WO2012081570A1 - Composé de lactame ou d'un sel de ce dernier, et activateur de ppar - Google Patents
Composé de lactame ou d'un sel de ce dernier, et activateur de ppar Download PDFInfo
- Publication number
- WO2012081570A1 WO2012081570A1 PCT/JP2011/078767 JP2011078767W WO2012081570A1 WO 2012081570 A1 WO2012081570 A1 WO 2012081570A1 JP 2011078767 W JP2011078767 W JP 2011078767W WO 2012081570 A1 WO2012081570 A1 WO 2012081570A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- isoindoline
- mmol
- group
- alkyl
- ring
- Prior art date
Links
- 0 CC(C1CC2)=C(CSc3cc(C)c(*)cc3)S[C@@]12c1ccc(C(F)(F)F)cc1 Chemical compound CC(C1CC2)=C(CSc3cc(C)c(*)cc3)S[C@@]12c1ccc(C(F)(F)F)cc1 0.000 description 1
- WSHKDCLCTRYHAA-UHFFFAOYSA-N CC(OCc1ccc(C(CCl)=O)c(O)c1)=O Chemical compound CC(OCc1ccc(C(CCl)=O)c(O)c1)=O WSHKDCLCTRYHAA-UHFFFAOYSA-N 0.000 description 1
- VWFACMNHSAFHLZ-GQCTYLIASA-N CCOC(/C=C/CCc1cc(N=C=S)ccc1O)=O Chemical compound CCOC(/C=C/CCc1cc(N=C=S)ccc1O)=O VWFACMNHSAFHLZ-GQCTYLIASA-N 0.000 description 1
- VZVPYBBXKYRXEE-UHFFFAOYSA-N CCOC(CC(CCc1c2)c1ccc2OCCCl)=O Chemical compound CCOC(CC(CCc1c2)c1ccc2OCCCl)=O VZVPYBBXKYRXEE-UHFFFAOYSA-N 0.000 description 1
- IALUSPPUCYDSJX-UHFFFAOYSA-N CCOC(CC(COc1c2)c1ccc2OCC(C1CN2c(cc3)ccc3OC(F)(F)F)C=CC=C1C2=O)=O Chemical compound CCOC(CC(COc1c2)c1ccc2OCC(C1CN2c(cc3)ccc3OC(F)(F)F)C=CC=C1C2=O)=O IALUSPPUCYDSJX-UHFFFAOYSA-N 0.000 description 1
- NEDJANZPWGVFBE-UHFFFAOYSA-N CCOC(CN(CCCc1c2)c1ccc2OCc1cccc(C2=O)c1CN2c1ccc(C(F)(F)F)cc1)=O Chemical compound CCOC(CN(CCCc1c2)c1ccc2OCc1cccc(C2=O)c1CN2c1ccc(C(F)(F)F)cc1)=O NEDJANZPWGVFBE-UHFFFAOYSA-N 0.000 description 1
- PRPYPKSGAFJIMU-UHFFFAOYSA-N CCOC(COc(c1c2CCCC1)ccc2S)=O Chemical compound CCOC(COc(c1c2CCCC1)ccc2S)=O PRPYPKSGAFJIMU-UHFFFAOYSA-N 0.000 description 1
- PHDVAXMGOIZCBJ-UHFFFAOYSA-N CCOC(COc(c1c2CCCC1)ccc2Sc1cccc(C2O)c1CN2c1ccc(C(F)(F)F)cc1)=O Chemical compound CCOC(COc(c1c2CCCC1)ccc2Sc1cccc(C2O)c1CN2c1ccc(C(F)(F)F)cc1)=O PHDVAXMGOIZCBJ-UHFFFAOYSA-N 0.000 description 1
- NIEBBBVEONGDMO-IBGZPJMESA-N CCOC(C[C@H](CCc1c2)c1ccc2OCc1cccc(C2=O)c1CN2c1ccc(C(F)(F)F)cc1)=O Chemical compound CCOC(C[C@H](CCc1c2)c1ccc2OCc1cccc(C2=O)c1CN2c1ccc(C(F)(F)F)cc1)=O NIEBBBVEONGDMO-IBGZPJMESA-N 0.000 description 1
- ASRCALVKWKRKTR-UHFFFAOYSA-N CCOC(C[n](ccc1c2)c1ccc2Br)=O Chemical compound CCOC(C[n](ccc1c2)c1ccc2Br)=O ASRCALVKWKRKTR-UHFFFAOYSA-N 0.000 description 1
- BTFPDKMGMAAMLP-UHFFFAOYSA-N CCOC(C[n]1c2ccc(C=C)cc2cc1)=O Chemical compound CCOC(C[n]1c2ccc(C=C)cc2cc1)=O BTFPDKMGMAAMLP-UHFFFAOYSA-N 0.000 description 1
- UHKASHRHZKVSIG-UHFFFAOYSA-N CCOC(Cc1c[o]c2c1ccc(OCc1c(CN(C3=O)c(cc4)ccc4Cl)c3ccc1)c2)=O Chemical compound CCOC(Cc1c[o]c2c1ccc(OCc1c(CN(C3=O)c(cc4)ccc4Cl)c3ccc1)c2)=O UHKASHRHZKVSIG-UHFFFAOYSA-N 0.000 description 1
- POLLAQACGCVQPK-UHFFFAOYSA-N CCOC(Cc1c[o]c2c1ccc(OCc1cccc(C3=O)c1CN3c1ccc(C)cc1)c2)=O Chemical compound CCOC(Cc1c[o]c2c1ccc(OCc1cccc(C3=O)c1CN3c1ccc(C)cc1)c2)=O POLLAQACGCVQPK-UHFFFAOYSA-N 0.000 description 1
