ME03432B - Piridonski derivati korišćeni kao inhibitori kinaze reorganizovane tokom transfekcije (ret) - Google Patents

Piridonski derivati korišćeni kao inhibitori kinaze reorganizovane tokom transfekcije (ret)

Info

Publication number
ME03432B
ME03432B MEP-2019-136A MEP2019136A ME03432B ME 03432 B ME03432 B ME 03432B ME P2019136 A MEP2019136 A ME P2019136A ME 03432 B ME03432 B ME 03432B
Authority
ME
Montenegro
Prior art keywords
ret
rearranged
kinase inhibitors
during transfection
pyridone derivatives
Prior art date
Application number
MEP-2019-136A
Other languages
German (de)
English (en)
French (fr)
Inventor
Michael P Demartino
Huiping Amy Guan
Original Assignee
Glaxosmithкiine Lntellectual Property Development 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 Glaxosmithкiine Lntellectual Property Development Ltd filed Critical Glaxosmithкiine Lntellectual Property Development Ltd
Publication of ME03432B publication Critical patent/ME03432B/me

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
    • A61K31/435Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/69Two or more oxygen atoms
    • 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
    • A61K31/4412Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • 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
    • A61K31/4418Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (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)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
MEP-2019-136A 2014-09-10 2015-09-09 Piridonski derivati korišćeni kao inhibitori kinaze reorganizovane tokom transfekcije (ret) ME03432B (me)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
CN2014086197 2014-09-10
CN2015086995 2015-08-14
PCT/IB2015/056905 WO2016038552A1 (en) 2014-09-10 2015-09-09 Pyridone derivatives as rearranged during transfection (ret) kinase inhibitors
EP15767599.2A EP3191450B1 (en) 2014-09-10 2015-09-09 Pyridone derivatives as rearranged during transfection (ret) kinase inhibitors

Publications (1)

Publication Number Publication Date
ME03432B true ME03432B (me) 2020-01-20

Family

ID=54186249

Family Applications (1)

Application Number Title Priority Date Filing Date
MEP-2019-136A ME03432B (me) 2014-09-10 2015-09-09 Piridonski derivati korišćeni kao inhibitori kinaze reorganizovane tokom transfekcije (ret)

Country Status (36)

