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      Six New Phragmalin Limonoids from the Stems of Chukrasia tabularis A. Juss

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          Abstract

          Six new phragmalin limonoids, named moluccensin Z1 ( 1), moluccensin Z2 ( 2), carapanolide Y ( 3), tabulalin N ( 4), chukvelutilide A1 ( 5), and velutinasin J ( 6), as well as two known compounds, chukvelutilide A ( 7) and velutinasin D ( 8) were isolated from the stems of Chukrasia tabularis A. Juss. The structures of the new compounds 16 were confirmed by spectroscopic methods, including IR and HRESIMS, as well as 1D and 2D NMR, and by comparisons with the data of known analogues. All compounds were tested for α-glucosidase and acetylcholinesterase inhibitory activities. However, none of the compounds was active against α-glucosidase and acetylcholinesterase in vitro.

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          Meliaceous limonoids: chemistry and biological activities.

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            Phragmalin limonoids from Chukrasia tabularis.

            Six phragmalin limonoids, named tabulalin and tabulalides A-E, were isolated from the root bark of Chukrasia tabularis (Meliaceae). Their structures were determined by spectroscopic methods, and their antifeedant properties evaluated.
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              Chuktabrins A and B, two novel limonoids from the twigs and leaves of Chukrasia tabularis.

              Two novel limonoids, chuktabrin A (1), featuring the unique motifs of a 1,3-dioxolan-2-one and a 3,4-dihydro-2 H-pyran, and chuktabrin B (2), possessing an unprecedented polycyclic skeleton, were isolated from Chukrasia tabularis. The structures of 1 and 2 bearing a biosynthetically extended C3 and C2 unit at C-15, respectively, were elucidated on the basis of spectroscopic data, and that of 1 was confirmed by a single-crystal X-ray diffraction.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                20 November 2018
                November 2018
                : 23
                : 11
                : 3024
                Affiliations
                [1 ]Hainan Key Laboratory for Research and Development of Natural Products from Li Folk Medicine, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China; wangyancui.mail@ 123456163.com (Y.-C.W.); kongfandong@ 123456itbb.org.cn (F.-D.K.); wanghao@ 123456itbb.org.cn (H.W.); meiwenli@ 123456itbb.org.cn (W.-L.M.); zhaoyouxing@ 123456itbb.org.cn (Y.-X.Z.)
                [2 ]Institute of Tropical Agriculture and Forestry, Hainan University, Haikou 570228, China; zhiwu19831113@ 123456163.com
                Author notes
                [* ]Correspondence: daihaofu@ 123456itbb.org.cn ; Tel.: +86-898-6696-1869
                Article
                molecules-23-03024
                10.3390/molecules23113024
                6278448
                30463280
                65dd5281-e9a6-4684-ad0d-1449a9df8367
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 31 October 2018
                : 16 November 2018
                Categories
                Article

                chukrasia tabularis a. juss,meliaceae,phragmalin limonoid,α-glucosidase inhibition activity,acetylcholinesterase inhibitory activity

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