JP4698591B2 - 非鎮静a−2アゴニスト1−(2,3−ジメチル−フェニル)−エチル−1、3−ジヒドロ−イミダゾール−2−チオン - Google Patents
非鎮静a−2アゴニスト1−(2,3−ジメチル−フェニル)−エチル−1、3−ジヒドロ−イミダゾール−2−チオン Download PDFInfo
- Publication number
- JP4698591B2 JP4698591B2 JP2006526107A JP2006526107A JP4698591B2 JP 4698591 B2 JP4698591 B2 JP 4698591B2 JP 2006526107 A JP2006526107 A JP 2006526107A JP 2006526107 A JP2006526107 A JP 2006526107A JP 4698591 B2 JP4698591 B2 JP 4698591B2
- Authority
- JP
- Japan
- Prior art keywords
- agonist
- compound
- pain
- adrenergic
- agonists
- 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.)
- Expired - Fee Related
Links
- WFXNKTPHRUEJDR-UHFFFAOYSA-O CC(C(N1)=CNC1=S)c1cccc(C)c1[NH3+] Chemical compound CC(C(N1)=CNC1=S)c1cccc(C)c1[NH3+] WFXNKTPHRUEJDR-UHFFFAOYSA-O 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
- C07D233/84—Sulfur atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Otolaryngology (AREA)
- Hospice & Palliative Care (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
本発明は、一般的には、痛みの処置および慢性の痛みの長期間にわたる緩和に関し、詳細には、α−アドレナリン作動性アゴニスト、およびα−2Aアドレナリン作動性受容体の選択的アンタゴニストに関する。
臨床での痛みには、侵害受容性の痛みおよび神経障害性の痛みが含まれる。それぞれのタイプの痛みは、損傷部位および隣接する正常な組織における感覚過敏によって特徴づけられる。侵害受容性の痛みは、通常、継続時間が限定され、利用可能なオピオイド治療によく応答するが、神経障害性の痛みは、例えば、切断術の後で生じることが多い「ゴースト痛み」において明らかであるように、開始事象が治癒した後も長く持続し得る。慢性の痛み症候群(例えば、慢性の神経障害性の痛みなど)は、手術、圧迫傷害もしくは外傷、感染性因子、毒性薬物、炎症性障害、または代謝性疾患(例えば、糖尿病または虚血など)を含む様々な傷害のいずれかによって引き起こされる。
本発明は、
α−2Aアドレナリン作動性受容体、α−2Bアドレナリン作動性受容体およびα−2Cアドレナリン作動性受容体のそれぞれにおいて、ブリモニジンと比べて25%を超える効力を有する化合物を意味し、汎α−1汎α−2アゴニストを包含する。様々な汎α−2アゴニストがこの分野では知られており、これらに、クロニジン、ブリモニジン、チザニジン、デキセメデトミジンおよびノルエピネフリンが含まれる。汎α−2アゴニストは、α−2A受容体、α−2B受容体およびα−2C受容体のそれぞれにおいて、ブリモニジンと比べて25%を超える効力を少なくとも有する。本発明は、現在までその痛みを抑えるために生涯にわたる毎日の薬物療法に直面している、慢性の痛みで苦しんでいる人々に対する新しい治療方法を提供する。そのような薬物は、脊椎投与されたとき、有用な鎮痛剤である。α−アドレナリン作動性アゴニストの望ましくない薬理学的性質、特に、鎮静作用および血圧低下により、これらの薬物の有用性が、経口投与または他の末梢経路によって投与されたときには制限されている。従って、経口経路または他の末梢経路によって投与することができ、かつ、鎮静作用および血圧低下などの望ましくない副作用を有しない効果的な鎮痛剤が求められている。本発明はこの要求を満たし、関連した利点もまた提供する。
化合物1の製造
本実施例は、α−2A/α−1A選択的アゴニスト、化合物1の製造を記載する。
A.化合物1((+)−(S)−4−[1−(2,3−ジメチル−フェニル)−エチル]−1、3−ジヒドロ−イミダゾール−2−チエン)の製造
ブリモニジンよりも高いα−2A/α−1A機能的選択性を有するα−2アゴニストのキャラクタリゼーション
α−アドレナリン作動性アゴニストを使用したα2−A受容体ノックアウトマウスにおける痛みの末梢での処置
本実施例では、α−アドレナリン作動性アゴニストが、α−2A受容体活性化の不存在下で末梢投与されたとき、効果的な鎮痛剤であることが明らかにされる。非特異的なα−アドレナリン作動性アゴニストが、スルプロストン感作された痛みのマウスモデルを使用してα−2A受容体欠損(「ノックアウト」)マウス(Hein他、上掲、1999)においてアッセイされた。このマウスモデルでは、本質的には、Minami他、Pain 57:217−223(1994)に記載されるように、異疼痛が、選択的プロスタグランジンE2受容体アゴニストを意識のあるマウスにクモ膜下投与することによって誘発される。このモデルにおいて、はけで側腹をなでることに対する痛み応答が、スルプロストンの脊髄投与および薬物またはコントロールビヒクルのクモ膜下投与または腹腔内投与の15分後から開始して35分間の期間にわたって8回スコア化される。スルプロストンは、16点の測定尺度で12点〜13点の「痛み」のスコアを誘発する。
α−2B/C選択的アゴニストの化合物8が、神経障害性の痛みの別のラット神経傷害モデルであるBennett部分坐骨神経結紮モデルにおいて試験された。このラットモデルは、ヒトにおいて認められる痛み感覚と類似した痛み感覚の障害を伴う末梢単神経障害をもたらす(BennettおよびXie、Pain、33:87−107(1988))。Bennettモデルでは、神経傷害が、締め付ける結紮糸で坐骨神経の周囲をゆるく縛り、これにより、締め付け部から遠位側の神経の変性を引き起こすことによってもたらされる。異疼痛および痛覚過敏が、無意識での痛みに加えて、締め付け傷害によってもたらされる(BennettおよびXie、上掲(1988))。具体的には、冷たさに対する異疼痛、すなわち、冷刺激からの痛み感覚が、変化した痛み感覚の1つの発現である:Bennettモデル動物は、コントロール動物とは対照的に、冷たい表面から、手術された肢の足を頻繁に持ち上げる。
