JP2007522178A - 心臓血管疾患の治療に有用なベンゾフランおよびベンゾチオフェン誘導体 - Google Patents
心臓血管疾患の治療に有用なベンゾフランおよびベンゾチオフェン誘導体 Download PDFInfo
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- JP2007522178A JP2007522178A JP2006552575A JP2006552575A JP2007522178A JP 2007522178 A JP2007522178 A JP 2007522178A JP 2006552575 A JP2006552575 A JP 2006552575A JP 2006552575 A JP2006552575 A JP 2006552575A JP 2007522178 A JP2007522178 A JP 2007522178A
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- methyl
- oxy
- trifluoromethyl
- benzothien
- acetic acid
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- 208000024172 Cardiovascular disease Diseases 0.000 title claims abstract description 9
- 238000011282 treatment Methods 0.000 title abstract description 12
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 title 2
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical class C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 312
- 150000003839 salts Chemical class 0.000 claims abstract description 17
- 150000002148 esters Chemical class 0.000 claims abstract description 14
- 239000012453 solvate Substances 0.000 claims abstract description 11
- 101000741788 Homo sapiens Peroxisome proliferator-activated receptor alpha Proteins 0.000 claims abstract description 7
- 102100038831 Peroxisome proliferator-activated receptor alpha Human genes 0.000 claims abstract 5
- -1 (methyloxy) ethylpropyloxy Chemical group 0.000 claims description 45
- 238000000034 method Methods 0.000 claims description 30
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims description 23
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- 201000010099 disease Diseases 0.000 claims description 11
- 239000003814 drug Substances 0.000 claims description 10
- 230000001404 mediated effect Effects 0.000 claims description 10
- 239000008194 pharmaceutical composition Substances 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 229910052717 sulfur Inorganic materials 0.000 claims description 9
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 8
- 208000008589 Obesity Diseases 0.000 claims description 6
- 235000020824 obesity Nutrition 0.000 claims description 6
- FXJJDFJCUSKROR-UHFFFAOYSA-N 2-[2-[3-[3-methyl-6-(trifluoromethyl)-1-benzothiophen-2-yl]heptylsulfanyl]-1,3-thiazol-4-yl]acetic acid Chemical compound S1C2=CC(C(F)(F)F)=CC=C2C(C)=C1C(CCCC)CCSC1=NC(CC(O)=O)=CS1 FXJJDFJCUSKROR-UHFFFAOYSA-N 0.000 claims description 5
- OEVMGZTXXMKIRO-UHFFFAOYSA-N 2-[2-methyl-4-[3-[3-methyl-6-(trifluoromethyl)-1-benzothiophen-2-yl]heptoxy]phenoxy]acetic acid Chemical compound S1C2=CC(C(F)(F)F)=CC=C2C(C)=C1C(CCCC)CCOC1=CC=C(OCC(O)=O)C(C)=C1 OEVMGZTXXMKIRO-UHFFFAOYSA-N 0.000 claims description 5
- UGRIRRAVVNVIJK-UHFFFAOYSA-N 2-[4-[3-(6-methoxy-3-methyl-1-benzothiophen-2-yl)heptoxy]-2-methylphenoxy]acetic acid Chemical compound S1C2=CC(OC)=CC=C2C(C)=C1C(CCCC)CCOC1=CC=C(OCC(O)=O)C(C)=C1 UGRIRRAVVNVIJK-UHFFFAOYSA-N 0.000 claims description 5
