Barbara Malawska , Katarzyna Kulig , Annika Gippert , Barbara Filipek , Jacek Sapa , Dorota Maciąg
{"title":"新2-取代1-[3-(4-芳基哌嗪-1-基)丙基]-吡咯烷酮-2- 1衍生物的合成与开发,具有抗心律失常、降压和α-溶肾上腺活性","authors":"Barbara Malawska , Katarzyna Kulig , Annika Gippert , Barbara Filipek , Jacek Sapa , Dorota Maciąg","doi":"10.1016/j.farmac.2005.08.002","DOIUrl":null,"url":null,"abstract":"<div><p>A series of new 1-[3-(4-arylpiperazinyl-1-yl)-2-(<em>N</em>-alkylcarbamoyloxy)propyl]-pyrrolidin-2-one derivatives (<strong>4a</strong>–<strong>12a</strong><span>) were synthesised and tested for their electrocardiographic, antiarrhythmic and antihypertensive activity, as well as for the α</span><sub>1</sub>- and α<sub>2</sub>-adrenoceptor binding affinities. Of the newly synthesised derivatives, 1-{2-(<em>N</em>-2-methylethylcarbamoiloxy)-3-[4-(2-methoxyphenyl)piperazin-1-yl)]propyl}pyrrolidin-2-one dihydrochloride (<strong>10a)</strong> was the most active in prophylactic antiarrhythmic tests, its ED<sub>50</sub> value equalling 2.7 mg kg<sup>–1</sup>, and the therapeutic index being 75.2; moreover, compound <strong>10a</strong> was also found to possess hypotensive activity. A preliminary molecular modelling study suggested that the selected α<sub>1</sub>-AR antagonist distances and angles between pharmacophoric features, estimated for the tested compounds, were in good agreement with the parameters evaluated for ligands.</p></div>","PeriodicalId":77128,"journal":{"name":"Farmaco (Societa chimica italiana : 1989)","volume":"60 10","pages":"Pages 793-803"},"PeriodicalIF":0.0000,"publicationDate":"2005-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.farmac.2005.08.002","citationCount":"17","resultStr":"{\"title\":\"Synthesis and development of new 2-substituted 1-[3-(4-arylpiperazin-1-yl)propyl]-pyrrolidin-2-one derivatives with antiarrhythmic, hypotensive, and α-adrenolytic activity\",\"authors\":\"Barbara Malawska , Katarzyna Kulig , Annika Gippert , Barbara Filipek , Jacek Sapa , Dorota Maciąg\",\"doi\":\"10.1016/j.farmac.2005.08.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A series of new 1-[3-(4-arylpiperazinyl-1-yl)-2-(<em>N</em>-alkylcarbamoyloxy)propyl]-pyrrolidin-2-one derivatives (<strong>4a</strong>–<strong>12a</strong><span>) were synthesised and tested for their electrocardiographic, antiarrhythmic and antihypertensive activity, as well as for the α</span><sub>1</sub>- and α<sub>2</sub>-adrenoceptor binding affinities. Of the newly synthesised derivatives, 1-{2-(<em>N</em>-2-methylethylcarbamoiloxy)-3-[4-(2-methoxyphenyl)piperazin-1-yl)]propyl}pyrrolidin-2-one dihydrochloride (<strong>10a)</strong> was the most active in prophylactic antiarrhythmic tests, its ED<sub>50</sub> value equalling 2.7 mg kg<sup>–1</sup>, and the therapeutic index being 75.2; moreover, compound <strong>10a</strong> was also found to possess hypotensive activity. A preliminary molecular modelling study suggested that the selected α<sub>1</sub>-AR antagonist distances and angles between pharmacophoric features, estimated for the tested compounds, were in good agreement with the parameters evaluated for ligands.</p></div>\",\"PeriodicalId\":77128,\"journal\":{\"name\":\"Farmaco (Societa chimica italiana : 1989)\",\"volume\":\"60 10\",\"pages\":\"Pages 793-803\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.farmac.2005.08.002\",\"citationCount\":\"17\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Farmaco (Societa chimica italiana : 1989)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0014827X05001734\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Farmaco (Societa chimica italiana : 1989)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0014827X05001734","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis and development of new 2-substituted 1-[3-(4-arylpiperazin-1-yl)propyl]-pyrrolidin-2-one derivatives with antiarrhythmic, hypotensive, and α-adrenolytic activity
A series of new 1-[3-(4-arylpiperazinyl-1-yl)-2-(N-alkylcarbamoyloxy)propyl]-pyrrolidin-2-one derivatives (4a–12a) were synthesised and tested for their electrocardiographic, antiarrhythmic and antihypertensive activity, as well as for the α1- and α2-adrenoceptor binding affinities. Of the newly synthesised derivatives, 1-{2-(N-2-methylethylcarbamoiloxy)-3-[4-(2-methoxyphenyl)piperazin-1-yl)]propyl}pyrrolidin-2-one dihydrochloride (10a) was the most active in prophylactic antiarrhythmic tests, its ED50 value equalling 2.7 mg kg–1, and the therapeutic index being 75.2; moreover, compound 10a was also found to possess hypotensive activity. A preliminary molecular modelling study suggested that the selected α1-AR antagonist distances and angles between pharmacophoric features, estimated for the tested compounds, were in good agreement with the parameters evaluated for ligands.