Claims (6)
- 前記選択的アゴニストのα−1A効果がブリモニジンよりも低いまたはα−1A/α−2A効力がブリモニジンの効力よりも低い、請求項1記載のα−2A/α−1A選択的アゴニスト。
- 前記選択的アゴニストのα−1A効果がブリモニジンよりも低いまたはα−1A/α−2A効力がブリモニジンの効力よりも低い、請求項4記載の医薬組成物。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US50256203P | 2003-09-12 | 2003-09-12 | |
US60/502,562 | 2003-09-12 | ||
US10/891,953 US7141597B2 (en) | 2003-09-12 | 2004-07-15 | Nonsedating α-2 agonists |
US10/891.953 | 2004-07-15 | ||
PCT/US2004/027134 WO2005034946A1 (en) | 2003-09-12 | 2004-08-20 | Nonsedating α-2 agonist 1- (2, 3-dimethyl-phenyl) -ethyl-1, 3-dihydro-imizadole-2-thione |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2007505111A JP2007505111A (ja) | 2007-03-08 |
JP4698591B2 true JP4698591B2 (ja) | 2011-06-08 |
Family
ID=34278841
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006526107A Expired - Fee Related JP4698591B2 (ja) | 2003-09-12 | 2004-08-20 | 非鎮静a−2アゴニスト1−(2,3−ジメチル−フェニル)−エチル−1、3−ジヒドロ−イミダゾール−2−チオン |
Country Status (26)
Country | Link |
---|---|
US (4) | US7141597B2 (ja) |
EP (2) | EP1800679B1 (ja) |
JP (1) | JP4698591B2 (ja) |
KR (1) | KR101145046B1 (ja) |
CN (1) | CN100417379C (ja) |
AT (2) | ATE358479T1 (ja) |
AU (1) | AU2004279332B2 (ja) |
BR (1) | BRPI0413719A (ja) |
CA (1) | CA2537832C (ja) |
CO (1) | CO5680444A2 (ja) |
CY (1) | CY1107608T1 (ja) |
DE (2) | DE602004030051D1 (ja) |
DK (2) | DK1663206T3 (ja) |
ES (1) | ES2285522T3 (ja) |
HK (2) | HK1092704A1 (ja) |
IL (1) | IL173530A (ja) |
MX (1) | MXPA06002668A (ja) |
NO (1) | NO20060667L (ja) |
NZ (1) | NZ545181A (ja) |
PL (2) | PL379561A1 (ja) |
PT (1) | PT1663206E (ja) |
RU (1) | RU2345987C2 (ja) |
SI (1) | SI1663206T1 (ja) |
TW (1) | TWI337999B (ja) |
WO (1) | WO2005034946A1 (ja) |
ZA (1) | ZA200601002B (ja) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5869079A (en) * | 1995-06-02 | 1999-02-09 | Oculex Pharmaceuticals, Inc. | Formulation for controlled release of drugs by combining hydrophilic and hydrophobic agents |
US6726918B1 (en) | 2000-07-05 | 2004-04-27 | Oculex Pharmaceuticals, Inc. | Methods for treating inflammation-mediated conditions of the eye |
ATE306951T1 (de) * | 2000-11-29 | 2005-11-15 | Allergan Inc | Verhinderung von transplantatabstossung im auge |
US7091232B2 (en) * | 2002-05-21 | 2006-08-15 | Allergan, Inc. | 4-(substituted cycloalkylmethyl) imidazole-2-thiones, 4-(substituted cycloalkenylmethyl) imidazole-2-thiones, 4-(substituted cycloalkylmethyl) imidazol-2-ones and 4-(substituted cycloalkenylmethyl) imidazol-2-ones and related compounds |
US7358269B2 (en) * | 2002-05-21 | 2008-04-15 | Allergan, Inc. | 2-((2-Thioxo-2,3-dihydro-1H-imidazol-4-yl)methyl)-3,4-dihydronapthalen-1(2H)-one |
US7323485B2 (en) * | 2002-05-21 | 2008-01-29 | Allergan, Inc. | 4-(substituted cycloalkylmethyl) imidazole-2-thiones, 4-(substituted cycloalkenylmethyl) imidazole-2-thiones, 4-(substituted cycloalkylmethyl) imidazol-2-ones and 4-(substituted cycloalkenylmethyl) imidazol-2-ones and related compounds |
