CN106928341B - 定点单取代聚乙二醇化Exendin类似物及其制备方法 - Google Patents
定点单取代聚乙二醇化Exendin类似物及其制备方法 Download PDFInfo
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- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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| CN201710091006.8A CN106928341B (zh) | 2011-03-30 | 2011-03-30 | 定点单取代聚乙二醇化Exendin类似物及其制备方法 |
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| CN201710091006.8A CN106928341B (zh) | 2011-03-30 | 2011-03-30 | 定点单取代聚乙二醇化Exendin类似物及其制备方法 |
| CN201110078314XA CN102718868A (zh) | 2011-03-30 | 2011-03-30 | 定点单取代聚乙二醇化Exendin类似物及其制备方法 |
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| CN201110078314XA Pending CN102718868A (zh) | 2011-03-30 | 2011-03-30 | 定点单取代聚乙二醇化Exendin类似物及其制备方法 |
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| UA116217C2 (uk) | 2012-10-09 | 2018-02-26 | Санофі | Пептидна сполука як подвійний агоніст рецепторів glp1-1 та глюкагону |
| PT2934568T (pt) | 2012-12-21 | 2018-01-04 | Sanofi Sa | Agonistas duplos de glp1/gip ou trigonais de glp1/gip/glucagina |
| TW201609799A (zh) | 2013-12-13 | 2016-03-16 | 賽諾菲公司 | 雙重glp-1/gip受體促效劑 |
| TW201609795A (zh) | 2013-12-13 | 2016-03-16 | 賽諾菲公司 | 作為雙重glp-1/gip受體促效劑的艾塞那肽-4(exendin-4)胜肽類似物 |
| TW201609797A (zh) | 2013-12-13 | 2016-03-16 | 賽諾菲公司 | 雙重glp-1/升糖素受體促效劑 |
| TW201609796A (zh) | 2013-12-13 | 2016-03-16 | 賽諾菲公司 | 非醯化之艾塞那肽-4(exendin-4)胜肽類似物 |
| KR101768446B1 (ko) * | 2014-03-21 | 2017-08-17 | 애니젠 주식회사 | 신규한 엑세나타이드 유사체 및 그의 용도 |
| TW201625669A (zh) | 2014-04-07 | 2016-07-16 | 賽諾菲公司 | 衍生自艾塞那肽-4(Exendin-4)之肽類雙重GLP-1/升糖素受體促效劑 |
| TW201625668A (zh) | 2014-04-07 | 2016-07-16 | 賽諾菲公司 | 作為胜肽性雙重glp-1/昇糖素受體激動劑之艾塞那肽-4衍生物 |
| TW201625670A (zh) | 2014-04-07 | 2016-07-16 | 賽諾菲公司 | 衍生自exendin-4之雙重glp-1/升糖素受體促效劑 |
| US9932381B2 (en) | 2014-06-18 | 2018-04-03 | Sanofi | Exendin-4 derivatives as selective glucagon receptor agonists |
| AR105319A1 (es) | 2015-06-05 | 2017-09-27 | Sanofi Sa | Profármacos que comprenden un conjugado agonista dual de glp-1 / glucagón conector ácido hialurónico |
| TW201706291A (zh) | 2015-07-10 | 2017-02-16 | 賽諾菲公司 | 作為選擇性肽雙重glp-1/升糖素受體促效劑之新毒蜥外泌肽(exendin-4)衍生物 |
| GB201603510D0 (en) * | 2016-02-29 | 2016-04-13 | Univ Ulster | Compositions for use in the treatment of neurological disease |
| CN115703825A (zh) * | 2021-08-17 | 2023-02-17 | 派格生物医药(苏州)股份有限公司 | 艾塞那肽变体及其聚乙二醇缀合物的制备方法 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1363559A (zh) * | 2001-05-10 | 2002-08-14 | 上海华谊生物技术有限公司 | 促胰岛素分泌肽衍生物 |
| CN1745091A (zh) * | 2003-01-18 | 2006-03-08 | 派格斯菲尔有限公司 | 非靶位点胺基被保护的肽,其制备方法以及使用该肽制备特异性地结合的peg肽的方法 |
| KR20070115602A (ko) * | 2006-06-01 | 2007-12-06 | 이강춘 | 폴리에틸렌글리콜 또는 이의 유도체로 단일 수식된 엑센딘,이의 제조방법 및 이의 용도 |
| CN101125207A (zh) * | 2006-11-14 | 2008-02-20 | 上海华谊生物技术有限公司 | 带有聚乙二醇基团的Exendin或其类似物及其制剂和用途 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0407936A (pt) * | 2003-03-19 | 2006-02-21 | Lilly Co Eli | composto de glp-1 peguilado, método de estimular o receptor de glp-1 em um indivìduo, e, uso de composto glp-1 peguilado |
| WO2006037811A2 (en) * | 2004-10-07 | 2006-04-13 | Novo Nordisk A/S | Protracted exendin-4 compounds |
| WO2007061148A1 (en) * | 2005-11-24 | 2007-05-31 | Pegsphere Co., Ltd. | Site-specific peg conjugates of glp-1 and methods for production thereof |
