JP2010530901A - 障害を治療するための方法および組成物 - Google Patents

障害を治療するための方法および組成物 Download PDF

Info

Publication number
JP2010530901A
JP2010530901A JP2010513485A JP2010513485A JP2010530901A JP 2010530901 A JP2010530901 A JP 2010530901A JP 2010513485 A JP2010513485 A JP 2010513485A JP 2010513485 A JP2010513485 A JP 2010513485A JP 2010530901 A JP2010530901 A JP 2010530901A
Authority
JP
Japan
Prior art keywords
pain
alkyl
trpa1
heteroaryl
halo
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
JP2010513485A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010530901A5 (enExample
Inventor
フォワード エヌジー,
マンフレッド ウェイゲル,
マグダレン モーラン,
ジェイホン チョン,
クリストファー ファンガー,
グレン アール. ラーセン,
カミーノ, ドナト デル
ニール ヘイワード,
スティーブン ピー. アダムス,
アミー リプカ,
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hydra Biosciences LLC
Original Assignee
Hydra Biosciences LLC
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 Hydra Biosciences LLC filed Critical Hydra Biosciences LLC
Publication of JP2010530901A publication Critical patent/JP2010530901A/ja
Publication of JP2010530901A5 publication Critical patent/JP2010530901A5/ja
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/095Sulfur, selenium, or tellurium compounds, e.g. thiols
    • A61K31/105Persulfides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/11Aldehydes
    • 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
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine 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]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/08Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • A61K31/522Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Dermatology (AREA)
  • Rheumatology (AREA)
  • Neurology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
JP2010513485A 2007-06-22 2008-06-23 障害を治療するための方法および組成物 Withdrawn JP2010530901A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US94586607P 2007-06-22 2007-06-22
US94584007P 2007-06-22 2007-06-22
PCT/US2008/067901 WO2009002933A1 (en) 2007-06-22 2008-06-23 Methods and compositions for treating disorders

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2014100946A Division JP5932883B2 (ja) 2007-06-22 2014-05-14 障害を処置するための方法および組成物

Publications (2)

Publication Number Publication Date
JP2010530901A true JP2010530901A (ja) 2010-09-16
JP2010530901A5 JP2010530901A5 (enExample) 2012-07-26

Family

ID=40186010

Family Applications (5)

Application Number Title Priority Date Filing Date
JP2010513485A Withdrawn JP2010530901A (ja) 2007-06-22 2008-06-23 障害を治療するための方法および組成物
JP2014100946A Expired - Fee Related JP5932883B2 (ja) 2007-06-22 2014-05-14 障害を処置するための方法および組成物
JP2015139797A Expired - Fee Related JP6258266B2 (ja) 2007-06-22 2015-07-13 障害を処置するための方法および組成物
JP2017131268A Withdrawn JP2017165790A (ja) 2007-06-22 2017-07-04 障害を処置するための方法および組成物
JP2019076011A Withdrawn JP2019147808A (ja) 2007-06-22 2019-04-12 障害を治療するための方法および組成物

Family Applications After (4)

Application Number Title Priority Date Filing Date
JP2014100946A Expired - Fee Related JP5932883B2 (ja) 2007-06-22 2014-05-14 障害を処置するための方法および組成物
JP2015139797A Expired - Fee Related JP6258266B2 (ja) 2007-06-22 2015-07-13 障害を処置するための方法および組成物
JP2017131268A Withdrawn JP2017165790A (ja) 2007-06-22 2017-07-04 障害を処置するための方法および組成物
JP2019076011A Withdrawn JP2019147808A (ja) 2007-06-22 2019-04-12 障害を治療するための方法および組成物

Country Status (11)

