CN104487435A - 用于抑制白三烯生成的苯并二氧杂环己烷与其他活性剂的组合 - Google Patents
用于抑制白三烯生成的苯并二氧杂环己烷与其他活性剂的组合 Download PDFInfo
- Publication number
- CN104487435A CN104487435A CN201380022189.8A CN201380022189A CN104487435A CN 104487435 A CN104487435 A CN 104487435A CN 201380022189 A CN201380022189 A CN 201380022189A CN 104487435 A CN104487435 A CN 104487435A
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- Prior art keywords
- dihydro
- benzyl
- benzodioxin
- pyridin
- dioxino
- Prior art date
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- ZSUDRFSFONYWNQ-HXUWFJFHSA-N NC1CCN(Cc2ccc([C@@H]3Oc4ccccc4OC3)cc2)CC1 Chemical compound NC1CCN(Cc2ccc([C@@H]3Oc4ccccc4OC3)cc2)CC1 ZSUDRFSFONYWNQ-HXUWFJFHSA-N 0.000 description 2
- MRSNPTMJHJKUAY-UHFFFAOYSA-N C(c1ccc(C2OC3NC=CC=C3OC2)cc1)N1CCOCC1 Chemical compound C(c1ccc(C2OC3NC=CC=C3OC2)cc1)N1CCOCC1 MRSNPTMJHJKUAY-UHFFFAOYSA-N 0.000 description 1
- ZWUUPDYTGUTSJH-KRWDZBQOSA-N C(c1ccc([C@H]2Oc3ncccc3OC2)cc1)N1CCOCC1 Chemical compound C(c1ccc([C@H]2Oc3ncccc3OC2)cc1)N1CCOCC1 ZWUUPDYTGUTSJH-KRWDZBQOSA-N 0.000 description 1
- MTJXVNHBIYNAHL-IQHZPMLTSA-N CC(C)(C)OC(N(C1)c2ccccc2C11CCN(CC2=CCC([C@@H]3Oc4ncccc4OC3)C=C2)CC1)=O Chemical compound CC(C)(C)OC(N(C1)c2ccccc2C11CCN(CC2=CCC([C@@H]3Oc4ncccc4OC3)C=C2)CC1)=O MTJXVNHBIYNAHL-IQHZPMLTSA-N 0.000 description 1
- HJMSTIKEZKTZED-JOCHJYFZSA-N CC(C)(C1CCN(Cc2ccc([C@@H]3Oc4ccccc4OC3)cc2)CC1)C(O)=O Chemical compound CC(C)(C1CCN(Cc2ccc([C@@H]3Oc4ccccc4OC3)cc2)CC1)C(O)=O HJMSTIKEZKTZED-JOCHJYFZSA-N 0.000 description 1
- SDIFFRCHBAENSZ-XMMPIXPASA-N CCOC(C(C)(C)C1CCN(Cc2ccc([C@@H]3Oc4ccccc4OC3)cc2)CC1)=O Chemical compound CCOC(C(C)(C)C1CCN(Cc2ccc([C@@H]3Oc4ccccc4OC3)cc2)CC1)=O SDIFFRCHBAENSZ-XMMPIXPASA-N 0.000 description 1
- TWGOBCCPOSEQIA-HXUWFJFHSA-N CCOC(C1CCN(Cc2ccc([C@@H]3Oc4ncccc4OC3)cc2)CC1)=O Chemical compound CCOC(C1CCN(Cc2ccc([C@@H]3Oc4ncccc4OC3)cc2)CC1)=O TWGOBCCPOSEQIA-HXUWFJFHSA-N 0.000 description 1
- LKHCONQEXOYJIZ-HHHXNRCGSA-N COC(c1ccc(CN2CCN(Cc3ccc([C@@H]4Oc(cccc5)c5OC4)cc3)CC2)cc1)=O Chemical compound COC(c1ccc(CN2CCN(Cc3ccc([C@@H]4Oc(cccc5)c5OC4)cc3)CC2)cc1)=O LKHCONQEXOYJIZ-HHHXNRCGSA-N 0.000 description 1
- MSDDPTBJKVNZGD-IIBYNOLFSA-N C[C@H](C(NC1CCN(Cc2ccc([C@@H]3Oc4ncccc4OC3)cc2)CC1)=O)NC Chemical compound C[C@H](C(NC1CCN(Cc2ccc([C@@H]3Oc4ncccc4OC3)cc2)CC1)=O)NC MSDDPTBJKVNZGD-IIBYNOLFSA-N 0.000 description 1
- VLHQXRIIQSTJCQ-ZCFIWIBFSA-O C[C@H](C([OH2+])=O)N(C)C(OC(C)(C)C)=O Chemical compound C[C@H](C([OH2+])=O)N(C)C(OC(C)(C)C)=O VLHQXRIIQSTJCQ-ZCFIWIBFSA-O 0.000 description 1
- AMHUMMCEAZPFIC-RUZDIDTESA-N Cc1ccc2OC[C@H](c3ccc(CN(CC4)CCC44c(cccc5)c5NC4)cc3)Oc2n1 Chemical compound Cc1ccc2OC[C@H](c3ccc(CN(CC4)CCC44c(cccc5)c5NC4)cc3)Oc2n1 AMHUMMCEAZPFIC-RUZDIDTESA-N 0.000 description 1
- YFLIVPLAEITJMX-GOSISDBHSA-N NC1CCN(Cc2ccc([C@@H]3Oc4ncccc4OC3)cc2)CC1 Chemical compound NC1CCN(Cc2ccc([C@@H]3Oc4ncccc4OC3)cc2)CC1 YFLIVPLAEITJMX-GOSISDBHSA-N 0.000 description 1
- LHJIYRIMYXKDLW-FKAXQMLKSA-N O=C(C1CCN(Cc2ccc([C@@H]3Oc4nc(COC(C5CCN(Cc6ccc([C@@H]7Oc8ncccc8OC7)cc6)CC5)=O)ccc4OC3)cc2)CC1)NC[C@H]1OCCC1 Chemical compound O=C(C1CCN(Cc2ccc([C@@H]3Oc4nc(COC(C5CCN(Cc6ccc([C@@H]7Oc8ncccc8OC7)cc6)CC5)=O)ccc4OC3)cc2)CC1)NC[C@H]1OCCC1 LHJIYRIMYXKDLW-FKAXQMLKSA-N 0.000 description 1
