Mahmoud A. Al-Qudah, Abdulrahman G. Alhamzani, Hala I. Al-Jaber, Zain F. Migdadi, Sultan T. Abu Orabi and Abbas I. Alakhras
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The known compounds included calycopterine (<strong>3</strong>), 17α-hydroxycabraleahydroxylactone (<strong>4</strong>), cleocarpanol (<strong>5</strong>), ambylone (<strong>6</strong>), β-sitosterol (<strong>7</strong>), β-sitosteryl glucoside (<strong>8</strong>), isorhamnetin-3-<em>O</em>-rhamnoside (<strong>9</strong>), kaempferol-3,7-<em>O</em>-dirhamnose (<strong>10</strong>) and 3′-<em>O</em>-methylquercetin-3,7-di-<em>O</em>-rhamnopyranoside (<strong>11</strong>). Structural elucidation of all isolated compounds was based on thorough investigation of their spectroscopic data including NMR (1D and 2D), HRESIMS, IR, and UV-Vis spectroscopy. LC-MS/MS analysis <em>versus</em> a selected set of authentic samples led to the detection of 21 constituents, including <strong>9</strong> of the isolated compounds. Antioxidant activities of isolated pure compounds were assessed individually and compared to ascorbic acid and α-tocopherol using DPPH<small><sup>˙</sup></small> and ABTS<small><sup>˙+</sup></small> assay methods. Compounds <strong>9–11</strong> showed strong antioxidant activities whereas compounds <strong>4–6</strong> exhibited low activity. New compounds <strong>1</strong> and <strong>2</strong> demonstrated moderate DPPH<small><sup>˙</sup></small> radical scavenging power (IC<small><sub>50</sub></small> = 14.70 ± 2.52 and 77.90 ± 3.77 μg mL<small><sup>−1</sup></small>, respectively) and a moderate ABTS<small><sup>˙+</sup></small> scavenging effect (IC<small><sub>50</sub></small> = 22.6 ± 0.04 and 78.30 ± 1.13 μg mL<small><sup>−1</sup></small>).</p>","PeriodicalId":102,"journal":{"name":"RSC Advances","volume":" 46","pages":" 38577-38584"},"PeriodicalIF":4.6000,"publicationDate":"2025-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/ra/d5ra04113a?page=search","citationCount":"0","resultStr":"{\"title\":\"Triterpenes isolated from Cleome amblyocarpa: evaluation of antioxidant potential\",\"authors\":\"Mahmoud A. Al-Qudah, Abdulrahman G. Alhamzani, Hala I. Al-Jaber, Zain F. Migdadi, Sultan T. Abu Orabi and Abbas I. 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引用次数: 0
摘要
对生长在约旦的野生木香的化学成分进行了研究,分离出两个新的达玛烷三萜,并对其他9个已知化合物进行了结构鉴定。新化合物鉴定为17-hydroxyambylone(1)和15β-acetoxy-17α-hydroxycabralealactone(2)。已知化合物包括花萼黄碱(3)、17α-羟基苦参内酯(4)、cleocarpanol(5)、ambylone(6)、β-谷甾醇(7)、β-谷甾醇基葡萄糖苷(8)、异鼠李糖素-3- o -鼠李糖苷(9)、山奈酚-3,7- o -鼠李糖(10)和3′- o -甲基槲皮素-3,7-二- o -鼠李糖pyranoside(11)。所有分离化合物的结构解析是基于对其光谱数据的彻底调查,包括核磁共振(1D和2D), hresms, IR和UV-Vis光谱。LC-MS/MS分析与选定的一组真实样品相比较,检测到21种成分,其中包括9种分离化合物。采用DPPH˙和ABTS˙+测定方法,对分离纯化化合物的抗氧化活性进行了单独评估,并与抗坏血酸和α-生育酚进行了比较。化合物9 ~ 11表现出较强的抗氧化活性,而化合物4 ~ 6表现出较低的抗氧化活性。新化合物1和2具有中等的DPPH˙自由基清除能力(IC50分别为14.70±2.52和77.90±3.77 μg mL−1)和中等的ABTS˙+清除能力(IC50分别为22.6±0.04和78.30±1.13 μg mL−1)。
Triterpenes isolated from Cleome amblyocarpa: evaluation of antioxidant potential
Investigation of the chemical constituents of Cleome amblyocarpa growing wild in Jordan resulted in the isolation and structural elucidation of two new dammarane triterpenes along with 9 other known compounds. The new compounds were identified as 17-hydroxyambylone (1) and 15β-acetoxy-17α-hydroxycabralealactone (2). The known compounds included calycopterine (3), 17α-hydroxycabraleahydroxylactone (4), cleocarpanol (5), ambylone (6), β-sitosterol (7), β-sitosteryl glucoside (8), isorhamnetin-3-O-rhamnoside (9), kaempferol-3,7-O-dirhamnose (10) and 3′-O-methylquercetin-3,7-di-O-rhamnopyranoside (11). Structural elucidation of all isolated compounds was based on thorough investigation of their spectroscopic data including NMR (1D and 2D), HRESIMS, IR, and UV-Vis spectroscopy. LC-MS/MS analysis versus a selected set of authentic samples led to the detection of 21 constituents, including 9 of the isolated compounds. Antioxidant activities of isolated pure compounds were assessed individually and compared to ascorbic acid and α-tocopherol using DPPH˙ and ABTS˙+ assay methods. Compounds 9–11 showed strong antioxidant activities whereas compounds 4–6 exhibited low activity. New compounds 1 and 2 demonstrated moderate DPPH˙ radical scavenging power (IC50 = 14.70 ± 2.52 and 77.90 ± 3.77 μg mL−1, respectively) and a moderate ABTS˙+ scavenging effect (IC50 = 22.6 ± 0.04 and 78.30 ± 1.13 μg mL−1).
期刊介绍:
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