JP2007520556A - Ccr3アンタゴニストとして有用なピペリジン誘導体 - Google Patents
Ccr3アンタゴニストとして有用なピペリジン誘導体 Download PDFInfo
- Publication number
- JP2007520556A JP2007520556A JP2006552160A JP2006552160A JP2007520556A JP 2007520556 A JP2007520556 A JP 2007520556A JP 2006552160 A JP2006552160 A JP 2006552160A JP 2006552160 A JP2006552160 A JP 2006552160A JP 2007520556 A JP2007520556 A JP 2007520556A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hydrogen
- mmol
- compound
- phenyl
- 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.)
- Pending
Links
- 0 CC1C(*)(Cc(cc2)cc(Cl)c2Cl)CCNC1 Chemical compound CC1C(*)(Cc(cc2)cc(Cl)c2Cl)CCNC1 0.000 description 11
- HDRXESCDVUCCBX-UHFFFAOYSA-N C=CC(C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c(cc1)cc2c1nccc2)=O Chemical compound C=CC(C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c(cc1)cc2c1nccc2)=O HDRXESCDVUCCBX-UHFFFAOYSA-N 0.000 description 1
- USVGNWKAZFLESS-UHFFFAOYSA-O C=CC1C(Cc(cc2Cl)ccc2Cl)CC[NH2+]C1 Chemical compound C=CC1C(Cc(cc2Cl)ccc2Cl)CC[NH2+]C1 USVGNWKAZFLESS-UHFFFAOYSA-O 0.000 description 1
- USVGNWKAZFLESS-JHJMLUEUSA-N C=C[C@H]1C(Cc(cc2Cl)ccc2Cl)CCNC1 Chemical compound C=C[C@H]1C(Cc(cc2Cl)ccc2Cl)CCNC1 USVGNWKAZFLESS-JHJMLUEUSA-N 0.000 description 1
- GFRNPXNOCOHYBF-KITAHSCOSA-N CC(C(OC(C)(C)C)=O)N(CC1)CCC1N(CCC1Cc(cc2C)ccc2Cl)C[C@H]1C#N Chemical compound CC(C(OC(C)(C)C)=O)N(CC1)CCC1N(CCC1Cc(cc2C)ccc2Cl)C[C@H]1C#N GFRNPXNOCOHYBF-KITAHSCOSA-N 0.000 description 1
- YMZHUBIUCAQFIX-UHFFFAOYSA-N CC(C1C(Cc(cc2C)ccc2Cl)CCN(CC(OC(C)(C)C)=O)C1)O Chemical compound CC(C1C(Cc(cc2C)ccc2Cl)CCN(CC(OC(C)(C)C)=O)C1)O YMZHUBIUCAQFIX-UHFFFAOYSA-N 0.000 description 1
- WPSLPOKBUUBFDE-UHFFFAOYSA-N CC(CNCC1)C1(Cc(cc1)cc(Cl)c1Cl)F Chemical compound CC(CNCC1)C1(Cc(cc1)cc(Cl)c1Cl)F WPSLPOKBUUBFDE-UHFFFAOYSA-N 0.000 description 1
- VWNGYVHWAIBKSL-UHFFFAOYSA-N CC(CNCC1)C1(Cc(cc1)cc(Cl)c1Cl)O Chemical compound CC(CNCC1)C1(Cc(cc1)cc(Cl)c1Cl)O VWNGYVHWAIBKSL-UHFFFAOYSA-N 0.000 description 1
- LTAATZPAPBUKOQ-UHFFFAOYSA-N CC(CNCC1)C1=C Chemical compound CC(CNCC1)C1=C LTAATZPAPBUKOQ-UHFFFAOYSA-N 0.000 description 1
- ARYIMOASXQFMAS-FOIFJWKZSA-N CCC(C1)[C@@H](Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c(cc1)cc2c1nccc2)=O Chemical compound CCC(C1)[C@@H](Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c(cc1)cc2c1nccc2)=O ARYIMOASXQFMAS-FOIFJWKZSA-N 0.000 description 1
- CBTRUZAXGMHJDO-UHFFFAOYSA-N CCC(CN(CC1)C(OC(C)(C)C)=O)C1O Chemical compound CCC(CN(CC1)C(OC(C)(C)C)=O)C1O CBTRUZAXGMHJDO-UHFFFAOYSA-N 0.000 description 1
- NSNANZVISWMXJP-UHFFFAOYSA-N CC[O-](C)(C)(=[NH+]C)#C Chemical compound CC[O-](C)(C)(=[NH+]C)#C NSNANZVISWMXJP-UHFFFAOYSA-N 0.000 description 1
- OTRJGARPBIJRKG-IAIRZMIISA-N CO[C@H](C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c(cc1)cc2c1nccc2)=O Chemical compound CO[C@H](C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c(cc1)cc2c1nccc2)=O OTRJGARPBIJRKG-IAIRZMIISA-N 0.000 description 1
