KR101368228B1 - 락탐 화합물 및 약제로서의 이의 용도 - Google Patents
락탐 화합물 및 약제로서의 이의 용도 Download PDFInfo
- Publication number
- KR101368228B1 KR101368228B1 KR1020077012990A KR20077012990A KR101368228B1 KR 101368228 B1 KR101368228 B1 KR 101368228B1 KR 1020077012990 A KR1020077012990 A KR 1020077012990A KR 20077012990 A KR20077012990 A KR 20077012990A KR 101368228 B1 KR101368228 B1 KR 101368228B1
- Authority
- KR
- South Korea
- Prior art keywords
- diazaspiro
- alkyl
- trans
- hydroxycyclohexyl
- compound
- 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
- SJPZNPMHFHQWSJ-MEQCVUQCSA-N CC(C)OC(Nc(cc1F)ccc1N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)=O Chemical compound CC(C)OC(Nc(cc1F)ccc1N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)=O SJPZNPMHFHQWSJ-MEQCVUQCSA-N 0.000 description 1
- PATAGDNVVKNJSD-IQHDZCMKSA-N CC(Nc(cc1)cc(F)c1N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)=O Chemical compound CC(Nc(cc1)cc(F)c1N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)=O PATAGDNVVKNJSD-IQHDZCMKSA-N 0.000 description 1
- BBQPGRPPLBXHSL-UHFFFAOYSA-N COC(C1(CC1)N(CCC1(CCC2)CN2c(cccc2)c2F)C1=O)=O Chemical compound COC(C1(CC1)N(CCC1(CCC2)CN2c(cccc2)c2F)C1=O)=O BBQPGRPPLBXHSL-UHFFFAOYSA-N 0.000 description 1
- STMNVSDVSXMZKR-UHFFFAOYSA-N CS(Nc(cc1F)ccc1N(CCC1)CC1(CCN1C2(CC3CC(C4)C2)CC4C3O)C1=O)(=O)=O Chemical compound CS(Nc(cc1F)ccc1N(CCC1)CC1(CCN1C2(CC3CC(C4)C2)CC4C3O)C1=O)(=O)=O STMNVSDVSXMZKR-UHFFFAOYSA-N 0.000 description 1
- FGCSKMFYVNVXTB-UHFFFAOYSA-N Cc(c(S(N(CCC1)CC1(CCN1C2CCCCCC2)C1=O)(=O)=O)ccc1)c1Cl Chemical compound Cc(c(S(N(CCC1)CC1(CCN1C2CCCCCC2)C1=O)(=O)=O)ccc1)c1Cl FGCSKMFYVNVXTB-UHFFFAOYSA-N 0.000 description 1
- HMOMWLAUCLSOHI-UYJZDEDHSA-N Cc(c(S(N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)(=O)=O)ccc1)c1Cl Chemical compound Cc(c(S(N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)(=O)=O)ccc1)c1Cl HMOMWLAUCLSOHI-UYJZDEDHSA-N 0.000 description 1
- JCPMZCUCXFDRMX-HPCXZVJPSA-N Cc1ccccc1N(CC1)CCN1C(N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)=O Chemical compound Cc1ccccc1N(CC1)CCN1C(N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)=O JCPMZCUCXFDRMX-HPCXZVJPSA-N 0.000 description 1
- YPRGYYBHIYWKHG-UHFFFAOYSA-N N#CC(CC1)CCC1N(CCC1(CCC2)CN2c2ccc(C(F)(F)F)cc2)C1=O Chemical compound N#CC(CC1)CCC1N(CCC1(CCC2)CN2c2ccc(C(F)(F)F)cc2)C1=O YPRGYYBHIYWKHG-UHFFFAOYSA-N 0.000 description 1
- AWULZLWAYLIPEH-UHFFFAOYSA-N N#CC(CC1)CCC1N(CCC1(CCC2)CN2c2cccc(F)n2)C1=O Chemical compound N#CC(CC1)CCC1N(CCC1(CCC2)CN2c2cccc(F)n2)C1=O AWULZLWAYLIPEH-UHFFFAOYSA-N 0.000 description 1
- HEMAMPMUSKSDBW-FCDKUWBWSA-N N#CC[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2c2ccc(C(F)(F)F)cc2)C1=O Chemical compound N#CC[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2c2ccc(C(F)(F)F)cc2)C1=O HEMAMPMUSKSDBW-FCDKUWBWSA-N 0.000 description 1
- SGKSVPIMQIQSKO-PTEGZUARSA-N N#Cc(cc1)ccc1N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O Chemical compound N#Cc(cc1)ccc1N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O SGKSVPIMQIQSKO-PTEGZUARSA-N 0.000 description 1
- ZHEWCNALCGWHGA-UHFFFAOYSA-N N#Cc(cc1F)ccc1N(CCC1)CC1(CCN1C2(CC3C(C4)C2)CC4C3O)C1=O Chemical compound N#Cc(cc1F)ccc1N(CCC1)CC1(CCN1C2(CC3C(C4)C2)CC4C3O)C1=O ZHEWCNALCGWHGA-UHFFFAOYSA-N 0.000 description 1
- SSLFXXYDSIDQMZ-UHFFFAOYSA-N N#Cc(cc1F)ccc1N(CCC1)CC1(CCN1C2(CC3CC(C4)C2)CC4C3O)C1=O Chemical compound N#Cc(cc1F)ccc1N(CCC1)CC1(CCN1C2(CC3CC(C4)C2)CC4C3O)C1=O SSLFXXYDSIDQMZ-UHFFFAOYSA-N 0.000 description 1
