{"title":"红树Lumnitzera littorea叶中化合物体外α-葡萄糖苷酶抑制活性的研究","authors":"T. Nguyen, T. Pham, P. Hansen, P. K. Nguyen","doi":"10.32508/STDJ.V22I1.1009","DOIUrl":null,"url":null,"abstract":"Introduction: Lumnitzera littorea grown at CanGio Mangrove Forest has been investigated. The present study reports the isolation, characterization and evaluation of the alpha-glucosidase inhibitory activity of isolated compounds from Lumnitzera littorea leaves. \nMethods: Their structures were elucidated by spectroscopic methods (including MS, 1D and 2D–NMR) and comparison with values from the literature. From the n-hexane extract, nine compounds including lupeol (1), betulin (2), betulinic acid (3), oleanolic acid (4), corosolic acid (5), -sitosterol (6), beta-sitosterol 3-O- beta-D-glucopyranoside (7), stigmast-5-ene-3beta-O-(6-O-hexadecanoyl-beta-D-glucopyranoside) (8), and stigmast-4-ene-3-one (9) were isolated and identified. \nResults: The results of the alpha-glucosidase inhibitory activity showed thatcorosolic acid (5) and oleanolic acid (4) were the most potent, with IC50 values of 17.86 +/- 0.42 and 18.82 +/- 0.59 ug/mL, respectively. Five of the other seven compounds exhibited inhibitory activity with IC50 values below 100 ug/mL, and higher than the positive control acarbose (127.64 +/- 0.64 ug/mL). \n ","PeriodicalId":285953,"journal":{"name":"Science and Technology Development Journal","volume":"66 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"In vitro α-glucosidase inhibitory activity of compounds isolated from mangrove Lumnitzera littorea leaves\",\"authors\":\"T. Nguyen, T. Pham, P. Hansen, P. K. Nguyen\",\"doi\":\"10.32508/STDJ.V22I1.1009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Lumnitzera littorea grown at CanGio Mangrove Forest has been investigated. The present study reports the isolation, characterization and evaluation of the alpha-glucosidase inhibitory activity of isolated compounds from Lumnitzera littorea leaves. \\nMethods: Their structures were elucidated by spectroscopic methods (including MS, 1D and 2D–NMR) and comparison with values from the literature. From the n-hexane extract, nine compounds including lupeol (1), betulin (2), betulinic acid (3), oleanolic acid (4), corosolic acid (5), -sitosterol (6), beta-sitosterol 3-O- beta-D-glucopyranoside (7), stigmast-5-ene-3beta-O-(6-O-hexadecanoyl-beta-D-glucopyranoside) (8), and stigmast-4-ene-3-one (9) were isolated and identified. \\nResults: The results of the alpha-glucosidase inhibitory activity showed thatcorosolic acid (5) and oleanolic acid (4) were the most potent, with IC50 values of 17.86 +/- 0.42 and 18.82 +/- 0.59 ug/mL, respectively. Five of the other seven compounds exhibited inhibitory activity with IC50 values below 100 ug/mL, and higher than the positive control acarbose (127.64 +/- 0.64 ug/mL). \\n \",\"PeriodicalId\":285953,\"journal\":{\"name\":\"Science and Technology Development Journal\",\"volume\":\"66 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-01-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science and Technology Development Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32508/STDJ.V22I1.1009\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science and Technology Development Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32508/STDJ.V22I1.1009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4
摘要
前言:本文对生长在CanGio红树林中的柳杉进行了调查。本研究报道了从littorea Lumnitzera叶片中分离的化合物的分离、表征和α -葡萄糖苷酶抑制活性的评价。方法:采用质谱、一维、二维核磁共振等波谱方法对其结构进行鉴定,并与文献值进行比较。从正己烷提取液中分离鉴定出九种化合物,分别为鹿皮醇(1)、白桦素(2)、白桦酸(3)、齐墩果酸(4)、花椰果酸(5)、-谷甾醇(6)、-谷甾醇3-o - β - d -葡萄糖苷(7)、柱头甾-5-烯-3-o -(6- o -hexadecanoyl- β - d -glucopyranoside)(8)和柱头甾-4-烯-3-one(9)。结果:α -葡萄糖苷酶抑制活性结果显示,花椰菜酸(5)和齐墩果酸(4)的抑制作用最强,IC50值分别为17.86 +/- 0.42和18.82 +/- 0.59 ug/mL。其中5个化合物的IC50值低于100 ug/mL,均高于阳性对照阿卡波糖(127.64 +/- 0.64 ug/mL)。
In vitro α-glucosidase inhibitory activity of compounds isolated from mangrove Lumnitzera littorea leaves
Introduction: Lumnitzera littorea grown at CanGio Mangrove Forest has been investigated. The present study reports the isolation, characterization and evaluation of the alpha-glucosidase inhibitory activity of isolated compounds from Lumnitzera littorea leaves.
Methods: Their structures were elucidated by spectroscopic methods (including MS, 1D and 2D–NMR) and comparison with values from the literature. From the n-hexane extract, nine compounds including lupeol (1), betulin (2), betulinic acid (3), oleanolic acid (4), corosolic acid (5), -sitosterol (6), beta-sitosterol 3-O- beta-D-glucopyranoside (7), stigmast-5-ene-3beta-O-(6-O-hexadecanoyl-beta-D-glucopyranoside) (8), and stigmast-4-ene-3-one (9) were isolated and identified.
Results: The results of the alpha-glucosidase inhibitory activity showed thatcorosolic acid (5) and oleanolic acid (4) were the most potent, with IC50 values of 17.86 +/- 0.42 and 18.82 +/- 0.59 ug/mL, respectively. Five of the other seven compounds exhibited inhibitory activity with IC50 values below 100 ug/mL, and higher than the positive control acarbose (127.64 +/- 0.64 ug/mL).