- HQBOQKZRRLZKPO-UHFFFAOYSA-N 2-[4-methyl-2-[3-[3-methyl-6-(trifluoromethyl)-1-benzothiophen-2-yl]heptylsulfanyl]-1,3-thiazol-5-yl]acetic acid Chemical compound S1C2=CC(C(F)(F)F)=CC=C2C(C)=C1C(CCCC)CCSC1=NC(C)=C(CC(O)=O)S1 HQBOQKZRRLZKPO-UHFFFAOYSA-N 0.000 claims description 5
- YLWDHISOLHDLNW-UHFFFAOYSA-N 3-[3-methoxy-4-[3-[3-methyl-6-(trifluoromethyl)-1-benzothiophen-2-yl]heptoxy]phenyl]propanoic acid Chemical compound S1C2=CC(C(F)(F)F)=CC=C2C(C)=C1C(CCCC)CCOC1=CC=C(CCC(O)=O)C=C1OC YLWDHISOLHDLNW-UHFFFAOYSA-N 0.000 claims description 5
- IRZOSBKFGJKJDZ-UHFFFAOYSA-N 3-[4-[3-[3-methyl-6-(trifluoromethyl)-1-benzothiophen-2-yl]heptoxy]phenyl]propanoic acid Chemical compound S1C2=CC(C(F)(F)F)=CC=C2C(C)=C1C(CCCC)CCOC1=CC=C(CCC(O)=O)C=C1 IRZOSBKFGJKJDZ-UHFFFAOYSA-N 0.000 claims description 5
- 208000017170 Lipid metabolism disease Diseases 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- VGXJHTHNYSRSHN-UHFFFAOYSA-N 2-[2-[3-(6-methoxy-3-methyl-1-benzothiophen-2-yl)heptylsulfanyl]-1,3-thiazol-4-yl]acetic acid Chemical compound S1C2=CC(OC)=CC=C2C(C)=C1C(CCCC)CCSC1=NC(CC(O)=O)=CS1 VGXJHTHNYSRSHN-UHFFFAOYSA-N 0.000 claims description 4
- YYGXSXXJQJNXKQ-UHFFFAOYSA-N 2-[2-ethyl-4-[3-[3-methyl-6-(trifluoromethyl)-1-benzothiophen-2-yl]hexoxy]phenoxy]acetic acid Chemical compound S1C2=CC(C(F)(F)F)=CC=C2C(C)=C1C(CCC)CCOC1=CC=C(OCC(O)=O)C(CC)=C1 YYGXSXXJQJNXKQ-UHFFFAOYSA-N 0.000 claims description 4
- ZRROAQMJVLVQBL-UHFFFAOYSA-N 2-[2-methyl-4-[3-[3-methyl-6-(trifluoromethyl)-1-benzothiophen-2-yl]-3-propoxypropyl]sulfanylphenoxy]acetic acid Chemical compound S1C2=CC(C(F)(F)F)=CC=C2C(C)=C1C(OCCC)CCSC1=CC=C(OCC(O)=O)C(C)=C1 ZRROAQMJVLVQBL-UHFFFAOYSA-N 0.000 claims description 4
- XCHRMFXHHRIWKD-UHFFFAOYSA-N 2-[3-methoxy-4-[3-(6-methoxy-3-methyl-1-benzothiophen-2-yl)heptoxy]phenyl]acetic acid Chemical compound S1C2=CC(OC)=CC=C2C(C)=C1C(CCCC)CCOC1=CC=C(CC(O)=O)C=C1OC XCHRMFXHHRIWKD-UHFFFAOYSA-N 0.000 claims description 4
- 206010022489 Insulin Resistance Diseases 0.000 claims description 4
- 208000011580 syndromic disease Diseases 0.000 claims description 4
- WHXIFNNKMPBSRB-UHFFFAOYSA-N 2-[2-(trifluoromethyl)-4-[3-[6-(trifluoromethyl)-1-benzothiophen-2-yl]heptylsulfanyl]phenoxy]acetic acid Chemical compound C=1C2=CC=C(C(F)(F)F)C=C2SC=1C(CCCC)CCSC1=CC=C(OCC(O)=O)C(C(F)(F)F)=C1 WHXIFNNKMPBSRB-UHFFFAOYSA-N 0.000 claims description 3
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- YRZCISGCWQPMOS-UHFFFAOYSA-N 2-[2-[3-(3,6-dimethyl-1-benzofuran-2-yl)heptylsulfanyl]-4-methyl-1,3-thiazol-5-yl]acetic acid Chemical compound O1C2=CC(C)=CC=C2C(C)=C1C(CCCC)CCSC1=NC(C)=C(CC(O)=O)S1 YRZCISGCWQPMOS-UHFFFAOYSA-N 0.000 claims description 3
- VOWULFOXILZTAV-UHFFFAOYSA-N 2-[2-[5-methoxy-3-[3-methyl-6-(trifluoromethyl)-1-benzothiophen-2-yl]pentyl]sulfanyl-4-methyl-1,3-thiazol-5-yl]acetic acid Chemical compound S1C2=CC(C(F)(F)F)=CC=C2C(C)=C1C(CCOC)CCSC1=NC(C)=C(CC(O)=O)S1 VOWULFOXILZTAV-UHFFFAOYSA-N 0.000 claims description 3