- GEHUCVSRHYNIBO-UHFFFAOYSA-N O=C1OCCN1Cc1ccc(C2Oc3ncccc3OC2)cc1 Chemical compound O=C1OCCN1Cc1ccc(C2Oc3ncccc3OC2)cc1 GEHUCVSRHYNIBO-UHFFFAOYSA-N 0.000 description 1
- ZLTGUVXUZAHLER-OAHLLOKOSA-N O=Cc1ccc([C@@H]2Oc3ccccc3OC2)cc1 Chemical compound O=Cc1ccc([C@@H]2Oc3ccccc3OC2)cc1 ZLTGUVXUZAHLER-OAHLLOKOSA-N 0.000 description 1
- ITBOMVWBEIYVLY-GOSISDBHSA-N OC(C1CCN(Cc2ccc([C@@H]3Oc4ncccc4OC3)cc2)CC1)=O Chemical compound OC(C1CCN(Cc2ccc([C@@H]3Oc4ncccc4OC3)cc2)CC1)=O ITBOMVWBEIYVLY-GOSISDBHSA-N 0.000 description 1
- VPZVETXXMUYAKD-AREMUKBSSA-N OC(c1ccc(CN2CCN(Cc3ccc([C@@H]4Oc(cccc5)c5OC4)cc3)CC2)cc1)=O Chemical compound OC(c1ccc(CN2CCN(Cc3ccc([C@@H]4Oc(cccc5)c5OC4)cc3)CC2)cc1)=O VPZVETXXMUYAKD-AREMUKBSSA-N 0.000 description 1
- GFTQSTZTKFGGLL-OAQYLSRUSA-N OCC(NC1CCN(Cc2ccc([C@@H]3Oc4ccccc4OC3)cc2)CC1)=O Chemical compound OCC(NC1CCN(Cc2ccc([C@@H]3Oc4ccccc4OC3)cc2)CC1)=O GFTQSTZTKFGGLL-OAQYLSRUSA-N 0.000 description 1
Classifications
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- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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| CN112076189A (zh) * | 2020-09-23 | 2020-12-15 | 唐怡庭 | 一种酰胺化合物在制备治疗脓毒症药物中的应用 |
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| CN103415513B (zh) | 2011-03-14 | 2016-01-20 | 勃林格殷格翰国际有限公司 | 白三烯产物的苯并二氧杂环己烷抑制剂 |
| EP2734516B1 (en) | 2011-07-19 | 2015-06-17 | Boehringer Ingelheim International GmbH | Arylpyrazole ethers as inhibitors of leukotriene a4 hydrolase |
| JP6080226B2 (ja) | 2012-03-06 | 2017-02-15 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 他の活性物質と組み合わせたロイコトリエン産生阻害用ベンゾジオキサン |
| WO2013134226A1 (en) * | 2012-03-06 | 2013-09-12 | Boehringer Ingelheim International Gmbh | Benzodioxanes for inhibiting leukotriene production |
| US9255154B2 (en) | 2012-05-08 | 2016-02-09 | Alderbio Holdings, Llc | Anti-PCSK9 antibodies and use thereof |
| WO2014014874A1 (en) | 2012-07-17 | 2014-01-23 | Boehringer Ingelheim International Gmbh | Pyrazole derivatives which inhibit leukotriene production |
| PL2978859T3 (pl) | 2013-03-27 | 2018-10-31 | F.Hoffmann-La Roche Ag | Markery genetyczne do przewidywania reakcji na terapię |
| JP2016523982A (ja) | 2013-07-15 | 2016-08-12 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ロイコトリエン生成の阻害剤 |
| EP3022193B1 (en) | 2013-07-15 | 2017-04-26 | Boehringer Ingelheim International GmbH | Inhibitors of leukotriene production |
| EP3795695A1 (en) | 2014-07-30 | 2021-03-24 | F. Hoffmann-La Roche AG | Genetic markers for predicting responsiveness to therapy |
| US10968193B2 (en) * | 2014-08-08 | 2021-04-06 | Merck Sharp & Dohme Corp. | Antidiabetic bicyclic compounds |
| CN104181252B (zh) * | 2014-09-01 | 2015-12-02 | 广东东阳光药业有限公司 | 一种分离检测安塞曲匹及其异构体的方法 |
| CN105748469B (zh) * | 2016-02-24 | 2019-07-23 | 长沙佰顺生物科技有限公司 | 一种安塞曲匹辛伐他汀药物组合物 |
| WO2017170830A1 (ja) * | 2016-03-31 | 2017-10-05 | 武田薬品工業株式会社 | 複素環化合物 |
| KR20230051227A (ko) | 2020-08-14 | 2023-04-17 | 노파르티스 아게 | 헤테로아릴 치환된 스피로피페리디닐 유도체 및 이의 제약 용도 |
| US11957671B2 (en) | 2021-11-01 | 2024-04-16 | Alkahest, Inc. | Benzodioxane modulators of leukotriene A4 hydrolase (LTA4H) for prevention and treatment of aging-associated diseases |
