J. Mpetga, A. R. N. Donfack, J. Tamokou, Iréne Chinda Kengne, P. Tane, Xiao-jiang Hao, Mathieu Tene
{"title":"海苔叶中的三萜类化合物及具有抗菌活性的半合成衍生物","authors":"J. Mpetga, A. R. N. Donfack, J. Tamokou, Iréne Chinda Kengne, P. Tane, Xiao-jiang Hao, Mathieu Tene","doi":"10.4236/abc.2021.114011","DOIUrl":null,"url":null,"abstract":"Chemical investigation of the MeOH extract from the \nleaves of C. glauca yielded nine known triterpenoids (1-9) \nbelonging to the cycloartane and friedelane series. Two of these \ncompounds namely glaucartanoic acid A (1) and 3β,21β-dihydroxy-30-nor-(D:A)-friedoolean-20(29)-en-27-oic \nacid (5) were subjected to chemical derivatizations and afforded five \nnew derivatives: diacetylglaucartanoic acid A (1a), \n24-acetylglaucartanoic acid A (1b), glaucartanoic acid A methyl ester (1c), \n24-methoxyglaucartanoic acid A methyl ester \n(1d), and 3β,21β-diacetoxy-30-nor-(D:A)-friedoolean-20(29)-en-27-oic acid (5a). Their structures were assigned based on their NMR and MS data \nand by comparison with literature values. \nThe MeOH extract, isolated compounds and some new semi-synthetic \nderivatives were subjected to in vitro antimicrobial assays \nagainst a panel of pathogenic microorganisms, including Gram-positive \nand Gram-negative bacteria, and fungi using broth microdilution method. The \nMeOH extract displayed activity towards all the tested pathogenic bacterial and fungal strains with good \nactivity (MIC against Staphylococcus aureus ATCC25923 and Shigella flexneri SDINT. Compounds 3 and 5 showed the most potent antimicrobial effect.","PeriodicalId":59114,"journal":{"name":"生物化学进展(英文)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Triterpenoids and Semisynthetic Derivatives with Antimicrobial Activities from the Leaves of Caloncoba glauca (Flacourtiaceae)\",\"authors\":\"J. Mpetga, A. R. N. Donfack, J. Tamokou, Iréne Chinda Kengne, P. Tane, Xiao-jiang Hao, Mathieu Tene\",\"doi\":\"10.4236/abc.2021.114011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Chemical investigation of the MeOH extract from the \\nleaves of C. glauca yielded nine known triterpenoids (1-9) \\nbelonging to the cycloartane and friedelane series. Two of these \\ncompounds namely glaucartanoic acid A (1) and 3β,21β-dihydroxy-30-nor-(D:A)-friedoolean-20(29)-en-27-oic \\nacid (5) were subjected to chemical derivatizations and afforded five \\nnew derivatives: diacetylglaucartanoic acid A (1a), \\n24-acetylglaucartanoic acid A (1b), glaucartanoic acid A methyl ester (1c), \\n24-methoxyglaucartanoic acid A methyl ester \\n(1d), and 3β,21β-diacetoxy-30-nor-(D:A)-friedoolean-20(29)-en-27-oic acid (5a). Their structures were assigned based on their NMR and MS data \\nand by comparison with literature values. \\nThe MeOH extract, isolated compounds and some new semi-synthetic \\nderivatives were subjected to in vitro antimicrobial assays \\nagainst a panel of pathogenic microorganisms, including Gram-positive \\nand Gram-negative bacteria, and fungi using broth microdilution method. The \\nMeOH extract displayed activity towards all the tested pathogenic bacterial and fungal strains with good \\nactivity (MIC against Staphylococcus aureus ATCC25923 and Shigella flexneri SDINT. Compounds 3 and 5 showed the most potent antimicrobial effect.\",\"PeriodicalId\":59114,\"journal\":{\"name\":\"生物化学进展(英文)\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"生物化学进展(英文)\",\"FirstCategoryId\":\"1089\",\"ListUrlMain\":\"https://doi.org/10.4236/abc.2021.114011\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"生物化学进展(英文)","FirstCategoryId":"1089","ListUrlMain":"https://doi.org/10.4236/abc.2021.114011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Triterpenoids and Semisynthetic Derivatives with Antimicrobial Activities from the Leaves of Caloncoba glauca (Flacourtiaceae)
Chemical investigation of the MeOH extract from the
leaves of C. glauca yielded nine known triterpenoids (1-9)
belonging to the cycloartane and friedelane series. Two of these
compounds namely glaucartanoic acid A (1) and 3β,21β-dihydroxy-30-nor-(D:A)-friedoolean-20(29)-en-27-oic
acid (5) were subjected to chemical derivatizations and afforded five
new derivatives: diacetylglaucartanoic acid A (1a),
24-acetylglaucartanoic acid A (1b), glaucartanoic acid A methyl ester (1c),
24-methoxyglaucartanoic acid A methyl ester
(1d), and 3β,21β-diacetoxy-30-nor-(D:A)-friedoolean-20(29)-en-27-oic acid (5a). Their structures were assigned based on their NMR and MS data
and by comparison with literature values.
The MeOH extract, isolated compounds and some new semi-synthetic
derivatives were subjected to in vitro antimicrobial assays
against a panel of pathogenic microorganisms, including Gram-positive
and Gram-negative bacteria, and fungi using broth microdilution method. The
MeOH extract displayed activity towards all the tested pathogenic bacterial and fungal strains with good
activity (MIC against Staphylococcus aureus ATCC25923 and Shigella flexneri SDINT. Compounds 3 and 5 showed the most potent antimicrobial effect.