JP5570435B2 - アミド−チオフェン化合物およびその使用 - Google Patents
アミド−チオフェン化合物およびその使用 Download PDFInfo
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- JP5570435B2 JP5570435B2 JP2010550262A JP2010550262A JP5570435B2 JP 5570435 B2 JP5570435 B2 JP 5570435B2 JP 2010550262 A JP2010550262 A JP 2010550262A JP 2010550262 A JP2010550262 A JP 2010550262A JP 5570435 B2 JP5570435 B2 JP 5570435B2
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- 0 CS(C)*1CCCC1 Chemical compound CS(C)*1CCCC1 0.000 description 6
- CAQYTJRDMJJATR-UHFFFAOYSA-N C1CNC2OCCOC2C1 Chemical compound C1CNC2OCCOC2C1 CAQYTJRDMJJATR-UHFFFAOYSA-N 0.000 description 1
- ZKVLVEZQSYNVOP-PKPIPKONSA-N C=CSC[C@@H]1NN=CCC1O Chemical compound C=CSC[C@@H]1NN=CCC1O ZKVLVEZQSYNVOP-PKPIPKONSA-N 0.000 description 1
- RFRJIPUPEWOSSC-UHFFFAOYSA-N CC(C)(C)OC(N(CCCC1O)C1O)=O Chemical compound CC(C)(C)OC(N(CCCC1O)C1O)=O RFRJIPUPEWOSSC-UHFFFAOYSA-N 0.000 description 1
- WFUOOGHHXGAOAX-UHFFFAOYSA-N CC(C)(CCC1)CCN1C(c1c[s]c(Br)c1)=O Chemical compound CC(C)(CCC1)CCN1C(c1c[s]c(Br)c1)=O WFUOOGHHXGAOAX-UHFFFAOYSA-N 0.000 description 1
- OMZVXZWLMBXIIK-LYKKTTPLSA-N CC(C)(CCC1)CCN1C1[C@H](CSC=C)N(CCO)N=CC1 Chemical compound CC(C)(CCC1)CCN1C1[C@H](CSC=C)N(CCO)N=CC1 OMZVXZWLMBXIIK-LYKKTTPLSA-N 0.000 description 1
- QKWSMHMXDXDQHD-UHFFFAOYSA-N CC(C)(CCC1)CCN1NNC=C Chemical compound CC(C)(CCC1)CCN1NNC=C QKWSMHMXDXDQHD-UHFFFAOYSA-N 0.000 description 1
- RFUOIZRBKSOXRB-UHFFFAOYSA-N CC1(C)CCN(C)CCC1 Chemical compound CC1(C)CCN(C)CCC1 RFUOIZRBKSOXRB-UHFFFAOYSA-N 0.000 description 1
- RTMBVIAUHVXGJX-UHFFFAOYSA-N CC1(C)CN(C)CCCC1 Chemical compound CC1(C)CN(C)CCCC1 RTMBVIAUHVXGJX-UHFFFAOYSA-N 0.000 description 1
- ZMJDNMLWLIQAFG-UHFFFAOYSA-N CC1(C)N(C)CCCCC1 Chemical compound CC1(C)N(C)CCCCC1 ZMJDNMLWLIQAFG-UHFFFAOYSA-N 0.000 description 1
- FBAPTUAEBQMVEY-UHFFFAOYSA-N CC1(C)OB(c2c[n](CCN3CCOCC3)nc2)OC1(C)C Chemical compound CC1(C)OB(c2c[n](CCN3CCOCC3)nc2)OC1(C)C FBAPTUAEBQMVEY-UHFFFAOYSA-N 0.000 description 1
- FIHGDOQUUMSOIX-UHFFFAOYSA-N CC1NOC(C)=C1CO Chemical compound CC1NOC(C)=C1CO FIHGDOQUUMSOIX-UHFFFAOYSA-N 0.000 description 1
- PHFSMEGEFNVGSS-UHFFFAOYSA-N CN(CC1)CCC1C1=CCCC=C1 Chemical compound CN(CC1)CCC1C1=CCCC=C1 PHFSMEGEFNVGSS-UHFFFAOYSA-N 0.000 description 1
- WKNUFWGXWRFSEZ-UHFFFAOYSA-N CN(CCC1)CCC1(N)F Chemical compound CN(CCC1)CCC1(N)F WKNUFWGXWRFSEZ-UHFFFAOYSA-N 0.000 description 1
- GLXOHWLGZMRLRM-UHFFFAOYSA-N CN(CCC1)CCC1O Chemical compound CN(CCC1)CCC1O GLXOHWLGZMRLRM-UHFFFAOYSA-N 0.000 description 1
- WENDHYNQFFCYLQ-UHFFFAOYSA-N CN(CCC=C1)C1c1cnccc1 Chemical compound CN(CCC=C1)C1c1cnccc1 WENDHYNQFFCYLQ-UHFFFAOYSA-N 0.000 description 1
- QXZRRKPSLHBRRW-UHFFFAOYSA-N CN(CCCC1)C1c1ncccc1 Chemical compound CN(CCCC1)C1c1ncccc1 QXZRRKPSLHBRRW-UHFFFAOYSA-N 0.000 description 1
