[go: up one dir, main page]

PE20150974A1 - Derivados de piridina - Google Patents

Derivados de piridina

Info

Publication number
PE20150974A1
PE20150974A1 PE2015000616A PE2015000616A PE20150974A1 PE 20150974 A1 PE20150974 A1 PE 20150974A1 PE 2015000616 A PE2015000616 A PE 2015000616A PE 2015000616 A PE2015000616 A PE 2015000616A PE 20150974 A1 PE20150974 A1 PE 20150974A1
Authority
PE
Peru
Prior art keywords
pyridin
prodrug
imidazole
methyl
carboxylic acid
Prior art date
Application number
PE2015000616A
Other languages
English (en)
Inventor
Akinobu Maruyama
Hirofumi Kamada
Mika Fujinuma
Susumu Takeuchi
Hiroshi Saitoh
Yoshimasa Takahashi
Original Assignee
Teijin Pharma 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 Teijin Pharma Ltd filed Critical Teijin Pharma Ltd
Publication of PE20150974A1 publication Critical patent/PE20150974A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C07D233/58Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary 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
    • A61P19/00Drugs for skeletal disorders
    • A61P19/06Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • 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
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/048Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Diabetes (AREA)
  • Epidemiology (AREA)
  • Urology & Nephrology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Vascular Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Beans For Foods Or Fodder (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)

Abstract

Un derivado de piridina representado por la formula (I), un profarmaco del mismo, una sal farmaceuticamente aceptable del derivado de piridina o del profarmaco, donde A es O, S, entre otros; R1 es N o CH; uno de X1 a X5 es N y los cuatro restantes son CH; R3 es H, halogeno, entre otros; R4 es un grupo carboxilo, grupo tetrazolilo, entre otros, que es util para el tratamiento o profilaxis de enfermedades asociadas con URAT1 tales como gota, hiperuricemia, hipertension, enfermedades renales tales como nefritis intersticial, diabetes, arterioesclerosis y sindrome de Lesch-Nyhan. Los compuestos preferidos son: acido 1-(2,5-dimetilbencil)-4-metil-2-(piridin-3-il)-1H-imidazol-5-carboxilico; acido 4-metil-1-(naftalen-1-ilmetil)-2-(piridin-3-il)-1H-imidazol-5-carboxilico; entre otros
PE2015000616A 2012-11-14 2013-11-13 Derivados de piridina PE20150974A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2012250661 2012-11-14

Publications (1)

Publication Number Publication Date
PE20150974A1 true PE20150974A1 (es) 2015-07-04

Family

ID=50731196

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2015000616A PE20150974A1 (es) 2012-11-14 2013-11-13 Derivados de piridina

Country Status (36)

