Dibenzocyclooctadiene lignans from Kadsura heteroclita.[Pubmed: 28457823]

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δ-Cadinene, Calarene and .δ-4-Carene from Kadsura heteroclita Essential Oil as Novel Larvicides Against Malaria, Dengue and Filariasis Mosquitoes.[Pubmed: 27151483]

Mosquitoes (Diptera: Culicidae) are major vectors of important pathogens and parasites. Malaria, dengue fever, yellow fever, filariasis, schistosomiasis and Japanese encephalitis cause millions of deaths every year. Mosquito control is being challenging due to the development of pesticide resistance and negative environmental concerns. In this scenario, plants employed in traditional Asian medicine may be alternative sources of newer and effective mosquitocides. In this research, we evaluated the larvicidal activity of Kadsura heteroclita leaf essential oil (EO) and its major chemical constituents (δ-Cadinene, Calarene and δ-4-Carene) against the malaria vector Anopheles stephensi, the dengue vector Aedes aegypti and the filariasis vector Culex quinquefasciatus. The chemical composition of the EO was analyzed by gas chromatography-mass spectroscopy. GC-MS revealed that the essential oil of K. heteroclita contained 33 compounds. The major chemical components were δ-Cadinene (18.3%), Calarene (14.8%) and δ-4-Carene (12.5%). The EO had a significant toxic effect against early third-stage larvae of An. stephensi, Ae. aegypti and Cx. quinquefasciatus, with LC50 values of 102.86, 111.79 and 121.97 µg/mL. The three major constituents extracted from the K. heteroclita EO were tested individually for acute toxicity against larvae of the three mosquito vectors. δ-Cadinene, Calarene and δ-4-Carene appeared most effective against An. stephensi (LC50 = 8.23, 12.34 and 16.37 µg/mL, r espectively) followed by Ae. aegypti (LC50 = 9.03, 13.33 and 17.91 µg/mL), and Cx. quinquefasciatus (LC50; = 9.86, 14.49 and 19.50 µg/mL). Overall, this study adds knowledge to develop newer and safer natural larvicides against malaria, dengue and filariasis mosquito.

A coumarin lignanoid from the stems of Kadsura heteroclita.[Pubmed: 25736995]

Coumarinlignan (1), possessing a unique coumarin-containing lignan skeleton, was isolated from the stems of Kadsura heteroclita. Its structure and absolute configuration were determined by spectroscopic techniques, especially 2D NMR and X-ray crystallographic data analyses. The proposed biosynthetic pathway is discussed. This new compound showed good anti-HBV activity against HBeAg and HBsAg, and moderate anti-fibrotic and neuroprotective activities.

Heteroclitins R-S: new dibenzocylooctadiene lignans from Kadsura heteroclita.[Pubmed: 25263981]

To study the dibenzocylooctadiene lignans from the stems of Kadsura heteroclita.

Two new bicyclic sesquiterpenes from the stems of Kadsura heteroclita.[Pubmed: 24784326]

Two new bicyclic sesquiterpenes, namely 6α,9α-dihydroxycadinan-4-en-3-one (1) and guai-3-en-10α-ol (2), together with one known sesquiterpene were isolated from the stems of Kadsura heteroclita, which is a Tujia ethnomedicine called 'Xue Tong'. Their structures were elucidated by using spectroscopic analyses and by comparing the NMR data with those reported previously.

[GC-MS study on fingerprint of volatile oil from Kadsura heteroclita].[Pubmed: 23451498]

To study the fingerprint of volatile oil from Kadsura heteroclita by GC-MS.

[Comparative study on macroscopic and microscopic identification of Celastrus aculeatus and Kadsura heteroclite].[Pubmed: 23213733]

To compare and identify Celastrus aculeatus and Kadsura heteroclita with pharmacognosy methods for analyzing the quality of the crude drug.

[A novel lignan dimer from stems of Kadsura heteroclita].[Pubmed: 20931848]

As a part of our search for bioactive material, the chemical investigation of the stems of Kadsura heteroclita led up to the isolation of a new lignan, heteroclitin R. The structure was elucidated on the basis of nuclear magnetic resonance spectroscopic data. Heteroclitin R was a new compound as a lignan dimer obtained from Schisandraceae family for the first time.

Bioactive triterpenoids from Kadsura heteroclita.[Pubmed: 20860030]

A phytochemical study of Kadsura heteroclita led to the isolation of eight triterpenoids, including two new compounds, named kadheterilactone A (1) and kadheterilactone B (2), as well as six known compounds, longipedlactone H (3), longipedlactone A (4), longipedlactone F (5), kadsuranic acid A (6), nigranoic acid (7), and schisandronic acid (8). Their structures were elucidated on the basis of spectroscopic methods, including 2D NMR techniques. The cytotoxic activities of 1-8 were tested against several tumor cell lines by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium hydrobromide (MTT) assay in vitro. As a result, 4 and 5 turned out to be significantly cytotoxic against Hep-G2 and Bel-7402 tumor cell lines. All compounds were also tested for inhibition on HIV-1 protease (PR) and reverse transcriptase (RT). Compounds 6 and 7 showed strong inhibition on HIV-1 PR, while 8 exhibited moderate activity, others were only weakly active. No compounds were active against HIV-1 RT.