- IMTYCTKSIBCEFR-UHFFFAOYSA-N CN(CCCC1)CC1=C Chemical compound CN(CCCC1)CC1=C IMTYCTKSIBCEFR-UHFFFAOYSA-N 0.000 description 1
- FTWKAHYVKOSDON-UHFFFAOYSA-N CN(CCCC1)CC1c1ccccc1 Chemical compound CN(CCCC1)CC1c1ccccc1 FTWKAHYVKOSDON-UHFFFAOYSA-N 0.000 description 1
- VYLGWVNPNMMXFQ-UHFFFAOYSA-N CN1C(CC2)CCN2CC1 Chemical compound CN1C(CC2)CCN2CC1 VYLGWVNPNMMXFQ-UHFFFAOYSA-N 0.000 description 1
- KRWGMASCMXYNOJ-UHFFFAOYSA-N COC(c1c[s]c(-c2cnc(N)[o]2)c1)=O Chemical compound COC(c1c[s]c(-c2cnc(N)[o]2)c1)=O KRWGMASCMXYNOJ-UHFFFAOYSA-N 0.000 description 1
- HZMGZDFTUBHMEX-UHFFFAOYSA-N COC(c1c[s]c(C(CBr)=O)c1)=O Chemical compound COC(c1c[s]c(C(CBr)=O)c1)=O HZMGZDFTUBHMEX-UHFFFAOYSA-N 0.000 description 1
- XLWKVBCRWLCYNE-UHFFFAOYSA-N O=C(c1c[s]c(-c2c[nH]nc2)c1)N1CC2OCCOC2CC1 Chemical compound O=C(c1c[s]c(-c2c[nH]nc2)c1)N1CC2OCCOC2CC1 XLWKVBCRWLCYNE-UHFFFAOYSA-N 0.000 description 1
- GPWYKMSIVSQEPG-UHFFFAOYSA-N O=C(c1c[s]c(Br)c1)N1C(CCCC2)C2CCC1 Chemical compound O=C(c1c[s]c(Br)c1)N1C(CCCC2)C2CCC1 GPWYKMSIVSQEPG-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
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- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Physical Education & Sports Medicine (AREA)
- Endocrinology (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Psychiatry (AREA)
- Emergency Medicine (AREA)
- Psychology (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Child & Adolescent Psychology (AREA)
- Toxicology (AREA)
- Vascular Medicine (AREA)
- Dermatology (AREA)
- Immunology (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3611108P | 2008-03-13 | 2008-03-13 | |
| US61/036,111 | 2008-03-13 | ||
| GB0804685.6 | 2008-03-13 | ||
| GBGB0804685.6A GB0804685D0 (en) | 2008-03-13 | 2008-03-13 | Therapeutic compounds and their use |
| PCT/GB2009/000686 WO2009112845A1 (en) | 2008-03-13 | 2009-03-13 | Amido-thiophene compounds and their use |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011513476A JP2011513476A (ja) | 2011-04-28 |
| JP2011513476A5 JP2011513476A5 (enExample) | 2012-04-26 |
| JP5570435B2 true JP5570435B2 (ja) | 2014-08-13 |
Family
ID=39328066
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010550262A Active JP5570435B2 (ja) | 2008-03-13 | 2009-03-13 | アミド−チオフェン化合物およびその使用 |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US8299063B2 (enExample) |
| EP (1) | EP2283004B1 (enExample) |
| JP (1) | JP5570435B2 (enExample) |
| KR (1) | KR101626627B1 (enExample) |
| AU (1) | AU2009224017B2 (enExample) |
| CA (1) | CA2716679C (enExample) |
| DK (1) | DK2283004T3 (enExample) |
| ES (1) | ES2545489T3 (enExample) |
| GB (1) | GB0804685D0 (enExample) |
| IL (1) | IL208081A (enExample) |