US20050048099A1 (en) | 2003-01-09 | 2005-03-03 | Allergan, Inc. | Ocular implant made by a double extrusion process |
US20060293359A1 (en) * | 2003-06-25 | 2006-12-28 | Allergan, Inc. | Methods and compositions for the treatment of diabetes |
US20050059664A1 (en) * | 2003-09-12 | 2005-03-17 | Allergan, Inc. | Novel methods for identifying improved, non-sedating alpha-2 agonists |
US7141597B2 (en) * | 2003-09-12 | 2006-11-28 | Allergan, Inc. | Nonsedating α-2 agonists |
US7812049B2 (en) * | 2004-01-22 | 2010-10-12 | Vicept Therapeutics, Inc. | Method and therapeutic/cosmetic topical compositions for the treatment of rosacea and skin erythema using α1-adrenoceptor agonists |
US20050244469A1 (en) | 2004-04-30 | 2005-11-03 | Allergan, Inc. | Extended therapeutic effect ocular implant treatments |
AU2005290075A1 (en) * | 2004-09-24 | 2006-04-06 | Allergan, Inc. | 4-(phenylmethyl and substituted phenylmethyl)-imidazole-2-thiones acting as specific alpha2 adrenergic agonists |
MX2007003094A (es) | 2004-09-24 | 2007-06-07 | Allergan Inc | 4-(metilo ciclico condensado)-imidazol-2-tionas como agonistas alfa2 adrenergicos. |
BRPI0613077A2 (pt) * | 2005-06-29 | 2010-12-21 | Allergan Inc | agonistas alfa-2 andrenérgicos para o tratamento de dor |
US20070203144A1 (en) * | 2006-01-17 | 2007-08-30 | Allergan, Inc. | Use of Memantine and Brimonidine to Attenuate Vitreoretinal Vascular Endothelial Growth Factor (VEGF) Protein Levels in Animals |
WO2007117923A2 (en) * | 2006-04-07 | 2007-10-18 | Allergan, Inc. | Compositions including relatively water insoluble/unwettable drugs and methods for using same |
US20070298073A1 (en) * | 2006-06-23 | 2007-12-27 | Allergan, Inc. | Steroid-containing sustained release intraocular implants and related methods |
US8802128B2 (en) | 2006-06-23 | 2014-08-12 | Allergan, Inc. | Steroid-containing sustained release intraocular implants and related methods |
US20080153874A1 (en) * | 2006-12-22 | 2008-06-26 | Allergan Inc. | Alpha-2b receptor agonist and anticonvulsant compositions for treating chronic pain |
JP2010528034A (ja) | 2007-05-23 | 2010-08-19 | アラーガン、インコーポレイテッド | 医薬としての((フェニル)イミダゾリル)メチルキノリニル化合物 |
PT2155733E (pt) * | 2007-05-23 | 2013-01-07 | Allergan Inc | Lactamas cíclicas para o tratamento de glaucoma ou pressão intra-ocular elevada |
US20110028559A1 (en) * | 2007-07-06 | 2011-02-03 | Fang Wenkui K | Substituted fluoroethyl ureas as alpha 2 adrenergic agents |
EP2188262A1 (en) * | 2007-08-15 | 2010-05-26 | Allergan, Inc. | Heterocyclyl substituted fused carbocyles useful in the treatment of conditions such as glaucoma and pain |
EP2190835B1 (en) * | 2007-08-15 | 2012-10-03 | Allergan, Inc. | Adrenergic compounds |
AU2008286823A1 (en) * | 2007-08-15 | 2009-02-19 | Allergan, Inc. | Therapeutic compounds |