Country Link
US (3) US8163761B2 (enExample)
EP (3) EP3184527B1 (enExample)
JP (5) JP2010530901A (enExample)
CN (4) CN103751194B (enExample)
AU (1) AU2008268463B2 (enExample)
CA (2) CA2691468C (enExample)
DK (1) DK2170309T3 (enExample)
ES (1) ES2609912T3 (enExample)
HR (1) HRP20200357T1 (enExample)
SI (1) SI3184527T1 (enExample)
WO (1) WO2009002933A1 (enExample)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012521406A (ja) * 2009-03-23 2012-09-13 グレンマーク ファーマシューティカルズ, エセ.アー. Trpa1調節因子としてのフロピリミジンジオン誘導体
JP2012521401A (ja) * 2009-03-23 2012-09-13 グレンマーク ファーマシューティカルズ, エセ.アー. Trpa1調節因子としての縮合ピリミジンジオン誘導体
WO2013146754A1 (ja) * 2012-03-27 2013-10-03 塩野義製薬株式会社 Trpv4阻害活性を有する芳香族複素5員環誘導体
JP2014501755A (ja) * 2010-12-20 2014-01-23 グレンマーク ファーマシューティカルズ, エセ.アー. Trpa1アンタゴニストとしての2−アミノ−4−アリールチアゾール化合物
JP2017516763A (ja) * 2014-04-23 2017-06-22 ハイドラ バイオサイエンシズ インコーポレイテッドHydra Biosciences,Inc. 一過性受容体電位a1イオンチャネルの阻害
JP2017528490A (ja) * 2014-09-19 2017-09-28 ハイドラ バイオサイエンシズ インコーポレイテッドHydra Biosciences,Inc. 一過性受容体電位a1イオンチャネルの阻害
JP2020510031A (ja) * 2017-03-07 2020-04-02 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft オキサジアゾール一過性受容器電位チャネル阻害剤