| WO (1) | WO2009112845A1 (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0724251D0 (en) | 2007-12-12 | 2008-02-06 | Univ Edinburgh | Therapeutic compounds and their use |
| GB0804685D0 (en) | 2008-03-13 | 2008-04-16 | Univ Edinburgh | Therapeutic compounds and their use |
| JP2012506375A (ja) * | 2008-10-21 | 2012-03-15 | メルク・シャープ・エンド・ドーム・コーポレイション | 2,5−二置換ピペリジンオレキシン受容体アンタゴニスト |
| WO2010146338A1 (en) * | 2009-06-15 | 2010-12-23 | The University Of Edinburgh | Amido-isothiazole compounds and their use as inhibitors of 11beta-hsd1 for the treatment of metabolic syndrome and related disorders |
| AU2010297068B2 (en) * | 2009-09-16 | 2015-10-01 | The University Of Edinburgh | (4-phenyl-piperidin-1-yl)-[5-1H-pyrazol-4yl)-thiophen-3-yl]-methanone compounds and their use |
| US9051296B2 (en) | 2009-11-16 | 2015-06-09 | Raqualia Pharma Inc. | Aryl carboxamide derivatives as TTX-S blockers |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| KR101714820B1 (ko) | 2010-04-29 | 2017-03-09 | 더 유니버시티 오브 에든버러 | 11(베타)-hsd1의 억제제로서 3,3-이치환된-(8-아자-비시클로[3.2.1]옥트-8-일)-[5-(1h-피라졸-4-일)-티오펜-3-일]-메탄온 |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| EP2630133A1 (de) | 2010-10-22 | 2013-08-28 | Bayer Intellectual Property GmbH | Neue heterocylische verbindungen als schädlingsbekämpfungsmittel |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP3373920A4 (en) | 2015-11-13 | 2019-07-17 | Pietro Paolo Sanna | METHOD AND COMPOSITIONS FOR TREATING ALCOHOL CONSUMPTION MALFUNCTIONS |
| CN106854189A (zh) * | 2015-12-08 | 2017-06-16 | 湖南华腾制药有限公司 | 一种哌嗪化合物的合成方法 |
| WO2018177993A1 (de) | 2017-03-31 | 2018-10-04 | Bayer Cropscience Aktiengesellschaft | Pyrazole zur bekämpfung von arthropoden |
| US11825838B2 (en) | 2017-03-31 | 2023-11-28 | Bayer Cropscience Aktiengesellschaft | Tricyclic carboxamides for controlling arthropods |
| CN111566105A (zh) * | 2018-01-08 | 2020-08-21 | 豪夫迈·罗氏有限公司 | 作为MAGL抑制剂的八氢吡啶并[1,2-α]吡嗪类化合物 |
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| US5087631A (en) | 1990-12-18 | 1992-02-11 | Glaxo Inc. | Oxathi(SIV)azol-5-one compounds |
| AR011913A1 (es) * | 1997-03-06 | 2000-09-13 | Yamano Masaki | Derivados de 4,4-difluoro-2,3,4,5-tetrahidro-1h-1-benzoazepina y composiciones farmaceuticas de los mismos. |
| US6303593B1 (en) * | 1999-03-02 | 2001-10-16 | Merck & Co., Inc. | 3-thienyl and 3-furanyl pyrrolidine modulators of chemokine receptor activity |
| MXPA04004837A (es) | 2001-11-22 | 2004-08-02 | Biovitrum Ab | Inhibidores de 11-??-hidroxiesteroide deshidrogenasa de tipo 1. |
| SE0202430D0 (sv) * | 2002-08-14 | 2002-08-14 | Astrazeneca Ab | New Compounds |
| US20050256159A1 (en) * | 2002-10-11 | 2005-11-17 | Astrazeneca Ab | 1,4-disubstituted piperidine derivatives and their use as 11,betahsd1 inhibitors |
