MA51664A - Formes cristallines de l'antagoniste du récepteur cxcr7 d'acide (3s,4s)-1-cyclopropylméthyl-4-([5-(2,4-difluoro-phényl)-isoxazole-3-carbonyl]-amino)-pipéridine-3-carboxylique (1-pyrimidin-2-yl-cyclopropyl)-amide - Google Patents

Formes cristallines de l'antagoniste du récepteur cxcr7 d'acide (3s,4s)-1-cyclopropylméthyl-4-([5-(2,4-difluoro-phényl)-isoxazole-3-carbonyl]-amino)-pipéridine-3-carboxylique (1-pyrimidin-2-yl-cyclopropyl)-amide

Info

Publication number
MA51664A
MA51664A MA051664A MA51664A MA51664A MA 51664 A MA51664 A MA 51664A MA 051664 A MA051664 A MA 051664A MA 51664 A MA51664 A MA 51664A MA 51664 A MA51664 A MA 51664A
Authority
MA
Morocco
Prior art keywords
cyclopropylmethyl
isoxazole
pyrimidin
difluoro
cyclopropyl
Prior art date
Application number
MA051664A
Other languages
English (en)
Other versions
MA51664B1 (fr
Inventor
Philippe Guerry
Raumer Markus Von
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 MA51664A publication Critical patent/MA51664A/fr
Publication of MA51664B1 publication Critical patent/MA51664B1/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
    • C07D413/14Heterocyclic 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
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • 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
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
MA51664A 2018-01-26 2019-01-25 Formes cristallines de l'antagoniste du récepteur cxcr7 d'acide (3s,4s)-1-cyclopropylméthyl-4-([5-(2,4-difluoro-phényl)-isoxazole-3-carbonyl]-amino)-pipéridine-3-carboxylique (1-pyrimidin-2-yl-cyclopropyl)-amide MA51664B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP2018051938 2018-01-26
PCT/EP2019/051819 WO2019145460A1 (fr) 2018-01-26 2019-01-25 Formes cristallines de l'antagoniste du récepteur cxcr7 d'acide (3s,4s)-1-cyclopropylméthyl-4-{[5-(2,4-difluoro-phényl)-isoxazole-3-carbonyl]-amino}-pipéridine-3-carboxylique (1-pyrimidin-2-yl-cyclopropyl)-amide

Publications (2)

Publication Number Publication Date
MA51664A true MA51664A (fr) 2021-05-05
MA51664B1 MA51664B1 (fr) 2024-05-31

Family

ID=65139016

Family Applications (1)

Application Number Title Priority Date Filing Date
MA51664A MA51664B1 (fr) 2018-01-26 2019-01-25 Formes cristallines de l'antagoniste du récepteur cxcr7 d'acide (3s,4s)-1-cyclopropylméthyl-4-([5-(2,4-difluoro-phényl)-isoxazole-3-carbonyl]-amino)-pipéridine-3-carboxylique (1-pyrimidin-2-yl-cyclopropyl)-amide

Country Status (25)

Country Link
US (1) US11339148B2 (fr)
EP (1) EP3743422B1 (fr)
JP (1) JP7076010B2 (fr)
KR (1) KR102502046B1 (fr)
CN (1) CN111683945B (fr)
AU (1) AU2019212888B8 (fr)
BR (1) BR112020015024A2 (fr)
CA (1) CA3088478A1 (fr)
CL (1) CL2020001928A1 (fr)
EA (1) EA202091746A1 (fr)
ES (1) ES2976567T3 (fr)
HR (1) HRP20240552T1 (fr)
HU (1) HUE066704T2 (fr)
IL (1) IL276227B2 (fr)
MA (1) MA51664B1 (fr)
MX (1) MX392844B (fr)
MY (1) MY206631A (fr)
PH (1) PH12020551121A1 (fr)
PL (1) PL3743422T3 (fr)
RS (1) RS65594B1 (fr)
SG (1) SG11202006943TA (fr)
TW (1) TWI822724B (fr)
UA (1) UA125327C2 (fr)
WO (1) WO2019145460A1 (fr)
ZA (1) ZA202005286B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA45782B1 (fr) 2016-07-28 2021-12-31 Idorsia Pharmaceuticals Ltd Modulateurs du récepteur de cxcr7 pipéridine
JP7749552B2 (ja) * 2019-10-31 2025-10-06 イドルシア・ファーマシューティカルズ・リミテッド Cxcr7アンタゴニストのs1p1受容体調節剤との合剤

