JP5739527B2 - RhoキナーゼインヒビターとしてのN−環式−3−(環状カルボニルアミノメチル)ベンズアミド誘導体 - Google Patents
RhoキナーゼインヒビターとしてのN−環式−3−(環状カルボニルアミノメチル)ベンズアミド誘導体 Download PDFInfo
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- JP5739527B2 JP5739527B2 JP2013518686A JP2013518686A JP5739527B2 JP 5739527 B2 JP5739527 B2 JP 5739527B2 JP 2013518686 A JP2013518686 A JP 2013518686A JP 2013518686 A JP2013518686 A JP 2013518686A JP 5739527 B2 JP5739527 B2 JP 5739527B2
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- 0 CCc1c(CC*)nc(N)[s]1 Chemical compound CCc1c(CC*)nc(N)[s]1 0.000 description 3
- RGTMILHZLXZRGF-UHFFFAOYSA-N CC(C)C/N=C(/N)\S Chemical compound CC(C)C/N=C(/N)\S RGTMILHZLXZRGF-UHFFFAOYSA-N 0.000 description 1
- PZRJDDJZXAGGSX-UHFFFAOYSA-N CCC(CC1=C(C)NC(N)S1)CN(C)C Chemical compound CCC(CC1=C(C)NC(N)S1)CN(C)C PZRJDDJZXAGGSX-UHFFFAOYSA-N 0.000 description 1
- VTNCRCDILUUKAV-UHFFFAOYSA-N CCC/N=C(/N)\SCC Chemical compound CCC/N=C(/N)\SCC VTNCRCDILUUKAV-UHFFFAOYSA-N 0.000 description 1
- RWSHANIPAAVDKE-ZETCQYMHSA-N CCCNC[C@H](C)S/C(/N)=N\C Chemical compound CCCNC[C@H](C)S/C(/N)=N\C RWSHANIPAAVDKE-ZETCQYMHSA-N 0.000 description 1
- GWSRENOMIBUYJQ-UHFFFAOYSA-N CC[n](c(C(NCc1cccc(C(Nc2ccc(CCN(C)C3)c3c2)=O)c1)=O)cc1c2)c1ccc2C#N Chemical compound CC[n](c(C(NCc1cccc(C(Nc2ccc(CCN(C)C3)c3c2)=O)c1)=O)cc1c2)c1ccc2C#N GWSRENOMIBUYJQ-UHFFFAOYSA-N 0.000 description 1
- SMAHIGCEYQYKLG-IBGZPJMESA-N CN(C)[C@@H](CC1)Cc2c1nc(NC(c1cc(CNC(c3c[n](cc(cc4)C#N)c4n3)=O)ccc1)=O)[s]2 Chemical compound CN(C)[C@@H](CC1)Cc2c1nc(NC(c1cc(CNC(c3c[n](cc(cc4)C#N)c4n3)=O)ccc1)=O)[s]2 SMAHIGCEYQYKLG-IBGZPJMESA-N 0.000 description 1
- NOBLKTZCRYVNMU-UHFFFAOYSA-N CN(CC1)Cc2c1ccc(NC(c1cc(CNC(C(C3)=NN=C3c3cccnc3)=O)ccc1)=O)c2 Chemical compound CN(CC1)Cc2c1ccc(NC(c1cc(CNC(C(C3)=NN=C3c3cccnc3)=O)ccc1)=O)c2 NOBLKTZCRYVNMU-UHFFFAOYSA-N 0.000 description 1
- KSVOONKKPUEFTJ-UHFFFAOYSA-N CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c(cc3)cc(CC4)c3NC4=O)=O)ccc1)=O)c2 Chemical compound CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c(cc3)cc(CC4)c3NC4=O)=O)ccc1)=O)c2 KSVOONKKPUEFTJ-UHFFFAOYSA-N 0.000 description 1
- NPYVDQGHCCYYBU-UHFFFAOYSA-N CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c(cc3)cc(N4)c3SCC4=O)=O)ccc1)=O)c2 Chemical compound CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c(cc3)cc(N4)c3SCC4=O)=O)ccc1)=O)c2 NPYVDQGHCCYYBU-UHFFFAOYSA-N 0.000 description 1
- BVOZVTOSIIZJFB-UHFFFAOYSA-N CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c(cc3)ccc3-c3ccc(CO)[o]3)=O)ccc1)=O)c2 Chemical compound CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c(cc3)ccc3-c3ccc(CO)[o]3)=O)ccc1)=O)c2 BVOZVTOSIIZJFB-UHFFFAOYSA-N 0.000 description 1