| US7700583B2 (en) * | 2003-04-11 | 2010-04-20 | High Point Pharmaceuticals, Llc | 11β-hydroxysteroid dehydrogenase type 1 active compounds |
| GB0325745D0 (en) | 2003-11-05 | 2003-12-10 | Astrazeneca Ab | Chemical compounds |
| GB0326029D0 (en) | 2003-11-07 | 2003-12-10 | Astrazeneca Ab | Chemical compounds |
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| TW200716576A (en) | 2005-06-07 | 2007-05-01 | Shionogi & Co | Heterocyclic derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
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| KR101081293B1 (ko) | 2006-01-18 | 2011-11-08 | 에프. 호프만-라 로슈 아게 | 11 베타-에이치에스디1 억제제로서 티아졸 |
| ATE509921T1 (de) | 2006-06-08 | 2011-06-15 | Lilly Co Eli | Substituierte carbonsäureamide als antagonisten des gruppe-i-metabotropen rezeptors |
| AU2007275301A1 (en) | 2006-07-20 | 2008-01-24 | Amgen Inc. | Substituted azole aromatic heterocycles as inhibitors of 11-beta-HSD-1 |
| GB0724251D0 (en) | 2007-12-12 | 2008-02-06 | Univ Edinburgh | Therapeutic compounds and their use |
| US20100022590A1 (en) | 2008-01-17 | 2010-01-28 | Biovitrum Ab (Publ.) | Novel compounds |
| GB0804685D0 (en) | 2008-03-13 | 2008-04-16 | Univ Edinburgh | Therapeutic compounds and their use |
| US8609690B2 (en) | 2008-08-25 | 2013-12-17 | Boehringer Ingelheim International Gmbh | Aryl- and heteroarylcarbonyl derivatives of substituted nortropanes, medicaments containing such compounds and their use |
| WO2010146338A1 (en) | 2009-06-15 | 2010-12-23 | The University Of Edinburgh | Amido-isothiazole compounds and their use as inhibitors of 11beta-hsd1 for the treatment of metabolic syndrome and related disorders |
| AU2010297068B2 (en) | 2009-09-16 | 2015-10-01 | The University Of Edinburgh | (4-phenyl-piperidin-1-yl)-[5-1H-pyrazol-4yl)-thiophen-3-yl]-methanone compounds and their use |
| KR101714820B1 (ko) | 2010-04-29 | 2017-03-09 | 더 유니버시티 오브 에든버러 | 11(베타)-hsd1의 억제제로서 3,3-이치환된-(8-아자-비시클로[3.2.1]옥트-8-일)-[5-(1h-피라졸-4-일)-티오펜-3-일]-메탄온 |
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| IL208081A (en) | 2017-04-30 |
| KR20110008170A (ko) | 2011-01-26 |
| ES2545489T3 (es) | 2015-09-11 |
| US20110015178A1 (en) | 2011-01-20 |
| CA2716679C (en) | 2016-07-12 |
| JP2011513476A (ja) | 2011-04-28 |
| IL208081A0 (en) | 2010-12-30 |
| AU2009224017B2 (en) | 2014-11-27 |
| AU2009224017A1 (en) | 2009-09-17 |
| DK2283004T3 (en) | 2015-08-24 |
| WO2009112845A1 (en) | 2009-09-17 |
| US8614209B2 (en) | 2013-12-24 |
| US20130012545A1 (en) | 2013-01-10 |
| CA2716679A1 (en) | 2009-09-17 |
| EP2283004B1 (en) | 2015-05-27 |
| EP2283004A1 (en) | 2011-02-16 |
| KR101626627B1 (ko) | 2016-06-01 |
| GB0804685D0 (en) | 2008-04-16 |
| US8299063B2 (en) | 2012-10-30 |
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