (fr) 2014-06-04 2018-01-10 Thomas Helledays Stiftelse För Medicinsk Forskning Inhibiteurs de mth1 destinés au traitement des états inflammatoires et auto-immuns
CA2949793C (fr) 2014-06-19 2024-02-27 Ariad Pharmaceuticals, Inc. Composes heteroaryle 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
NZ733575A (en) 2015-01-09 2022-10-28 Ono Pharmaceutical Co Tricyclic spiro compound
WO2017014323A1 (fr) 2015-07-23 2017-01-26 Takeda Pharmaceutical Company Limited Dérivés substitués en 1 de 1,2,3,4-tétrahydro-1,7-naphtyridin-8-amine et leur utilisation comme antagonistes du récepteur ep4
CN108473497B (zh) 2015-10-16 2021-09-10 卫材R&D 管理有限公司 Ep4拮抗剂
CR20180323A (es) 2015-11-20 2018-08-06 Idorsia Pharmaceuticals Ltd Derivados de indol n-sustituídos como moduladores de los receptores de pge2
JP7033583B2 (ja) 2016-07-13 2022-03-10 バーテックス ファーマシューティカルズ インコーポレイテッド ゲノム編集効率を高めるための方法、組成物及びキット
CA3063788A1 (fr) 2017-05-18 2018-11-22 Idorsia Pharmaceuticals Ltd Derives de pyrimidine
TW201900179A (zh) 2017-05-18 2019-01-01 瑞士商愛杜西亞製藥有限公司 作為pge2受體調節劑之苯并呋喃及苯并噻吩衍生物
UA124748C2 (uk) 2017-05-18 2021-11-10 Ідорсія Фармасьютікалз Лтд N-заміщені індольні похідні
MA49126B1 (fr) 2017-05-18 2021-10-29 Idorsia Pharmaceuticals Ltd Dérivés de phényle utilisés en tant que modulateurs des récepteurs des pge2

Also Published As

Publication number Publication date
LT3625228T (lt) 2021-10-25
SG11201908097YA (en) 2019-10-30
AU2018268311B2 (en) 2022-02-10
KR20200007932A (ko) 2020-01-22
EP3625228A1 (fr) 2020-03-25
PH12019502564A1 (en) 2020-09-14
AU2018268311A1 (en) 2020-01-16
PT3625228T (pt) 2021-09-16
CA3060394A1 (fr) 2018-11-22
AR111808A1 (es) 2019-08-21
PE20191811A1 (es) 2019-12-26
BR112019024105A2 (pt) 2020-06-02
IL270620A (en) 2022-12-01
EA201992677A1 (ru) 2020-04-23
CL2019003274A1 (es) 2020-05-04
CY1124799T1 (el) 2022-11-25
HUE056382T2 (hu) 2022-02-28
ES2887041T3 (es) 2021-12-21
CN110612299A (zh) 2019-12-24
UA125124C2 (uk) 2022-01-12
JP7159215B2 (ja) 2022-10-24
PL3625228T3 (pl) 2021-12-20
WO2018210988A1 (fr) 2018-11-22
KR102626982B1 (ko) 2024-01-18
US20210113559A1 (en) 2021-04-22
TW201900178A (zh) 2019-01-01
DK3625228T3 (da) 2021-10-11
JP2020520358A (ja) 2020-07-09
MX2019013638A (es) 2020-01-21
IL270620B2 (en) 2023-04-01
US11839613B2 (en) 2023-12-12
EP3625228B1 (fr) 2021-07-07
CO2019010505A2 (es) 2019-10-21
HRP20211380T1 (hr) 2021-11-26
CR20190560A (es) 2020-02-10
RS62398B1 (sr) 2021-10-29
SI3625228T1 (sl) 2021-11-30

Similar Documents

Publication Publication Date Title
MA49128A (fr) Dérivés de pyrimidine utilisés en tant que modulateurs des récepteurs des pge2
MA49126A (fr) Dérivés de phényle utilisés en tant que modulateurs des récepteurs des pge2
MA54169A (fr) Tolyles substitués utilisés en tant que fongicides
MA54452A (fr) Dérivés de 2-oxoquinazoline utilisés en tant qu'inhibiteurs de la méthionine adénosyltransférase 2a
MA47123A (fr) Dérivés de benzooxazole en tant qu'mmunomodulateurs
MA47120A (fr) Dérivés pyridine utilisés en tant qu'immunomodulateurs
MA47125A (fr) Dérivés de pyrazole en tant qu'inhibiteurs de malt1
MA46196A (fr) Composés et compositions en tant qu'inhibiteurs de récepteurs de type toll endosomal
MA43169A (fr) Composés hétérocycliques utilisés en tant qu'inhibiteurs de pi3k-gamma
MA42659A (fr) Dérivés hétéroaryle utilisés en tant qu'inhibiteurs de parp
MA51438A (fr) Composés hétérocycliques utilisés en tant qu'inhibiteurs de lsd1
MA43512A (fr) Composés hétérocycliques utiles en tant que modulateurs du tnf alpha
MA51429A (fr) Dérivés amino-fluoropipéridines utilisés en tant qu'inhibiteur de kinase
MA44498A (fr) Dérivés d'indoline substituée utilisés en tant qu'inhibiteurs de la réplication du virus de la dengue
MA47086A (fr) Dérivés de dihydropyrimidine-carboxamide bicycliques utilisés en tant qu'inhibiteurs de rho-kinase
MA44502A (fr) Dérivés d'indole substitués utilisés en tant qu'inhibiteurs de réplication du virus de la dengue
MA55046A (fr) Utilisation de dérivés d'indole n-substitués comme modulateurs des récepteurs des pge2
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
CL2015002121A1 (es) Modulares de receptores nmda de espiro-lactama y sus usos.
MA40774A (fr) Dérivés de diaryle-urée en tant qu'inhibiteurs de kinase p38
MA48943A (fr) Dérivés d'indoline substitués utilisés en tant qu'inhibiteurs de réplication du virus de la dengue
MA46981A (fr) Dérivés de benzimidazole en tant qu'inhibiteurs de bromodomaine
MA47370A (fr) Dérivés bis-hétéroaryliques en tant que modulateurs de l'agrégation des protéines
MA42810A (fr) Dérivés d'indole monosubstitués ou disubstitués utilisés en tant qu'inhibiteurs de la réplication du virus de la dengue