Families Citing this family (61)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7767685B2 (en) * 2006-06-29 2010-08-03 King Pharmaceuticals Research And Development, Inc. Adenosine A2B receptor antagonists
US20120108614A1 (en) * 2008-05-14 2012-05-03 Chong Jayhong A Compounds and compositions for treating chemical warfare agent-induced injuries
WO2010039289A2 (en) 2008-05-14 2010-04-08 Hydra Biosciences, Inc. Compounds and compositions for treating chemical warfare agent-induced injuries
WO2009140517A1 (en) * 2008-05-14 2009-11-19 Hydra Biosciences, Inc. Compounds and compositions for treating chemical warfare agent-induced injuries
WO2010004390A1 (en) 2008-06-17 2010-01-14 Glenmark Pharmaceuticals, S.A. Quinazoline dione derivatives as trpa1 modulators
US8722896B2 (en) 2008-12-17 2014-05-13 The Regents Of The University Of California Prokineticin receptor antagonists and uses thereof
US8362025B2 (en) * 2008-12-22 2013-01-29 Hydra Biosciences, Inc. Compositions useful for treating disorders related to TRPA1
ES2424340T3 (es) 2009-03-23 2013-10-01 Glenmark Pharmaceuticals S.A. Derivados de isotiazolo-pirimidindiona como moduladores de TRPA1
US8623880B2 (en) 2009-03-23 2014-01-07 Glenmark Pharmaceuticals S.A. Fused pyrimidine-dione derivatives as TRPA1 modulators
CN102498107A (zh) * 2009-09-04 2012-06-13 诺瓦提斯公司 作为激酶抑制剂的杂芳基化合物
WO2012098281A2 (es) 2011-01-19 2012-07-26 Universidad Miguel Hernández De Elche Péptidos moduladores de receptores trp y sus usos
JP2014517031A (ja) 2011-06-13 2014-07-17 グレンマーク ファーマシューティカルズ, エセ.アー. Trpa1アンタゴニストを使用した呼吸器疾患の治療
WO2012176105A1 (en) 2011-06-22 2012-12-27 Glenmark Pharmaceuticals Sa Pharmaceutical composition comprising a trpa1 antagonist and a leukotriene receptor antagonist
US20140107113A1 (en) 2011-06-22 2014-04-17 Glenmark Pharmaceuticals S.A. Pharmaceutical composition comprising a trpa1 antagonist and a beta-2 agonist
WO2013014597A1 (en) * 2011-07-25 2013-01-31 Glenmark Pharmaceuticals Sa Pharmaceutical composition comprising a trpa1 antagonist and a steroid
BR112014002960A2 (pt) * 2011-08-09 2017-02-21 Cubist Pharm Inc inibição de canal de íons potencial receptor transiente trpa1
US20140364445A1 (en) 2011-12-05 2014-12-11 Glenmark Pharmaceuticals S.A. Pharmaceutical composition comprising a trpa1 antagonist and an anticholinergic agent
WO2013122979A1 (en) 2012-02-15 2013-08-22 Chirhoclin, Inc. Methods for treating pain associated with chronic pancreatitis
US11406718B2 (en) 2012-05-29 2022-08-09 Chirhoclin, Inc. Methods of detecting pancreobiliary ductal leaks
US9221821B2 (en) 2012-06-05 2015-12-29 Forest Laboratories Holdings, Limited Methods for the synthesis of 1,3-substituted aminouracils and other xanthine-related compounds
HK1207643A1 (en) * 2012-06-08 2016-02-05 Glenmark Pharmaceuticals S.A. Amides of 2-amino-4-arylthiazole compounds and their salts
US20140163048A1 (en) * 2012-08-09 2014-06-12 Cubist Pharmaceuticals, Inc. Compositions with increased stability for inhibiting transient receptor potential ion channel trpa1
DK2928474T3 (en) 2012-12-07 2019-02-11 Chemocentryx Inc Diazollactamer
WO2014100735A2 (en) 2012-12-21 2014-06-26 Chemocentryx, Inc. Diazole amides
TW201441225A (zh) * 2013-01-18 2014-11-01 Cubist Pharm Inc 瞬時受體電位a1離子通道之抑制
US9394308B2 (en) 2013-01-18 2016-07-19 Merck Sharp & Dohme Corp. Inhibiting the transient receptor potential A1 ion channel
GB201309333D0 (en) * 2013-05-23 2013-07-10 Agency Science Tech & Res Purine diones as WNT pathway modulators
CN105492444B (zh) 2013-07-02 2018-09-07 百时美施贵宝公司 作为rock抑制剂的三环吡啶-甲酰胺衍生物
EP3016950B1 (en) 2013-07-02 2017-06-07 Bristol-Myers Squibb Company Tricyclic pyrido-carboxamide derivatives as rock inhibitors
US9532988B2 (en) 2013-10-15 2017-01-03 Glenmark Pharmaceuticals S.A. Pharmaceutical composition comprising a TRPA1 antagonist and an analgesic agent
CN107739372A (zh) * 2013-11-03 2018-02-27 黑龙江福和华星制药集团股份有限公司 一种多索茶碱注射液
CN103788095A (zh) * 2014-01-20 2014-05-14 四川大学华西医院 2,4(1h,3h)-嘧啶二酮衍生物及其制备方法
WO2015134790A1 (en) * 2014-03-07 2015-09-11 Sanford-Burnham Medical Research Institute Small molecule fatty acid synthase inhibitors
US20190175599A1 (en) 2014-09-16 2019-06-13 Glemark Pharmaceuticals S.A. Trpa1 antagonist for the treatment of pain associated to diabetic neuropathic pain
WO2017060488A1 (en) 2015-10-09 2017-04-13 Almirall, S.A. New trpa1 antagonists
WO2017064068A1 (en) 2015-10-14 2017-04-20 Almirall, S.A. New trpa1 antagonists
RU2745195C2 (ru) 2016-04-07 2021-03-22 Кемосентрикс, Инк. Уменьшение массы опухоли путем введения ccr1 антагонистов в комбинации с pd-1 ингибиторами или pd-l1 ингибиторами
JP6788476B2 (ja) 2016-10-21 2020-11-25 株式会社ミツトヨ クロマティック共焦点センサ及び測定方法
US20190374552A1 (en) * 2016-11-02 2019-12-12 George Edward Hoag Multifunctional formulations and methods to control dermatitis and pruritus
CN111655693B (zh) 2018-01-31 2023-03-28 伊莱利利公司 抑制瞬时型感受器电位a1离子通道
US10710994B2 (en) 2018-03-19 2020-07-14 Genentech, Inc. Oxadiazole transient receptor potential channel inhibitors
CN108997350B (zh) * 2018-07-03 2021-03-02 南昌立德生物技术有限公司 一种周期蛋白依赖性激酶8抑制剂
US10828287B2 (en) 2019-03-11 2020-11-10 Nocion Therapeutics, Inc. Charged ion channel blockers and methods for use
JP7630439B2 (ja) 2019-03-11 2025-02-17 ノシオン セラピューティクス,インコーポレイテッド エステル置換イオンチャンネル遮断薬および使用方法
WO2020185928A1 (en) 2019-03-11 2020-09-17 Nocion Therapeutics, Inc. Charged ion channel blockers and methods for use
KR20210143791A (ko) 2019-03-11 2021-11-29 녹시온 테라퓨틱스 인코포레이티드 하전된 이온 채널 차단제 및 사용 방법
CN110343759A (zh) * 2019-06-03 2019-10-18 张鹏 Trpv4的用途及其抑制剂的用途和药物筛选方法
CN110526878A (zh) * 2019-09-16 2019-12-03 成都睿智化学研究有限公司 一种2-(噁唑基)乙胺的制备方法
CN112691094B (zh) * 2019-10-22 2022-09-23 中国科学院分子细胞科学卓越创新中心 防治病毒的新型化合物及其应用
JP7513713B2 (ja) 2019-11-06 2024-07-09 ノシオン セラピューティクス,インコーポレイテッド 荷電したイオンチャンネル遮断薬および使用方法
US10842798B1 (en) 2019-11-06 2020-11-24 Nocion Therapeutics, Inc. Charged ion channel blockers and methods for use
CN119118953A (zh) 2020-03-11 2024-12-13 诺西恩医疗公司 带电的离子通道阻滞剂及其使用方法
US12162851B2 (en) 2020-03-11 2024-12-10 Nocion Therapeutics, Inc. Charged ion channel blockers and methods for use
US11744878B2 (en) 2020-08-19 2023-09-05 Chirhoclin, Inc. Methods for treatment of COVID-19 syndrome
AU2021350916A1 (en) * 2020-09-24 2023-06-08 Shanghai Yao Yuan Biotechnology Co., Ltd. Alpha protein kinase 1 inhibitors and methods of use
EP4079304A1 (en) * 2021-04-21 2022-10-26 Fundació Privada Institut d'Investigació Oncològica de Vall-Hebron Compounds for use in the treatment of hyperproliferative disorders
CN115477626B (zh) * 2021-06-16 2024-08-02 上海璃道医药科技有限公司 N-取代苯基磺酰胺类化合物及其用途
CN114671875A (zh) * 2022-04-27 2022-06-28 成都施贝康生物医药科技有限公司 新型二氢嘧啶类化合物、异构体或盐及其制备方法和用途
US11951082B2 (en) 2022-08-22 2024-04-09 Ford Therapeutics, Llc Composition of chlorhexidine
CN117986195A (zh) * 2023-01-10 2024-05-07 四川大学 一种新型杂环化合物及其制备方法和用途
CN116655635B (zh) * 2023-05-19 2024-01-26 济南爱思医药科技有限公司 黑茶茶碱衍生物及在制备药物中的应用