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- OJVUVIXYAHGQPV-UHFFFAOYSA-N 2-[2-ethyl-4-[3-[3-methyl-6-(trifluoromethyl)-1-benzothiophen-2-yl]heptoxy]phenoxy]acetic acid Chemical compound S1C2=CC(C(F)(F)F)=CC=C2C(C)=C1C(CCCC)CCOC1=CC=C(OCC(O)=O)C(CC)=C1 OJVUVIXYAHGQPV-UHFFFAOYSA-N 0.000 claims description 3
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- DFJCXQJTYVAQDE-UHFFFAOYSA-N 2-[2-ethyl-4-[3-[5-(trifluoromethyl)-1-benzothiophen-2-yl]heptoxy]phenoxy]acetic acid Chemical compound C=1C2=CC(C(F)(F)F)=CC=C2SC=1C(CCCC)CCOC1=CC=C(OCC(O)=O)C(CC)=C1 DFJCXQJTYVAQDE-UHFFFAOYSA-N 0.000 claims description 3
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- VYGAYXVFXNMYAS-UHFFFAOYSA-N 2-[2-ethyl-4-[5-methoxy-3-[3-methyl-6-(trifluoromethyl)-1-benzothiophen-2-yl]pentoxy]phenoxy]acetic acid Chemical compound C1=C(OCC(O)=O)C(CC)=CC(OCCC(CCOC)C2=C(C3=CC=C(C=C3S2)C(F)(F)F)C)=C1 VYGAYXVFXNMYAS-UHFFFAOYSA-N 0.000 claims description 3
- GMKXJFUYVOVIJS-ONEGZZNKSA-N 2-[2-methyl-4-[(e)-3-[3-methyl-5-(trifluoromethyl)-1-benzothiophen-2-yl]prop-2-enyl]sulfanylphenoxy]acetic acid Chemical compound S1C2=CC=C(C(F)(F)F)C=C2C(C)=C1\C=C\CSC1=CC=C(OCC(O)=O)C(C)=C1 GMKXJFUYVOVIJS-ONEGZZNKSA-N 0.000 claims description 3
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
-
- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D307/80—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/54—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/54—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D333/56—Radicals substituted by oxygen atoms
-
- 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
- C07D417/02—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 containing two hetero rings
- C07D417/12—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 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
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- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Child & Adolescent Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0403148.0A GB0403148D0 (en) | 2004-02-12 | 2004-02-12 | Chemical compounds |
| PCT/EP2005/001540 WO2005077926A2 (en) | 2004-02-12 | 2005-02-10 | Benzofuran and benzothiophene derivatives useful for the treatment of cardiovascular disease |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007522178A true JP2007522178A (ja) | 2007-08-09 |
| JP2007522178A5 JP2007522178A5 (enExample) | 2007-11-15 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2006552575A Pending JP2007522178A (ja) | 2004-02-12 | 2005-02-10 | 心臓血管疾患の治療に有用なベンゾフランおよびベンゾチオフェン誘導体 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20070155805A1 (enExample) |
| EP (1) | EP1740568B1 (enExample) |
| JP (1) | JP2007522178A (enExample) |
| AT (1) | ATE415395T1 (enExample) |