Country Link
US (2) US9637469B2 (es)
EP (2) EP2944633B1 (es)
JP (2) JP5774238B2 (es)
KR (1) KR20150082194A (es)
CN (2) CN104797570B (es)
AR (1) AR093468A1 (es)
AU (2) AU2013345894B2 (es)
BR (1) BR112015010977A2 (es)
CA (1) CA2891408A1 (es)
CL (1) CL2015001279A1 (es)
CY (1) CY1120127T1 (es)
DK (1) DK2944633T3 (es)
ES (1) ES2662444T3 (es)
HR (1) HRP20180451T1 (es)
HU (1) HUE037736T2 (es)
IL (2) IL238539A (es)
LT (1) LT2944633T (es)
MA (1) MA38078B1 (es)
ME (1) ME03016B (es)
MX (1) MX2015003672A (es)
NO (1) NO2944633T3 (es)
NZ (1) NZ708031A (es)
PE (1) PE20150974A1 (es)
PH (1) PH12015501037A1 (es)
PL (1) PL2944633T3 (es)
PT (1) PT2944633T (es)
RS (1) RS57090B1 (es)
RU (1) RU2640588C2 (es)
SA (1) SA515360431B1 (es)
SG (2) SG11201503770VA (es)
SI (1) SI2944633T1 (es)
SM (1) SMT201800322T1 (es)
TW (1) TWI666205B (es)
UA (1) UA117359C2 (es)
WO (1) WO2014077285A1 (es)
ZA (1) ZA201503322B (es)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3144306B1 (en) * 2014-05-13 2017-11-15 Teijin Pharma Limited Pyrazine derivative
MX2016014692A (es) * 2014-05-13 2017-02-23 Teijin Pharma Ltd Polimorfos cristalinos novedosos de derivados de piridina y metodo para producirlos.
MX2018011214A (es) * 2016-03-15 2019-03-28 Bayer Cropscience Ag Sulfonamidas sustituidas para controlar plagas animales.
CN107286156A (zh) * 2016-04-05 2017-10-24 江苏新元素医药科技有限公司 新型urat1抑制剂及其在医药上的应用
CN106008488B (zh) * 2016-05-20 2018-10-30 广东东阳光药业有限公司 氰基吲哚类衍生物及其制备方法和用途
ES2961901T3 (es) * 2016-05-23 2024-03-14 Dongbao Purple Star Hangzhou Biopharmaceutical Co Ltd Tiofeno, método de fabricación del mismo y aplicación farmacéutica del mismo
TW201822637A (zh) 2016-11-07 2018-07-01 德商拜耳廠股份有限公司 用於控制動物害蟲的經取代磺醯胺類
UY37556A (es) 2017-01-10 2018-07-31 Bayer Ag Derivados heterocíclicos como pesticidas
CN110312718B (zh) 2017-01-10 2023-02-28 拜耳公司 作为害虫防治剂的杂环烯衍生物
CN108658879A (zh) * 2017-03-29 2018-10-16 天津药物研究院有限公司 一种urat1抑制剂及其制备方法和用途
CN109251184B (zh) * 2017-07-13 2021-06-15 浙江海正药业股份有限公司 一种2-三氟甲基苯磺酰胺类衍生物的医药用途
CA3093445A1 (en) 2018-03-08 2019-11-28 Incyte Corporation Aminopyrazine diol compounds as pi3k-.gamma. inhibitors
US11046658B2 (en) 2018-07-02 2021-06-29 Incyte Corporation Aminopyrazine derivatives as PI3K-γ inhibitors
TWI820231B (zh) 2018-10-11 2023-11-01 德商拜耳廠股份有限公司 用於製備經取代咪唑衍生物之方法
CN111943957B (zh) * 2019-05-17 2023-01-06 中国医学科学院药物研究所 喹啉甲酰胺类化合物及其制备方法和用途
WO2021089673A1 (de) 2019-11-07 2021-05-14 Bayer Aktiengesellschaft Substituierte sulfonylamide zur bekämpfung tierischer schädlinge
JP2023532548A (ja) 2020-07-02 2023-07-28 バイエル・アクチエンゲゼルシヤフト 有害生物防除剤としてのヘテロサイクレン誘導体
CN114315729B (zh) * 2021-12-09 2024-01-26 大连理工大学 1-苄基-2,4-二芳基咪唑类化合物、合成方法及其在抗肿瘤上的应用
WO2025026738A1 (en) 2023-07-31 2025-02-06 Bayer Aktiengesellschaft 6-[5-(ethylsulfonyl)-1-methyl-1h-imidazol-4-yl]-7-methyl-3-(pentafluoroethyl)-7h-imidazo[4,5-c]pyridazine derivatives as pesticides