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2083470A (en) * 1980-09-04 1982-03-24 Eisai Co Ltd Theophylline and theobromine derivatives
EP0087810A1 (en) * 1982-03-02 1983-09-07 Eisai Co., Ltd. Antiphlogistic/antipyretic/analgesic pharmaceutical compositions containing theophylline derivatives as active ingredient
JPS5910586A (ja) * 1982-03-12 1984-01-20 キノイン・ジヨ−ジセル・エ−シユ・ヴエジエ−セテイ・テルメ−ケク・ジヤ−ラ・エルテ− オキサジアゾリルアルキルテオフイリン,その製法及びそれを含む薬剤組成物
JPS6187681A (ja) * 1984-10-01 1986-05-06 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 1h‐インドル‐3‐イルを含む1,3‐ジメチル‐1h‐プリン‐2,6‐ジオン類、その製法および用途
FR2761068A1 (fr) * 1997-03-20 1998-09-25 Synthelabo Derives de piperazin-4-ylthieno[3,2-c]pyridin-4-yl-2- carboxamide, leur preparation et leur application en therapeutique
US20030199693A1 (en) * 2000-07-28 2003-10-23 Ing-Jun Chen Theophylline and 3-isobutyl-1-methylxanthine based N-7 substituted derivatives displaying inhibitory activies on PDE-5 phosphodiesterase
US20050209243A1 (en) * 2002-09-27 2005-09-22 Ing-Jun Chen Theophylline-based soluble guanylyl cyclase activators KMUP-1 analogues enhanced cyclic GMP and K+ channel activities on rabbit corpus cavernosum smooth muscle and intercavernous pressure activities
JP2009521485A (ja) * 2005-12-22 2009-06-04 ハイドラ バイオサイエンシズ インコーポレイテッド 疼痛を処置するためのtrpa1阻害剤

