A. V. Petrova, Ya. L. Esaulkova, M. G. Mikhalsky, V. V. Zarubaev, O. B. Kazakova
{"title":"C(28)位连接a -二萜的曼尼希碱基的抗病毒活性","authors":"A. V. Petrova, Ya. L. Esaulkova, M. G. Mikhalsky, V. V. Zarubaev, O. B. Kazakova","doi":"10.1007/s11172-025-4575-9","DOIUrl":null,"url":null,"abstract":"<div><p>Novel derivatives of A-secooleanolic and A-secobetulinic acids containing a propargylamine substituent at the C(28) position were synthesized <i>via</i> the Cu-catalyzed Mannich reaction. Antiviral properties of the compounds were evaluated on MDCK cell culture against influenza A/Puerto Rico/8/34 (H1N1) virus. It was demonstrated that among the Mannich bases of A-secooleanolic acid, the derivative containing the piperazine moiety exhibited the highest activity (IC<sub>50</sub> = 5 µmol L<sup>−1</sup> and SI >100). In the case of A-secobetulinic acid, a positive effect was caused by the introduction of <i>N</i>-methylpiperazine (IC<sub>50</sub> = 1 µmol L<sup>−1</sup> and SI >25) and morpholine (IC<sub>50</sub> = 3 µmol L<sup>−1</sup> and SI = 42) moieties.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"74 3","pages":"818 - 823"},"PeriodicalIF":1.7000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Antiviral activity of Mannich bases linked to A-secotriterpenoids at the C(28) position\",\"authors\":\"A. V. Petrova, Ya. L. Esaulkova, M. G. Mikhalsky, V. V. Zarubaev, O. B. Kazakova\",\"doi\":\"10.1007/s11172-025-4575-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Novel derivatives of A-secooleanolic and A-secobetulinic acids containing a propargylamine substituent at the C(28) position were synthesized <i>via</i> the Cu-catalyzed Mannich reaction. Antiviral properties of the compounds were evaluated on MDCK cell culture against influenza A/Puerto Rico/8/34 (H1N1) virus. It was demonstrated that among the Mannich bases of A-secooleanolic acid, the derivative containing the piperazine moiety exhibited the highest activity (IC<sub>50</sub> = 5 µmol L<sup>−1</sup> and SI >100). In the case of A-secobetulinic acid, a positive effect was caused by the introduction of <i>N</i>-methylpiperazine (IC<sub>50</sub> = 1 µmol L<sup>−1</sup> and SI >25) and morpholine (IC<sub>50</sub> = 3 µmol L<sup>−1</sup> and SI = 42) moieties.</p></div>\",\"PeriodicalId\":756,\"journal\":{\"name\":\"Russian Chemical Bulletin\",\"volume\":\"74 3\",\"pages\":\"818 - 823\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-04-28\",\"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/s11172-025-4575-9\",\"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/s11172-025-4575-9","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Antiviral activity of Mannich bases linked to A-secotriterpenoids at the C(28) position
Novel derivatives of A-secooleanolic and A-secobetulinic acids containing a propargylamine substituent at the C(28) position were synthesized via the Cu-catalyzed Mannich reaction. Antiviral properties of the compounds were evaluated on MDCK cell culture against influenza A/Puerto Rico/8/34 (H1N1) virus. It was demonstrated that among the Mannich bases of A-secooleanolic acid, the derivative containing the piperazine moiety exhibited the highest activity (IC50 = 5 µmol L−1 and SI >100). In the case of A-secobetulinic acid, a positive effect was caused by the introduction of N-methylpiperazine (IC50 = 1 µmol L−1 and SI >25) and morpholine (IC50 = 3 µmol L−1 and SI = 42) moieties.
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.