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1599032A (en) * 1977-03-04 1981-09-30 May & Baker Ltd Imidazole derivatives having herbicidal activity
JPS5671073A (en) 1979-11-12 1981-06-13 Takeda Chem Ind Ltd Imidazole derivative
US4770689A (en) 1986-03-10 1988-09-13 Janssen Pharmaceutica N.V. Herbicidal imidazole-5-carboxylic acid derivatives
PL149675B1 (pl) 1986-03-10 1990-03-31 Sposób wytwarzania nowych pochodnych kwasu 1-metyl0-1h-imidaz0l0karb0ksyl0weg0-5
DD260928A5 (de) 1986-06-06 1988-10-12 Ciba-Geigy Ag,Ch Verfahren zur herstellung neuer aralkylimidizolderivate
US4851424A (en) 1986-06-06 1989-07-25 Ciba-Geigy Corporation 1-Phenyl-lower alkyl-imidazole 4- or 5-carboxamide compounds which are useful in the treatment of epilepsy
JPH08119936A (ja) 1994-10-18 1996-05-14 Fujisawa Pharmaceut Co Ltd 複素環式誘導体
IT1295405B1 (it) 1997-09-30 1999-05-12 Merck Sharp & Dohme Italia S P Uso di un antagonista recettoriale di angiotensina ii per la preparazione di farmaci per aumentare il tasso di sopravvivenza di
AU2001275794A1 (en) 2000-07-28 2002-02-13 Sumitomo Pharmaceuticals Co. Ltd. Pyrrole derivatives
JP3999128B2 (ja) 2001-02-22 2007-10-31 帝人株式会社 ベンゾ[b]チオフェン誘導体、およびその製造方法
AU2003902828A0 (en) * 2003-06-05 2003-06-26 Fujisawa Pharmaceutical Co., Ltd. Dpp-iv inhibitor
CA2706858C (en) * 2007-11-27 2013-12-24 Ardea Biosciences, Inc. Imidazole and triazole derivatives and methods of use
WO2009148599A1 (en) * 2008-06-04 2009-12-10 Synta Pharmaceuticals Corp. Pyrrole compunds that modulate hsp90 activity
JP2012502049A (ja) * 2008-09-04 2012-01-26 アルディア バイオサイエンス,インク. 尿酸値を調節するための化合物、組成物及びそれを使用する方法。
JP2010202575A (ja) 2009-03-03 2010-09-16 Takeda Chem Ind Ltd 複素環化合物
BR112012000606A2 (pt) * 2009-07-10 2016-11-22 Brigham & Womens Hospital análogos de etomidato que não inibem a síntese de esteróides adrenocorticais
CN102035579B (zh) * 2009-09-28 2014-09-03 夏普株式会社 信息反馈方法和用户设备
AR081930A1 (es) * 2010-06-16 2012-10-31 Ardea Biosciences Inc Compuestos de tioacetato
JP5485811B2 (ja) * 2010-06-23 2014-05-07 株式会社ジャパンディスプレイ 双方向シフトレジスタ、及びこれを用いた画像表示装置
SG187795A1 (en) * 2010-08-11 2013-03-28 Millennium Pharm Inc Heteroaryls and uses thereof

Also Published As

Publication number Publication date
TWI666205B (zh) 2019-07-21
JP2015091865A (ja) 2015-05-14
IL243193A0 (en) 2016-02-29
PL2944633T3 (pl) 2018-08-31
IL238539A (en) 2017-11-30
AR093468A1 (es) 2015-06-10
PH12015501037A1 (en) 2015-07-27
UA117359C2 (uk) 2018-07-25
MA38078B1 (fr) 2017-04-28
JP6293068B2 (ja) 2018-03-14
EP2944633B1 (en) 2018-01-31
JPWO2014077285A1 (ja) 2017-01-05
DK2944633T3 (en) 2018-03-12
RS57090B1 (sr) 2018-06-29
ES2662444T3 (es) 2018-04-06
CN104797570B (zh) 2017-11-07
ME03016B (me) 2018-10-20
CN107721931A (zh) 2018-02-23
ZA201503322B (en) 2016-01-27
KR20150082194A (ko) 2015-07-15
LT2944633T (lt) 2018-03-12
CN104797570A (zh) 2015-07-22
EP2944633A4 (en) 2016-01-06
SG11201503770VA (en) 2015-06-29
HRP20180451T1 (hr) 2018-06-01
SI2944633T1 (en) 2018-06-29
EP3339302A1 (en) 2018-06-27
SMT201800322T1 (it) 2018-07-17
US20150284358A1 (en) 2015-10-08
IL238539A0 (en) 2015-06-30
PT2944633T (pt) 2018-05-09
US20170190694A1 (en) 2017-07-06
SA515360431B1 (ar) 2017-11-15
EP2944633A1 (en) 2015-11-18
RU2015122698A (ru) 2017-01-10
CL2015001279A1 (es) 2015-06-26
HUE037736T2 (hu) 2018-09-28
MX2015003672A (es) 2015-06-15
TW201422603A (zh) 2014-06-16
US9637469B2 (en) 2017-05-02
AU2013345894B2 (en) 2017-05-25
AU2013345894A1 (en) 2015-05-21
NZ708031A (en) 2018-04-27
RU2640588C2 (ru) 2018-01-10
HK1211940A1 (en) 2016-06-03
WO2014077285A1 (ja) 2014-05-22
CA2891408A1 (en) 2014-05-22
AU2013345894A9 (en) 2015-11-12
NO2944633T3 (es) 2018-06-30
CY1120127T1 (el) 2018-12-12
BR112015010977A2 (pt) 2017-07-11
JP5774238B2 (ja) 2015-09-09
AU2017204665A1 (en) 2017-07-27
MA38078A1 (fr) 2016-09-30
SG10201705852PA (en) 2017-08-30

