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HRP20160044T1 - Novi spojevi fenilamino izonikotinamida - Google Patents

Novi spojevi fenilamino izonikotinamida Download PDF

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Publication number
HRP20160044T1
HRP20160044T1 HRP20160044TT HRP20160044T HRP20160044T1 HR P20160044 T1 HRP20160044 T1 HR P20160044T1 HR P20160044T T HRP20160044T T HR P20160044TT HR P20160044 T HRP20160044 T HR P20160044T HR P20160044 T1 HRP20160044 T1 HR P20160044T1
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HR
Croatia
Prior art keywords
hydrogen
hal
pharmaceutically acceptable
cancer
subformula
Prior art date
Application number
HRP20160044TT
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English (en)
Inventor
Andreas Goutopoulos
Henry Yu
Benny C. Askew
Lesley Liu-Bujalski
Original Assignee
Merck Patent Gmbh
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.)
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Publication date
Application filed by Merck Patent Gmbh filed Critical Merck Patent Gmbh
Publication of HRP20160044T1 publication Critical patent/HRP20160044T1/hr

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    • 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
    • C07D213/82Amides; Imides in position 3
    • 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
    • A61P1/18Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • 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
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/04Antipruritics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • 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
    • 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
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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
    • 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/79Acids; Esters
    • 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Urology & Nephrology (AREA)
  • Dermatology (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Neurology (AREA)
  • Vascular Medicine (AREA)
  • Neurosurgery (AREA)
  • Ophthalmology & Optometry (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Obesity (AREA)
  • Biomedical Technology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Claims (10)

1. Spoj s Formulom (II) [image] i njegove farmaceutski prihvatljive soli, ili solvati, naznačen time da: R1 je vodik, metil, etil, n-propil, i-propil, SH ili Hal, R2 je vodik, metoksi, etoksi, acetilen, cijano, SH ili Hal, R3, R4 su neovisno izabrani od vodika, SH ili Hal, i Hal je F, Cl, Br ili I.
2. Spoj prema zahtjevu 1, u kojem radikali koji nisu naznačeni s više detalja imaju značenje navedeno za Formulu (II) prema zahtjevu 1, ali u kojem u Podformuli IA R1 je Hal, metil ili etil, R2 je vodik, Hal, metoksi ili acetilen, R3 je vodik ili Hal, R4 je vodik ili Hal, Hal je F, Cl, Br ili I, u Podformuli IB R1 je Hal, R2 je vodik ili Hal, R3 je vodik ili Hal, R4 je vodik ili Hal, Hal je F, Cl, Br ili I, u Podformuli IC R1 je F, Cl, metil ili etil, R2 je vodik, I, Br, metoksi ili acetilen, R3 je vodik ili Hal, R4 je vodik ili Hal, Hal je F, Cl, Br ili I, u Podformuli ID R1 je F, Cl, metil ili etil, R2 je vodik, I, Br, metoksi ili acetilen, R3 je vodik ili F, R4 je vodik ili Cl u Podformuli IE R1 je F ili Cl, R2 je I ili Br, R3 je vodik ili F, R4 je vodik ili Cl u Podformuli IF R1 je F ili Cl, R2 je I ili Br, R3 je vodik ili F, R4 je vodik ili Cl, u Podformuli IG R1 je F ili Cl, R2 je I ili Br, R3 je vodik, R4 je vodik, te u Podformuli IH R1 je F, R2 je I, R3 je vodik ili F, R4 je vodik ili Cl, i njegove farmaceutski prihvatljive soli, ili solvati.
3. Spoj prema zahtjevu 1, naznačen time da je spoj odabran iz skupine koju čine: [image] i njegove farmaceutski prihvatljive soli, ili solvati.
4. Farmaceutski pripravak naznačen time da kao aktivni sastojak sadrži spoj prema bilo kojem od zahtjeva 1 do 3, ili njegovu farmaceutski prihvatljivu sol ili solvat, zajedno s farmaceutski prihvatljivim nosačem.
5. Spoj prema bilo kojem od zahtjeva 1 do 3, ili njegova farmaceutski prihvatljiva sol ili solvat, naznačen time da je za uporabu kao lijek.
6. Spoj prema bilo kojem od zahtjeva 1 do 3, ili njegova farmaceutski prihvatljiva sol ili solvat, naznačen time da je za uporabu za liječenje hiperproliferativnih bolesti povezanih s hiperaktivnošću MEK kao i bolesti koje su modulirane pomoću MEK kaskade kod sisavaca
7. Spoj prema zahtjevu 6, ili njegova farmaceutski prihvatljiva sol ili solvat, za uporabu prema zahtjevu 6 naznačen time da je bolest odabrana iz skupine koju čine karcinom, upala, pankreatitis ili bolest bubrega, bol, benigna hiperplazija kože, restenoza, prostate, bolesti povezane s vaskulogenezom ili angiogenezom, angiogenezom tumora, kožne bolesti koje su odabrane od psorijaze, ekcema, i sklerodermije, dijabetes, dijabetička retinopatija, retinopatija zbog preuranjenog porođaja, makularna degeneracija povezana sa starenjem, hemangiom, gliom, melanom i Kapozijev sarkom.
8. Spoj prema zahtjevu 7, ili njegova farmaceutski prihvatljiva sol ili solvat, za uporabu prema zahtjevu 7 naznačen time da bolest je rak.
9. Spoj prema zahtjevu 8, ili njegova farmaceutski prihvatljiva sol ili solvat, za uporabu prema zahtjevu 8 naznačen time da rak je rak mozga, pluća, skvamoznih stanica, mjehura, rak želuca, gušterače, dojke, glave, vrata, bubrega, jajnika, prostate, rak debelog crijeva, jednjaka, rak testisa, ginekološki rak ili rak štitnjače, melanom, mijelogena leukemija, multipli mijelom, kronična mijelogena leukemija ili leukemija mijeloidnih stanica.
10. Komplet (kit) naznačen time da sadrži odvojena pakiranja učinkovite količine spoja prema jednom ili više zahtjeva 1 do 3 ili njegove farmaceutski prihvatljive soli ili solvata, te učinkovite količine spoja dodatnog lijeka u vidu aktivnog sastojka.
HRP20160044TT 2008-08-04 2016-01-14 Novi spojevi fenilamino izonikotinamida HRP20160044T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US13785808P 2008-08-04 2008-08-04
EP09790842.0A EP2307376B1 (en) 2008-08-04 2009-07-27 Novel phenylamino isonicotinamide compounds
PCT/US2009/051817 WO2010017051A1 (en) 2008-08-04 2009-07-27 Novel phenylamino isonicotinamide compounds

