JP2007521286A5 - - Google Patents
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- JP2007521286A5 JP2007521286A5 JP2006517746A JP2006517746A JP2007521286A5 JP 2007521286 A5 JP2007521286 A5 JP 2007521286A5 JP 2006517746 A JP2006517746 A JP 2006517746A JP 2006517746 A JP2006517746 A JP 2006517746A JP 2007521286 A5 JP2007521286 A5 JP 2007521286A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- group
- alkyl
- aryl
- heteroaryl
- 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.)
- Granted
Links
- 0 CCN(*)CCN(C)C(*)(*)C[Al]* Chemical compound CCN(*)CCN(C)C(*)(*)C[Al]* 0.000 description 43
- HUSMPKZBAOSVGH-MSOLQXFVSA-N C[C@@H](c(cc1)ccc1Br)N(CC1)[C@H](C)CN1C(CC1)CCN1C(OC(C)(C)C)=O Chemical compound C[C@@H](c(cc1)ccc1Br)N(CC1)[C@H](C)CN1C(CC1)CCN1C(OC(C)(C)C)=O HUSMPKZBAOSVGH-MSOLQXFVSA-N 0.000 description 3
- JHUBNQSPUZXGKI-UHFFFAOYSA-N CC(C)c(cc1)cc2c1OCO2 Chemical compound CC(C)c(cc1)cc2c1OCO2 JHUBNQSPUZXGKI-UHFFFAOYSA-N 0.000 description 2
- LWYFMTMRWRGREZ-UHFFFAOYSA-N CC(C)c1cc(C#N)ccc1 Chemical compound CC(C)c1cc(C#N)ccc1 LWYFMTMRWRGREZ-UHFFFAOYSA-N 0.000 description 2
- RPQZZDWFWOIRAN-UHFFFAOYSA-N CC(C)c1ccc(C(F)(F)F)cc1 Chemical compound CC(C)c1ccc(C(F)(F)F)cc1 RPQZZDWFWOIRAN-UHFFFAOYSA-N 0.000 description 2
- FRGXNJWEDDQLFH-UHFFFAOYSA-N CC(C)c1ccncc1 Chemical compound CC(C)c1ccncc1 FRGXNJWEDDQLFH-UHFFFAOYSA-N 0.000 description 2
- OXHKQGRHPLZUGH-UHFFFAOYSA-N Cc([s]cc1)c1OC Chemical compound Cc([s]cc1)c1OC OXHKQGRHPLZUGH-UHFFFAOYSA-N 0.000 description 2
- IKNQPNLSEBWZKX-UHFFFAOYSA-N Cc(cc1)cc(Cl)c1F Chemical compound Cc(cc1)cc(Cl)c1F IKNQPNLSEBWZKX-UHFFFAOYSA-N 0.000 description 2
- HGDGACBSGVRCSM-UHFFFAOYSA-N Cc1c[s]cc1OC Chemical compound Cc1c[s]cc1OC HGDGACBSGVRCSM-UHFFFAOYSA-N 0.000 description 2
- FBOYMIDCHINJKC-UHFFFAOYSA-N Brc(cc1)cc2c1OCO2 Chemical compound Brc(cc1)cc2c1OCO2 FBOYMIDCHINJKC-UHFFFAOYSA-N 0.000 description 1
- QQNIQRMNEKOPBX-UHFFFAOYSA-N CCCCOc1c(C)[s]cc1 Chemical compound CCCCOc1c(C)[s]cc1 QQNIQRMNEKOPBX-UHFFFAOYSA-N 0.000 description 1
- MXZNLZCPCFVLEH-UHFFFAOYSA-N CCCOc(cc[s]1)c1I Chemical compound CCCOc(cc[s]1)c1I MXZNLZCPCFVLEH-UHFFFAOYSA-N 0.000 description 1
- JSBSMNUHMWSUGB-ITXNJQJZSA-N CCCOc1c(C(CC(CC2)=CCCC2N(CC2)C[C@@H](C)N2[C@@H](C)c2ccc(CCc(cc3)ccc3Cl)cc2)=O)[s]cc1 Chemical compound CCCOc1c(C(CC(CC2)=CCCC2N(CC2)C[C@@H](C)N2[C@@H](C)c2ccc(CCc(cc3)ccc3Cl)cc2)=O)[s]cc1 JSBSMNUHMWSUGB-ITXNJQJZSA-N 0.000 description 1
