AP2008004432A0 - Substituted benzofused derivatives and their use as vanilloid receptor ligands - Google Patents

Substituted benzofused derivatives and their use as vanilloid receptor ligands

Info

Publication number
AP2008004432A0
AP2008004432A0 AP2008004432A AP2008004432A AP2008004432A0 AP 2008004432 A0 AP2008004432 A0 AP 2008004432A0 AP 2008004432 A AP2008004432 A AP 2008004432A AP 2008004432 A AP2008004432 A AP 2008004432A AP 2008004432 A0 AP2008004432 A0 AP 2008004432A0
Authority
AP
ARIPO
Prior art keywords
receptor ligands
vanilloid receptor
substituted benzofused
benzofused derivatives
derivatives
Prior art date
Application number
AP2008004432A
Other languages
English (en)
Inventor
Laxmikant Atmaram Gharat
Uday Mukundib Joshi
Neelima Khairatkar Joshi
Original Assignee
Glenmark Pharmaceuticals Sa
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=37603267&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AP2008004432(A0) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Glenmark Pharmaceuticals Sa filed Critical Glenmark Pharmaceuticals Sa
Publication of AP2008004432A0 publication Critical patent/AP2008004432A0/xx

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    • C07D491/02—Heterocyclic 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
    • C07D491/10—Spiro-condensed systems
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    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
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    • C07D413/12—Heterocyclic 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
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    • C07D417/02—Heterocyclic 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 two hetero rings
    • C07D417/12—Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
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    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Dermatology (AREA)
  • Pulmonology (AREA)
  • Diabetes (AREA)
  • Urology & Nephrology (AREA)
  • Pain & Pain Management (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Obesity (AREA)
  • Rheumatology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Otolaryngology (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Immunology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Psychology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Vascular Medicine (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
AP2008004432A 2005-10-07 2006-10-09 Substituted benzofused derivatives and their use as vanilloid receptor ligands AP2008004432A0 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
IN1269MU2005 2005-10-07
US73066005P 2005-10-26 2005-10-26
IN996MU2006 2006-06-26
US80720506P 2006-07-13 2006-07-13
PCT/IB2006/002814 WO2007042906A1 (en) 2005-10-07 2006-10-09 Substituted benzofused derivatives and their use as vanilloid receptor ligands

Publications (1)

Publication Number Publication Date
AP2008004432A0 true AP2008004432A0 (en) 2008-04-30

Family

ID=37603267

Family Applications (1)

Application Number Title Priority Date Filing Date
AP2008004432A AP2008004432A0 (en) 2005-10-07 2006-10-09 Substituted benzofused derivatives and their use as vanilloid receptor ligands

Country Status (12)

Country Link
US (4) US7842703B2 (xx)
EP (1) EP1931681B1 (xx)
JP (1) JP2009511465A (xx)
KR (1) KR20080064972A (xx)
AP (1) AP2008004432A0 (xx)
AR (1) AR057543A1 (xx)
CA (1) CA2624307C (xx)
EA (1) EA200801013A1 (xx)
IL (1) IL190587A0 (xx)
NO (1) NO20082125L (xx)
TW (1) TW200801013A (xx)
WO (1) WO2007042906A1 (xx)