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1565436B1 (fr) 2002-11-27 2012-04-25 Incyte Corporation Derives de la 3-aminopyrrolidine modulateurs des recepteurs de la chemoquine
TW200526626A (en) 2003-09-13 2005-08-16 Astrazeneca Ab Chemical compounds
US7115646B2 (en) 2003-10-08 2006-10-03 Bristol Myers Squibb, Co. Cyclic diamines and derivatives as factor Xa inhibitors
JP4058106B2 (ja) 2005-02-18 2008-03-05 アストラゼネカ アクチボラグ 抗菌性のピペリジン誘導体
WO2009011850A2 (fr) * 2007-07-16 2009-01-22 Abbott Laboratories Nouveaux composés thérapeutiques
JP6094578B2 (ja) 2011-06-09 2017-03-15 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 代謝性障害の治療のためのgpr119モジュレーターとしての置換ピペリジン
WO2013084241A1 (fr) 2011-12-09 2013-06-13 Cadila Healthcare Limited Composés inhibiteurs de rénine
AR091516A1 (es) 2012-06-22 2015-02-11 Actelion Pharmaceuticals Ltd Derivados de 1-[m-carboxamido(hetero)aril-metil]-heterociclil-carboxamida
MX359651B (es) * 2012-11-29 2018-10-05 Chemocentryx Inc Antagonistas de cxcr7.
MA38679B1 (fr) 2013-05-30 2019-12-31 Idorsia Pharmaceuticals Ltd Modulateurs du récepteur de cxcr7
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
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
US20170253601A1 (en) * 2014-09-10 2017-09-07 Epizyme, Inc. Substituted Pyrrolidine Compounds
CA2960280A1 (fr) 2014-09-10 2016-03-17 Epizyme, Inc. Composes piperidines substitues
JP6582056B2 (ja) * 2014-12-01 2019-09-25 イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd Cxcr7受容体調節剤
MA45782B1 (fr) * 2016-07-28 2021-12-31 Idorsia Pharmaceuticals Ltd Modulateurs du récepteur de cxcr7 pipéridine

Also Published As

Publication number Publication date
TW201932460A (zh) 2019-08-16
CL2020001928A1 (es) 2020-12-18
KR20200116115A (ko) 2020-10-08
IL276227B1 (en) 2024-06-01
WO2019145460A1 (fr) 2019-08-01
IL276227A (en) 2020-09-30
SG11202006943TA (en) 2020-08-28
EP3743422C0 (fr) 2024-03-13
CN111683945A (zh) 2020-09-18
AU2019212888B8 (en) 2024-01-04
RS65594B1 (sr) 2024-06-28
PH12020551121A1 (en) 2021-05-31
CA3088478A1 (fr) 2019-08-01
ZA202005286B (en) 2025-02-26
CN111683945B (zh) 2023-11-10
MY206631A (en) 2024-12-27
AU2019212888B2 (en) 2023-12-21
HUE066704T2 (hu) 2024-08-28
JP7076010B2 (ja) 2022-05-26
MX392844B (es) 2025-03-24
EP3743422B1 (fr) 2024-03-13
UA125327C2 (uk) 2022-02-16
MX2020007881A (es) 2022-06-02
US20210115033A1 (en) 2021-04-22
KR102502046B1 (ko) 2023-02-20
AU2019212888A8 (en) 2024-01-04
JP2021511382A (ja) 2021-05-06
EP3743422A1 (fr) 2020-12-02
HRP20240552T1 (hr) 2024-07-19
BR112020015024A2 (pt) 2021-01-19
EA202091746A1 (ru) 2020-11-26
ES2976567T3 (es) 2024-08-05
US11339148B2 (en) 2022-05-24
MA51664B1 (fr) 2024-05-31
PL3743422T3 (pl) 2024-07-01
IL276227B2 (en) 2024-10-01
TWI822724B (zh) 2023-11-21
AU2019212888A1 (en) 2020-09-10