| DE (1) | DE602005011267D1 (enExample) |
| ES (1) | ES2317192T3 (enExample) |
| GB (1) | GB0403148D0 (enExample) |
| WO (1) | WO2005077926A2 (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009128558A1 (ja) * | 2008-04-15 | 2009-10-22 | 日本ケミファ株式会社 | ペルオキシソーム増殖剤活性化受容体の活性化剤 |
| JP2012250979A (ja) * | 2011-05-10 | 2012-12-20 | Sumitomo Chemical Co Ltd | 植物の生長を促進する方法 |
| JP2012250978A (ja) * | 2011-05-10 | 2012-12-20 | Sumitomo Chemical Co Ltd | 植物の生長を促進する方法 |
| JP2022516922A (ja) * | 2019-01-02 | 2022-03-03 | 上海 インスティテュート オブ マテリア メディカ、チャイニーズ アカデミー オブ サイエンシーズ | フッ素含有置換ベンゾチオフェン化合物ならびにその医薬組成物および応用 |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2565205A1 (en) * | 2004-05-03 | 2005-11-24 | Janssen Pharmaceutica N.V. | Benzofuran derivatives as selective androgen receptor modulators (sarms) |
| TWI359810B (en) * | 2004-11-04 | 2012-03-11 | Mitsubishi Tanabe Pharma Corp | Carboxylic acid derivative containing thiazole rin |
| WO2006101454A1 (en) * | 2005-03-21 | 2006-09-28 | S*Bio Pte Ltd | Benzothiophene derivatives: preparation and pharmaceutical applications |
| AU2007239283B2 (en) | 2006-04-18 | 2013-02-07 | Nippon Chemiphar Co., Ltd. | Activating agent for peroxisome proliferator activated receptor delta |
| US20090163481A1 (en) * | 2007-12-13 | 2009-06-25 | Murphy Brian J | Ppar-delta ligands and methods of their use |
| EP2464349A2 (en) * | 2009-08-14 | 2012-06-20 | Cerenis Therapeutics S.A. | Use of ppar delta ligands for the treatment or prevention of inflammation or energy metabolism/production related diseases |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2000504021A (ja) * | 1996-02-02 | 2000-04-04 | メルク エンド カンパニー インコーポレーテッド | 糖尿病及び関連疾患状態を治療する方法 |
| JP2001511767A (ja) * | 1996-12-23 | 2001-08-14 | メルク エンド カンパニー インコーポレーテッド | 糖尿病薬 |
| JP2001261674A (ja) * | 2000-03-22 | 2001-09-26 | Mitsui Chemicals Inc | ベンゾチオフェン誘導体およびそれを有効成分として含有する核内レセプター作動薬 |
| WO2002092590A1 (en) * | 2001-05-11 | 2002-11-21 | Glaxo Group Limited | Furan and thiophene derivatives that activate human peroxisome proliferator activated receptors |
| JP2003520838A (ja) * | 2000-01-28 | 2003-07-08 | ノボ ノルディスク アクティーゼルスカブ | 新規化合物、それらの製造および使用。 |
| WO2003084916A2 (en) * | 2002-04-05 | 2003-10-16 | Warner-Lambert Company Llc | Compounds that modulate ppar activity and methods for their preparation |
| WO2004010936A2 (en) * | 2002-07-30 | 2004-02-05 | Merck & Co., Inc. | Ppar alpha selective compounds for the treatment of dyslipidemia and other lipid disorders |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5859051A (en) * | 1996-02-02 | 1999-01-12 | Merck & Co., Inc. | Antidiabetic agents |
| WO1997028149A1 (en) * | 1996-02-02 | 1997-08-07 | Merck & Co., Inc. | Method for raising hdl cholesterol levels |
| BR0315667A (pt) * | 2002-10-28 | 2005-09-06 | Novo Nordisk As | Composto, uso de um composto, composição farmacêutica, e, método para o tratamento |