| WO2008130066A1 (en) * | 2007-04-20 | 2008-10-30 | Kang Choon Lee | Mono modified exendin with polyethylene glycol or its derivatives and uses thereof |
| US7935877B2 (en) * | 2007-04-20 | 2011-05-03 | Master Key, Llc | System and method for music composition |
| AU2010225523B2 (en) * | 2009-03-20 | 2012-05-24 | Hanmi Science Co., Ltd. | Method for preparing a site-specific physiologically active polypeptide conjugate |
| CN101870728A (zh) * | 2009-04-23 | 2010-10-27 | 派格生物医药(苏州)有限公司 | 新型Exendin变体及其缀合物 |
| CN101559041B (zh) * | 2009-05-19 | 2014-01-15 | 中国科学院过程工程研究所 | 粒径均一的多肽药物缓释微球或微囊制剂及制备方法 |
| BR112012007374A2 (pt) * | 2009-09-30 | 2019-09-24 | Glaxo Group Ltd | composição, formulação oral, injetável, inalável ou nebulizável, e, ácido nucleico isolado ou recombinante |
| CN102397558B (zh) * | 2010-09-09 | 2013-08-14 | 中国人民解放军军事医学科学院毒物药物研究所 | Exendin-4类似物的定位聚乙二醇化修饰物及其用途 |
-
2011
- 2011-03-30 CN CN201710091006.8A patent/CN106928341B/zh active Active
- 2011-03-30 CN CN201110078314XA patent/CN102718868A/zh active Pending
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2012
- 2012-03-05 WO PCT/CN2012/071910 patent/WO2012130015A1/zh not_active Ceased
- 2012-03-05 JP JP2014501409A patent/JP6297969B2/ja active Active
- 2012-03-05 CA CA2829122A patent/CA2829122C/en active Active
- 2012-03-05 EP EP12765410.1A patent/EP2692730B1/en active Active
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- 2012-03-05 RU RU2013147468A patent/RU2625015C2/ru active
- 2012-03-05 AU AU2012237899A patent/AU2012237899B2/en active Active
- 2012-03-05 BR BR112013024706-1A patent/BR112013024706B1/pt active IP Right Grant
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2013
- 2013-09-30 US US14/042,544 patent/US20140142037A1/en not_active Abandoned
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1363559A (zh) * | 2001-05-10 | 2002-08-14 | 上海华谊生物技术有限公司 | 促胰岛素分泌肽衍生物 |
| CN1745091A (zh) * | 2003-01-18 | 2006-03-08 | 派格斯菲尔有限公司 | 非靶位点胺基被保护的肽,其制备方法以及使用该肽制备特异性地结合的peg肽的方法 |
| KR20070115602A (ko) * | 2006-06-01 | 2007-12-06 | 이강춘 | 폴리에틸렌글리콜 또는 이의 유도체로 단일 수식된 엑센딘,이의 제조방법 및 이의 용도 |
| CN101125207A (zh) * | 2006-11-14 | 2008-02-20 | 上海华谊生物技术有限公司 | 带有聚乙二醇基团的Exendin或其类似物及其制剂和用途 |
Non-Patent Citations (2)
| Title |
|---|
| Preparation and PEGylation of exendin-4 peptide secreted from yeast Pichia pastoris;Jin Zhou et al.;《European Journal of Pharmaceutics and Biopharmaceutics》;20090207;第72卷;第412-417页 * |
| 蛋白质和肽类分子的聚乙二醇化化学;姜忠义等;《有机化学》;20031231;第23卷(第12期);第1340-1347页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN106928341A (zh) | 2017-07-07 |
| RU2013147468A (ru) | 2015-05-10 |
| JP2014510735A (ja) | 2014-05-01 |
| CA2829122A1 (en) | 2012-10-04 |
| KR102005385B1 (ko) | 2019-07-30 |
| US20140142037A1 (en) | 2014-05-22 |
| BR112013024706B1 (pt) | 2022-10-11 |
| KR20140033023A (ko) | 2014-03-17 |
| AU2012237899A1 (en) | 2013-09-19 |
| CA2829122C (en) | 2022-05-03 |
| BR112013024706A2 (pt) | 2016-09-06 |
| EP2692730B1 (en) | 2018-11-14 |
| WO2012130015A1 (zh) | 2012-10-04 |
| EP2692730A1 (en) | 2014-02-05 |
| JP6297969B2 (ja) | 2018-03-20 |
| EP2692730A4 (en) | 2015-04-01 |
| RU2625015C2 (ru) | 2017-07-11 |
| CN102718868A (zh) | 2012-10-10 |
| AU2012237899B2 (en) | 2017-04-13 |
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