Country Link
US (4) US9918974B2 (me)
EP (2) EP3191450B1 (me)
JP (2) JP6538154B2 (me)
KR (1) KR20170045350A (me)
CN (1) CN107074768B (me)
AU (1) AU2015313841B2 (me)
BR (1) BR112017004900A2 (me)
CA (1) CA2960768A1 (me)
CL (1) CL2017000588A1 (me)
CO (1) CO2017002273A2 (me)
CR (1) CR20170093A (me)
CY (1) CY1121661T1 (me)
DK (1) DK3191450T3 (me)
DO (1) DOP2017000059A (me)
EA (1) EA033544B1 (me)
ES (2) ES2816453T3 (me)
HR (1) HRP20190815T1 (me)
HU (1) HUE044604T2 (me)
IL (1) IL250908B (me)
LT (1) LT3191450T (me)
MA (1) MA40581A (me)
ME (1) ME03432B (me)
MX (1) MX373863B (me)
MY (1) MY181913A (me)
PE (1) PE20170705A1 (me)
PH (1) PH12017500425B1 (me)
PL (1) PL3191450T3 (me)
PT (1) PT3191450T (me)
RS (1) RS58813B1 (me)
SG (1) SG11201701694QA (me)
SI (1) SI3191450T1 (me)
SM (1) SMT201900304T1 (me)
TW (1) TWI683807B (me)
UA (1) UA122213C2 (me)
UY (1) UY36293A (me)
WO (1) WO2016038552A1 (me)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112012029405B1 (pt) 2010-05-20 2021-01-05 Array Biopharma Inc. compostos macrocíclicos como inibidores de trk quinase, composição farmacêutica, uso de um composto de fórmula i ou um sal farmaceuticamente aceitável do mesmo, processo para a preparação de um composto
EP3191450B1 (en) 2014-09-10 2019-04-10 GlaxoSmithKline Intellectual Property Development Limited Pyridone derivatives as rearranged during transfection (ret) kinase inhibitors
PE20170677A1 (es) * 2014-09-10 2017-05-13 Glaxosmithkline Ip Dev Ltd Nuevos compuestos como inhibidores de reorganizado durante la transfeccion (ret)
US10202365B2 (en) 2015-02-06 2019-02-12 Blueprint Medicines Corporation 2-(pyridin-3-yl)-pyrimidine derivatives as RET inhibitors
EP3322706B1 (en) 2015-07-16 2020-11-11 Array Biopharma, Inc. Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors
IL302209B2 (en) 2015-11-02 2024-06-01 Blueprint Medicines Corp Inhibitors of ret
WO2017161269A1 (en) 2016-03-17 2017-09-21 Blueprint Medicines Corporation Inhibitors of ret receptor tyrosine kinases
WO2018017983A1 (en) 2016-07-22 2018-01-25 Blueprint Medicines Corporation Compounds useful for treating disorders related to ret
JP2018052878A (ja) * 2016-09-29 2018-04-05 第一三共株式会社 ピリジン化合物
TWI704148B (zh) 2016-10-10 2020-09-11 美商亞雷生物製藥股份有限公司 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物
JOP20190077A1 (ar) 2016-10-10 2019-04-09 Array Biopharma Inc مركبات بيرازولو [1، 5-a]بيريدين بها استبدال كمثبطات كيناز ret
WO2018136663A1 (en) 2017-01-18 2018-07-26 Array Biopharma, Inc. Ret inhibitors
CN110267960B (zh) 2017-01-18 2022-04-26 阿雷生物药品公司 作为RET激酶抑制剂的取代的吡唑并[1,5-a]吡嗪化合物
JOP20190213A1 (ar) 2017-03-16 2019-09-16 Array Biopharma Inc مركبات حلقية ضخمة كمثبطات لكيناز ros1
JP2020519672A (ja) 2017-05-15 2020-07-02 ブループリント メディシンズ コーポレイション RET阻害剤とmTORC1阻害剤との組合せ及び異常なRET活性によって媒介されるがんを処置するためのその使用
TWI791053B (zh) 2017-10-10 2023-02-01 美商亞雷生物製藥股份有限公司 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之結晶形式及其醫藥組合物
TWI876442B (zh) 2017-10-10 2025-03-11 美商絡速藥業公司 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之調配物
EP3740491A1 (en) 2018-01-18 2020-11-25 Array Biopharma, Inc. Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors
EP3740490A1 (en) 2018-01-18 2020-11-25 Array Biopharma, Inc. Substituted pyrazolo[3,4-d]pyrimidine compounds as ret kinase inhibitors
TW201932464A (zh) 2018-01-18 2019-08-16 美商亞雷生物製藥股份有限公司 作為ret激酶抑制劑之經取代吡唑基[4,3-c]吡啶化合物
PT3773589T (pt) 2018-04-03 2024-02-06 Blueprint Medicines Corp Inibidor de ret para utilização no tratamento de cancro com alteração de ret
WO2020055672A1 (en) 2018-09-10 2020-03-19 Array Biopharma Inc. Fused heterocyclic compounds as ret kinase inhibitors
TWI786742B (zh) * 2020-07-23 2022-12-11 大陸商深圳晶泰科技有限公司 吡啶酮類化合物及其製備方法和應用
EP4578458A1 (en) 2022-08-24 2025-07-02 Toray Industries, Inc. Medicament for treatment and/or prevention of cancer

