HRP20120762T1 - Tetrasupstituirani piridazini kao inhibitori hedgehog puta - Google Patents

Tetrasupstituirani piridazini kao inhibitori hedgehog puta Download PDF

Info

Publication number
HRP20120762T1
HRP20120762T1 HRP20120762AT HRP20120762T HRP20120762T1 HR P20120762 T1 HRP20120762 T1 HR P20120762T1 HR P20120762A T HRP20120762A T HR P20120762AT HR P20120762 T HRP20120762 T HR P20120762T HR P20120762 T1 HRP20120762 T1 HR P20120762T1
Authority
HR
Croatia
Prior art keywords
pharmaceutically acceptable
cancer
compound according
acceptable salt
image
Prior art date
Application number
HRP20120762AT
Other languages
English (en)
Croatian (hr)
Inventor
Jolie Anne Bastian
Julia Marie Clay
Jeffrey Daniel Cohen
Philip Arthur Hipskind
Karen Lynn Lobb
Daniel Jon Sall
Wilson (Nee Takakuwa), Takako
Michelle Lee Thompson
Original Assignee
Eli Lilly And Company
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 Eli Lilly And Company filed Critical Eli Lilly And Company
Publication of HRP20120762T1 publication Critical patent/HRP20120762T1/hr

Links

Classifications

    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
HRP20120762AT 2008-11-17 2009-11-05 Tetrasupstituirani piridazini kao inhibitori hedgehog puta HRP20120762T1 (hr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11533208P 2008-11-17 2008-11-17
PCT/US2009/063370 WO2010056588A1 (en) 2008-11-17 2009-11-05 Tetrasubstituted pyridazine hedgehog pathway antagonists

Publications (1)

Publication Number Publication Date
HRP20120762T1 true HRP20120762T1 (hr) 2012-10-31

Family

ID=41722877

Family Applications (1)

Application Number Title Priority Date Filing Date
HRP20120762AT HRP20120762T1 (hr) 2008-11-17 2009-11-05 Tetrasupstituirani piridazini kao inhibitori hedgehog puta

Country Status (18)

Country Link
US (1) US8507490B2 (enExample)
EP (1) EP2358698B1 (enExample)
JP (1) JP5518887B2 (enExample)
KR (1) KR101342184B1 (enExample)
CN (1) CN102216285B (enExample)
AU (1) AU2009314349B2 (enExample)
BR (1) BRPI0921782A2 (enExample)
CA (1) CA2743483C (enExample)
CY (1) CY1113377T1 (enExample)
DK (1) DK2358698T3 (enExample)
EA (1) EA017386B1 (enExample)
ES (1) ES2392759T3 (enExample)
HR (1) HRP20120762T1 (enExample)
MX (1) MX2011005177A (enExample)
PL (1) PL2358698T3 (enExample)
PT (1) PT2358698E (enExample)
SI (1) SI2358698T1 (enExample)
WO (1) WO2010056588A1 (enExample)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GT200700057A (es) * 2006-07-17 2008-03-05 Nuevos derivados de piridazina
JP5442717B2 (ja) 2008-04-29 2014-03-12 イーライ リリー アンド カンパニー 二置換フタラジンヘッジホッグ経路アンタゴニスト
CA2742539C (en) 2008-11-03 2014-05-06 Eli Lilly And Company Disubstituted phthalazine hedgehog pathway antagonists
EP2358703B1 (en) 2008-11-17 2013-12-25 Eli Lilly and Company Tetrasubstituted pyridazines hedgehog pathway antagonists
AR077014A1 (es) 2009-06-19 2011-07-27 Lilly Co Eli Compuesto derivado de ftalazina 1,4-disustituida, composicion farmaceutica que lo comprende y uso para preparar un medicamento util para el tratamiento de cancer
GB201309508D0 (en) 2013-05-28 2013-07-10 Redx Pharma Ltd Compounds
US9814703B2 (en) 2013-11-14 2017-11-14 The Board Of Trustees Of The Leland Stanford Junior University Methods for treating cancer by activation of BMP signaling
GB2528298A (en) * 2014-07-16 2016-01-20 Redx Pharma Plc Compounds
CN105130980B (zh) * 2015-09-09 2018-05-22 沈阳药科大学 N-3-苯并咪唑噻唑胺类衍生物及其制备方法与应用
CN107163028B (zh) * 2017-05-24 2019-07-12 东南大学 一种苯甲酰胺类Hedgehog抑制剂及其制备方法和应用
CN110208424A (zh) * 2019-06-28 2019-09-06 江苏恒生检测有限公司 一种农药氟啶虫酰胺中含有杂质的分析方法
WO2021071981A1 (en) * 2019-10-08 2021-04-15 Skyhawk Therapeutics, Inc. Compounds for modulating splicing
JP2023546536A (ja) 2020-10-13 2023-11-02 エンデバー バイオメディシンズ, インコーポレイテッド 線維症を処置する方法
EP4395890A1 (en) * 2021-08-30 2024-07-10 Remix Therapeutics Inc. Compounds and methods for modulating splicing
WO2025188802A1 (en) 2024-03-05 2025-09-12 Endeavor Biomedicines, Inc. Methods of improving lung function