- GGZTXYSRXXLBBR-UHFFFAOYSA-N N#Cc1c(N(CCC2)CC2(CCN2C3(CC4CC(C5)C3)CC5C4O)C2=O)nccc1 Chemical compound N#Cc1c(N(CCC2)CC2(CCN2C3(CC4CC(C5)C3)CC5C4O)C2=O)nccc1 GGZTXYSRXXLBBR-UHFFFAOYSA-N 0.000 description 1
- XELSRHDOXRXLRI-UHFFFAOYSA-N O=C(C(CC1)(CCC2)CN2c2ccc(C(F)(F)F)cn2)N1c1cccc2c1cccn2 Chemical compound O=C(C(CC1)(CCC2)CN2c2ccc(C(F)(F)F)cn2)N1c1cccc2c1cccn2 XELSRHDOXRXLRI-UHFFFAOYSA-N 0.000 description 1
- CBCHCHUYFVOWOX-SFHVURJKSA-N O=C([C@](CC1)(CCC2)CN2c2ccc(C(F)(F)F)cn2)N1C1CCOCC1 Chemical compound O=C([C@](CC1)(CCC2)CN2c2ccc(C(F)(F)F)cn2)N1C1CCOCC1 CBCHCHUYFVOWOX-SFHVURJKSA-N 0.000 description 1
- DDWGKUUKGKVXRK-UHFFFAOYSA-N O=C(c1ccncc1)N(CCC1)CC1(CCN1C2CCCCC2)C1=O Chemical compound O=C(c1ccncc1)N(CCC1)CC1(CCN1C2CCCCC2)C1=O DDWGKUUKGKVXRK-UHFFFAOYSA-N 0.000 description 1
- YZARSKMLBOLSFS-UHFFFAOYSA-N O=C(c1cnccc1)N(CCC1)CC1(CCN1C2CCCCC2)C1=O Chemical compound O=C(c1cnccc1)N(CCC1)CC1(CCN1C2CCCCC2)C1=O YZARSKMLBOLSFS-UHFFFAOYSA-N 0.000 description 1
- ULLKRKMWFZHZEO-DUNBPCILSA-N O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2C(N(CC2)CCN2c2cc(C(F)(F)F)ccc2)=O)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2C(N(CC2)CCN2c2cc(C(F)(F)F)ccc2)=O)C1=O ULLKRKMWFZHZEO-DUNBPCILSA-N 0.000 description 1
- FQXWJFDFQDAMMN-YYSPQECZSA-N O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2C(N(CC2)CCN2c2ccccc2Cl)=O)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2C(N(CC2)CCN2c2ccccc2Cl)=O)C1=O FQXWJFDFQDAMMN-YYSPQECZSA-N 0.000 description 1
- HGSMANHDPUPKJV-OPYUEGPBSA-N O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2C(N(CC2)CCN2c2ncc(C(F)(F)F)cc2)=O)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2C(N(CC2)CCN2c2ncc(C(F)(F)F)cc2)=O)C1=O HGSMANHDPUPKJV-OPYUEGPBSA-N 0.000 description 1
- FDMLOJXVQKRTBM-JDVJWJCPSA-N O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2c(cc2)ccc2NC(C2CC2)=O)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2c(cc2)ccc2NC(C2CC2)=O)C1=O FDMLOJXVQKRTBM-JDVJWJCPSA-N 0.000 description 1
- GQQPVPCOCYLUDS-DBTMUERSSA-N O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2c2ccc(C(F)(F)F)cn2)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2c2ccc(C(F)(F)F)cn2)C1=O GQQPVPCOCYLUDS-DBTMUERSSA-N 0.000 description 1
- QCWLUDVUOHLREO-RSBROLRWSA-N O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2c2ccccc2)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2c2ccccc2)C1=O QCWLUDVUOHLREO-RSBROLRWSA-N 0.000 description 1
- BEUJVDNNIASPQJ-DBTMUERSSA-N O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2c2ncccc2)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2c2ncccc2)C1=O BEUJVDNNIASPQJ-DBTMUERSSA-N 0.000 description 1
- GOVLKWZKLWIJEE-ONXXMXGDSA-N O[C@H](CC1)CC[C@H]1N(CCC12CNCCC1)C2=O Chemical compound O[C@H](CC1)CC[C@H]1N(CCC12CNCCC1)C2=O GOVLKWZKLWIJEE-ONXXMXGDSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/20—Spiro-condensed ring systems
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4747—Quinolines; Isoquinolines spiro-condensed
-
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- 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
- A61K31/495—Heterocyclic 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Epidemiology (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Urology & Nephrology (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US62661704P | 2004-11-10 | 2004-11-10 | |
| US60/626,617 | 2004-11-10 | ||
| US71502005P | 2005-09-08 | 2005-09-08 | |
| US60/715,020 | 2005-09-08 | ||
| PCT/US2005/040550 WO2006053024A2 (en) | 2004-11-10 | 2005-11-09 | Lactam compounds and their use as pharmaceuticals |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20070085944A KR20070085944A (ko) | 2007-08-27 |
