K. Yu. Parkhoma, E. D. Davydenkova, R. R. Makhmudov, I. A. Gorbunova, D. A. Shipilovskikh
{"title":"4-(het)芳基-4-氧-2-[(3-乙氧羰基-5,6,7,8-四氢- 4h -环庚[b]-噻吩-2-基)氨基]- 2-烯酸的合成、分子内环化及其抑菌活性","authors":"K. Yu. Parkhoma, E. D. Davydenkova, R. R. Makhmudov, I. A. Gorbunova, D. A. Shipilovskikh","doi":"10.1007/s11172-024-4452-y","DOIUrl":null,"url":null,"abstract":"<div><p>The synthetic procedure was developed and the scope of the substituted 4-(het)aryl-2-[(3-ethoxycarbonyl-5,6,7,8-tetrahydro-4<i>H</i>-cyclohepta[<i>b</i>]thiophen-2-yl)amino]-4-oxobut-2-enoic acids was broadened. Antinociceptive activity and acute toxicity of the synthesized compounds were studied. It was found that the synthesized substituted acids show pronounced antinociceptive activity and were classified as being practically non-toxic.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"73 11","pages":"3359 - 3366"},"PeriodicalIF":1.7000,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis, intramolecular cyclization, and antinociceptive activity of 4-(het)aryl-4-oxo-2-[(3-ethoxycarbonyl-5,6,7,8-tetrahydro-4H-cyclohepta[b]-thiophen-2-yl)amino]but-2-enoic acids\",\"authors\":\"K. Yu. Parkhoma, E. D. Davydenkova, R. R. Makhmudov, I. A. Gorbunova, D. A. Shipilovskikh\",\"doi\":\"10.1007/s11172-024-4452-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The synthetic procedure was developed and the scope of the substituted 4-(het)aryl-2-[(3-ethoxycarbonyl-5,6,7,8-tetrahydro-4<i>H</i>-cyclohepta[<i>b</i>]thiophen-2-yl)amino]-4-oxobut-2-enoic acids was broadened. Antinociceptive activity and acute toxicity of the synthesized compounds were studied. It was found that the synthesized substituted acids show pronounced antinociceptive activity and were classified as being practically non-toxic.</p></div>\",\"PeriodicalId\":756,\"journal\":{\"name\":\"Russian Chemical Bulletin\",\"volume\":\"73 11\",\"pages\":\"3359 - 3366\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-01-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Chemical Bulletin\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11172-024-4452-y\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Chemical Bulletin","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11172-024-4452-y","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Synthesis, intramolecular cyclization, and antinociceptive activity of 4-(het)aryl-4-oxo-2-[(3-ethoxycarbonyl-5,6,7,8-tetrahydro-4H-cyclohepta[b]-thiophen-2-yl)amino]but-2-enoic acids
The synthetic procedure was developed and the scope of the substituted 4-(het)aryl-2-[(3-ethoxycarbonyl-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophen-2-yl)amino]-4-oxobut-2-enoic acids was broadened. Antinociceptive activity and acute toxicity of the synthesized compounds were studied. It was found that the synthesized substituted acids show pronounced antinociceptive activity and were classified as being practically non-toxic.
期刊介绍:
Publishing nearly 500 original articles a year, by leading Scientists from Russia and throughout the world, Russian Chemical Bulletin is a prominent international journal. The coverage of the journal spans practically all areas of fundamental chemical research and is presented in five sections:
General and Inorganic Chemistry;
Physical Chemistry;
Organic Chemistry;
Organometallic Chemistry;
Chemistry of Natural Compounds and Bioorganic Chemistry.