JP2012509940A5 - - Google Patents

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Publication number
JP2012509940A5
JP2012509940A5 JP2011538682A JP2011538682A JP2012509940A5 JP 2012509940 A5 JP2012509940 A5 JP 2012509940A5 JP 2011538682 A JP2011538682 A JP 2011538682A JP 2011538682 A JP2011538682 A JP 2011538682A JP 2012509940 A5 JP2012509940 A5 JP 2012509940A5
Authority
JP
Japan
Prior art keywords
pyrrol
octahydrocyclopenta
trifluoromethyl
methyl
phenyl
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.)
Pending
Application number
JP2011538682A
Other languages
English (en)
Japanese (ja)
Other versions
JP2012509940A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2009/065847 external-priority patent/WO2010062927A2/en
Publication of JP2012509940A publication Critical patent/JP2012509940A/ja
Publication of JP2012509940A5 publication Critical patent/JP2012509940A5/ja
Pending legal-status Critical Current

Links

JP2011538682A 2008-11-26 2009-11-25 カルシウムチャンネル遮断薬としての置換されたオクタヒドロシクロペンタ[c]ピロール−4−アミン類 Pending JP2012509940A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US11799508P 2008-11-26 2008-11-26
US61/117,995 2008-11-26
PCT/US2009/065847 WO2010062927A2 (en) 2008-11-26 2009-11-25 Novel substituted octahydrocyclopenta(c)pyrrol-4-amines as calcium channel blockers

Publications (2)

Publication Number Publication Date
JP2012509940A JP2012509940A (ja) 2012-04-26
JP2012509940A5 true JP2012509940A5 (enExample) 2013-01-17

Family

ID=42124348

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011538682A Pending JP2012509940A (ja) 2008-11-26 2009-11-25 カルシウムチャンネル遮断薬としての置換されたオクタヒドロシクロペンタ[c]ピロール−4−アミン類

Country Status (23)

Country Link
US (1) US8129417B2 (enExample)
EP (1) EP2367790A2 (enExample)
JP (1) JP2012509940A (enExample)
KR (1) KR20110091784A (enExample)
CN (1) CN102292319A (enExample)
AR (1) AR074226A1 (enExample)
AU (1) AU2009319796A1 (enExample)
BR (1) BRPI0921184A2 (enExample)
CA (1) CA2742350A1 (enExample)
CL (1) CL2011001176A1 (enExample)
CO (1) CO6382118A2 (enExample)
CR (1) CR20110304A (enExample)
EC (1) ECSP11011160A (enExample)
IL (1) IL212484A0 (enExample)
MX (1) MX2011005537A (enExample)
NZ (1) NZ592507A (enExample)
PA (1) PA8850301A1 (enExample)
PE (1) PE20110833A1 (enExample)
RU (1) RU2011126215A (enExample)
TW (1) TW201028378A (enExample)
UY (1) UY32261A (enExample)
WO (1) WO2010062927A2 (enExample)
ZA (1) ZA201103538B (enExample)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2009319796A1 (en) 2008-11-26 2010-06-03 Abbvie Inc. Substituted octahydrocyclopnta (c) pyrrol-4 -amines as calcium channel blockers
US8211933B2 (en) * 2008-12-12 2012-07-03 Vanderbilt University 3.3.0 bicyclic GlyT1 inhibitors and methods of making and using same
US8815869B2 (en) 2010-03-18 2014-08-26 Abbvie Inc. Lactam acetamides as calcium channel blockers
US8796470B2 (en) 2010-05-25 2014-08-05 Abbvie Inc. Substituted octahydrocyclopenta[c]pyrroles as calcium channel modulators
WO2011149995A1 (en) * 2010-05-25 2011-12-01 Abbott Laboratories Novel substituted octahydrocyclopenta [c]pyrrol-4-amines as calcium channel blockers
FR2976285B1 (fr) * 2011-06-08 2013-05-24 Servier Lab Procede de synthese et forme cristalline du chlorhydrate de 4-{3-[cis-hexahydrocypenta[c]pyrrol-2(1h)-yl]propoxy}benzamide ainsi que les compositions pharmaceutiques qui la contiennent
WO2013049164A1 (en) 2011-09-29 2013-04-04 Abbvie Inc. SUBSTITUTED OCTAHYDROPYRROLO[1,2-a]PYRAZINES AS CALCIUM CHANNEL BLOCKERS
WO2013049174A1 (en) 2011-09-29 2013-04-04 Abbvie Inc. Substituted octahydropyrrolo[1,2-a]pyrazine sulfonamides as calcium channel blockers
CN105008361A (zh) 2012-12-12 2015-10-28 艾伯维公司 作为钙通道阻滞剂用于治疗疼痛的的二氮杂*衍生物
CN106565674B (zh) * 2015-10-13 2021-02-05 四川海思科制药有限公司 一种八氢环戊烷并[c]吡咯衍生物及其制备方法和在医药上的用途
TWI851542B (zh) * 2017-09-11 2024-08-11 美商克魯松藥物公司 Shp2之八氫環戊烷并[c]吡咯別構抑制劑
KR102656571B1 (ko) 2018-03-05 2024-04-11 아르커스 바이오사이언시즈 인코포레이티드 아르기나아제 억제제
CA3214469A1 (en) * 2021-04-01 2022-10-06 Ono Pharmaceutical Co., Ltd. Abhd6 antagonist
TW202421635A (zh) 2022-09-30 2024-06-01 日商小野藥品工業股份有限公司 Abhd6拮抗劑
KR20240046089A (ko) 2022-09-30 2024-04-08 오노 야꾸힝 고교 가부시키가이샤 Abhd6 길항제를 함유하는 약학 조성물

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0278659A (ja) 1988-09-12 1990-03-19 Shionogi & Co Ltd アザビシクロアルカン類化合物
ATE269848T1 (de) * 1999-04-07 2004-07-15 Univ Virginia Calciumkanalblocker als antikrebsmittel
US8163769B2 (en) * 2002-03-12 2012-04-24 Abbott Laboratories Antibacterial compounds
US7223754B2 (en) * 2003-03-10 2007-05-29 Dynogen Pharmaceuticals, Inc. Thiazolidinone, oxazolidinone, and imidazolone derivatives for treating lower urinary tract and related disorders
EP1631570A1 (en) * 2003-03-12 2006-03-08 Abbott Laboratories Naphthyridine derivatives as antibacterial agents
US7230022B2 (en) * 2004-02-19 2007-06-12 Bristol-Myers Squibb Company Substituted fused bicyclic amines as modulators of chemokine receptor activity
US7381738B2 (en) * 2004-02-19 2008-06-03 Bristol-Myers Squibb Company Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity
JP2008507543A (ja) * 2004-07-22 2008-03-13 グラクソ グループ リミテッド 抗細菌剤
DE102004039789A1 (de) * 2004-08-16 2006-03-02 Sanofi-Aventis Deutschland Gmbh Arylsubstituierte polycyclische Amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
JP2008536927A (ja) * 2005-04-19 2008-09-11 メルク エンド カムパニー インコーポレーテッド N−アルキル−アザシクロアルキルnmda/nr2b拮抗物質
WO2010039947A1 (en) 2008-10-02 2010-04-08 Abbott Laboratories Novel compounds as calcium channel blockers
AU2009319796A1 (en) 2008-11-26 2010-06-03 Abbvie Inc. Substituted octahydrocyclopnta (c) pyrrol-4 -amines as calcium channel blockers
US8211933B2 (en) * 2008-12-12 2012-07-03 Vanderbilt University 3.3.0 bicyclic GlyT1 inhibitors and methods of making and using same

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