HRP20210040T1 - (2r,4r)-5-(5′-klor-2’-fluorbifenil-4-il)-2-hidroksi-4-[(5-metiloksazol-2-karbonil)amino]pentanska kiselina - Google Patents

(2r,4r)-5-(5′-klor-2’-fluorbifenil-4-il)-2-hidroksi-4-[(5-metiloksazol-2-karbonil)amino]pentanska kiselina Download PDF

Info

Publication number
HRP20210040T1
HRP20210040T1 HRP20210040TT HRP20210040T HRP20210040T1 HR P20210040 T1 HRP20210040 T1 HR P20210040T1 HR P20210040T T HRP20210040T T HR P20210040TT HR P20210040 T HRP20210040 T HR P20210040T HR P20210040 T1 HRP20210040 T1 HR P20210040T1
Authority
HR
Croatia
Prior art keywords
crystalline form
compound
compound according
methyloxazole
fluorobiphenyl
Prior art date
Application number
HRP20210040TT
Other languages
English (en)
Croatian (hr)
Inventor
Melissa Fleury
Adam D. Hughes
Anne-Marie Beausoleil
Erik FENSTER
Venkat R. Thalladi
Miroslav Rapta
Original Assignee
Theravance Biopharma R&D Ip, Llc
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 Theravance Biopharma R&D Ip, Llc filed Critical Theravance Biopharma R&D Ip, Llc
Publication of HRP20210040T1 publication Critical patent/HRP20210040T1/hr

Links

Classifications

    • 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
    • A61K31/42Oxazoles
    • A61K31/4211,3-Oxazoles, e.g. pemoline, trimethadione
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/12Carboxylic acids; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4816Wall or shell material
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4816Wall or shell material
    • A61K9/4825Proteins, e.g. gelatin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/54Organic compounds
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B7/00Single-crystal growth from solutions using solvents which are liquid at normal temperature, e.g. aqueous solutions
    • C30B7/14Single-crystal growth from solutions using solvents which are liquid at normal temperature, e.g. aqueous solutions the crystallising materials being formed by chemical reactions in the solution
    • 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)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Hospice & Palliative Care (AREA)
  • Pulmonology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Medicinal Preparation (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
HRP20210040TT 2015-02-19 2016-02-12 (2r,4r)-5-(5′-klor-2’-fluorbifenil-4-il)-2-hidroksi-4-[(5-metiloksazol-2-karbonil)amino]pentanska kiselina HRP20210040T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562118067P 2015-02-19 2015-02-19
PCT/US2016/017699 WO2016133803A1 (en) 2015-02-19 2016-02-12 (2r,4r)-5-(5'-chloro-2'-fluorobiphenyl-4-yl)-2-hydroxy-4-[(5-methyloxazole-2-carbonyl)amino]pentanoic acid
EP16708268.4A EP3259255B1 (en) 2015-02-19 2016-02-12 (2r,4r)-5-(5'-chloro-2'-fluorobiphenyl-4-yl)-2-hydroxy-4-[(5-methyloxazole-2-carbonyl)amino]pentanoic acid

Publications (1)

Publication Number Publication Date
HRP20210040T1 true HRP20210040T1 (hr) 2021-04-02

Family

ID=55456914

Family Applications (1)

Application Number Title Priority Date Filing Date
HRP20210040TT HRP20210040T1 (hr) 2015-02-19 2016-02-12 (2r,4r)-5-(5′-klor-2’-fluorbifenil-4-il)-2-hidroksi-4-[(5-metiloksazol-2-karbonil)amino]pentanska kiselina

Country Status (29)