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4599337A (en) * 1977-08-09 1986-07-08 Eisai Co., Ltd. Antiphlogistic/antipyretic/analgesic agents containing theobromine or theophylline derivatives as active ingredient
GB9524812D0 (en) 1995-12-05 1996-02-07 Leo Pharm Prod Ltd Chemical compounds
US7818808B1 (en) 2000-12-27 2010-10-19 Intel Corporation Processor mode for limiting the operation of guest software running on a virtual machine supported by a virtual machine monitor
GB0108770D0 (en) * 2001-04-06 2001-05-30 Eisai London Res Lab Ltd Inhibitors
KR20040080939A (ko) * 2002-02-01 2004-09-20 킹 파머슈티칼스 리서치 앤드 디벨로프먼트 아이엔씨 8-헤테로아릴 크산틴 아데노신 에이투비 수용체 길항제
US20030203847A1 (en) * 2002-02-28 2003-10-30 Millennium Pharmaceuticals, Inc. Methods and compositions in treating pain and painful disorders using 9949, 14230, 760, 62553, 12216, 17719, 41897, 47174, 33408, 10002, 16209, 314, 636, 27410, 33260, 619, 15985, 69112, 2158, 224, 615, 44373, 95431, 22245, 2387, 16658, 55054, 16314, 1613, 1675, 9569 or 13424 molecules
GB0213869D0 (en) * 2002-06-17 2002-07-31 Arakis Ltd The treatment of pain
US20070196866A1 (en) * 2004-03-13 2007-08-23 Irm Llc Modulators of ion channel trpa1
KR20060129411A (ko) * 2004-03-30 2006-12-15 패러다임 테라퓨틱스 리미티드 이온 채널
CA2549577A1 (en) 2004-09-09 2006-03-16 Avaya Technology Corp. Methods of and systems for network traffic security
US20070021992A1 (en) * 2005-07-19 2007-01-25 Srinivas Konakalla Method and system for generating a business intelligence system based on individual life cycles within a business process
WO2007054480A1 (en) * 2005-11-08 2007-05-18 N.V. Organon 2-(benzimidazol-1-yl)-acetamide biaryl derivatives and their use as inhibitors of the trpv1 receptor
WO2007125405A2 (en) * 2006-05-01 2007-11-08 Pfizer Products Inc. Substituted 2-amino-fused heterocyclic compounds
US20120108614A1 (en) 2008-05-14 2012-05-03 Chong Jayhong A Compounds and compositions for treating chemical warfare agent-induced injuries
WO2009140517A1 (en) 2008-05-14 2009-11-19 Hydra Biosciences, Inc. Compounds and compositions for treating chemical warfare agent-induced injuries

