{"title":"Sandoricum koetjape 叶子中的环木菠萝烷类三萜及其对 α-葡萄糖苷酶抑制活性的功效。","authors":"Tai-Xuan-Hoa Hang, Suekanya Jarupinthusophon, Rita Hairani, Van-Kieu Nguyen, Warinthorn Chavasiri","doi":"10.1007/s11418-023-01778-8","DOIUrl":null,"url":null,"abstract":"<div><p>The preliminary α-glucosidase inhibitory activity of the methanol extract of the leaves of <i>Sandoricum koetjape</i> Merr. exhibited promising results. The leaves was extracted with methanol to obtain\nthe methanol extract that was continuedly partitioned with hexane and ethyl acetate. Those fractions were further purified by various chromatographic techniques. The isolation of the potent fractions furnished two new cycloartane-type triterpenoids (<b>1</b> and <b>2</b>) along with ten known compounds (<b>3</b>–<b>12</b>). Their chemical structures were unambiguously established by interpretation of NMR (1 D & 2 D) and high-resolution electrospray ionization mass spectrometry (HRESIMS) data. Furthermore, the configurations of two new compounds were determined by using NOESY spectrum as well as comparing their NMR data to the reference. These compounds were evaluated against α-glucosidase. All tested compounds revealed potent activity with IC<sub>50</sub> value in the range of 2.17–49.2 µM compared to that of acarbose (IC<sub>50</sub> 100.6 µM). Compound <b>10</b> showed the lowest IC<sub>50</sub> value. This compound was reported as a mixed-type inhibitor. Compound <b>3</b> possessed the second strong activity with an IC<sub>50</sub> value of 14.0 μM and was further investigated on kinetic analysis which revealed as a mixed-type inhibitor with K<sub>i</sub> and K<sub>i</sub>′ values of 59.1 and 155.2 μM, respectively.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":654,"journal":{"name":"Journal of Natural Medicines","volume":"78 3","pages":"655 - 663"},"PeriodicalIF":2.5000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s11418-023-01778-8.pdf","citationCount":"0","resultStr":"{\"title\":\"Cycloartane-type triterpenoids from the leaves of Sandoricum koetjape and their efficacy on α-glucosidase inhibition activity\",\"authors\":\"Tai-Xuan-Hoa Hang, Suekanya Jarupinthusophon, Rita Hairani, Van-Kieu Nguyen, Warinthorn Chavasiri\",\"doi\":\"10.1007/s11418-023-01778-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The preliminary α-glucosidase inhibitory activity of the methanol extract of the leaves of <i>Sandoricum koetjape</i> Merr. exhibited promising results. The leaves was extracted with methanol to obtain\\nthe methanol extract that was continuedly partitioned with hexane and ethyl acetate. Those fractions were further purified by various chromatographic techniques. The isolation of the potent fractions furnished two new cycloartane-type triterpenoids (<b>1</b> and <b>2</b>) along with ten known compounds (<b>3</b>–<b>12</b>). Their chemical structures were unambiguously established by interpretation of NMR (1 D & 2 D) and high-resolution electrospray ionization mass spectrometry (HRESIMS) data. Furthermore, the configurations of two new compounds were determined by using NOESY spectrum as well as comparing their NMR data to the reference. These compounds were evaluated against α-glucosidase. All tested compounds revealed potent activity with IC<sub>50</sub> value in the range of 2.17–49.2 µM compared to that of acarbose (IC<sub>50</sub> 100.6 µM). Compound <b>10</b> showed the lowest IC<sub>50</sub> value. This compound was reported as a mixed-type inhibitor. Compound <b>3</b> possessed the second strong activity with an IC<sub>50</sub> value of 14.0 μM and was further investigated on kinetic analysis which revealed as a mixed-type inhibitor with K<sub>i</sub> and K<sub>i</sub>′ values of 59.1 and 155.2 μM, respectively.</p><h3>Graphical abstract</h3>\\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":654,\"journal\":{\"name\":\"Journal of Natural Medicines\",\"volume\":\"78 3\",\"pages\":\"655 - 663\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://link.springer.com/content/pdf/10.1007/s11418-023-01778-8.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Natural Medicines\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11418-023-01778-8\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Medicines","FirstCategoryId":"3","ListUrlMain":"https://link.springer.com/article/10.1007/s11418-023-01778-8","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Cycloartane-type triterpenoids from the leaves of Sandoricum koetjape and their efficacy on α-glucosidase inhibition activity
The preliminary α-glucosidase inhibitory activity of the methanol extract of the leaves of Sandoricum koetjape Merr. exhibited promising results. The leaves was extracted with methanol to obtain
the methanol extract that was continuedly partitioned with hexane and ethyl acetate. Those fractions were further purified by various chromatographic techniques. The isolation of the potent fractions furnished two new cycloartane-type triterpenoids (1 and 2) along with ten known compounds (3–12). Their chemical structures were unambiguously established by interpretation of NMR (1 D & 2 D) and high-resolution electrospray ionization mass spectrometry (HRESIMS) data. Furthermore, the configurations of two new compounds were determined by using NOESY spectrum as well as comparing their NMR data to the reference. These compounds were evaluated against α-glucosidase. All tested compounds revealed potent activity with IC50 value in the range of 2.17–49.2 µM compared to that of acarbose (IC50 100.6 µM). Compound 10 showed the lowest IC50 value. This compound was reported as a mixed-type inhibitor. Compound 3 possessed the second strong activity with an IC50 value of 14.0 μM and was further investigated on kinetic analysis which revealed as a mixed-type inhibitor with Ki and Ki′ values of 59.1 and 155.2 μM, respectively.
期刊介绍:
The Journal of Natural Medicines is an international journal publishing original research in naturally occurring medicines and their related foods and cosmetics. It covers:
-chemistry of natural products
-biochemistry of medicinal plants
-pharmacology of natural products and herbs, including Kampo formulas and traditional herbs
-botanical anatomy
-cultivation of medicinal plants.
The journal accepts Original Papers, Notes, Rapid Communications and Natural Resource Letters. Reviews and Mini-Reviews are generally invited.