Country Link
US (6) US9533962B2 (enExample)
EP (1) EP3259255B1 (enExample)
JP (1) JP6714009B2 (enExample)
KR (1) KR102573351B1 (enExample)
CN (1) CN107250119B (enExample)
AU (1) AU2016220348B2 (enExample)
BR (1) BR112017017783A2 (enExample)
CA (1) CA2975269C (enExample)
CO (1) CO2017008426A2 (enExample)
CY (1) CY1123728T1 (enExample)
DK (1) DK3259255T3 (enExample)
ES (1) ES2857101T3 (enExample)
HR (1) HRP20210040T1 (enExample)
HU (1) HUE052732T2 (enExample)
IL (1) IL253759B (enExample)
LT (1) LT3259255T (enExample)
MX (1) MX370065B (enExample)
MY (1) MY191183A (enExample)
PH (1) PH12017501444A1 (enExample)
PL (1) PL3259255T3 (enExample)
PT (1) PT3259255T (enExample)
RS (1) RS61325B1 (enExample)
RU (1) RU2715241C2 (enExample)
SG (1) SG11201706662YA (enExample)
SI (1) SI3259255T1 (enExample)
SM (1) SMT202100028T1 (enExample)
TW (1) TWI707846B (enExample)
WO (1) WO2016133803A1 (enExample)
ZA (1) ZA201705487B (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX356260B (es) * 2012-06-08 2018-05-21 Theravance Biopharma R&D Ip Llc Inhibidores de la neprilisina.
HRP20210040T1 (hr) 2015-02-19 2021-04-02 Theravance Biopharma R&D Ip, Llc (2r,4r)-5-(5′-klor-2’-fluorbifenil-4-il)-2-hidroksi-4-[(5-metiloksazol-2-karbonil)amino]pentanska kiselina
KR102238177B1 (ko) 2017-09-15 2021-04-07 주식회사 엘지화학 전지셀 및 전극 리드 제조방법
UY38072A (es) 2018-02-07 2019-10-01 Novartis Ag Compuestos derivados de éster butanoico sustituido con bisfenilo como inhibidores de nep, composiciones y combinaciones de los mismos
RS65436B1 (sr) 2019-07-03 2024-05-31 Merck Patent Gmbh Postupak za proizvodnju (s)-3-hidroksi-1-(1h-indol-5-il)-2-okso-pirolidin-3-karboksilne kiseline 3,5-difluoro-benzilamida