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999032106A1 (en) * 1997-12-22 1999-07-01 Bayer Corporation Inhibition of raf kinase using substituted heterocyclic ureas
US20120046290A1 (en) 1997-12-22 2012-02-23 Jacques Dumas Inhibition of p38 kinase activity using substituted heterocyclic ureas
US20070244120A1 (en) 2000-08-18 2007-10-18 Jacques Dumas Inhibition of raf kinase using substituted heterocyclic ureas
ES2154253T3 (es) 1997-12-22 2012-01-27 Bayer Healthcare Llc Inhibición de la actividad de p38 cinasa usando ureas heterocíclicas sustituidas.
US7034049B1 (en) 1999-08-12 2006-04-25 Pharmacia Italia S.P.A. 3(5)-amino-pyrazole derivatives, process for their preparation and their use as antitumor agents
CA2430151A1 (en) 2000-11-27 2002-06-20 Pharmacia Italia S.P.A. Phenylacetamido- pyrazole derivatives and their use as antitumor agents
DE10201764A1 (de) 2002-01-18 2003-07-31 Bayer Cropscience Ag Substituierte 4-Aminopyridin-Derivate
AR037647A1 (es) 2002-05-29 2004-12-01 Novartis Ag Derivados de diarilurea utiles para el tratamiento de enfermedades dependientes de la cinasa de proteina
JPWO2004024694A1 (ja) 2002-09-10 2006-01-05 杏林製薬株式会社 4−置換アリール−5−ヒドロキシイソキノリノン誘導体
CA2536293A1 (en) 2003-08-22 2005-03-03 Boehringer Ingelheim Pharmaceuticals, Inc. Methods of treating copd and pulmonary hypertension
TW200530236A (en) * 2004-02-23 2005-09-16 Chugai Pharmaceutical Co Ltd Heteroaryl phenylurea
US7968574B2 (en) 2004-12-28 2011-06-28 Kinex Pharmaceuticals, Llc Biaryl compositions and methods for modulating a kinase cascade
BRPI0519424B8 (pt) * 2004-12-28 2021-05-25 Athenex Inc compostos, composição e uso dos ditos compostos para a preparação de um medicamento para prevenção ou tratamento de um distúrbio de proliferação celular ou infecção microbiana
GB0507575D0 (en) * 2005-04-14 2005-05-18 Novartis Ag Organic compounds
US8247556B2 (en) * 2005-10-21 2012-08-21 Amgen Inc. Method for preparing 6-substituted-7-aza-indoles
TW200804349A (en) * 2005-12-23 2008-01-16 Kalypsys Inc Novel substituted pyrimidinyloxy ureas as inhibitors of protein kinases
ES2500165T3 (es) 2006-06-29 2014-09-30 Kinex Pharmaceuticals, Llc Composiciones de biarilo y métodos para modular una cascada de quinasas
AU2007294686B2 (en) * 2006-09-15 2013-10-31 Equinox Sciences, Llc Kinase inhibitor compounds
AU2007312310A1 (en) * 2006-10-16 2008-04-24 Novartis Ag Phenylacetamides useful as protein kinase inhibitors
AU2007321719B2 (en) * 2006-11-15 2013-11-21 Ym Biosciences Australia Pty Ltd Inhibitors of kinase activity
MX2012001974A (es) 2009-08-19 2012-04-11 Ambit Biosciences Corp Compuestos de biarilo y metodos de uso de los mismos.
US9073895B2 (en) 2010-12-16 2015-07-07 Boehringer Ingelheim International Gmbh Biarylamide inhibitors of leukotriene production
WO2014141187A1 (en) * 2013-03-15 2014-09-18 Glaxosmithkline Intellectual Property Development Limited Pyridine derivatives as rearranged during transfection (ret) kinase inhibitors
US8937071B2 (en) 2013-03-15 2015-01-20 Glaxosmithkline Intellectual Property Development Limited Compounds as rearranged during transfection (RET) inhibitors
EP3191450B1 (en) 2014-09-10 2019-04-10 GlaxoSmithKline Intellectual Property Development Limited Pyridone derivatives as rearranged during transfection (ret) kinase inhibitors
PE20170677A1 (es) 2014-09-10 2017-05-13 Glaxosmithkline Ip Dev Ltd Nuevos compuestos como inhibidores de reorganizado durante la transfeccion (ret)