- IICYHOZEEWHDDO-UHFFFAOYSA-N CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c(cc3)ccc3-c3cncnc3)=O)ccc1)=O)c2 Chemical compound CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c(cc3)ccc3-c3cncnc3)=O)ccc1)=O)c2 IICYHOZEEWHDDO-UHFFFAOYSA-N 0.000 description 1
- AVCZTAYFQCNLLG-UHFFFAOYSA-N CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c(cc3)cnc3-c3cc(C#N)ccc3)=O)ccc1)=O)c2 Chemical compound CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c(cc3)cnc3-c3cc(C#N)ccc3)=O)ccc1)=O)c2 AVCZTAYFQCNLLG-UHFFFAOYSA-N 0.000 description 1
- JKVINGMBDITKAB-UHFFFAOYSA-N CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c3cc(-[n]4cncc4)ccc3)=O)ccc1)=O)c2 Chemical compound CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c3cc(-[n]4cncc4)ccc3)=O)ccc1)=O)c2 JKVINGMBDITKAB-UHFFFAOYSA-N 0.000 description 1
- SYKGIXVMJZXJTH-UHFFFAOYSA-N CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c3cc(ccc(C#N)c4)c4[nH]3)=O)ccc1)=O)c2 Chemical compound CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c3cc(ccc(C#N)c4)c4[nH]3)=O)ccc1)=O)c2 SYKGIXVMJZXJTH-UHFFFAOYSA-N 0.000 description 1
- VICNOHNTTMWFIN-UHFFFAOYSA-N CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c3ccc(-c4ccncc4)[s]3)=O)ccc1)=O)c2 Chemical compound CN(CC1)Cc2c1ccc(NC(c1cc(CNC(c3ccc(-c4ccncc4)[s]3)=O)ccc1)=O)c2 VICNOHNTTMWFIN-UHFFFAOYSA-N 0.000 description 1
- BYSSCYBLIXTBMA-UHFFFAOYSA-N CN(CC1)Cc2c1nc(NC(c1cc(CNC(c(cc3)ccc3-c3ccncc3)=O)ccc1)=O)[s]2 Chemical compound CN(CC1)Cc2c1nc(NC(c1cc(CNC(c(cc3)ccc3-c3ccncc3)=O)ccc1)=O)[s]2 BYSSCYBLIXTBMA-UHFFFAOYSA-N 0.000 description 1
- UOMWJXFLQYIMLU-UHFFFAOYSA-N CN(CC1)Cc2c1nc(NC(c1cc(CNC(c3ccc(-c4c[nH]nc4)[s]3)=O)ccc1)=O)[s]2 Chemical compound CN(CC1)Cc2c1nc(NC(c1cc(CNC(c3ccc(-c4c[nH]nc4)[s]3)=O)ccc1)=O)[s]2 UOMWJXFLQYIMLU-UHFFFAOYSA-N 0.000 description 1
- YPVUFKHLPDWRHK-UHFFFAOYSA-N CN(c(cc1)ncc1C(NCc1cccc(C(Nc2cc(CN(C)CC3)c3cc2)=O)c1)=O)S(c(cccc1)c1O)(=O)=O Chemical compound CN(c(cc1)ncc1C(NCc1cccc(C(Nc2cc(CN(C)CC3)c3cc2)=O)c1)=O)S(c(cccc1)c1O)(=O)=O YPVUFKHLPDWRHK-UHFFFAOYSA-N 0.000 description 1
- CKIJOWCUTDBWQT-UHFFFAOYSA-N CN1Cc2cc(NC(c3cc(CNC(c(cc4)cc(C(N5CCO)=O)c4C5=O)=O)ccc3)=O)ccc2CC1 Chemical compound CN1Cc2cc(NC(c3cc(CNC(c(cc4)cc(C(N5CCO)=O)c4C5=O)=O)ccc3)=O)ccc2CC1 CKIJOWCUTDBWQT-UHFFFAOYSA-N 0.000 description 1
- GFMNRPSQBYBMKY-UHFFFAOYSA-N C[n]1ncc(C(C2)=NOC2C(NCc2cccc(C(Nc3ccc(CCN(C)C4)c4c3)=O)c2)=O)c1 Chemical compound C[n]1ncc(C(C2)=NOC2C(NCc2cccc(C(Nc3ccc(CCN(C)C4)c4c3)=O)c2)=O)c1 GFMNRPSQBYBMKY-UHFFFAOYSA-N 0.000 description 1
- BDANDTMOVORWHP-UHFFFAOYSA-N Cc1c(C(NCc2cccc(C(Nc3nc(CCN(C)C4)c4[s]3)=O)c2)=O)[nH]c(-c2ccncc2)n1 Chemical compound Cc1c(C(NCc2cccc(C(Nc3nc(CCN(C)C4)c4[s]3)=O)c2)=O)[nH]c(-c2ccncc2)n1 BDANDTMOVORWHP-UHFFFAOYSA-N 0.000 description 1