Family Cites Families (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4189604A (en) 1975-07-22 1980-02-19 Zaidan Hojin Biseibutsu Kagaku Kenkyu Kai Bestatin
US4206232A (en) 1976-05-10 1980-06-03 E. R. Squibb & Sons, Inc. Relieving hypertension with carboxyalkylacylamino acids
IL58849A (en) 1978-12-11 1983-03-31 Merck & Co Inc Carboxyalkyl dipeptides and derivatives thereof,their preparation and pharmaceutical compositions containing them
FR2480747A1 (fr) 1980-04-17 1981-10-23 Roques Bernard Derives d'acides amines et leur application therapeutique
US4906615A (en) 1980-12-18 1990-03-06 Schering Corporation Substituted dipeptides as inhibitors of enkephalinases
US4722810A (en) 1984-08-16 1988-02-02 E. R. Squibb & Sons, Inc. Enkephalinase inhibitors
US4939261A (en) 1984-06-08 1990-07-03 Ciba-Geigy Corporation N-substituted butyramide derivatives useful for treatment of conditions responsive to inhibition of enkephalinase
EP0225292A3 (en) 1985-12-06 1988-11-30 Ciba-Geigy Ag Certain n-substituted butyramide derivatives
US4929641B1 (en) 1988-05-11 1994-08-30 Schering Corp Mercapto-acylamino acid antihypertensives
KR880007441A (ko) 1986-12-11 1988-08-27 알렌 제이.스피겔 스피로-치환된 글루타르아미드 이뇨제
FR2623498B1 (fr) 1987-11-24 1990-04-06 Bioprojet Soc Civ Nouveaux composes enantiomeres derives d'amino-acides, leur procede de preparation et leurs applications therapeutiques
GB8820844D0 (en) 1988-09-05 1988-10-05 Pfizer Ltd Therapeutic agents
US5599951A (en) 1989-09-15 1997-02-04 Societe Civile Bioprojet Amino acid derivatives, the process for their preparation and their applications to therapy
US5155100A (en) 1991-05-01 1992-10-13 Ciba-Geigy Corporation Phosphono/biaryl substituted dipeptide derivatives
US5294632A (en) 1991-05-01 1994-03-15 Ciba-Geigy Corporation Phosphono/biaryl substituted dipetide derivatives
US5217996A (en) 1992-01-22 1993-06-08 Ciba-Geigy Corporation Biaryl substituted 4-amino-butyric acid amides
US5508272A (en) 1993-06-15 1996-04-16 Bristol-Myers Squibb Company Compounds containing a fused bicycle ring and processes therefor
DE19510566A1 (de) 1995-03-23 1996-09-26 Kali Chemie Pharma Gmbh Benzazepin-, Benzoxazepin- und Benzothiazepin-N-essigsäurederivate sowie Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel
CA2218716A1 (en) 1995-04-21 1996-10-24 Novartis Ag N-aroylamino acid amides as endothelin inhibitors
US6660756B2 (en) 2001-03-28 2003-12-09 Pfizer Inc. N-phenpropylcyclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase
GB0119305D0 (en) 2001-04-12 2001-10-03 Aventis Pharma Gmbh Mercaptoacetylamide derivatives,a process for their preparation and their use
WO2006027680A1 (en) 2004-09-10 2006-03-16 Pfizer Limited 3-(1-carbamoylcyclohexyl) propionic acid derivatives as inhibitors of neutral endopeptidase enzyme
AR057882A1 (es) 2005-11-09 2007-12-26 Novartis Ag Compuestos de accion doble de bloqueadores del receptor de angiotensina e inhibidores de endopeptidasa neutra
WO2007106708A2 (en) 2006-03-10 2007-09-20 Novartis Ag Combinations of the angiotensin ii antagonist valsartan and the nep inhibitor daglutril
SG185318A1 (en) 2007-01-12 2012-11-29 Novartis Ag Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid
TWI448284B (zh) 2007-04-24 2014-08-11 Theravance Inc 雙效抗高血壓劑
AR070176A1 (es) 2008-01-17 2010-03-17 Novartis Ag Procesos de sintesis de inhibidores de nep, compuestos intermediarios y uso de los mismos en la sintesis
EP2435402B1 (en) * 2009-05-28 2016-04-13 Novartis AG Substituted aminobutyric derivatives as neprilysin inhibitors
BRPI1011657A2 (pt) * 2009-05-28 2019-04-16 Novartis Ag derivados aminopropiônicos substituídos como inibidores de neprilisina
US8372984B2 (en) * 2009-07-22 2013-02-12 Theravance, Inc. Dual-acting oxazole antihypertensive agents
JO2967B1 (en) 2009-11-20 2016-03-15 نوفارتس ايه جي Acetic acid derivatives of carbamoyl methyl amino are substituted as new NEP inhibitors
CN104262228B (zh) 2010-01-22 2017-01-18 诺华股份有限公司 中性内肽酶抑制剂中间体和其制备方法
US8673974B2 (en) 2010-11-16 2014-03-18 Novartis Ag Substituted amino bisphenyl pentanoic acid derivatives as NEP inhibitors
US8993631B2 (en) 2010-11-16 2015-03-31 Novartis Ag Method of treating contrast-induced nephropathy
RS54348B1 (sr) 2010-12-15 2016-02-29 Theravance Biopharma R&D Ip, Llc Inhibitori neprilizina
KR101892611B1 (ko) 2010-12-15 2018-08-28 세라밴스 바이오파마 알앤디 아이피, 엘엘씨 네프릴리신 억제제
CN103380119B (zh) * 2011-02-17 2016-02-17 施万生物制药研发Ip有限责任公司 作为脑啡肽酶抑制剂的经取代的氨基丁酸衍生物
WO2012154249A1 (en) 2011-02-17 2012-11-15 Theravance, Inc. Substituted aminobutyric derivatives as neprilysin inhibitors
EP2714660B1 (en) 2011-05-31 2018-09-26 Theravance Biopharma R&D IP, LLC Neprilysin inhibitors
US8686184B2 (en) 2011-05-31 2014-04-01 Theravance, Inc. Neprilysin inhibitors
JP5959074B2 (ja) 2011-05-31 2016-08-02 セラヴァンス バイオファーマ アール&ディー アイピー, エルエルシー ネプリライシン阻害剤
TWI560172B (en) 2011-11-02 2016-12-01 Theravance Biopharma R&D Ip Llc Neprilysin inhibitors
CA2871292A1 (en) 2012-05-31 2013-12-05 Theravance Biopharma R&D Ip, Llc Nitric oxide donor neprilysin inhibitors
MX356260B (es) 2012-06-08 2018-05-21 Theravance Biopharma R&D Ip Llc Inhibidores de la neprilisina.
CA2873328A1 (en) 2012-06-08 2013-12-12 Theravance Biopharma R&D Ip, Llc Neprilysin inhibitors
CN104520277B (zh) 2012-08-08 2018-01-19 施万生物制药研发Ip有限责任公司 脑啡肽酶抑制剂
HRP20171097T1 (hr) 2013-03-05 2017-10-06 Theravance Biopharma R&D Ip, Llc Inhibitori neprilizina
JP2017504625A (ja) * 2014-01-30 2017-02-09 セラヴァンス バイオファーマ アール&ディー アイピー, エルエルシー ネプリライシン阻害剤としての5−ビフェニル−4−ヘテロアリールカルボニルアミノ−ペンタン酸誘導体
JP6766055B2 (ja) 2015-02-11 2020-10-07 セラヴァンス バイオファーマ アール&ディー アイピー, エルエルシー ネプリライシン阻害剤としての(2s,4r)−5−(5’−クロロ−2’−フルオロビフェニル−4−イル)−4−(エトキシオキサリルアミノ)−2−ヒドロキシメチル−2−メチルペンタン酸
HRP20210040T1 (hr) * 2015-02-19 2021-04-02 Theravance Biopharma R&D Ip, Llc (2r,4r)-5-(5′-klor-2’-fluorbifenil-4-il)-2-hidroksi-4-[(5-metiloksazol-2-karbonil)amino]pentanska kiselina