US20100216857A1 (en) * | 2007-10-18 | 2010-08-26 | Luhrs Lauren M B | Method of treating motor disorders with 4-(1-(2,3-dimethylphenyl)ethyl)-1h-imidazole-2(3h)-thione |
US20110269805A1 (en) * | 2007-10-18 | 2011-11-03 | Gil Daniel W | Method of treating sensorimotor disorders with 4-(1-(2,3-dimethylphenyl)ethyl)-1h-imidazole-2(3h)-thione |
WO2009052073A2 (en) * | 2007-10-18 | 2009-04-23 | Allergan, Inc. | Method of treating sensorimotor disorders with alpha-2 adrenergic receptor agonists |
WO2009089448A1 (en) * | 2008-01-11 | 2009-07-16 | Allergan, Inc. | Therapeutic disulfide compounds for treating pain and diabetes |
US8420114B2 (en) * | 2008-04-18 | 2013-04-16 | Warsaw Orthopedic, Inc. | Alpha and beta adrenergic receptor agonists for treatment of pain and / or inflammation |
US8956641B2 (en) | 2008-04-18 | 2015-02-17 | Warsaw Orthopedic, Inc. | Alpha adrenergic receptor agonists for treatment of inflammatory diseases |
US9072727B2 (en) | 2008-04-18 | 2015-07-07 | Warsaw Orthopedic, Inc. | Alpha adrenergic receptor agonists for treatment of degenerative disc disease |
US20090263451A1 (en) * | 2008-04-18 | 2009-10-22 | Warsaw Orthopedic, Inc. | Anti-Inflammatory and/or Analgesic Agents for Treatment of Myofascial Pain |
US20090264477A1 (en) * | 2008-04-18 | 2009-10-22 | Warsaw Orthopedic, Inc., An Indiana Corporation | Beta adrenergic receptor agonists for treatment of pain and/or inflammation |
US8889173B2 (en) * | 2008-04-18 | 2014-11-18 | Warsaw Orthopedic, Inc. | Alpha adrenergic receptor agonists for treatment of pain and/or inflammation |
USRE48948E1 (en) | 2008-04-18 | 2022-03-01 | Warsaw Orthopedic, Inc. | Clonidine compounds in a biodegradable polymer |
JP2012518005A (ja) | 2009-02-13 | 2012-08-09 | アラーガン インコーポレイテッド | 4‐(1‐(3‐(ヒドロキシメチル)‐2‐メチルフェニル)エチル)‐1h‐イミダゾール‐2(3h)‐チオン |
US20100239632A1 (en) | 2009-03-23 | 2010-09-23 | Warsaw Orthopedic, Inc. | Drug depots for treatment of pain and inflammation in sinus and nasal cavities or cardiac tissue |
US8394800B2 (en) * | 2009-11-19 | 2013-03-12 | Galderma Laboratories, L.P. | Method for treating psoriasis |
US9050274B2 (en) * | 2010-01-28 | 2015-06-09 | Warsaw Orthopedic, Inc. | Compositions and methods for treating an intervertebral disc using bulking agents or sealing agents |
US9125902B2 (en) * | 2010-01-28 | 2015-09-08 | Warsaw Orthopedic, Inc. | Methods for treating an intervertebral disc using local analgesics |
US9486500B2 (en) | 2010-01-28 | 2016-11-08 | Warsaw Orthopedic, Inc. | Osteoimplant and methods for making |
US9060978B2 (en) | 2011-01-24 | 2015-06-23 | Warsaw Orthopedic, Inc. | Method for treating an intervertebral disc disorder by administering a dominant negative tumor necrosis factor antagonist |
US9511077B2 (en) | 2011-04-25 | 2016-12-06 | Warsaw Orthopedic, Inc. | Medical devices and methods comprising an anabolic agent for wound healing |
US9592243B2 (en) | 2011-04-25 | 2017-03-14 | Warsaw Orthopedic, Inc. | Medical devices and methods comprising an anabolic agent for treatment of an injury |