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2083470A (en) * 1980-09-04 1982-03-24 Eisai Co Ltd Theophylline and theobromine derivatives
EP0087810A1 (en) * 1982-03-02 1983-09-07 Eisai Co., Ltd. Antiphlogistic/antipyretic/analgesic pharmaceutical compositions containing theophylline derivatives as active ingredient
JPS5910586A (ja) * 1982-03-12 1984-01-20 キノイン・ジヨ−ジセル・エ−シユ・ヴエジエ−セテイ・テルメ−ケク・ジヤ−ラ・エルテ− オキサジアゾリルアルキルテオフイリン,その製法及びそれを含む薬剤組成物
JPS6187681A (ja) * 1984-10-01 1986-05-06 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 1h‐インドル‐3‐イルを含む1,3‐ジメチル‐1h‐プリン‐2,6‐ジオン類、その製法および用途
FR2761068A1 (fr) * 1997-03-20 1998-09-25 Synthelabo Derives de piperazin-4-ylthieno[3,2-c]pyridin-4-yl-2- carboxamide, leur preparation et leur application en therapeutique
US20030199693A1 (en) * 2000-07-28 2003-10-23 Ing-Jun Chen Theophylline and 3-isobutyl-1-methylxanthine based N-7 substituted derivatives displaying inhibitory activies on PDE-5 phosphodiesterase
US20050209243A1 (en) * 2002-09-27 2005-09-22 Ing-Jun Chen Theophylline-based soluble guanylyl cyclase activators KMUP-1 analogues enhanced cyclic GMP and K+ channel activities on rabbit corpus cavernosum smooth muscle and intercavernous pressure activities
JP2009521485A (ja) * 2005-12-22 2009-06-04 ハイドラ バイオサイエンシズ インコーポレイテッド 疼痛を処置するためのtrpa1阻害剤

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
JOURNAL OF MEDICINAL CHEMISTRY, vol. 48(14), JPN6013018244, 2005, pages 4697 - 4701, ISSN: 0002509029 *

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012521406A (ja) * 2009-03-23 2012-09-13 グレンマーク ファーマシューティカルズ, エセ.アー. Trpa1調節因子としてのフロピリミジンジオン誘導体
JP2012521401A (ja) * 2009-03-23 2012-09-13 グレンマーク ファーマシューティカルズ, エセ.アー. Trpa1調節因子としての縮合ピリミジンジオン誘導体
JP2014501755A (ja) * 2010-12-20 2014-01-23 グレンマーク ファーマシューティカルズ, エセ.アー. Trpa1アンタゴニストとしての2−アミノ−4−アリールチアゾール化合物
WO2013146754A1 (ja) * 2012-03-27 2013-10-03 塩野義製薬株式会社 Trpv4阻害活性を有する芳香族複素5員環誘導体
JPWO2013146754A1 (ja) * 2012-03-27 2015-12-14 塩野義製薬株式会社 Trpv4阻害活性を有する芳香族複素5員環誘導体
US9499533B2 (en) 2012-03-27 2016-11-22 Shionogi & Co., Ltd. Aromatic 5-membered heterocyclic derivative having TRPV4-Inhibiting activity
JP2017516763A (ja) * 2014-04-23 2017-06-22 ハイドラ バイオサイエンシズ インコーポレイテッドHydra Biosciences,Inc. 一過性受容体電位a1イオンチャネルの阻害
JP2017528490A (ja) * 2014-09-19 2017-09-28 ハイドラ バイオサイエンシズ インコーポレイテッドHydra Biosciences,Inc. 一過性受容体電位a1イオンチャネルの阻害
JP2019206577A (ja) * 2014-09-19 2019-12-05 イーライ リリー アンド カンパニー 一過性受容体電位a1イオンチャネルの阻害
JP2021120403A (ja) * 2014-09-19 2021-08-19 イーライ リリー アンド カンパニー 一過性受容体電位a1イオンチャネルの阻害
JP7181967B2 (ja) 2014-09-19 2022-12-01 イーライ リリー アンド カンパニー 一過性受容体電位a1イオンチャネルの阻害
JP2020510031A (ja) * 2017-03-07 2020-04-02 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft オキサジアゾール一過性受容器電位チャネル阻害剤
JP7178357B2 (ja) 2017-03-07 2022-11-25 エフ.ホフマン-ラ ロシュ アーゲー オキサジアゾール一過性受容器電位チャネル阻害剤