- PLUPXRGZDHFZNH-UHFFFAOYSA-N COC(CC(CSc1cccc(O)c1)=O)=O Chemical compound COC(CC(CSc1cccc(O)c1)=O)=O PLUPXRGZDHFZNH-UHFFFAOYSA-N 0.000 description 1
- XIHGEIOYZYJPME-UHFFFAOYSA-N O=C(c1c(C2)c(Br)ccc1)N2c1ccc(C(F)(F)F)cc1 Chemical compound O=C(c1c(C2)c(Br)ccc1)N2c1ccc(C(F)(F)F)cc1 XIHGEIOYZYJPME-UHFFFAOYSA-N 0.000 description 1
- KLXDZJGRVXVRLB-UHFFFAOYSA-N OC(CC(CC1)c(cc2)c1cc2OCCCOc1c(CN(C2=O)c(cc3)ccc3OC(F)(F)F)c2ccc1)=O Chemical compound OC(CC(CC1)c(cc2)c1cc2OCCCOc1c(CN(C2=O)c(cc3)ccc3OC(F)(F)F)c2ccc1)=O KLXDZJGRVXVRLB-UHFFFAOYSA-N 0.000 description 1
- JPXXWCVGNZQMHS-GQCTYLIASA-N OC(CC1c2ccc(/C=C/c3cccc(C4=O)c3CN4c(cc3)ccc3OC(F)(F)F)cc2CC1)=O Chemical compound OC(CC1c2ccc(/C=C/c3cccc(C4=O)c3CN4c(cc3)ccc3OC(F)(F)F)cc2CC1)=O JPXXWCVGNZQMHS-GQCTYLIASA-N 0.000 description 1
- SFIOMRRDURWOMU-UHFFFAOYSA-N OCc1cccc(C2=O)c1CN2c(cc1)ccc1Br Chemical compound OCc1cccc(C2=O)c1CN2c(cc1)ccc1Br SFIOMRRDURWOMU-UHFFFAOYSA-N 0.000 description 1
- GBGNQVQRSXGIBK-UHFFFAOYSA-N Oc1cccc(C2=O)c1CN2c(cc1)ccc1OC(F)(F)F Chemical compound Oc1cccc(C2=O)c1CN2c(cc1)ccc1OC(F)(F)F GBGNQVQRSXGIBK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- 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
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- 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
- 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
- C07D401/02—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 containing two hetero rings
- C07D401/12—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 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
- C07D405/02—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 containing two hetero rings
- C07D405/12—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 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D409/02—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
- C07D409/12—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 chain containing hetero atoms as chain links
Abstract
Cette invention concerne un composé de lactame ou d'un sel de ce dernier représenté par la formule (1), lequel composé possède un squelette de lactame ou d'un sel de lactame et convient comme activateur de PPAR. [Dans cette formule, le noyau Z correspond à un noyau hydrocarboné condensé ou un noyau hétérocyclique ; R1 désigne des atomes d'halogène identiques ou différents, des groupes alkyle pouvant avoir un groupe substitué, des groupes hydroxyle, ou des groupes alkoxy pouvant avoir un groupe substitué ; R2 désigne un groupe alkylène pouvant avoir une liaison directe ou un groupe substitué ; R3 désigne un groupe alkoxy pouvant avoir un groupe hydroxyle ou un groupe substitué ; le lieur (X) compte 1-10 atomes dans la chaine principale pris dans des atomes de carbone et des hétéro atomes, et la chaîne principale peut avoir un groupe substitué ; Y désigne une liaison directe, un atome d'oxygène ou un atome de soufre ; et k est un entier compris entre 0 et 5.]