-
2004
- 2004-02-12 GB GBGB0403148.0A patent/GB0403148D0/en not_active Ceased
-
2005
- 2005-02-10 AT AT05707417T patent/ATE415395T1/de not_active IP Right Cessation
- 2005-02-10 WO PCT/EP2005/001540 patent/WO2005077926A2/en not_active Ceased
- 2005-02-10 ES ES05707417T patent/ES2317192T3/es not_active Expired - Lifetime
- 2005-02-10 JP JP2006552575A patent/JP2007522178A/ja active Pending
- 2005-02-10 DE DE602005011267T patent/DE602005011267D1/de not_active Expired - Fee Related
- 2005-02-10 EP EP05707417A patent/EP1740568B1/en not_active Expired - Lifetime
- 2005-02-10 US US10/597,870 patent/US20070155805A1/en not_active Abandoned
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000504021A (ja) * | 1996-02-02 | 2000-04-04 | メルク エンド カンパニー インコーポレーテッド | 糖尿病及び関連疾患状態を治療する方法 |
| JP2001511767A (ja) * | 1996-12-23 | 2001-08-14 | メルク エンド カンパニー インコーポレーテッド | 糖尿病薬 |
| JP2003520838A (ja) * | 2000-01-28 | 2003-07-08 | ノボ ノルディスク アクティーゼルスカブ | 新規化合物、それらの製造および使用。 |
| JP2001261674A (ja) * | 2000-03-22 | 2001-09-26 | Mitsui Chemicals Inc | ベンゾチオフェン誘導体およびそれを有効成分として含有する核内レセプター作動薬 |
| WO2002092590A1 (en) * | 2001-05-11 | 2002-11-21 | Glaxo Group Limited | Furan and thiophene derivatives that activate human peroxisome proliferator activated receptors |
| WO2003084916A2 (en) * | 2002-04-05 | 2003-10-16 | Warner-Lambert Company Llc | Compounds that modulate ppar activity and methods for their preparation |
| WO2004010936A2 (en) * | 2002-07-30 | 2004-02-05 | Merck & Co., Inc. | Ppar alpha selective compounds for the treatment of dyslipidemia and other lipid disorders |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009128558A1 (ja) * | 2008-04-15 | 2009-10-22 | 日本ケミファ株式会社 | ペルオキシソーム増殖剤活性化受容体の活性化剤 |
| JP5474769B2 (ja) * | 2008-04-15 | 2014-04-16 | 日本ケミファ株式会社 | ペルオキシソーム増殖剤活性化受容体の活性化剤 |
| KR20170021918A (ko) * | 2008-04-15 | 2017-02-28 | 닛뽕 케미파 가부시키가이샤 | 퍼옥시좀 증식제 활성화 수용체의 활성화제 |
| KR101871665B1 (ko) * | 2008-04-15 | 2018-06-27 | 닛뽕 케미파 가부시키가이샤 | 퍼옥시좀 증식제 활성화 수용체의 활성화제 |
| JP2012250979A (ja) * | 2011-05-10 | 2012-12-20 | Sumitomo Chemical Co Ltd | 植物の生長を促進する方法 |
| JP2012250978A (ja) * | 2011-05-10 | 2012-12-20 | Sumitomo Chemical Co Ltd | 植物の生長を促進する方法 |
| JP2022516922A (ja) * | 2019-01-02 | 2022-03-03 | 上海 インスティテュート オブ マテリア メディカ、チャイニーズ アカデミー オブ サイエンシーズ | フッ素含有置換ベンゾチオフェン化合物ならびにその医薬組成物および応用 |
| JP7329052B2 (ja) | 2019-01-02 | 2023-08-17 | 上海 インスティテュート オブ マテリア メディカ、チャイニーズ アカデミー オブ サイエンシーズ | フッ素含有置換ベンゾチオフェン化合物ならびにその医薬組成物および応用 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20070155805A1 (en) | 2007-07-05 |
| DE602005011267D1 (de) | 2009-01-08 |
| EP1740568B1 (en) | 2008-11-26 |
| GB0403148D0 (en) | 2004-03-17 |
| WO2005077926A2 (en) | 2005-08-25 |
| EP1740568A2 (en) | 2007-01-10 |
| ES2317192T3 (es) | 2009-04-16 |
| WO2005077926A3 (en) | 2005-12-08 |
| ATE415395T1 (de) | 2008-12-15 |
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