- KTLZURZEOPZMKJ-RPBOFIJWSA-N CCCOc1c(C(N(CC2)CCC2N(CC2)C[C@@H](C)N2[C@@H](C)c(cc2)ccc2-c2cc(C#N)ccc2)=O)[s]cc1 Chemical compound CCCOc1c(C(N(CC2)CCC2N(CC2)C[C@@H](C)N2[C@@H](C)c(cc2)ccc2-c2cc(C#N)ccc2)=O)[s]cc1 KTLZURZEOPZMKJ-RPBOFIJWSA-N 0.000 description 1
- MNCDTFLKJRBXBT-FTJBHMTQSA-N CCCOc1c(C(N(CC2)CCC2N(CC2)C[C@@H](C)N2[C@@H](C)c2ccc(CCc(cc3)ccc3Cl)cc2)=O)[s]cc1 Chemical compound CCCOc1c(C(N(CC2)CCC2N(CC2)C[C@@H](C)N2[C@@H](C)c2ccc(CCc(cc3)ccc3Cl)cc2)=O)[s]cc1 MNCDTFLKJRBXBT-FTJBHMTQSA-N 0.000 description 1
- ZGIXPQMXXDPWKF-FTJBHMTQSA-N CCCOc1c(C(N(CC2)CCC2N(CC2)C[C@@H](C)N2[C@@H](C)c2ccc(CCc3ccc4OCOc4c3)cc2)=O)[s]cc1 Chemical compound CCCOc1c(C(N(CC2)CCC2N(CC2)C[C@@H](C)N2[C@@H](C)c2ccc(CCc3ccc4OCOc4c3)cc2)=O)[s]cc1 ZGIXPQMXXDPWKF-FTJBHMTQSA-N 0.000 description 1
- QDZYLJJZEADFNS-CQSZACIVSA-N CCCOc1c(C(N(CC2)CCC2N2C[C@@H](C)NCC2)=O)[s]cc1 Chemical compound CCCOc1c(C(N(CC2)CCC2N2C[C@@H](C)NCC2)=O)[s]cc1 QDZYLJJZEADFNS-CQSZACIVSA-N 0.000 description 1
- NOCGTFKCRFTUQN-UHFFFAOYSA-N CCCOc1c(C(O)=O)[s]cc1 Chemical compound CCCOc1c(C(O)=O)[s]cc1 NOCGTFKCRFTUQN-UHFFFAOYSA-N 0.000 description 1
- KFBUGBFIQMNIEO-UHFFFAOYSA-N CCCOc1c(C(OC)=O)[s]cc1 Chemical compound CCCOc1c(C(OC)=O)[s]cc1 KFBUGBFIQMNIEO-UHFFFAOYSA-N 0.000 description 1
- MBYMHSDIEZNZCE-PKTZIBPZSA-N CCCOc1c[s]cc1C(N(CC1)CCC1N(CC1)C[C@@H](C)N1[C@@H](C)c(cc1)ccc1-c1cc(Cl)cc(Cl)c1)=O Chemical compound CCCOc1c[s]cc1C(N(CC1)CCC1N(CC1)C[C@@H](C)N1[C@@H](C)c(cc1)ccc1-c1cc(Cl)cc(Cl)c1)=O MBYMHSDIEZNZCE-PKTZIBPZSA-N 0.000 description 1
- MQDRVHOWRJXGJQ-YADHBBJMSA-N C[C@@H](C(CC1)=CC=C1c1ccncc1)N(CC1)[C@H](C)CN1C(CC1)CCN1C(OC(C)(C)C)=O Chemical compound C[C@@H](C(CC1)=CC=C1c1ccncc1)N(CC1)[C@H](C)CN1C(CC1)CCN1C(OC(C)(C)C)=O MQDRVHOWRJXGJQ-YADHBBJMSA-N 0.000 description 1
- CMYFCWNDXUVHMJ-RPWUZVMVSA-N C[C@@H](c(cc1)ccc1-c1cc(Cl)cc(Cl)c1)N(CC1)[C@H](C)CN1C(CC1)CCN1C(c1c(COCC2CC2)cc[s]1)=O Chemical compound C[C@@H](c(cc1)ccc1-c1cc(Cl)cc(Cl)c1)N(CC1)[C@H](C)CN1C(CC1)CCN1C(c1c(COCC2CC2)cc[s]1)=O CMYFCWNDXUVHMJ-RPWUZVMVSA-N 0.000 description 1
- KIQFKJQHLHAUOR-AGQFNQOXSA-N C[C@@H](c(cc1)ccc1Br)N(CC1)[C@H](C)CN1C(CC1)C[C@@H](C)N1C(OC(C)(C)C)=O Chemical compound C[C@@H](c(cc1)ccc1Br)N(CC1)[C@H](C)CN1C(CC1)C[C@@H](C)N1C(OC(C)(C)C)=O KIQFKJQHLHAUOR-AGQFNQOXSA-N 0.000 description 1
- TZLLCNOMYATBLU-UXHICEINSA-N C[C@@H](c1ccc(C=C)cc1)N(CC1)[C@H](C)CN1C(CC1)CCN1C(OC(C)(C)C)=O Chemical compound C[C@@H](c1ccc(C=C)cc1)N(CC1)[C@H](C)CN1C(CC1)CCN1C(OC(C)(C)C)=O TZLLCNOMYATBLU-UXHICEINSA-N 0.000 description 1
