PE20121050A1 - Compuestos de n-(1-(4-(1h-pirazol-5-il)ftalazin-1-il)piperidin-4-il)-benzamida sustituidos como antagonistas de la trayectoria hedgehog - Google Patents

Compuestos de n-(1-(4-(1h-pirazol-5-il)ftalazin-1-il)piperidin-4-il)-benzamida sustituidos como antagonistas de la trayectoria hedgehog

Info

Publication number
PE20121050A1
PE20121050A1 PE2011002119A PE2011002119A PE20121050A1 PE 20121050 A1 PE20121050 A1 PE 20121050A1 PE 2011002119 A PE2011002119 A PE 2011002119A PE 2011002119 A PE2011002119 A PE 2011002119A PE 20121050 A1 PE20121050 A1 PE 20121050A1
Authority
PE
Peru
Prior art keywords
ftalazin
hedgehog
piperidin
trajectory
pyrazole
Prior art date
Application number
PE2011002119A
Other languages
English (en)
Spanish (es)
Inventor
Philip Arthur Hipskind
Bharvin Kumar Patel
Takako Wilson
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of PE20121050A1 publication Critical patent/PE20121050A1/es

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
    • C07D401/14Heterocyclic 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
    • 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
    • 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
    • A61K31/502Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
PE2011002119A 2009-06-19 2010-06-15 Compuestos de n-(1-(4-(1h-pirazol-5-il)ftalazin-1-il)piperidin-4-il)-benzamida sustituidos como antagonistas de la trayectoria hedgehog PE20121050A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US21862809P 2009-06-19 2009-06-19

Publications (1)

Publication Number Publication Date
PE20121050A1 true PE20121050A1 (es) 2012-08-09

Family

ID=42332981

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2011002119A PE20121050A1 (es) 2009-06-19 2010-06-15 Compuestos de n-(1-(4-(1h-pirazol-5-il)ftalazin-1-il)piperidin-4-il)-benzamida sustituidos como antagonistas de la trayectoria hedgehog

Country Status (35)