Similar Documents

Publication Publication Date Title
EP3949382A4 (fr) Architecture de capteur d'image
EA201170251A1 (ru) ЗАМЕЩЕННЫЕ ПРОИЗВОДНЫЕ 1,2,3,4-ТЕТРАГИДРОЦИКЛОПЕНТА[b]ИНДОЛ-3-ИЛ)УКСУСНОЙ КИСЛОТЫ, ПРИМЕНИМЫЕ В ЛЕЧЕНИИ АУТОИММУННЫХ И ВОСПАЛИТЕЛЬНЫХ РАССТРОЙСТВ
EP3767709A4 (fr) Composition d'électrode positive pour accumulateur au lithium-ion, électrode positive pour accumulateur au lithium-ion et accumulateur au lithium-ion
EP2049110A4 (fr) Diazépans pontés antagonistes du récepteur de l'oréxine
MA28358A1 (fr) Inhibiteurs de l'integrase du vih
EA201891267A1 (ru) Фармацевтическая композиция, содержащая действенный ингибитор urat1
MA28519B1 (fr) Inhibiteurs de l'integrase du vih
EP3930852A4 (fr) Protéines de liaison à l'antigène se liant à bcma
EP1725102A4 (fr) Inhibiteurs de l'integrase du vih
MA51664A (fr) Formes cristallines de l'antagoniste du récepteur cxcr7 d'acide (3s,4s)-1-cyclopropylméthyl-4-([5-(2,4-difluoro-phényl)-isoxazole-3-carbonyl]-amino)-pipéridine-3-carboxylique (1-pyrimidin-2-yl-cyclopropyl)-amide
MX2021010133A (es) Forma cristalina de 1-(1-oxo-1,2-dihidroisoquinolin-5-il)-5-(trifl uorometil)-n-(2-(trifluorometil)piridin-4-il)-1h-pirazol-4-carbox amida monohidratada.
EP4168985A4 (fr) Compression d'image multiplans
EP1881825A4 (fr) Inhibiteurs de l'intégrase du vih
MA54713A (fr) Forme posologique parentérale stable d'acétate de cétrorélix
EP4031039A4 (fr) Plaque d'ostéotomie de nivellement du plateau tibial avec décalage
CY1109694T1 (el) Παραγωγα πυρρολιδινης ως ανταγωνιστες υποδοχεα η3 ισταμινης
EP3920962A4 (fr) Purification d'analogues de glp-1
EP3445763A4 (fr) Nouvelles formes de sel cristallin du 3-(1,2,4-triazolo[4,3-a]pyridin-3-yléthynyl)-4-méthyl-n-(4-((4-méthylpipérazin-1-yl)méthyl)-3-trifluorométhylphényl)benzamide pour une application médicale
EA200702612A1 (ru) Соединения бензимидазолкарбоксамида в качестве агонистов рецепторов 5-нт
EP3902545A4 (fr) Nouveaux sels d'agents de dégradation sélectifs du récepteur des oestrogènes
JP2007523166A5 (fr)
EP3924324A4 (fr) Cocristal d'acide l-pipécolique de cannabidiol
ATE525360T1 (de) Neuartige imidazolinylmethyl-aryl-sulfonamide
EP3740204A4 (fr) Formes à l'état solide de fasoracétam
EP3880305A4 (fr) Forme cristalline d'acide 3- ((l-valyl) amino)-1-propanesulfonique