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| DE19705450A1 (de) | 1997-02-13 | 1998-08-20 | Merck Patent Gmbh | Bicyclische aromatische Aminosäuren |
| DE19821003A1 (de) | 1998-05-11 | 1999-11-18 | Dresden Arzneimittel | Neue 1,2,5-trisubstituierte 1,2-dihydro-indazol-3-one mit antiasthmatischer, antiallergischer, entzündungshemmender, immunmodulierender und neuroprotektiver Wirkung, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
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| EP2734516B1 (en) | 2011-07-19 | 2015-06-17 | Boehringer Ingelheim International GmbH | Arylpyrazole ethers as inhibitors of leukotriene a4 hydrolase |
| WO2013134226A1 (en) | 2012-03-06 | 2013-09-12 | Boehringer Ingelheim International Gmbh | Benzodioxanes for inhibiting leukotriene production |
| JP6080226B2 (ja) | 2012-03-06 | 2017-02-15 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 他の活性物質と組み合わせたロイコトリエン産生阻害用ベンゾジオキサン |
| WO2014014874A1 (en) | 2012-07-17 | 2014-01-23 | Boehringer Ingelheim International Gmbh | Pyrazole derivatives which inhibit leukotriene production |
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| US498770A (en) * | 1893-06-06 | Electrolytic apparatus | ||
| US4918092A (en) * | 1983-12-21 | 1990-04-17 | Merck Frosst Canada, Inc. | Leukotriene antagonists |
| WO2012125598A1 (en) * | 2011-03-14 | 2012-09-20 | Boehringer Ingelheim International Gmbh | Benzodioxane inhibitors of leukotriene production |
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| CHERYL A GRICE,等: "Current status of leukotriene A(4) hydrolase inhibitors", 《EXPERT OPINION ON THERAPEUTIC PATENTS》, vol. 18, no. 12, 1 December 2008 (2008-12-01), pages 1333 - 1350, XP 055024826, DOI: doi:10.1517/13543770802494100 * |
| VINCENT SANDANAYAKA,等: "Discovery of 4-[(2S)-2-{[4-(4-Chlorophenoxy)phenoxy]methyl}-1-pyrrolidinyl]butanoic Acid (DG-051) as a Novel Leukotriene A4 Hydrolase Inhibitor of Leukotriene B4 Biosynthesis", 《JOURNAL OF MEDICINAL CHEMISTRY》, vol. 53, no. 2, 1 December 2009 (2009-12-01), pages 573 - 585, XP 055024858, DOI: doi:10.1021/jm900838g * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112076189A (zh) * | 2020-09-23 | 2020-12-15 | 唐怡庭 | 一种酰胺化合物在制备治疗脓毒症药物中的应用 |
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| Publication number | Publication date |
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| EA201400976A1 (ru) | 2015-02-27 |
| CL2014002326A1 (es) | 2014-11-14 |
| AU2013229560A1 (en) | 2014-08-28 |
| CA2866471A1 (en) | 2013-09-12 |
| UY34661A (es) | 2013-09-30 |
| US20130236468A1 (en) | 2013-09-12 |
| TW201350475A (zh) | 2013-12-16 |
| EP2822941B1 (en) | 2017-05-10 |
| JP2015513552A (ja) | 2015-05-14 |
| EP2822941A1 (en) | 2015-01-14 |
| NZ628587A (en) | 2016-07-29 |
| AR090259A1 (es) | 2014-10-29 |
| PH12014501967B1 (en) | 2014-11-17 |
| MX2014010563A (es) | 2014-12-05 |
| KR20140138851A (ko) | 2014-12-04 |
| US9662339B2 (en) | 2017-05-30 |
| PH12014501967A1 (en) | 2014-11-17 |
| WO2013131901A1 (en) | 2013-09-12 |
| JP6080226B2 (ja) | 2017-02-15 |
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