Also Published As

Publication number Publication date
HUE044604T2 (hu) 2019-11-28
BR112017004900A2 (pt) 2017-12-12
CL2017000588A1 (es) 2017-10-06
PL3191450T3 (pl) 2019-08-30
TWI683807B (zh) 2020-02-01
PT3191450T (pt) 2019-05-29
US9918974B2 (en) 2018-03-20
MA40581A (fr) 2019-04-10
US10292975B2 (en) 2019-05-21
DK3191450T3 (da) 2019-05-20
RS58813B1 (sr) 2019-07-31
ES2725704T3 (es) 2019-09-26
CN107074768A (zh) 2017-08-18
US10709695B2 (en) 2020-07-14
CN107074768B (zh) 2019-12-10
AU2015313841B2 (en) 2018-03-08
JP2019163316A (ja) 2019-09-26
UA122213C2 (uk) 2020-10-12
KR20170045350A (ko) 2017-04-26
CR20170093A (es) 2017-07-17
CO2017002273A2 (es) 2017-06-20
TW201625534A (en) 2016-07-16
DOP2017000059A (es) 2017-03-31
SMT201900304T1 (it) 2019-07-11
SI3191450T1 (sl) 2019-07-31
JP2017527578A (ja) 2017-09-21
EP3517526B1 (en) 2020-08-19
US20170340617A1 (en) 2017-11-30
EP3191450A1 (en) 2017-07-19
CA2960768A1 (en) 2016-03-17
US20180147194A1 (en) 2018-05-31
JP6538154B2 (ja) 2019-07-03
MY181913A (en) 2021-01-14
US10111866B2 (en) 2018-10-30
AU2015313841A1 (en) 2017-03-23
HRP20190815T1 (hr) 2019-07-12
CY1121661T1 (el) 2020-07-31
EP3191450B1 (en) 2019-04-10
MX2017003114A (es) 2017-11-15
JP6728447B2 (ja) 2020-07-22
PE20170705A1 (es) 2017-05-21
SG11201701694QA (en) 2017-04-27
UY36293A (es) 2016-04-01
PH12017500425A1 (en) 2017-07-31
MX373863B (es) 2020-03-26
IL250908B (en) 2020-11-30
ES2816453T3 (es) 2021-04-05
EP3517526A1 (en) 2019-07-31
IL250908A0 (en) 2017-04-30
US20190022078A1 (en) 2019-01-24
LT3191450T (lt) 2019-06-10
US20190247382A1 (en) 2019-08-15
EA033544B1 (ru) 2019-10-31
EA201790546A1 (ru) 2017-07-31
WO2016038552A1 (en) 2016-03-17
PH12017500425B1 (en) 2017-07-31

Similar Documents

Publication Publication Date Title
ME03432B (me) Piridonski derivati korišćeni kao inhibitori kinaze reorganizovane tokom transfekcije (ret)
IL256898B (en) Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors
PL3958977T3 (pl) Pochodne kamptotecyny
LT3523301T (lt) Pakeistieji pirazolo[1,5-a]piridino junginiai kaip ret kinazės slopikliai
IL254124A0 (en) New 3-indole-transformed histories, medicinal preparations and methods of use
HUE054848T2 (hu) Vegyületek és készítmények EGFR mutáns kináz aktivitás módosítására
MA40774A (fr) Dérivés de diaryle-urée en tant qu'inhibiteurs de kinase p38
DK3466955T3 (da) Fremgangsmåde til fremstilling af oxazol[4,5-b]pyridin og thiazol[4,5-b]pyridinderivater som irak4-hæmmere til behandling af cancer
EP3283171A4 (en) DERIVATIVES OF AMPHOTERICIN B
PL3494120T3 (pl) Pochodne oksadiazolopirydyny do zastosowania jako inhibitory o-acylotransferazy greliny (goat)
IL253549B (en) Antibody-urease conjugates for therapeutic purposes
DK3452465T3 (da) Substituerede 2,4-diaminoquinolinderivater til anvendelse til behandling af proliferative sygdomme
DK3303323T3 (da) Heterocykliske forbindelser af 3,3-difluorpiperidincarbamat som NR2B-NMDA-receptorantagonister
HUE060654T2 (hu) Heterokondelzált piridonvegyületek és azok IDH-gátlóként történõ alkalmazása
HUE054815T2 (hu) 3,5-Difenil-diazol vegyületek vízoldható származékai
DK3512518T3 (da) Buprenophinformuleringer med langvarig frigivelse
EP3312172A4 (en) aminopyrazole
LT3500572T (lt) Citizino dariniai, skirti priklausomybių gydymui
IL252986B (en) 5,3-diaminopyrazole kinase inhibitors
MA42048A (fr) Dérivés d'aminoesters
HUE053725T2 (hu) Aminotiolészter vegyületek vagy azok gyógyászatilag elfogadható sói, rák kezelésében történõ alkalmazásra
DK3242877T3 (da) Fremgangsmåde til at fremstille thiazolderivat
MA41641A (fr) Dérivés de tétrahydropyranylbenzamide
GB201412045D0 (en) Tibial intra-medullary nail alignment support
TH1501005474A (th) อนุพันธ์ไพริดีนในรูปสารยับยั้งไคเนสถูกจัดเรียงใหม่ในระหว่างการทรานส์เฟคชั่น (ret)