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012548787A JPWO2012081570A1 (ja) | 2010-12-14 | 2011-12-13 | ラクタム化合物又はその塩及びppar活性化剤 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010277978 | 2010-12-14 | ||
JP2010-277978 | 2010-12-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2012081570A1 true WO2012081570A1 (fr) | 2012-06-21 |
Family
ID=46244669
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2011/078767 WO2012081570A1 (fr) | 2010-12-14 | 2011-12-13 | Composé de lactame ou d'un sel de ce dernier, et activateur de ppar |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPWO2012081570A1 (fr) |
WO (1) | WO2012081570A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015153410A1 (fr) * | 2014-03-31 | 2015-10-08 | The Trustees Of Columbia University In The City Of New York | Activateurs d'histone acétyltransférase et utilisation desdits activateurs |
CN106977478A (zh) * | 2017-04-21 | 2017-07-25 | 山东大学 | 一种2‑(6‑羟基‑2,3‑二氢苯并呋喃‑3‑基)乙酸甲酯的手性拆分方法 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112480047B (zh) * | 2020-12-01 | 2023-06-02 | 云南省第二人民医院 | 一种具有降糖调脂作用的化合物及其制剂与应用 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005056522A2 (fr) * | 2003-12-04 | 2005-06-23 | National Health Research Institutes | Composes indoles |
JP2006516254A (ja) * | 2003-01-06 | 2006-06-29 | イーライ・リリー・アンド・カンパニー | Pparモジュレータとしての縮合ヘテロ環誘導体 |
JP2006524220A (ja) * | 2003-04-17 | 2006-10-26 | ワーナー−ランバート カンパニー リミティド ライアビリティー カンパニー | Ppar活性を変調する化合物及び製造法 |
WO2009072581A1 (fr) * | 2007-12-05 | 2009-06-11 | Aska Pharmaceutical Co., Ltd. | Composé lactame ou sel de celui-ci, et activateur du ppar |
-
2011
- 2011-12-13 JP JP2012548787A patent/JPWO2012081570A1/ja active Pending
- 2011-12-13 WO PCT/JP2011/078767 patent/WO2012081570A1/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006516254A (ja) * | 2003-01-06 | 2006-06-29 | イーライ・リリー・アンド・カンパニー | Pparモジュレータとしての縮合ヘテロ環誘導体 |
JP2006524220A (ja) * | 2003-04-17 | 2006-10-26 | ワーナー−ランバート カンパニー リミティド ライアビリティー カンパニー | Ppar活性を変調する化合物及び製造法 |
WO2005056522A2 (fr) * | 2003-12-04 | 2005-06-23 | National Health Research Institutes | Composes indoles |
WO2009072581A1 (fr) * | 2007-12-05 | 2009-06-11 | Aska Pharmaceutical Co., Ltd. | Composé lactame ou sel de celui-ci, et activateur du ppar |
Non-Patent Citations (2)
Title |
---|
JOURNAL OF MEDICINAL CHEMISTRY, vol. 50, no. 5, 2007, pages 984 - 1000 * |
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, vol. 42, no. 5, 2006, pages 689 - 695 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015153410A1 (fr) * | 2014-03-31 | 2015-10-08 | The Trustees Of Columbia University In The City Of New York | Activateurs d'histone acétyltransférase et utilisation desdits activateurs |