Also Published As

Publication number Publication date
US10548879B2 (en) 2020-02-04
SI3259255T1 (sl) 2021-04-30
IL253759B (en) 2020-10-29
PL3259255T3 (pl) 2021-07-26
CA2975269C (en) 2023-09-19
TW201638074A (zh) 2016-11-01
CA2975269A1 (en) 2016-08-25
PH12017501444A1 (en) 2018-01-15
MX370065B (es) 2019-11-29
US11642332B2 (en) 2023-05-09
KR20170118855A (ko) 2017-10-25
RS61325B1 (sr) 2021-02-26
TWI707846B (zh) 2020-10-21
SG11201706662YA (en) 2017-09-28
US20170196841A1 (en) 2017-07-13
HUE052732T2 (hu) 2021-05-28
JP6714009B2 (ja) 2020-06-24
WO2016133803A1 (en) 2016-08-25
MX2017010666A (es) 2017-11-16
US10172834B2 (en) 2019-01-08
CO2017008426A2 (es) 2017-11-10
CN107250119A (zh) 2017-10-13
RU2017132430A3 (enExample) 2019-08-12
KR102573351B1 (ko) 2023-09-01
US20200281900A1 (en) 2020-09-10
MY191183A (en) 2022-06-04
AU2016220348A1 (en) 2017-08-17
US20210401808A1 (en) 2021-12-30
LT3259255T (lt) 2021-04-26
CN107250119B (zh) 2020-09-22
US20190269659A1 (en) 2019-09-05
AU2016220348B2 (en) 2019-10-17
NZ734623A (en) 2021-01-29
US9872855B2 (en) 2018-01-23
US20180228774A1 (en) 2018-08-16
RU2715241C2 (ru) 2020-02-26
IL253759A0 (en) 2017-09-28
ZA201705487B (en) 2018-05-30
RU2017132430A (ru) 2019-03-19
ES2857101T3 (es) 2021-09-28
US20160244416A1 (en) 2016-08-25
JP2018507207A (ja) 2018-03-15
DK3259255T3 (da) 2021-01-18
SMT202100028T1 (it) 2021-03-15
CY1123728T1 (el) 2022-05-27
EP3259255A1 (en) 2017-12-27
US11033533B2 (en) 2021-06-15
BR112017017783A2 (pt) 2018-07-17
HK1245772A1 (zh) 2018-08-31
EP3259255B1 (en) 2020-10-21
PT3259255T (pt) 2021-01-26
US9533962B2 (en) 2017-01-03

