PE20211963A1 - Formas cristalinas de un inhibidor de par4 - Google Patents

Formas cristalinas de un inhibidor de par4

Info

Publication number
PE20211963A1
PE20211963A1 PE2021000917A PE2021000917A PE20211963A1 PE 20211963 A1 PE20211963 A1 PE 20211963A1 PE 2021000917 A PE2021000917 A PE 2021000917A PE 2021000917 A PE2021000917 A PE 2021000917A PE 20211963 A1 PE20211963 A1 PE 20211963A1
Authority
PE
Peru
Prior art keywords
thromboembolic disorders
crystal forms
crystals
par4
par4 inhibitor
Prior art date
Application number
PE2021000917A
Other languages
English (en)
Inventor
Roxana F Schlam
Nicolas Cuniere
Victoria A Mbachu
Zhongping Shi
Petinka I Vlahova
Original Assignee
Bristol Myers Squibb Co
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 Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of PE20211963A1 publication Critical patent/PE20211963A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/433Thidiazoles
    • 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
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C55/00Saturated compounds having more than one carboxyl group bound to acyclic carbon atoms
    • C07C55/02Dicarboxylic acids
    • C07C55/10Succinic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/235Saturated compounds containing more than one carboxyl group
    • C07C59/245Saturated compounds containing more than one carboxyl group containing hydroxy or O-metal groups
    • C07C59/265Citric acid
    • 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

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Esta referido a co-cristales del antagonista del receptor 4 activado por proteasa (PAR4), 4-(4-(((6-metoxi-2-(2-metoxiimidazo [2,1-b][1,3, 4]tiadiazol-6-il)benzofuran-4-il)oxi) metil)tiazol-2-il)-N, N-dimetilbenzamida (compuesto de Formula I). La molecula co-formadora de los co-cristales es acido succinico o acido citrico. Estos compuestos se emplean para tratar o prevenir trastornos tromboembolicos como trastornos tromboembolicos cardiovasculares arteriales, trastornos tromboembolicos cardiovasculares venosos, trastornos tromboembolicos cerebrovasculares y trastornos tromboembolicos en las camaras del corazon o en la circulacion periferica
PE2021000917A 2018-12-21 2019-12-20 Formas cristalinas de un inhibidor de par4 PE20211963A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201862783223P 2018-12-21 2018-12-21
PCT/US2019/067717 WO2020132381A1 (en) 2018-12-21 2019-12-20 Crystalline forms of a par4 inhibitor

Publications (1)

Publication Number Publication Date
PE20211963A1 true PE20211963A1 (es) 2021-10-04

Family

ID=69187955

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2021000917A PE20211963A1 (es) 2018-12-21 2019-12-20 Formas cristalinas de un inhibidor de par4

Country Status (27)

Country Link
US (1) US20220064186A1 (es)
EP (1) EP3898638B1 (es)
JP (1) JP7473554B2 (es)
KR (1) KR20210109559A (es)
CN (1) CN113227102A (es)
AU (1) AU2019403348A1 (es)
BR (1) BR112021011688A2 (es)
CA (1) CA3124100A1 (es)
CL (1) CL2021001590A1 (es)
CO (1) CO2021008043A2 (es)
DK (1) DK3898638T3 (es)
EA (1) EA202191760A1 (es)
ES (1) ES2964404T3 (es)
FI (1) FI3898638T3 (es)
HR (1) HRP20231527T1 (es)
HU (1) HUE064830T2 (es)
IL (1) IL284222A (es)
LT (1) LT3898638T (es)
MX (1) MX2021007417A (es)
PE (1) PE20211963A1 (es)
PL (1) PL3898638T3 (es)
PT (1) PT3898638T (es)
RS (1) RS64900B1 (es)
SG (1) SG11202106561RA (es)
SI (1) SI3898638T1 (es)
WO (1) WO2020132381A1 (es)
ZA (1) ZA202105115B (es)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112014026643B1 (pt) * 2012-04-26 2023-03-07 Universite De Montreal Derivados de imidazotiadiazol e imidazopirazina como inibidores de receptor 4 ativado por protease (par4) para o tratamento de agregação de plaqueta, seus usos e composição farmacêutica

Also Published As

Publication number Publication date
CL2021001590A1 (es) 2021-12-03
MX2021007417A (es) 2021-08-05
SI3898638T1 (sl) 2023-12-29
EP3898638B1 (en) 2023-08-30
BR112021011688A2 (pt) 2021-09-08
FI3898638T3 (fi) 2023-11-15
JP2022514624A (ja) 2022-02-14
SG11202106561RA (en) 2021-07-29
KR20210109559A (ko) 2021-09-06
HUE064830T2 (hu) 2024-04-28
EP3898638A1 (en) 2021-10-27
CO2021008043A2 (es) 2021-06-30
ZA202105115B (en) 2024-02-28
HRP20231527T1 (hr) 2024-04-26
IL284222A (en) 2021-08-31
ES2964404T3 (es) 2024-04-05
CN113227102A (zh) 2021-08-06
RS64900B1 (sr) 2023-12-29
DK3898638T3 (da) 2023-11-20
PT3898638T (pt) 2023-11-13
PL3898638T3 (pl) 2023-12-04
WO2020132381A1 (en) 2020-06-25
EA202191760A1 (ru) 2021-10-07
CA3124100A1 (en) 2020-06-25
JP7473554B2 (ja) 2024-04-23
AU2019403348A1 (en) 2021-08-05
LT3898638T (lt) 2023-11-10
US20220064186A1 (en) 2022-03-03

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