US11191768B2 (en) | 2014-03-31 | 2021-12-07 | The Trustees Of Columbia University In The City Of New York | Histone acetyltransferase activators and uses thereof |
CN106977478A (zh) * | 2017-04-21 | 2017-07-25 | 山东大学 | 一种2‑(6‑羟基‑2,3‑二氢苯并呋喃‑3‑基)乙酸甲酯的手性拆分方法 |
CN106977478B (zh) * | 2017-04-21 | 2019-04-09 | 山东大学 | 一种2-(6-羟基-2,3-二氢苯并呋喃-3-基)乙酸甲酯的手性拆分方法 |
Also Published As
Publication number | Publication date |
---|---|
JPWO2012081570A1 (ja) | 2014-05-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5290749B2 (ja) | ペルオキシソーム増殖剤活性化受容体δの活性化剤 | |
KR100202463B1 (ko) | 아미노코우마란 유도체, 그들의 제조방법 및 용도 | |
KR101396606B1 (ko) | 신규 갑상선 호르몬 β 수용체 작동약 | |
EP3154954B1 (fr) | Modulateurs allostériques négatifs (nam) du récepteur métabotropique du glutamate et utilisations de ceux-ci | |
US7432392B2 (en) | Ester derivatives and medical use thereof | |
JPH10504836A (ja) | オルト置換芳香族エーテル化合物及び鎮痛のための薬剤組成物中へのこれらの使用 | |
WO2007085136A1 (fr) | Dérivés de 1,3-benzodioxolecyclopentène, procédé de préparation et applications médicales | |
CA2646430A1 (fr) | Derives bicycliques de l'acide carboxylique utiles dans le traitement de troubles metaboliques | |
WO2003072532A1 (fr) | Compose d'esters et ses utilisation en medecine | |
WO2007085135A1 (fr) | Dérivés d'acide 1,3-benzodioxolecyclopentène-2,2-dicarboxylique, procédé de préparation et applications médicales | |
JP2010533645A (ja) | 脂肪酸アミドヒドロラーゼの三環系阻害剤 | |
JP2010533645A5 (fr) | ||
WO2016108282A1 (fr) | Inhibiteur d'urat1 | |
AU2014241390A1 (en) | GPR120 agonists for the treatment of type II diabetes | |
JP5892550B2 (ja) | 縮合イミダゾール誘導体 | |
JP4191269B2 (ja) | 新規なアニリド化合物及びこれを含有する医薬 | |
WO2012081570A1 (fr) | Composé de lactame ou d'un sel de ce dernier, et activateur de ppar | |
KR100677013B1 (ko) | 헤테로시클릭 옥심 화합물, 이의 제조 방법 및 이를함유하는 약제학적 조성물 | |
US8524745B2 (en) | Benzisothiazol-3(1H)-one-5-sulfonyl derivatives as chemokine receptor modulators | |
CN107922375A (zh) | 靶向idh2突变的抗肿瘤化合物及其使用方法 | |
JP6303031B2 (ja) | Ii型糖尿病を処置するためのgpr120アゴニストとしてのイソチアゾール誘導体 | |
JPWO2006126714A1 (ja) | ペルオキシソーム増殖剤活性化受容体の活性化剤 | |
JP2018039733A (ja) | 新規複素環誘導体 | |
JP2007516986A (ja) | 酸性キノリン誘導体ならびに高血糖に関連する病状の予防および/または治療のためのその使用 | |
JP5436941B2 (ja) | ラクタム化合物又はその塩及びppar活性化剤 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 11849286 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2012548787 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 11849286 Country of ref document: EP Kind code of ref document: A1 |