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MY144307A (en) * 2006-04-18 2011-08-29 Abbott Lab Antagonists of the vanilloid receptor subtype 1 (vr1) and uses thereof
WO2007135026A2 (de) 2006-05-24 2007-11-29 Boehringer Ingelheim International Gmbh Substituierte pteridine als therapeutika
WO2008110863A1 (en) * 2007-03-15 2008-09-18 Glenmark Pharmaceuticals S.A. Indazole derivatives and their use as vanilloid receptor ligands
ES2431344T3 (es) * 2007-10-16 2013-11-26 Santen Pharmaceutical Co., Ltd Agente terapéutico para la vejiga hiperactiva
MX2010005704A (es) * 2007-12-18 2010-08-17 Glenmark Pharmaceuticals Sa Derivados de cromano como modulares del trpv3.
WO2009081219A1 (en) * 2007-12-20 2009-07-02 Glenmark Pharmaceuticals, S.A. Quinazoline derivatives as vanilloid receptor modulators
US8349846B2 (en) * 2008-01-11 2013-01-08 Glenmark Pharmaceuticals, S.A. Fused pyrimidine derivatives as TRPV3 modulators
CN101925575B (zh) 2008-01-28 2014-06-18 株式会社爱茉莉太平洋 作为香草酸受体拮抗剂的化合物、其异构体或其药物学可接受的盐、及包含这些化合物的药物组合物
WO2009095726A1 (en) * 2008-01-29 2009-08-06 Glenmark Pharmaceuticals, S.A. Acrylamide derivatives as vanilloid receptor 1 modulators
EA201071280A1 (ru) 2008-06-17 2012-05-30 Гленмарк Фармасьютикалс С.А. Производные хроманов как модуляторы trpv3
JP5438103B2 (ja) 2008-07-02 2014-03-12 アモーレパシフィック コーポレイション バニロイド受容体アンタゴニストとしての新規化合物、その異性体またはその薬学的に許容される塩、並びにそれを含む医薬組成物
WO2010023512A1 (en) * 2008-08-28 2010-03-04 Matrix Laboratories Ltd. Novel vanilloid receptor modulators, process for their preparation and pharmaceutical compositions containing them
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JP2012505907A (ja) * 2008-10-17 2012-03-08 アボット・ラボラトリーズ Ｔｒｐｖ１拮抗薬
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US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
WO2011092293A2 (en) 2010-02-01 2011-08-04 Novartis Ag Cyclohexyl amide derivatives as crf receptor antagonists
JP2013518085A (ja) 2010-02-01 2013-05-20 ノバルティス アーゲー ＣＲＦ−１受容体アンタゴニストとしてのピラゾロ［５，１ｂ］オキサゾール誘導体
JP5748777B2 (ja) 2010-02-02 2015-07-15 ノバルティス アーゲー Ｃｒｆ受容体アンタゴニストとしてのシクロヘキシルアミド誘導体
WO2012049555A1 (en) 2010-10-13 2012-04-19 Lupin Limited Spirocyclic compounds as voltage-gated sodium channel modulators
EP3348267B1 (en) * 2010-11-03 2024-01-10 University Of Hawaii Trpv1 inhibitor for prevention and treatment of cardiac hypertrophy
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US8969325B2 (en) 2011-12-19 2015-03-03 Abbvie Inc. TRPV1 antagonists
WO2013096223A1 (en) 2011-12-19 2013-06-27 Abbvie Inc. Trpv1 antagonists
US8796328B2 (en) 2012-06-20 2014-08-05 Abbvie Inc. TRPV1 antagonists
AU2014282769A1 (en) 2013-06-21 2015-12-17 Lupin Limited Substituted heterocyclic compounds as CRAC modulators
WO2014207648A1 (en) 2013-06-24 2014-12-31 Lupin Limited Chromane and chromene derivatives and their use as crac modulators
GB201401886D0 (en) 2014-02-04 2014-03-19 Lytix Biopharma As Neurodegenerative therapies
US11168068B2 (en) 2016-07-18 2021-11-09 Janssen Pharmaceutica Nv Tau PET imaging ligands
RU2755206C1 (ru) 2020-05-20 2021-09-14 Федеральное государственное бюджетное учреждение науки Тихоокеанский институт биоорганической химии им. Г.Б. Елякова Дальневосточного отделения Российской академии наук (ТИБОХ ДВО РАН) Средство пролонгированного анальгетического действия и лекарственный препарат на его основе

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EP1931681A1 (en) 2008-06-18
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US20080269253A1 (en) 2008-10-30
AU2006300871A1 (en) 2007-04-19
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US7842703B2 (en) 2010-11-30

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