Country Link
US (2) US8273742B2 (cg-RX-API-DMAC7.html)
EP (1) EP2443104B1 (cg-RX-API-DMAC7.html)
JP (1) JP5596139B2 (cg-RX-API-DMAC7.html)
KR (1) KR101389165B1 (cg-RX-API-DMAC7.html)
CN (1) CN102459233B (cg-RX-API-DMAC7.html)
AR (1) AR077014A1 (cg-RX-API-DMAC7.html)
AU (1) AU2010260244B2 (cg-RX-API-DMAC7.html)
BR (1) BRPI1011601A2 (cg-RX-API-DMAC7.html)
CA (1) CA2764542C (cg-RX-API-DMAC7.html)
CL (1) CL2011003147A1 (cg-RX-API-DMAC7.html)
CO (1) CO6480932A2 (cg-RX-API-DMAC7.html)
CR (1) CR20110658A (cg-RX-API-DMAC7.html)
DK (1) DK2443104T3 (cg-RX-API-DMAC7.html)
DO (1) DOP2011000386A (cg-RX-API-DMAC7.html)
EA (1) EA019059B1 (cg-RX-API-DMAC7.html)
EC (1) ECSP11011541A (cg-RX-API-DMAC7.html)
ES (1) ES2409054T3 (cg-RX-API-DMAC7.html)
HN (1) HN2011003139A (cg-RX-API-DMAC7.html)
HR (1) HRP20130408T1 (cg-RX-API-DMAC7.html)
IL (1) IL216599A (cg-RX-API-DMAC7.html)
JO (1) JO2931B1 (cg-RX-API-DMAC7.html)
MA (1) MA33363B1 (cg-RX-API-DMAC7.html)
MX (1) MX2011014029A (cg-RX-API-DMAC7.html)
MY (1) MY156667A (cg-RX-API-DMAC7.html)
NZ (1) NZ596882A (cg-RX-API-DMAC7.html)
PE (1) PE20121050A1 (cg-RX-API-DMAC7.html)
PL (1) PL2443104T3 (cg-RX-API-DMAC7.html)
PT (1) PT2443104E (cg-RX-API-DMAC7.html)
SG (1) SG177289A1 (cg-RX-API-DMAC7.html)
SI (1) SI2443104T1 (cg-RX-API-DMAC7.html)
TN (1) TN2011000627A1 (cg-RX-API-DMAC7.html)
TW (1) TWI385165B (cg-RX-API-DMAC7.html)
UA (1) UA106755C2 (cg-RX-API-DMAC7.html)
WO (1) WO2010147917A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA201108587B (cg-RX-API-DMAC7.html)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2723042A1 (en) * 2008-04-29 2009-11-05 Eli Lilly And Company Disubstituted phthalazine hedgehog pathway antagonists
DK2364185T3 (da) * 2008-11-03 2013-06-03 Lilly Co Eli Disubstituerede phthalazin-hedgehog-pathway-antagonister
CN102216292B (zh) * 2008-11-17 2014-08-13 伊莱利利公司 四取代的哒嗪hedgehog途径拮抗剂
AU2009314349B2 (en) 2008-11-17 2013-04-18 Eli Lilly And Company Tetrasubstituted pyridazine 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
AU2012232670A1 (en) 2011-03-23 2013-09-12 Ariel-University Research And Development Company Ltd. Treatment of proliferative disorders with a chemiluminescent agent
GB201309508D0 (en) * 2013-05-28 2013-07-10 Redx Pharma Ltd Compounds
GB201311953D0 (en) * 2013-07-03 2013-08-14 Redx Pharma Ltd Compounds
WO2015073691A1 (en) 2013-11-14 2015-05-21 The Board Of Trustees Of The Leland Stanford Junior University Methods for treating cancer by activation of bmp signaling
CN105017140B (zh) * 2014-04-28 2017-12-29 复旦大学 邻氨基苯甲酰胺化合物及其制备方法和用途
GB2528298A (en) * 2014-07-16 2016-01-20 Redx Pharma Plc Compounds
CN105985319B (zh) * 2015-02-11 2019-02-26 复旦大学 芳基酞嗪化合物及其制备方法和用途
CN105985320B (zh) * 2015-02-11 2018-10-26 复旦大学 苄基酞嗪化合物及其制备方法和用途
CN105985321B (zh) * 2015-02-11 2018-10-26 复旦大学 吡唑酞嗪化合物及其制备方法和用途
CA2988289C (en) 2015-06-04 2023-12-05 PellePharm, Inc. Topical formulations for delivery of hedgehog inhibitor compounds and use thereof
EP3303289A4 (en) * 2015-06-05 2018-11-14 Dana-Farber Cancer Institute, Inc. Compounds and methods for treating cancer
JP7158023B2 (ja) 2016-03-15 2022-10-21 オリソン ヘノミクス エセ. アー. 固形腫瘍の治療における使用のための、lsd1阻害剤の組合せ
CN106279114B (zh) * 2016-08-04 2019-01-29 东南大学 一种Taladegib的合成方法
US10548908B2 (en) * 2016-09-15 2020-02-04 Nostopharma, LLC Compositions and methods for preventing and treating heterotopic ossification and pathologic calcification
CN106831718B (zh) * 2016-12-30 2019-05-07 上海科技大学 平滑受体配体及其应用
WO2018211007A1 (en) 2017-05-18 2018-11-22 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and pharmaceutical compositions for the treatment of mast cell diseases
US20230301950A1 (en) 2020-06-26 2023-09-28 Raqualia Pharma Inc. Method for selecting cancer patients for whom combination therapy with retinoid and cancer therapeutic agent is effective, and combination medicament with retinoid and cancer therapeutic agent
AU2021360767A1 (en) * 2020-10-13 2023-04-27 Endeavor Biomedicines, Inc. Methods of treating fibrosis
WO2025188802A1 (en) 2024-03-05 2025-09-12 Endeavor Biomedicines, Inc. Methods of improving lung function
WO2025189041A1 (en) * 2024-03-07 2025-09-12 Endeavor Biomedicines, Inc. Methods of treating fibrosis
WO2025242197A1 (zh) * 2024-05-24 2025-11-27 成都思倍博医药科技有限公司 氘代的Hedgehog通路SMO受体抑制剂