BR112021020962A2 (pt) | 2019-05-01 | 2021-12-14 | Clexio Biosciences Ltd | Métodos de tratamento de prurido |
CN110894508B (zh) * | 2019-10-31 | 2021-08-06 | 内蒙古大学 | 一种调控白色脂肪棕色化的基因Adra1a的应用 |
WO2022093767A1 (en) * | 2020-10-26 | 2022-05-05 | Rush University Medical Center | Alpha-2 adrenergic receptor agonists to reduce mortality and improve outcomes in viral respiratory syndromes |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0302603A1 (en) * | 1987-07-09 | 1989-02-08 | Smithkline Beecham Corporation | Dopamine-beta-hydroxylase inhibitors |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63150266A (ja) * | 1986-12-12 | 1988-06-22 | Mitsui Petrochem Ind Ltd | ベンジルイミダゾ−ル誘導体 |
US4868197A (en) * | 1987-03-20 | 1989-09-19 | Merrell Dow Pharmaceuticals Inc. | Reducing reperfusion injury with 1,3-dihydro-4-methyl-5-(4-methylthio)benzoyl)-2H-imidazol-2-thione |
ZA881807B (en) | 1987-03-20 | 1988-09-05 | Merrell Dow Pharmaceuticals Inc. | Method for reducing reperfusion injury with imidazol-2-thiones |
GB2206880B (en) * | 1987-07-16 | 1991-04-24 | Farmos Oy | Optical isomers of an imidazole derivative |
BR9507595A (pt) | 1994-05-02 | 1997-09-16 | Zeneca Ltd | Composto composição herbicida processo para controlar vegetação indesejável |
AR015744A1 (es) * | 1998-04-01 | 2001-05-16 | Orion Corp | Uso de dexmedetomidina para sedacion en terapia intensiva |
US7091232B2 (en) * | 2002-05-21 | 2006-08-15 | Allergan, Inc. | 4-(substituted cycloalkylmethyl) imidazole-2-thiones, 4-(substituted cycloalkenylmethyl) imidazole-2-thiones, 4-(substituted cycloalkylmethyl) imidazol-2-ones and 4-(substituted cycloalkenylmethyl) imidazol-2-ones and related compounds |
US7141597B2 (en) * | 2003-09-12 | 2006-11-28 | Allergan, Inc. | Nonsedating α-2 agonists |
-
2004
- 2004-07-15 US US10/891,953 patent/US7141597B2/en not_active Expired - Fee Related
- 2004-08-20 EP EP07006921A patent/EP1800679B1/en not_active Not-in-force
- 2004-08-20 PL PL379561A patent/PL379561A1/pl unknown
- 2004-08-20 DE DE602004030051T patent/DE602004030051D1/de active Active
- 2004-08-20 AU AU2004279332A patent/AU2004279332B2/en not_active Ceased
- 2004-08-20 ES ES04781753T patent/ES2285522T3/es active Active
- 2004-08-20 DK DK04781753T patent/DK1663206T3/da active
- 2004-08-20 NZ NZ545181A patent/NZ545181A/en unknown
- 2004-08-20 RU RU2006113600/04A patent/RU2345987C2/ru not_active IP Right Cessation
- 2004-08-20 DK DK07006921.6T patent/DK1800679T3/da active
- 2004-08-20 CA CA2537832A patent/CA2537832C/en not_active Expired - Fee Related
- 2004-08-20 PL PL04781753T patent/PL1663206T3/pl unknown
- 2004-08-20 KR KR1020067005031A patent/KR101145046B1/ko not_active IP Right Cessation
- 2004-08-20 PT PT04781753T patent/PT1663206E/pt unknown
- 2004-08-20 AT AT04781753T patent/ATE358479T1/de active
- 2004-08-20 CN CNB2004800262738A patent/CN100417379C/zh not_active Expired - Fee Related