Publications (1)

Publication Number Publication Date
HRP20160044T1 true HRP20160044T1 (hr) 2016-02-26

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ID=41078311

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HRP20160044TT HRP20160044T1 (hr) 2008-08-04 2016-01-14 Novi spojevi fenilamino izonikotinamida

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US (2) US8404725B2 (hr)
EP (1) EP2307376B1 (hr)
JP (1) JP2011529963A (hr)
KR (1) KR101651700B1 (hr)
CN (1) CN102099336B (hr)
AR (1) AR072904A1 (hr)
AU (1) AU2009279940B2 (hr)
BR (1) BRPI0916566B8 (hr)
CA (1) CA2732828C (hr)
CL (1) CL2011000258A1 (hr)
CO (1) CO6341612A2 (hr)
DK (1) DK2307376T3 (hr)
EA (1) EA018539B1 (hr)
EC (1) ECSP11010867A (hr)
ES (1) ES2560878T3 (hr)
HK (1) HK1159097A1 (hr)
HR (1) HRP20160044T1 (hr)
HU (1) HUE027223T2 (hr)
IL (1) IL210937A (hr)
MX (1) MX2011001127A (hr)
MY (1) MY151342A (hr)
NZ (1) NZ591498A (hr)
PE (1) PE20110665A1 (hr)
PL (1) PL2307376T3 (hr)
PT (1) PT2307376E (hr)
SI (1) SI2307376T1 (hr)
UA (1) UA107183C2 (hr)
WO (1) WO2010017051A1 (hr)
ZA (1) ZA201101661B (hr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112012033228A2 (pt) * 2010-07-01 2015-09-15 Merck Patent Gmbh método para a preparação de cis-1,2-dióis na escala de quilograma
US9045429B2 (en) * 2010-10-29 2015-06-02 Bayer Intellectual Property Gmbh Substituted phenoxypyridines
EP2760821B1 (en) 2011-09-02 2017-10-11 Novartis AG Choline salt of an anti-inflammatory substituted cyclobutenedione compound
JP6599861B2 (ja) 2013-08-07 2019-10-30 リグスホスピタレット コペンハーゲン ユニバーシティ ホスピタル 男性不妊治療用の抗体、化合物、およびその誘導体
CA2964982C (en) 2014-11-20 2022-07-05 Merck Patent Gmbh Heteroaryl compounds as irak inhibitors and uses thereof
US20190008859A1 (en) 2015-08-21 2019-01-10 Acerta Pharma B.V. Therapeutic Combinations of a MEK Inhibitor and a BTK Inhibitor
CN106632021A (zh) * 2016-09-27 2017-05-10 中国药科大学 2‑取代异烟酸类化合物、其制备方法及其用途
KR20210142154A (ko) 2019-03-21 2021-11-24 옹쎄오 암 치료를 위한 키나제 억제제와 조합된 dbait 분자
AU2020378630A1 (en) 2019-11-08 2022-05-26 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
TW202342018A (zh) 2022-03-04 2023-11-01 美商奇奈特生物製藥公司 Mek激酶抑制劑