- RDSIIPUBKKQZFV-ZTDHTWSHSA-N CO[C@H](C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1cccc2c1nccc2)=O Chemical compound CO[C@H](C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1cccc2c1nccc2)=O RDSIIPUBKKQZFV-ZTDHTWSHSA-N 0.000 description 1
- AXAAKILJQSGHDI-CJFMBICVSA-N CO[C@H](C1)[C@@H](Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1ccc(cccn2)c2n1)=O Chemical compound CO[C@H](C1)[C@@H](Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1ccc(cccn2)c2n1)=O AXAAKILJQSGHDI-CJFMBICVSA-N 0.000 description 1
- JFTMOYZXGVYYQW-FIWHBWSRSA-N COc(cc1)c2nc(C(F)(F)F)ccc2c1C(N(CC1)CCC1N1CC(CO)[C@@H](Cc(cc2Cl)ccc2Cl)CC1)=O Chemical compound COc(cc1)c2nc(C(F)(F)F)ccc2c1C(N(CC1)CCC1N1CC(CO)[C@@H](Cc(cc2Cl)ccc2Cl)CC1)=O JFTMOYZXGVYYQW-FIWHBWSRSA-N 0.000 description 1
- WYUIWKFIFOJVKW-UHFFFAOYSA-N Cc(cc1)cc(Cl)c1Cl Chemical compound Cc(cc1)cc(Cl)c1Cl WYUIWKFIFOJVKW-UHFFFAOYSA-N 0.000 description 1
- MUDSDYNRBDKLGK-UHFFFAOYSA-N Cc1c(cccc2)c2ncc1 Chemical compound Cc1c(cccc2)c2ncc1 MUDSDYNRBDKLGK-UHFFFAOYSA-N 0.000 description 1
- ICEDQJZQQACDDP-UHFFFAOYSA-N Cc1ccc(CC(CC2)CCN2C2CCN(C)CC2)cc1C Chemical compound Cc1ccc(CC(CC2)CCN2C2CCN(C)CC2)cc1C ICEDQJZQQACDDP-UHFFFAOYSA-N 0.000 description 1
- JIVMLAUZOHRZPP-UHFFFAOYSA-N O=C(c(cc1)cc2c1nccc2)N(CC1)CCC1N1CCC(Cc(cc2Cl)ccc2Cl)CC1 Chemical compound O=C(c(cc1)cc2c1nccc2)N(CC1)CCC1N1CCC(Cc(cc2Cl)ccc2Cl)CC1 JIVMLAUZOHRZPP-UHFFFAOYSA-N 0.000 description 1
- WUPBGHRTKMOHRL-NHCUHLMSSA-N O=C(c1c(cccc2)c2ncc1)N(CC1)CCC1N1C[C@@H](CF)[C@@H](Cc(cc2Cl)ccc2Cl)CC1 Chemical compound O=C(c1c(cccc2)c2ncc1)N(CC1)CCC1N1C[C@@H](CF)[C@@H](Cc(cc2Cl)ccc2Cl)CC1 WUPBGHRTKMOHRL-NHCUHLMSSA-N 0.000 description 1
- WPWOBIYXOOJNTH-UHFFFAOYSA-N O=C(c1cnc(cccc2)c2c1)N(CC1)CCC1N1CCC(Cc(cc2Cl)ccc2Cl)CC1 Chemical compound O=C(c1cnc(cccc2)c2c1)N(CC1)CCC1N1CCC(Cc(cc2Cl)ccc2Cl)CC1 WPWOBIYXOOJNTH-UHFFFAOYSA-N 0.000 description 1
- VSBDCHHRACGZFL-UHFFFAOYSA-N O=C(c1nccc2c1cccc2)N(CC1)CCC1N1CCC(Cc(cc2Cl)ccc2Cl)CC1 Chemical compound O=C(c1nccc2c1cccc2)N(CC1)CCC1N1CCC(Cc(cc2Cl)ccc2Cl)CC1 VSBDCHHRACGZFL-UHFFFAOYSA-N 0.000 description 1
- BKSRLDUBSLBPQQ-UHFFFAOYSA-N OCC(C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1ccc2ncccc2c1)=O Chemical compound OCC(C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1ccc2ncccc2c1)=O BKSRLDUBSLBPQQ-UHFFFAOYSA-N 0.000 description 1
- UMAJFKLARLMOMU-ANYOKISRSA-N OC[C@H](C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1c(cccc2)c2nc(O)c1)=O Chemical compound OC[C@H](C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1c(cccc2)c2nc(O)c1)=O UMAJFKLARLMOMU-ANYOKISRSA-N 0.000 description 1
- LCPSFHDBHJGJMG-KEKNWZKVSA-N OC[C@H](C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1cccc2c1nccc2)=O Chemical compound OC[C@H](C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1cccc2c1nccc2)=O LCPSFHDBHJGJMG-KEKNWZKVSA-N 0.000 description 1