- 2004-08-20 EP EP04781753A patent/EP1663206B1/en not_active Not-in-force
- 2004-08-20 SI SI200430257T patent/SI1663206T1/sl unknown
- 2004-08-20 AT AT07006921T patent/ATE487477T1/de not_active IP Right Cessation
- 2004-08-20 WO PCT/US2004/027134 patent/WO2005034946A1/en active IP Right Grant
- 2004-08-20 DE DE602004005720T patent/DE602004005720T2/de active Active
- 2004-08-20 BR BRPI0413719-1A patent/BRPI0413719A/pt not_active IP Right Cessation
- 2004-08-20 MX MXPA06002668A patent/MXPA06002668A/es active IP Right Grant
- 2004-08-20 JP JP2006526107A patent/JP4698591B2/ja not_active Expired - Fee Related
- 2004-09-10 TW TW093127519A patent/TWI337999B/zh not_active IP Right Cessation
-
2006
- 2006-02-03 ZA ZA200601002A patent/ZA200601002B/en unknown
- 2006-02-05 IL IL173530A patent/IL173530A/en active IP Right Grant
- 2006-02-10 NO NO20060667A patent/NO20060667L/no not_active Application Discontinuation
- 2006-02-21 CO CO06017219A patent/CO5680444A2/es unknown
- 2006-07-20 US US11/458,731 patent/US7312238B2/en active Active
- 2006-12-06 HK HK06113430A patent/HK1092704A1/xx not_active IP Right Cessation
-
2007
- 2007-06-21 CY CY20071100823T patent/CY1107608T1/el unknown
- 2007-12-10 HK HK07113440.2A patent/HK1104979A1/xx not_active IP Right Cessation
- 2007-12-18 US US11/959,356 patent/US20080176918A1/en not_active Abandoned
-
2010
- 2010-09-09 US US12/878,593 patent/US8022226B2/en active Active
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0302603A1 (en) * | 1987-07-09 | 1989-02-08 | Smithkline Beecham Corporation | Dopamine-beta-hydroxylase inhibitors |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4698591B2 (ja) | 非鎮静a−2アゴニスト1−(2,3−ジメチル−フェニル)−エチル−1、3−ジヒドロ−イミダゾール−2−チオン | |
JP5673973B2 (ja) | 痛みを緩和するための新規な方法および組成物 | |
JP2007505112A (ja) | 改善された非沈静α2アゴニストを同定するための新規方法 | |
US7754768B2 (en) | Methods and compositions for modulating alpha adrenergic receptor activity | |
US6313172B1 (en) | Methods and compositions for modulating alpha adrenergic receptor activity | |
US7569595B2 (en) | 2-((2-thioxo-2,3-dihydro-1H-imidazol-4-yl)methyl)-3,4-dihydronaphthalen-1(2H)-one | |
US20230062049A1 (en) | Methods of treating alpha adrenergic mediated conditions | |
EP2932968B1 (en) | Compound for treating alpha adrenergic mediated conditions | |
US20090306398A1 (en) | Methods of treating alpha adrenergic mediated conditions |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20070508 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20101026 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20110126 |
|
RD03 | Notification of appointment of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7423 Effective date: 20110126 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20110222 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20110301 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
LAPS | Cancellation because of no payment of annual fees |