- VWHRGYATTNGULG-FQEVSTJZSA-N Cc1c(C(NCc2cccc(C(Nc3nc(CC[C@@H](C4)N(C)C)c4[s]3)=O)c2)=O)[s]c(-c2ccncc2)n1 Chemical compound Cc1c(C(NCc2cccc(C(Nc3nc(CC[C@@H](C4)N(C)C)c4[s]3)=O)c2)=O)[s]c(-c2ccncc2)n1 VWHRGYATTNGULG-FQEVSTJZSA-N 0.000 description 1
- LUOAIOLPDAAFJO-UHFFFAOYSA-N Cc1ncc(-c2ccc(C(NCc3cccc(C(Nc4nc(CCN(C)C5)c5[s]4)=O)c3)=O)[s]2)[o]1 Chemical compound Cc1ncc(-c2ccc(C(NCc3cccc(C(Nc4nc(CCN(C)C5)c5[s]4)=O)c3)=O)[s]2)[o]1 LUOAIOLPDAAFJO-UHFFFAOYSA-N 0.000 description 1
- GLKHVOTYDJEAHX-UHFFFAOYSA-N Cc1nnn[n]1-c(cc1)ccc1C(NCc1cccc(C(Nc2nc(CCN(C)C3)c3[s]2)=O)c1)=O Chemical compound Cc1nnn[n]1-c(cc1)ccc1C(NCc1cccc(C(Nc2nc(CCN(C)C3)c3[s]2)=O)c1)=O GLKHVOTYDJEAHX-UHFFFAOYSA-N 0.000 description 1
- MDMDDLBGJKODKN-NRFANRHFSA-N Cc1nnn[n]1-c(cc1)ccc1C(NCc1cccc(C(Nc2nc(CC[C@@H](C3)N(C)C)c3[s]2)=O)c1)=O Chemical compound Cc1nnn[n]1-c(cc1)ccc1C(NCc1cccc(C(Nc2nc(CC[C@@H](C3)N(C)C)c3[s]2)=O)c1)=O MDMDDLBGJKODKN-NRFANRHFSA-N 0.000 description 1
- OXSMZTRDGVTACF-UHFFFAOYSA-N NCC(C(F)(F)F)=O Chemical compound NCC(C(F)(F)F)=O OXSMZTRDGVTACF-UHFFFAOYSA-N 0.000 description 1
- NMMAOBDSOJXRMN-FQEVSTJZSA-N N[C@@H](CC1)Cc2c1nc(NC(c1cc(CNC(c3cccc(-c4c[nH]nc4)c3)=O)ccc1)=O)[s]2 Chemical compound N[C@@H](CC1)Cc2c1nc(NC(c1cc(CNC(c3cccc(-c4c[nH]nc4)c3)=O)ccc1)=O)[s]2 NMMAOBDSOJXRMN-FQEVSTJZSA-N 0.000 description 1
- HJFVYDJAEFHGGT-QHCPKHFHSA-N O=C(c(cc1)ccc1-c1cnc[o]1)NCc1cccc(C(Nc2nc(CC[C@@H](C3)N4CCOCC4)c3[s]2)=O)c1 Chemical compound O=C(c(cc1)ccc1-c1cnc[o]1)NCc1cccc(C(Nc2nc(CC[C@@H](C3)N4CCOCC4)c3[s]2)=O)c1 HJFVYDJAEFHGGT-QHCPKHFHSA-N 0.000 description 1
- HBELMBTYFXJPKJ-UHFFFAOYSA-N OC(c1ccc(-c2c[n](C(c3ccccc3)(c3ccccc3)c3ccccc3)nc2)[s]1)=O Chemical compound OC(c1ccc(-c2c[n](C(c3ccccc3)(c3ccccc3)c3ccccc3)nc2)[s]1)=O HBELMBTYFXJPKJ-UHFFFAOYSA-N 0.000 description 1
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- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
- C07D217/04—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
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- C—CHEMISTRY; METALLURGY
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- C07D401/00—Heterocyclic 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
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- 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
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- C—CHEMISTRY; METALLURGY
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- 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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- C—CHEMISTRY; METALLURGY