- FWORXIUSKYVBDG-AKRCKQFNSA-N OC[C@H](C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1cnc(cccc2)c2c1)=O Chemical compound OC[C@H](C1)C(Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1cnc(cccc2)c2c1)=O FWORXIUSKYVBDG-AKRCKQFNSA-N 0.000 description 1
- JQFHJJMJPITPRT-UXHICEINSA-N OC[C@H](C1)[C@@H](Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1ccnc(cc2)c1cc2Cl)=O Chemical compound OC[C@H](C1)[C@@H](Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1ccnc(cc2)c1cc2Cl)=O JQFHJJMJPITPRT-UXHICEINSA-N 0.000 description 1
- QMBSOOBEQAAHHB-RTWAWAEBSA-N OC[C@H](C1)[C@@H](Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1ccnc2c1cccc2)=O Chemical compound OC[C@H](C1)[C@@H](Cc(cc2Cl)ccc2Cl)CCN1C(CC1)CCN1C(c1ccnc2c1cccc2)=O QMBSOOBEQAAHHB-RTWAWAEBSA-N 0.000 description 1
Classifications
-
- 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
- C07D401/14—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 three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54201304P | 2004-02-05 | 2004-02-05 | |
| PCT/US2005/002664 WO2005077369A1 (en) | 2004-02-05 | 2005-02-02 | Piperidine derivatives useful as ccr3 antagonists |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2007520556A true JP2007520556A (ja) | 2007-07-26 |
Family
ID=34860249
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006552160A Pending JP2007520556A (ja) | 2004-02-05 | 2005-02-02 | Ccr3アンタゴニストとして有用なピペリジン誘導体 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7705153B2 (https=) |
| EP (1) | EP1725235B1 (https=) |
| JP (1) | JP2007520556A (https=) |
| CN (1) | CN1946402A (https=) |
| AT (1) | ATE428422T1 (https=) |
| CA (1) | CA2554465A1 (https=) |
| DE (1) | DE602005013931D1 (https=) |
| ES (1) | ES2324224T3 (https=) |
| WO (1) | WO2005077369A1 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012514024A (ja) * | 2009-04-08 | 2012-06-21 | 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 | Ccr3アンタゴニストとしての置換ピペリジン |
| JP2014520116A (ja) * | 2011-06-16 | 2014-08-21 | 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 | 新規の選択的ccr2拮抗薬 |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2006100190A (ru) * | 2003-06-13 | 2006-08-10 | Шеринг Акциенгезельшафт (De) | Производные хинолиламида в качестве антагонистов ccr-5 |
| US8067457B2 (en) | 2005-11-01 | 2011-11-29 | Millennium Pharmaceuticals, Inc. | Compounds useful as antagonists of CCR2 |
| WO2007053499A2 (en) | 2005-11-01 | 2007-05-10 | Millennium Pharmaceuticals, Inc. | Compounds useful as antagonists of ccr2 |
| TW200803855A (en) * | 2006-02-24 | 2008-01-16 | Kalypsys Inc | Quinolones useful as inducible nitric oxide synthase inhibitors |
| CN101460482B (zh) * | 2006-03-21 | 2013-03-27 | 默沙东公司 | 具有cxcr3拮抗剂活性的杂环取代的吡啶化合物 |
| MX2009000577A (es) * | 2006-07-14 | 2009-03-09 | Schering Corp | Compuestos de piperazina sustituida heterociclica con actividad antagonista de cxcr3. |