Similar Documents

Publication Publication Date Title
PE20150974A1 (es) Derivados de piridina
PE20170502A1 (es) ACIDO 4-(3-FLUORO-3-(2-(5,6,7,8-TETRAHIDRO-1,8-NAFTIRIDIN-2-IL)ETIL)PIRROLIDIN-1-IL)-3-(3-(2-METOXIETOXI)FENIL)BUTANOICO COMO ANTAGONISTA DE INTEGRINA aVß6
CR20120296A (es) Nuevos compuestos de espiropiperidina
EA201492281A1 (ru) Соединения n-арилтриазола в качестве антагонистов рецепторов лизофосфатидной кислоты (lpar)
ECSP12011799A (es) Compuestos de espiropiperidina y uso farmacéutico de los mismos
EA201492285A1 (ru) Соединения n-алкилтриазола в качестве антагонистов лизофосфатидной кислоты (lpar)
PH12016502382A1 (en) Substituted indazole compounds as irak4 inhibitors
GEP201706671B (en) Heterocyclyl compounds as mek inhibitors
EA201390969A1 (ru) Модуляторы глюкагонового рецептора
EA201691428A1 (ru) Бициклические гетероциклические производные в качестве ингибиторов irak4
PE20170141A1 (es) Procedimiento para la preparacion de (4s)-4-(4-ciano-2-metoxifenil)-5-etoxi-2,8-dimetil-1,4-dihidro-1,6-naftiridin-3-carbox-amida y su purificacion para su uso como principio activo farmaceutico
PE20141822A1 (es) Inhibidor de la quinasa reguladora de la senal de apoptosis
EA201500298A1 (ru) Алкоксипиразолы в качестве активаторов растворимой гуанилатциклазы
PE20150224A1 (es) Inhibidores del nampt
PE20170946A1 (es) 2-amino-6-(difluorometil)- 5,5-difluoro-6-fenil-3,4,5,6-tetrahidropiridinas como inhibidores de bace1
CU20160192A7 (es) Derivados de indano e indolina útiles como activadores de la guanilato ciclasa soluble
CU24330B1 (es) Derivados del ácido 4-((1,1) bifenil-4-il)-3-(3-fosfonopropanamido) butanoico, activos como inhibidores de nep (endopeptidasa neutral)
EA201492283A1 (ru) Замещенные соединения пиразола в качестве антагонистов рецепторов лизофосфатидной кислоты (lpar)
PE20201184A1 (es) Compuestos espirociclicos como moduladores del receptor farnesoide x
BR112014032229A2 (pt) método para produção de 4-[5-(piridin-4-il)-1h-1,2,4-triazol-3-il) piridina-2-carbonitrila, e intermediários da mesma
EA201692300A1 (ru) Производные карбоксамида
PE20181274A1 (es) Compuestos utiles para inhibir ror-gamma-t
PE20142399A1 (es) Compuestos de pirazol como inhibidores de sglt1
CL2017001720A1 (es) Nuevos derivados de bencimidazol como agentes antihistamínicos.
EA201391744A1 (ru) Производные 2-амино-3-(имидазол-2-ил)-пиридин-4-она и их применение в качестве ингибиторов киназы рецептора vegf

Legal Events

Date Code Title Description
FA Abandonment or withdrawal