Similar Documents

Publication Publication Date Title
HRP20210040T1 (hr) (2r,4r)-5-(5′-klor-2’-fluorbifenil-4-il)-2-hidroksi-4-[(5-metiloksazol-2-karbonil)amino]pentanska kiselina
KR101829595B1 (ko) 3-(1-{3-[5-(1-메틸-피페리딘-4일메톡시)-피리미딘-2-일]-벤질}-6-옥소-1,6-디히드로-피리다진-3-일)-벤조니트릴 히드로클로라이드 염의 신규한 다형체 및 이의 제조 방법
RU2016136823A (ru) Кристаллические формы 5-хлор-n2-(2-изопропокси-5-метил-4-пиперидин-4-ил-фенил)-n4-[2-(пропан-2-сульфонил)-фенил]-пиримидин-2,4-диамина
TW200813016A (en) Novel heterocyclic substituted pyridine compounds with CXCR3 antagonist activity
CN109923114A (zh) 作为hpk1调节剂的吡唑并吡啶衍生物和其用于治疗癌症的用途
HRP20170736T1 (hr) Indoli
HRP20201681T1 (hr) Inhibitor aurora a kinaze
HRP20171201T1 (hr) Postupak kristalizacije i biodostupnost
JP2016537366A5 (enExample)
CN102480966A (zh) 融合的杂环化合物及其用途
CN105837560A (zh) 调控jak激酶的喹唑啉衍生物和其使用方法
JP2015529234A5 (enExample)
HRP20180411T1 (hr) Predlijekovi inhibitora aminokinazolinske kinaze
HRP20241633T1 (hr) 2,4-disupstituirani derivat pirimidina, postupak njegove pripreme i njegova uporaba
JP2015529681A5 (enExample)
CN103565653A (zh) 取代的吡唑酮化合物及其使用方法和用途
RS61715B1 (sr) Inhibicija jonskog kanala tranzitornog receptorskog potencijala a1
JP6978003B2 (ja) 複素環式化合物およびその使用
HRP20171763T1 (hr) Derivati piridin-4-ila
JP6978002B2 (ja) チエノ−ピリミジン誘導体およびその使用
JP2018506535A5 (ja) ネプリライシン阻害剤としての(2s,4r)−5−(5’−クロロ−2’−フルオロビフェニル−4−イル)−4−(エトキシオキサリルアミノ)−2−ヒドロキシメチル−2−メチルペンタン酸
HRP20211046T1 (hr) Upotreba derivata benzimidazola kod noćnog proboja kiseline
RU2016141650A (ru) Амидные соединения
JP2018507207A5 (enExample)
CN104130265B (zh) 一种含有螺环或桥环的嘧啶类化合物