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IN148482B (cg-RX-API-DMAC7.html) * 1977-06-03 1981-03-07 Pfizer
ZA97288B (en) 1996-01-15 1998-07-14 Janssen Pharmaceutica Nv Angiogenesis inhibiting pyridazinamines
JP5067986B2 (ja) 1998-04-09 2012-11-07 ジョンズ ホプキンズ ユニヴァーシティー スクール オブ メディシン ヘッジホッグシグナリング経路の阻害剤としてのステロイドアルカロイド誘導体の使用
CA2376210A1 (en) 1999-06-08 2000-12-14 Lorantis Limited Therapeutic use of an inhibitor of a hedgehog or a hedgehog-related signalling pathway
MXPA04000803A (es) * 2001-07-27 2004-05-21 Curis Inc Mediadores de rutas de senalizacion de hedgehog, composiciones y usos relacionados a los mismos.
JP2005529876A (ja) * 2002-04-22 2005-10-06 ジョンズ ホプキンス ユニバーシティー スクール オブ メディシン Hedgehogシグナル伝達経路の調節因子、それに関連する組成物および使用
AU2003265853A1 (en) 2002-08-29 2004-03-19 Curis, Inc. Hedgehog antagonists, methods and uses related thereto
US8067608B2 (en) 2003-09-29 2011-11-29 The Johns Hopkins University Hedgehog pathway antagonists
TW200533356A (en) 2004-02-24 2005-10-16 Mitsubishi Pharma Corp Fused pyridazine derivatives
CA2564996A1 (en) 2004-05-08 2006-01-12 Taeyoung Yoon 3-aryl-5,6-disubstituted pyridazines
KR101225018B1 (ko) 2004-09-02 2013-01-23 쿠리스 인코퍼레이션 헤지호그 신호전달에 대한 피리딜 억제제
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
JP5550352B2 (ja) * 2007-03-15 2014-07-16 ノバルティス アーゲー 有機化合物およびその使用
EP2170866B1 (en) * 2007-06-25 2014-08-13 Amgen Inc. Phthalazine compounds, compositions and methods of use
CA2697682A1 (en) 2007-09-07 2009-03-19 Amgen Inc. Annelated pyridazines for the treatment of tumors driven by inapropriate hedgehog signalling
JP5620821B2 (ja) * 2007-12-13 2014-11-05 シエナ ビオテク ソシエタ ペル アチオニSiena Biotech S.P.A. ヘッジホッグ経路拮抗薬およびその治療用途
CA2723042A1 (en) * 2008-04-29 2009-11-05 Eli Lilly And Company Disubstituted phthalazine hedgehog pathway antagonists
US20100041663A1 (en) 2008-07-18 2010-02-18 Novartis Ag Organic Compounds as Smo Inhibitors
EP2321298B1 (en) * 2008-08-04 2013-10-02 Amgen Inc. Aurora kinase modulators and methods of use
DK2364185T3 (da) 2008-11-03 2013-06-03 Lilly Co Eli Disubstituerede phthalazin-hedgehog-pathway-antagonister
CN102216292B (zh) 2008-11-17 2014-08-13 伊莱利利公司 四取代的哒嗪hedgehog途径拮抗剂
AU2009314349B2 (en) 2008-11-17 2013-04-18 Eli Lilly And Company Tetrasubstituted pyridazine 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
CA2764542C (en) 2013-09-10
SG177289A1 (en) 2012-02-28
US9000023B2 (en) 2015-04-07
CN102459233B (zh) 2014-07-02
IL216599A0 (en) 2012-03-01
EP2443104A1 (en) 2012-04-25
UA106755C2 (uk) 2014-10-10
PL2443104T3 (pl) 2013-08-30
CR20110658A (es) 2012-02-20
DK2443104T3 (da) 2013-05-06
JP5596139B2 (ja) 2014-09-24
TW201113268A (en) 2011-04-16
AU2010260244A1 (en) 2012-01-19
BRPI1011601A2 (pt) 2016-03-22
KR20120024783A (ko) 2012-03-14
MX2011014029A (es) 2012-02-21
KR101389165B1 (ko) 2014-04-24
ECSP11011541A (es) 2012-01-31
MA33363B1 (fr) 2012-06-01
PT2443104E (pt) 2013-05-07
TN2011000627A1 (en) 2013-05-24
DOP2011000386A (es) 2012-02-29
HN2011003139A (es) 2013-07-29
CO6480932A2 (es) 2012-07-16
EP2443104B1 (en) 2013-04-17
EA201270049A1 (ru) 2012-05-30
SI2443104T1 (sl) 2013-07-31
NZ596882A (en) 2013-08-30
US20100324048A1 (en) 2010-12-23
WO2010147917A1 (en) 2010-12-23
TWI385165B (zh) 2013-02-11
EA019059B1 (ru) 2013-12-30
MY156667A (en) 2016-03-15
AU2010260244B2 (en) 2013-09-05
CN102459233A (zh) 2012-05-16
CL2011003147A1 (es) 2012-07-20
JP2012530705A (ja) 2012-12-06
JO2931B1 (en) 2015-09-15
ES2409054T3 (es) 2013-06-24
US20120316174A1 (en) 2012-12-13
ZA201108587B (en) 2013-05-29
US8273742B2 (en) 2012-09-25
AR077014A1 (es) 2011-07-27
HK1164872A1 (en) 2012-09-28
IL216599A (en) 2015-09-24
CA2764542A1 (en) 2010-12-23
HRP20130408T1 (en) 2013-06-30

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