Two new oleanane triterpenes from Maytenus hookeri
Two new triterpenes mayteneri A (1), mayteneri B (2), and seven known compounds (3-9) were isolated from stems of Maytenus hookeri Loes. The chemical structures of compounds 1 and 2 were established by 1D, 2D NMR, HRESIMS analysis, and calculating electronic circular dichroism (ECD). The structures...
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Published in | Journal of asian natural products research Vol. 26; no. 7; pp. 803 - 811 |
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Abstract | Two new triterpenes mayteneri A (1), mayteneri B (2), and seven known compounds (3-9) were isolated from stems of Maytenus hookeri Loes. The chemical structures of compounds 1 and 2 were established by 1D, 2D NMR, HRESIMS analysis, and calculating electronic circular dichroism (ECD). The structures of known compounds 3-9 were determined by comparison of their spectral with those reported. Compounds 4-7 showed significant inhibitory activity for NLRP3 inflammasome, with the IC
50
values of 2.36-3.44 μM. |
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AbstractList | Two new triterpenes mayteneri A (1), mayteneri B (2), and seven known compounds (3-9) were isolated from stems of Maytenus hookeri Loes. The chemical structures of compounds 1 and 2 were established by 1D, 2D NMR, HRESIMS analysis, and calculating electronic circular dichroism (ECD). The structures of known compounds 3-9 were determined by comparison of their spectral with those reported. Compounds 4-7 showed significant inhibitory activity for NLRP3 inflammasome, with the IC50 values of 2.36-3.44 mu M.
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. Two new triterpenes mayteneri A (1), mayteneri B (2), and seven known compounds (3-9) were isolated from stems of Maytenus hookeri Loes. The chemical structures of compounds 1 and 2 were established by 1D, 2D NMR, HRESIMS analysis, and calculating electronic circular dichroism (ECD). The structures of known compounds 3-9 were determined by comparison of their spectral with those reported. Compounds 4-7 showed significant inhibitory activity for NLRP3 inflammasome, with the IC50 values of 2.36–3.44 μM. Two new triterpenes mayteneri A (1), mayteneri B (2), and seven known compounds (3-9) were isolated from stems of Maytenus hookeri Loes. The chemical structures of compounds 1 and 2 were established by 1D, 2D NMR, HRESIMS analysis, and calculating electronic circular dichroism (ECD). The structures of known compounds 3-9 were determined by comparison of their spectral with those reported. Compounds 4-7 showed significant inhibitory activity for NLRP3 inflammasome, with the IC 50 values of 2.36-3.44 μM. Two new triterpenes mayteneri A ( ), mayteneri B ( ), and seven known compounds ( ) were isolated from stems of Loes. The chemical structures of compounds and were established by 1D, 2D NMR, HRESIMS analysis, and calculating electronic circular dichroism (ECD). The structures of known compounds - were determined by comparison of their spectral with those reported. Compounds - showed significant inhibitory activity for NLRP3 inflammasome, with the IC values of 2.36-3.44 M. |
Author | Li, Bo Li, Xiao-Li Yang, Quan-Yu Wei, Qiong Yang, Song-Xue Ma, Yan-Zi Zhang, Xing-Jie Xiao, Wei-Lie Wu, Xue-Wen Zhang, Rui-Han |
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Keywords | SESQUITERPENE ALKALOIDS ACID Celastraceae triterpenes Maytenus hookeri MEDICINE chemical composition anti-inflammatory activity |
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Snippet | Two new triterpenes mayteneri A (1), mayteneri B (2), and seven known compounds (3-9) were isolated from stems of Maytenus hookeri Loes. The chemical... Two new triterpenes mayteneri A ( ), mayteneri B ( ), and seven known compounds ( ) were isolated from stems of Loes. The chemical structures of compounds and... |
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SubjectTerms | anti-inflammatory activity Celastraceae chemical composition Chemical compounds Chemistry Chemistry, Applied Chemistry, Medicinal Circular dichroism Dichroism Inflammasomes Life Sciences & Biomedicine Maytenus Maytenus hookeri NMR Nuclear magnetic resonance Pharmacology & Pharmacy Physical Sciences Plant Sciences Science & Technology Triterpenes Two dimensional analysis |
Title | Two new oleanane triterpenes from Maytenus hookeri |
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