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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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D417/00—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
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D487/04—Ortho-condensed systems
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
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| US61/362,032 | 2010-07-07 | ||
| PCT/US2011/042508 WO2012006203A1 (en) | 2010-07-07 | 2011-06-30 | N-cyclyl-3 - (cyclylcarbonylaminomethyl) benzamide derivatives as rho kinase inhibitors |
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| JP2013531013A5 JP2013531013A5 (enExample) | 2014-08-14 |
| JP5739527B2 true JP5739527B2 (ja) | 2015-06-24 |
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| US9079880B2 (en) | 2010-07-07 | 2015-07-14 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
| US8697911B2 (en) | 2010-07-07 | 2014-04-15 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
| WO2012054367A1 (en) | 2010-10-19 | 2012-04-26 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
| CN103420917B (zh) * | 2012-05-18 | 2015-08-19 | 国药一心制药有限公司 | 含稠环结构的苯甲酰胺类化合物及其作为抗肿瘤药物应用 |
| EP2939675B1 (en) * | 2012-12-28 | 2019-09-04 | Shin Nippon Biomedical Laboratories, Ltd. | Oct3 activity inhibitor containing imidazopyridine derivative as active component, and oct3 detection agent |
| AR094929A1 (es) | 2013-02-28 | 2015-09-09 | Bristol Myers Squibb Co | Derivados de fenilpirazol como inhibidores potentes de rock1 y rock2 |
| CN105102448B (zh) | 2013-02-28 | 2018-03-06 | 百时美施贵宝公司 | 作为rock1和rock2抑制剂的苯基吡唑衍生物 |
| WO2015017335A1 (en) * | 2013-07-30 | 2015-02-05 | Boehringer Ingelheim International Gmbh | Azaindole compounds as modulators of rorc |
| JP6883173B2 (ja) | 2015-05-12 | 2021-06-09 | ヘモストッド エスエー | 改善された血小板産生のための薬理学的特徴およびマイクロ流体特徴の組み合わせ |
| JP2018515623A (ja) * | 2015-05-18 | 2018-06-14 | トランスレイショナル・ドラッグ・ディベロップメント・エルエルシー | キナーゼ阻害剤としての複素環式化合物 |
| US10738007B2 (en) | 2016-10-24 | 2020-08-11 | Translation Drug Development, LLC | Amide compounds as kinase inhibitors, compositions and methods of treatment |
| IL266150B2 (en) * | 2016-10-24 | 2023-12-01 | Translational Drug Dev Llc | 3-substituted benzamide derivatives as kinase inhibitors |
| CA3082254A1 (en) | 2016-11-21 | 2018-05-24 | Translational Drug Development, Llc | Heterocyclic compounds as kinase inhibitors |
| CN108203433B (zh) * | 2016-12-16 | 2020-07-03 | 成都先导药物开发股份有限公司 | 一种rock抑制剂及其应用 |
| JP7065951B2 (ja) | 2017-09-22 | 2022-05-12 | ジュビラント エピパッド エルエルシー | Pad阻害剤としての複素環式化合物 |