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1293565A (en) 1969-05-03 1972-10-18 Aspro Nicholas Ltd Aminophthalazines and pharmaceutical compositions thereof
AU717744B2 (en) 1996-01-15 2000-03-30 Janssen Pharmaceutica N.V. Angiogenesis inhibiting pyridazinamines
AU768130B2 (en) 1998-04-09 2003-12-04 Johns Hopkins University School Of Medicine, The Use of steroidal alkaloid derivatives as inhibitors of hedgehog signaling pathways
US6432970B2 (en) 1998-04-09 2002-08-13 Johns Hopkins University School Of Medicine Inhibitors of hedgehog signaling pathways, compositions and uses related thereto
ATE283700T1 (de) 1999-06-08 2004-12-15 Lorantis Ltd Therapeutische verwendung eines inhibitors des hedgehog signalübertragungsweges
US7655674B2 (en) 2002-04-22 2010-02-02 The Johns Hopkins University Modulators of hedgehog signaling pathways, compositions and uses related thereto
AU2003265853A1 (en) 2002-08-29 2004-03-19 Curis, Inc. Hedgehog antagonists, methods and uses related thereto
WO2005033288A2 (en) 2003-09-29 2005-04-14 The Johns Hopkins University Hedgehog pathway antagonists
TW200533356A (en) 2004-02-24 2005-10-16 Mitsubishi Pharma Corp Fused pyridazine derivatives
WO2006004589A2 (en) 2004-05-08 2006-01-12 Neurogen Corporation 3-aryl-5,6-disubstituted pyridazines
AU2005282722C1 (en) 2004-09-02 2011-08-18 Curis, Inc. Pyridyl inhibitors of hedgehog signalling
EP1900731A1 (de) 2006-09-07 2008-03-19 Bayer Schering Pharma Aktiengesellschaft N-(1-Phthalazin-1-yl-piperidin-4-yl)-amide als EP2-Rezeptor Modulatoren
KR101473504B1 (ko) * 2007-03-15 2014-12-16 노파르티스 아게 유기 화합물 및 그의 용도
CA2690378A1 (en) 2007-06-25 2008-12-31 Amgen Inc. Phthalazine compounds, compositions and methods of use
EP2188283B1 (en) 2007-09-07 2012-08-15 Amgen Inc. Annelated pyridazines for the treatment of tumors driven by inappropriate hedgehog signalling
JP5442717B2 (ja) 2008-04-29 2014-03-12 イーライ リリー アンド カンパニー 二置換フタラジンヘッジホッグ経路アンタゴニスト
US20100041663A1 (en) 2008-07-18 2010-02-18 Novartis Ag Organic Compounds as Smo Inhibitors
CA2742539C (en) 2008-11-03 2014-05-06 Eli Lilly And Company Disubstituted phthalazine hedgehog pathway antagonists
EP2358703B1 (en) 2008-11-17 2013-12-25 Eli Lilly and Company Tetrasubstituted pyridazines hedgehog pathway antagonists
AR077014A1 (es) 2009-06-19 2011-07-27 Lilly Co Eli Compuesto derivado de ftalazina 1,4-disustituida, composicion farmaceutica que lo comprende y uso para preparar un medicamento util para el tratamiento de cancer