| WO2010129351A1 (en) | 2009-04-28 | 2010-11-11 | Schepens Eye Research Institute | Method to identify and treat age-related macular degeneration |
| UA109290C2 (uk) | 2010-10-07 | 2015-08-10 | Спільні кристали і солі інгібіторів ccr3 | |
| EP2780015B1 (en) | 2011-11-18 | 2017-01-04 | Heptares Therapeutics Limited | Muscarinic m1 receptor agonists |
| US8680280B2 (en) | 2012-04-02 | 2014-03-25 | Boehringer Ingelheim International Gmbh | Process for the manufacturing of CRR inhibitors |
| US10213421B2 (en) | 2012-04-04 | 2019-02-26 | Alkahest, Inc. | Pharmaceutical formulations comprising CCR3 antagonists |
| KR20160098424A (ko) | 2013-12-19 | 2016-08-18 | 바이엘 파마 악티엔게젤샤프트 | 치환된 피페리디닐-테트라히드로퀴놀린 |
| EP3083610A1 (de) | 2013-12-19 | 2016-10-26 | Bayer Pharma Aktiengesellschaft | Substituierte bipiperidinyl-derivate als adrenrezeptor alpha 2c antagonisten |
| CR20160276A (es) | 2013-12-19 | 2016-10-20 | Bayer Pharma AG | "piperidiniltetrahidroquinolinas sustituidas y su uso como antagonistas de los adenoreceptores alpha-2c" |
| US20160318866A1 (en) | 2013-12-19 | 2016-11-03 | Bayer Pharma Aktiengesellschaft | Substituted bipiperidinyl derivatives |
| GB201404922D0 (en) | 2014-03-19 | 2014-04-30 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| GB201513743D0 (en) | 2015-08-03 | 2015-09-16 | Heptares Therapeutics Ltd | Muscarinic agonists |
| GB201519352D0 (en) | 2015-11-02 | 2015-12-16 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| GB201617454D0 (en) | 2016-10-14 | 2016-11-30 | Heptares Therapeutics Limited | Pharmaceutical compounds |
| CN110636844A (zh) | 2017-04-05 | 2019-12-31 | 万能溶剂有限公司 | 使用ccr3-抑制剂治疗衰老相关损伤的方法及组合物 |
| PL233595B1 (pl) | 2017-05-12 | 2019-11-29 | Celon Pharma Spolka Akcyjna | Pochodne pirazolo[1,5-a]pirymidyny jako inhibitory kinazy JAK |
| GB201810239D0 (en) | 2018-06-22 | 2018-08-08 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| GB201819960D0 (en) | 2018-12-07 | 2019-01-23 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| GB201819961D0 (en) | 2018-12-07 | 2019-01-23 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| GB202020191D0 (en) | 2020-12-18 | 2021-02-03 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| US20230312697A1 (en) | 2020-06-11 | 2023-10-05 | Alkahest Inc. | Methods of improving retina-associated disease outcome using ccr3-inhibitors |
| US12221463B2 (en) | 2020-08-07 | 2025-02-11 | The Board Of Regents Of The University Of Oklahoma | Method of promoting wound healing by inhibiting CCR3 |
| CN112250611B (zh) * | 2020-11-27 | 2022-04-22 | 济南大学 | 一种-2-(2,5-二氟苯基)吡咯烷盐酸盐的合成方法 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6387930B1 (en) * | 1999-05-04 | 2002-05-14 | Schering Corporation | Piperidine derivatives useful as CCR5 antagonists |