- OJXBIWMWVHZKRM-YADHBBJMSA-N C[C@@H](c1ccc(CCc2ccc3OCOc3c2)cc1)N(CC1)[C@H](C)CN1C1CCN(C)CC1 Chemical compound C[C@@H](c1ccc(CCc2ccc3OCOc3c2)cc1)N(CC1)[C@H](C)CN1C1CCN(C)CC1 OJXBIWMWVHZKRM-YADHBBJMSA-N 0.000 description 1
- HZJKLKAIQVELLV-UHFFFAOYSA-N Ic([s]cc1)c1OCC1CC1 Chemical compound Ic([s]cc1)c1OCC1CC1 HZJKLKAIQVELLV-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US48361903P | 2003-06-30 | 2003-06-30 | |
| PCT/US2004/020763 WO2005005419A1 (en) | 2003-06-30 | 2004-06-28 | Mch antagonists for the treatment of obesity |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007521286A JP2007521286A (ja) | 2007-08-02 |
| JP2007521286A5 true JP2007521286A5 (enExample) | 2008-02-28 |
| JP4605801B2 JP4605801B2 (ja) | 2011-01-05 |
Family
ID=34061963
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006517746A Expired - Fee Related JP4605801B2 (ja) | 2003-06-30 | 2004-06-28 | 肥満治療用のｍｃｈアンタゴニスト |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7345042B2 (enExample) |
| EP (1) | EP1644366A1 (enExample) |
| JP (1) | JP4605801B2 (enExample) |
| CN (1) | CN1812985A (enExample) |
| CA (1) | CA2526725A1 (enExample) |
| MX (1) | MXPA05013596A (enExample) |
| WO (1) | WO2005005419A1 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0509803A (pt) | 2004-04-13 | 2007-09-18 | Incyte Corp | derivados de piperazinilpiperidina como antagonistas de receptor de quimiocina |
| WO2007124045A2 (en) * | 2006-04-20 | 2007-11-01 | Ampla Pharmaceuticals, Inc. | Piperidine and piperazine compounds for use in the treatment of obesity, eating disorders and sexual dysfunction by potentiation of mc4 receptor activity |
| WO2008030853A2 (en) * | 2006-09-06 | 2008-03-13 | Incyte Corporation | Combination therapy for human immunodeficiency virus infection |
| US10556013B2 (en) | 2017-06-20 | 2020-02-11 | Imbria Pharmaceuticals, Inc. | Compositions and methods for increasing efficiency of cardiac metabolism |
| EP4497474A3 (en) | 2018-10-17 | 2025-04-23 | Imbria Pharmaceuticals, Inc. | Methods of treating rheumatic diseases using trimetazidine-based compounds |
| US11780811B2 (en) | 2020-06-30 | 2023-10-10 | Imbria Pharmaceuticals, Inc. | Methods of synthesizing 2-[4-[(2,3,4-trimethoxyphenyl)methyl]piperazin-1-yl]ethyl pyridine-3-carboxylate |
| US11530184B2 (en) | 2020-06-30 | 2022-12-20 | Imbria Pharmaceuticals, Inc. | Crystal forms of 2-[4-[(2,3,4-trimethoxyphenyl)methyl]piperazin-1-yl]ethyl pyridine-3-carboxylate |
