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)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (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 (18)

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)
IL (1) IL276227B1 (fr)
MA (1) MA51664B1 (fr)
MX (1) MX2020007881A (fr)
PH (1) PH12020551121A1 (fr)
SG (1) SG11202006943TA (fr)
TW (1) TWI822724B (fr)
UA (1) UA125327C2 (fr)
WO (1) WO2019145460A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3490986B1 (fr) 2016-07-28 2021-11-24 Idorsia Pharmaceuticals Ltd Modulateurs du récepteur de cxcr7 pipéridine
AU2020372647A1 (en) 2019-10-31 2022-06-16 Idorsia Pharmaceuticals Ltd Combination of a CXCR7 antagonist with an S1P1 receptor modulator

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004050024A2 (fr) 2002-11-27 2004-06-17 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
WO2005032490A2 (fr) 2003-10-08 2005-04-14 Bristol-Myers Squibb Company Diamines cycliques et derives comme inhibiteurs du facteur xa
BRPI0607756A2 (pt) 2005-02-18 2010-05-18 Astrazeneca Ab composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, método para inibição de dna girase bacteriana e/ou topoisomerase iv em um animal de sangue quente, uso de um composto ou um sal farmaceuticamente aceitável do mesmo, e, processo para preparar compostos ou sais farmaceuticamente aceitáveis dos mesmos
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
PT2925745T (pt) * 2012-11-29 2018-08-08 Chemocentryx Inc Antagonistas de cxcr7
CN105263924B (zh) 2013-05-30 2018-10-19 爱杜西亚制药有限公司 Cxcr7受体调节剂
AU2014315457B2 (en) 2013-09-04 2018-05-10 Bristol-Myers Squibb Company Compounds useful as immunomodulators
ES2788848T3 (es) 2013-09-06 2020-10-23 Aurigene Discovery Tech Ltd Derivados de 1,2,4-oxadiazol como inmunomoduladores
WO2015044900A1 (fr) 2013-09-27 2015-04-02 Aurigene Discovery Technologies Limited Composés immunomodulateurs thérapeutiques
KR20170047397A (ko) * 2014-09-10 2017-05-04 에피자임, 인코포레이티드 치환된 피페리딘 화합물
AU2015315173A1 (en) * 2014-09-10 2017-03-16 Epizyme, Inc. Substituted pyrrolidine compounds
WO2016087370A1 (fr) 2014-12-01 2016-06-09 Actelion Pharmaceuticals Ltd Modulateurs du récepteur cxcr7
EP3490986B1 (fr) * 2016-07-28 2021-11-24 Idorsia Pharmaceuticals Ltd Modulateurs du récepteur de cxcr7 pipéridine

Also Published As

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

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