| EP3691642B1 (en) | 2017-10-02 | 2024-03-06 | Boehringer Ingelheim International GmbH | [1,6]naphthyridine compounds and derivatives as cdk8/cdk19 inhibitors |
| WO2019077631A1 (en) | 2017-10-18 | 2019-04-25 | Jubilant Biosys Limited | IMIDAZO-PYRIDINE COMPOUNDS FOR USE AS PAD INHIBITORS |
| EP3707135A1 (en) | 2017-11-06 | 2020-09-16 | Jubilant Prodel LLC | Pyrimidine derivatives as inhibitors of pd1/pd-l1 activation |
| IL274762B2 (en) | 2017-11-24 | 2023-10-01 | Jubilant Episcribe Llc | Novel heterocyclic compounds as prmt5 inhibitors |
| WO2019175897A1 (en) | 2018-03-13 | 2019-09-19 | Jubilant Biosys Limited | Bicyclic compounds as inhibitors of pd1/pd-l1 interaction/activation |
| EP3784226B1 (en) | 2018-04-24 | 2024-08-14 | Translational Drug Development Llc | Pyrazole-phenylamide derivatives as inhibitors of the rho-associated protein kinase rock1 and rock2 for the treatment of cancer |
| CN109678815B (zh) * | 2019-01-09 | 2022-11-29 | 中国药科大学 | N-苄基苯甲酰胺类衍生物及其制备方法与制药用途 |
| WO2023091565A1 (en) * | 2021-11-17 | 2023-05-25 | The University Of North Carolina At Chapel Hill | Nsd2-targeted chemical degraders and compositions and methods of use thereof |
| CN116284045A (zh) * | 2023-05-18 | 2023-06-23 | 西南交通大学 | 一种手性吲哚单元取代的四氢异喹啉化合物及其合成方法 |
| WO2025242921A1 (en) * | 2024-05-23 | 2025-11-27 | Storm Therapeutics Limited | Processes for the preparation of inhibitory compounds |
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| US5210208A (en) | 1990-09-24 | 1993-05-11 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Disubstituted aryl compounds exhibiting selective leukotriene b4 antagonist activity |
| NZ240863A (en) | 1991-09-11 | 1995-04-27 | Mcneilab Inc | Substituted 4-aryl piperidine and 4-aryl piperazine derivatives, preparation and pharmaceutical compositions thereof |
| JPH11130751A (ja) | 1997-10-30 | 1999-05-18 | Yoshitomi Pharmaceut Ind Ltd | アミド化合物およびそれらの酸付加塩の標識化合物 |
| US7217722B2 (en) | 2000-02-01 | 2007-05-15 | Kirin Beer Kabushiki Kaisha | Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same |
| WO2002044126A2 (en) | 2000-11-28 | 2002-06-06 | Guilford Pharmaceuticals Inc. | Bisubstituted carbocyclic cyclophilin binding compounds and theirus |
| DE10112768A1 (de) | 2001-03-16 | 2002-09-19 | Merck Patent Gmbh | Phenylderivate 3 |
| WO2002100833A1 (en) | 2001-06-12 | 2002-12-19 | Sumitomo Pharmaceuticals Company, Limited | Rho KINASE INHIBITORS |
| SE0102764D0 (sv) | 2001-08-17 | 2001-08-17 | Astrazeneca Ab | Compounds |
| US20040186151A1 (en) | 2003-02-12 | 2004-09-23 | Mjalli Adnan M.M. | Substituted azole derivatives as therapeutic agents |
| FR2862965B1 (fr) | 2003-11-27 | 2007-09-07 | Merck Sante Sas | Nouveaux derives de phenoxyacetamides et leur utilisation pour la preparation de diphenylamides. |