Also Published As

Publication number Publication date
CY1113377T1 (el) 2016-06-22
EP2358698A1 (en) 2011-08-24
WO2010056588A1 (en) 2010-05-20
SI2358698T1 (sl) 2012-11-30
US8507490B2 (en) 2013-08-13
JP5518887B2 (ja) 2014-06-11
AU2009314349B2 (en) 2013-04-18
PT2358698E (pt) 2012-10-24
ES2392759T3 (es) 2012-12-13
PL2358698T3 (pl) 2013-01-31
KR20110070920A (ko) 2011-06-24
CA2743483A1 (en) 2010-05-20
BRPI0921782A2 (pt) 2019-09-24
EA017386B1 (ru) 2012-12-28
CN102216285B (zh) 2014-08-13
EA201170699A1 (ru) 2011-12-30
DK2358698T3 (da) 2012-10-08
AU2009314349A1 (en) 2010-05-20
CN102216285A (zh) 2011-10-12
EP2358698B1 (en) 2012-09-05
JP2012509263A (ja) 2012-04-19
CA2743483C (en) 2014-03-11
KR101342184B1 (ko) 2013-12-19
MX2011005177A (es) 2011-05-30
US20110263602A1 (en) 2011-10-27

Similar Documents

Publication Publication Date Title
HRP20120762T1 (hr) Tetrasupstituirani piridazini kao inhibitori hedgehog puta
HRP20191268T1 (hr) Derivati tieno[2,3-c]pirol-4-ona kao inhibitori erk
MX2009003157A (es) Pirazoliltienopiridinas terapeuticas.
UA99617C2 (ru) Производные пирролконденсированного азотсодержащего гетероцикла, их получение и фармацевтическое применение
MX2011011875A (es) Compuesto de carboxamida heterociclica diamino.
JP2012509263A5 (enExample)
EA200800815A1 (ru) 2-анилин-4-арилзамещенные тиазольные производные
TN2012000608A1 (en) Imidazopyridine derivatives, process for the preparation thereof and therapeutic use thereof
MX2009012117A (es) Composiciones y derivados heterociclicos sustituidos y su uso farmaceutico como antibacterianos.
MX2009011997A (es) Derivados de pirrolopirimidin-7-ona y su uso como farmaceuticos.
MX344276B (es) Compuesto de piperidina novedoso o sal del mismo.
MX2013004407A (es) Derivado de piridina y agente medicinal.
SI2134691T1 (sl) Derivati kvinolina kot PARP in TANK inhibitorji
SG170069A1 (en) Quinoline derivatives
TW200745067A (en) Novel compounds
MX2012003644A (es) Compuestos de 2-piridona empleados como inhibidores de la elastasa neutrofila.
JO3115B1 (ar) مركبات بيريدازينون واستخدامها كمثبطات daao
MX2009011579A (es) Pirimidinonas como moduladores de caseina cinasa ii (ck2).
MX2013005833A (es) Nuevos compuestos de piridina fusionada como inhibidores de caseina quinasa.
TW200833670A (en) Novel compounds 569
MY145795A (en) Pyrazoline compounds
MX2010009022A (es) Derivados 16 alfa, 17 alfa-acetal glucocorticoesteroideos y su uso.
MX2011011764A (es) Compuestos de carboxamida y su uso como inhibidores de calpaina.
IL200469A0 (en) Benzimidazole derivatives
MY183039A (en) Pyridin-2-yl derivatives as immunomodulating agents