| US11883396B2 (en) | 2021-05-03 | 2024-01-30 | Imbria Pharmaceuticals, Inc. | Methods of treating kidney conditions using modified forms of trimetazidine |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL117149A0 (en) | 1995-02-23 | 1996-06-18 | Schering Corp | Muscarinic antagonists |
| US5889006A (en) | 1995-02-23 | 1999-03-30 | Schering Corporation | Muscarinic antagonists |
| US5908830A (en) | 1996-10-31 | 1999-06-01 | Merck & Co., Inc. | Combination therapy for the treatment of diabetes and obesity |
| US6391865B1 (en) * | 1999-05-04 | 2002-05-21 | Schering Corporation | Piperazine derivatives useful as CCR5 antagonists |
| CA2371583C (en) | 1999-05-04 | 2005-09-13 | Schering Corporation | Piperazine derivatives useful as ccr5 antagonists |
| EP1366030A2 (en) * | 2000-07-06 | 2003-12-03 | Neurogen Corporation | Melanin concentrating hormone receptor ligands |
| US6900329B2 (en) * | 2001-03-21 | 2005-05-31 | Schering Corporation | MCH antagonists and their use in the treatment of obesity |
| CN1703401A (zh) * | 2001-05-22 | 2005-11-30 | 神经原公司 | 黑色素浓集激素受体的配体:取代的1－苄基－4－芳基哌嗪类似物 |
| DE60234116D1 (de) * | 2001-11-26 | 2009-12-03 | Schering Corp | Piperidin mch antagonisten und ihre verwendung in der behandlung von obesität und störungen des zentralnervensystems |
| WO2003059289A2 (en) * | 2002-01-10 | 2003-07-24 | Neurogen Corporation | Melanin concentrating hormone receptor ligands: substituted benzoimidazole analogues |
| AR043434A1 (es) * | 2003-03-03 | 2005-07-27 | Merck & Co Inc | Derivados de piperizacina acilados como agonistas del receptor de melanocortina-4. composiciones farmaceuticas y usos |
| WO2004113323A1 (en) * | 2003-06-13 | 2004-12-29 | Schering Aktiengesellschaft | Quinolyl amide derivatives as ccr-5 antagonists |
-
2004
- 2004-06-28 WO PCT/US2004/020763 patent/WO2005005419A1/en not_active Ceased
- 2004-06-28 US US10/878,788 patent/US7345042B2/en not_active Expired - Fee Related
- 2004-06-28 CA CA002526725A patent/CA2526725A1/en not_active Abandoned
- 2004-06-28 EP EP04777221A patent/EP1644366A1/en not_active Withdrawn
- 2004-06-28 CN CNA2004800183172A patent/CN1812985A/zh active Pending
- 2004-06-28 MX MXPA05013596A patent/MXPA05013596A/es not_active Application Discontinuation
- 2004-06-28 JP JP2006517746A patent/JP4605801B2/ja not_active Expired - Fee Related
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