| JP2002543185A (ja) * | 1999-05-04 | 2002-12-17 | シェーリング コーポレイション | Ccr5アンタゴニストとして有用なピペラジン誘導体 |
| JP2003530393A (ja) * | 2000-04-08 | 2003-10-14 | アストラゼネカ・アクチエボラーグ | 化学化合物 |
| JP2004524360A (ja) * | 2001-03-29 | 2004-08-12 | シェーリング コーポレイション | Ccr5アンタゴニストとして有用なアリールオキシム−ピペラジン |
| JP2004525157A (ja) * | 2001-03-29 | 2004-08-19 | シェーリング コーポレイション | Aidsの処置に有用なccr5アンタゴニスト |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5889006A (en) | 1995-02-23 | 1999-03-30 | Schering Corporation | Muscarinic antagonists |
| IL117149A0 (en) | 1995-02-23 | 1996-06-18 | Schering Corp | Muscarinic antagonists |
| KR0171169B1 (ko) * | 1996-01-20 | 1999-03-30 | 구자홍 | 엘시디 패널 구동을 위한 다계조 전압 발생 회로 |
| US5952349A (en) | 1996-07-10 | 1999-09-14 | Schering Corporation | Muscarinic antagonists for treating memory loss |
| US5977138A (en) | 1996-08-15 | 1999-11-02 | Schering Corporation | Ether muscarinic antagonists |
-
2005
- 2005-02-02 CA CA002554465A patent/CA2554465A1/en not_active Abandoned
- 2005-02-02 AT AT05712200T patent/ATE428422T1/de not_active IP Right Cessation
- 2005-02-02 US US11/049,460 patent/US7705153B2/en not_active Expired - Fee Related
- 2005-02-02 WO PCT/US2005/002664 patent/WO2005077369A1/en not_active Ceased
- 2005-02-02 JP JP2006552160A patent/JP2007520556A/ja active Pending
- 2005-02-02 EP EP05712200A patent/EP1725235B1/en not_active Expired - Lifetime
- 2005-02-02 CN CNA2005800121378A patent/CN1946402A/zh active Pending
- 2005-02-02 ES ES05712200T patent/ES2324224T3/es not_active Expired - Lifetime
- 2005-02-02 DE DE602005013931T patent/DE602005013931D1/de not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6387930B1 (en) * | 1999-05-04 | 2002-05-14 | Schering Corporation | Piperidine derivatives useful as CCR5 antagonists |
| JP2002543185A (ja) * | 1999-05-04 | 2002-12-17 | シェーリング コーポレイション | Ccr5アンタゴニストとして有用なピペラジン誘導体 |
| JP2003530393A (ja) * | 2000-04-08 | 2003-10-14 | アストラゼネカ・アクチエボラーグ | 化学化合物 |
| JP2004524360A (ja) * | 2001-03-29 | 2004-08-12 | シェーリング コーポレイション | Ccr5アンタゴニストとして有用なアリールオキシム−ピペラジン |
| JP2004525157A (ja) * | 2001-03-29 | 2004-08-19 | シェーリング コーポレイション | Aidsの処置に有用なccr5アンタゴニスト |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012514024A (ja) * | 2009-04-08 | 2012-06-21 | 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 | Ccr3アンタゴニストとしての置換ピペリジン |
| JP2014520116A (ja) * | 2011-06-16 | 2014-08-21 | 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 | 新規の選択的ccr2拮抗薬 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1946402A (zh) | 2007-04-11 |
| US20050182095A1 (en) | 2005-08-18 |
| WO2005077369A1 (en) | 2005-08-25 |
| CA2554465A1 (en) | 2005-08-25 |
| ATE428422T1 (de) | 2009-05-15 |
| ES2324224T3 (es) | 2009-08-03 |
| US7705153B2 (en) | 2010-04-27 |
| EP1725235A1 (en) | 2006-11-29 |
| DE602005013931D1 (https=) | 2009-05-28 |
| EP1725235B1 (en) | 2009-04-15 |
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