| US20050209284A1 (en) | 2004-02-12 | 2005-09-22 | Boehringer Ingelheim Pharmaceuticals, Inc. | Tec kinase inhibitors |
| MX2007003332A (es) | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores de estearoil-coa-desaturasa. |
| WO2006052542A2 (en) | 2004-11-04 | 2006-05-18 | Neurogen Corporation | Arylalkyl ureas as cb1 antagonists |
| GB0510139D0 (en) | 2005-05-18 | 2005-06-22 | Addex Pharmaceuticals Sa | Novel compounds B1 |
| US7470787B2 (en) | 2005-07-11 | 2008-12-30 | Aerie Pharmaceuticals, Inc. | Isoquinoline compounds |
| JP5235887B2 (ja) | 2006-09-20 | 2013-07-10 | アエリー ファーマシューティカルズ インコーポレイテッド | Rhoキナーゼ阻害剤 |
| WO2008053319A1 (en) | 2006-10-30 | 2008-05-08 | Pfizer Products Inc. | Amide resorcinol compounds |
| WO2008079277A1 (en) * | 2006-12-22 | 2008-07-03 | Millennium Pharmaceuticals, Inc. | Certain pyrazoline derivatives with kinase inhibitory activity |
| EP2079694B1 (en) | 2006-12-28 | 2017-03-01 | Rigel Pharmaceuticals, Inc. | N-substituted-heterocycloalkyloxybenzamide compounds and methods of use |
| CL2007003874A1 (es) | 2007-01-03 | 2008-05-16 | Boehringer Ingelheim Int | Compuestos derivados de benzamida; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar enfermedades cardiovasculares, hipertension, aterosclerosis, reestenosis, ictus, insuficiencia cardiaca, lesion isquemica, hipertensio |
| WO2008157330A1 (en) | 2007-06-14 | 2008-12-24 | Smithkline Beecham Corporation | Chemical compounds |
| EP2193119B1 (en) | 2007-08-27 | 2014-01-01 | Abbvie Deutschland GmbH & Co. KG | 4-(4-pyridinyl)-benzamides and their use as rock activity modulators |
| EP2194045A4 (en) | 2007-08-30 | 2011-09-21 | Takeda Pharmaceutical | Substituted pyrazole derivative |
| MX2010005298A (es) | 2007-11-16 | 2010-06-30 | Rigel Pharmaceuticals Inc | Compuestos de carboxamida, sulfonamida y amina para trastornos metabolicos. |
| TW200944506A (en) | 2008-03-26 | 2009-11-01 | Takeda Pharmaceutical | Substituted pyrazole derivatives and use thereof |
| US8697911B2 (en) | 2010-07-07 | 2014-04-15 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
| US9079880B2 (en) | 2010-07-07 | 2015-07-14 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
| WO2012054367A1 (en) | 2010-10-19 | 2012-04-26 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
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| JP2013531013A (ja) | 2013-08-01 |
| EP2590950A1 (en) | 2013-05-15 |
| EP2590950B1 (en) | 2014-10-15 |
| WO2012006203A1 (en) | 2012-01-12 |
| US8697911B2 (en) | 2014-04-15 |
| US20120165322A1 (en) | 2012-06-28 |
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