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5525625A (en) * 1995-01-24 1996-06-11 Warner-Lambert Company 2-(2-Amino-3-methoxyphenyl)-4-oxo-4H-[1]benzopyran for treating proliferative disorders
UA73073C2 (uk) 1997-04-03 2005-06-15 Уайт Холдінгз Корпорейшн Заміщені 3-ціанохіноліни, спосіб їх одержання та фармацевтична композиція
ES2274572T3 (es) 1997-07-01 2007-05-16 Warner-Lambert Company Llc Derivados de acido 2-(4-bromo- o 4-yodo-fenilamino) benzoico y su uso como inhibidor de mek.
CA2290506C (en) 1997-07-01 2005-12-27 Warner-Lambert Company 4-bromo or 4-iodo phenylamino benzhydroxamic acid derivatives and their use as mek inhibitors
ES2252996T3 (es) 1999-01-13 2006-05-16 Warner-Lambert Company Llc Derivados de bencenosulfonamida y su uso como inhibidores de mek.
AU2483400A (en) 1999-01-13 2000-08-01 Warner-Lambert Company 4'heteroaryl diarylamines
ATE302761T1 (de) 1999-01-13 2005-09-15 Warner Lambert Co 1-heterozyklus-substituierte diarylaminen
CA2348236A1 (en) 1999-01-13 2000-07-20 Stephen Douglas Barrett 4-arylamino, 4-aryloxy, and 4-arylthio diarylamines and derivatives thereof as selective mek inhibitors
CZ20012498A3 (cs) 1999-01-13 2002-08-14 Warner-Lambert Company Benzoheterocyklické sloučeniny a jejich pouľití jako inhibitorů MEK
WO2000042002A1 (en) 1999-01-13 2000-07-20 Warner-Lambert Company Sulphohydroxamic acids and sulphohydroxamates and their use as mek inhibitors
GB9910577D0 (en) 1999-05-08 1999-07-07 Zeneca Ltd Chemical compounds
CA2403017A1 (en) 2000-03-15 2001-09-20 Warner-Lambert Company 5-amide substituted diarylamines as mex inhibitors
IL153817A0 (en) 2000-07-19 2003-07-31 Warner Lambert Co Oxygenated esters of 4-iodo phenylamino benzhydroxamic acids
NZ535158A (en) 2002-03-13 2007-06-29 Array Biopharma Inc N3 alkylated benzimidazole derivatives as MEK inhibitors
RU2300528C2 (ru) 2002-03-13 2007-06-10 Эррэй Биофарма, Инк. N3-алкилированные бензимидазольные производные в качестве ингибиторов мек
GB0215823D0 (en) 2002-07-09 2002-08-14 Astrazeneca Ab Quinazoline derivatives
US20050004186A1 (en) 2002-12-20 2005-01-06 Pfizer Inc MEK inhibiting compounds
ZA200703912B (en) * 2004-10-20 2008-09-25 Serono Lab 3-arylamino pyridine derivatives
WO2007121269A2 (en) 2006-04-11 2007-10-25 Ardea Biosciences, Inc. N-aryl-n'alkyl sulfamides as mek inhibitors
BRPI0710817A2 (pt) 2006-04-18 2011-08-23 Ardea Biosciences Inc piridona sulfonamidas e piridona sulfamidas como inibidores mek
AU2007334402B2 (en) 2006-12-14 2014-02-13 Exelixis, Inc. Methods of using MEK inhibitors

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US20110184032A1 (en) 2011-07-28
ECSP11010867A (es) 2011-04-29
EP2307376A1 (en) 2011-04-13
KR101651700B1 (ko) 2016-08-26
CL2011000258A1 (es) 2011-07-29
US8889719B2 (en) 2014-11-18
US8404725B2 (en) 2013-03-26
BRPI0916566B1 (pt) 2020-03-10
MX2011001127A (es) 2011-03-21
AR072904A1 (es) 2010-09-29
AU2009279940A1 (en) 2010-02-11
HK1159097A1 (en) 2012-07-27
CN102099336A (zh) 2011-06-15
NZ591498A (en) 2012-09-28
CN102099336B (zh) 2013-11-06
IL210937A0 (en) 2011-04-28
BRPI0916566B8 (pt) 2021-05-25
IL210937A (en) 2015-07-30
JP2011529963A (ja) 2011-12-15
SI2307376T1 (sl) 2016-02-29
EP2307376B1 (en) 2015-11-04
MY151342A (en) 2014-05-15
UA107183C2 (uk) 2014-12-10
ES2560878T3 (es) 2016-02-23
CA2732828A1 (en) 2010-02-11
PL2307376T3 (pl) 2016-04-29
WO2010017051A1 (en) 2010-02-11
PT2307376E (pt) 2016-02-26
AU2009279940B2 (en) 2014-01-16
EA201100296A1 (ru) 2011-08-30
DK2307376T3 (en) 2016-01-11
US20130184314A1 (en) 2013-07-18
HUE027223T2 (en) 2016-08-29
BRPI0916566A2 (pt) 2015-11-10
PE20110665A1 (es) 2011-09-23
KR20110044768A (ko) 2011-04-29
CA2732828C (en) 2017-06-13
CO6341612A2 (es) 2011-11-21
ZA201101661B (en) 2011-11-30
EA018539B1 (ru) 2013-08-30

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