| KR101368228B1 true KR101368228B1 (ko) | 2014-02-27 |
Family
ID=36337171
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020077012990A Expired - Fee Related KR101368228B1 (ko) | 2004-11-10 | 2005-11-09 | 락탐 화합물 및 약제로서의 이의 용도 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US20060116382A1 (enExample) |
| EP (2) | EP1812005B1 (enExample) |
| JP (1) | JP5202954B2 (enExample) |
| KR (1) | KR101368228B1 (enExample) |
| CN (1) | CN102731499B (enExample) |
| AU (1) | AU2005304560C1 (enExample) |
| BR (1) | BRPI0518022A (enExample) |
| CA (1) | CA2585797C (enExample) |
| EA (1) | EA019747B1 (enExample) |
| ES (1) | ES2547724T3 (enExample) |
| GE (1) | GEP20125565B (enExample) |
| IL (1) | IL182876A (enExample) |
| MX (1) | MX2007005527A (enExample) |
| NO (1) | NO340365B1 (enExample) |
| NZ (1) | NZ554906A (enExample) |
| SG (1) | SG161261A1 (enExample) |
| TW (1) | TWI400239B (enExample) |
| WO (1) | WO2006053024A2 (enExample) |
| ZA (1) | ZA200703754B (enExample) |
Families Citing this family (92)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20100222316A1 (en) | 2004-04-29 | 2010-09-02 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| US7880001B2 (en) | 2004-04-29 | 2011-02-01 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme |
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- 2005-11-09 WO PCT/US2005/040550 patent/WO2006053024A2/en not_active Ceased
- 2005-11-09 BR BRPI0518022-8A patent/BRPI0518022A/pt not_active Application Discontinuation
- 2005-11-09 EA EA200701036A patent/EA019747B1/ru unknown
- 2005-11-09 NZ NZ554906A patent/NZ554906A/en not_active IP Right Cessation
- 2005-11-09 CN CN201210167780.XA patent/CN102731499B/zh not_active Expired - Lifetime
- 2005-11-09 CA CA2585797A patent/CA2585797C/en not_active Expired - Lifetime
-
2007
- 2007-04-30 IL IL182876A patent/IL182876A/en active IP Right Grant
- 2007-05-03 NO NO20072322A patent/NO340365B1/no unknown
- 2007-05-09 ZA ZA2007/03754A patent/ZA200703754B/en unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05213957A (ja) * | 1992-02-07 | 1993-08-24 | Tsumura & Co | 新規なスピロピロリジンイミダゾリン誘導体および新規なアミノピロリジンカルボン酸誘導体並びに該化合物を有効成分とする鎮けい剤 |
| US20040009998A1 (en) | 2001-10-01 | 2004-01-15 | Dhar T. G. Murali | Spiro-hydantoin compounds useful as anti-inflammatory agents |
Also Published As
| Publication number | Publication date |
|---|---|
| NO340365B1 (no) | 2017-04-10 |
| MX2007005527A (es) | 2007-07-09 |
| AU2005304560A1 (en) | 2006-05-18 |
| CN102731499B (zh) | 2016-01-13 |
| JP5202954B2 (ja) | 2013-06-05 |
| HK1113305A1 (zh) | 2008-10-03 |
| EA200701036A1 (ru) | 2007-12-28 |
| NZ554906A (en) | 2011-01-28 |
| WO2006053024A2 (en) | 2006-05-18 |
| NO20072322L (no) | 2007-07-19 |
| IL182876A0 (en) | 2007-08-19 |
| SG161261A1 (en) | 2010-05-27 |
| EA019747B1 (ru) | 2014-06-30 |
| AU2005304560C1 (en) | 2013-05-09 |
| TWI400239B (zh) | 2013-07-01 |
| ZA200703754B (en) | 2008-01-08 |
| WO2006053024A3 (en) | 2007-07-05 |
| JP2008519765A (ja) | 2008-06-12 |
| IL182876A (en) | 2015-10-29 |
| CA2585797A1 (en) | 2006-05-18 |
| TW200621763A (en) | 2006-07-01 |
| GEP20125565B (en) | 2012-07-10 |
| EP1812005A4 (en) | 2009-09-30 |
| EP1812005B1 (en) | 2015-09-16 |
| US20060116382A1 (en) | 2006-06-01 |
| BRPI0518022A (pt) | 2008-10-21 |
| EP1812005A2 (en) | 2007-08-01 |
| CA2585797C (en) | 2015-01-06 |
| AU2005304560B2 (en) | 2012-05-03 |
| CN102731499A (zh) | 2012-10-17 |
| EP2450351A1 (en) | 2012-05-09 |
| KR20070085944A (ko) | 2007-08-27 |
| ES2547724T3 (es) | 2015-10-08 |
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