Also Published As

Publication number Publication date
US8163761B2 (en) 2012-04-24
JP2019147808A (ja) 2019-09-05
HRP20200357T1 (hr) 2020-06-12
AU2008268463B2 (en) 2015-03-05
CA2962043A1 (en) 2008-12-31
CN103751194B (zh) 2018-01-05
CN101801362A (zh) 2010-08-11
US20090143377A1 (en) 2009-06-04
JP2014141535A (ja) 2014-08-07
CN101801362B (zh) 2014-01-22
EP3184527A1 (en) 2017-06-28
JP5932883B2 (ja) 2016-06-08
SI3184527T1 (sl) 2020-03-31
US20130059869A1 (en) 2013-03-07
EP2170309A1 (en) 2010-04-07
ES2609912T3 (es) 2017-04-25
JP2015180700A (ja) 2015-10-15
EP2170309A4 (en) 2010-11-03
AU2008268463A1 (en) 2008-12-31
EP3184527B1 (en) 2020-01-29
CA2691468C (en) 2017-05-09
CA2691468A1 (en) 2008-12-31
US20180133170A1 (en) 2018-05-17
WO2009002933A1 (en) 2008-12-31
CN103751194A (zh) 2014-04-30
CN104825457B (zh) 2019-11-19
DK2170309T3 (en) 2017-01-09
JP6258266B2 (ja) 2018-01-10
EP2170309B1 (en) 2016-10-26
EP3663295A1 (en) 2020-06-10
CN104825457A (zh) 2015-08-12
CN108042542A (zh) 2018-05-18
AU2008268463A2 (en) 2010-02-25
JP2017165790A (ja) 2017-09-21

Similar Documents

Publication Publication Date Title
JP6258266B2 (ja) 障害を処置するための方法および組成物
JP2010530901A5 (enExample)
US8389546B2 (en) Compounds for modulating TRPV3 function
JP5858557B2 (ja) 疼痛を処置するためのtrpa1阻害剤
US20100152209A1 (en) Compounds for Modulating TRPV3 Function
US20090018147A1 (en) Compounds for modulating TRPV3 function
AU2015202546B2 (en) Methods and Compositions for Treating Disorders
HK1240581B (en) 2,6-dioxo,-2,3-dihydro-1h-purine compounds useful for treating disorders related to the activity of the trpa1 channel

Legal Events

Date Code Title Description
A524 Written submission of copy of amendment under article 19 pct

Free format text: JAPANESE INTERMEDIATE CODE: A524

Effective date: 20110622

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20110622

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20120604

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20130417

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20130716

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20130723

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20131017

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20131114

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20140212

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20140219

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20140313

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20140320

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20140411

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20140418

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20140703

A761 Written withdrawal of application

Free format text: JAPANESE INTERMEDIATE CODE: A761

Effective date: 20140714