| In vitro: |
| Chem Pharm Bull (Tokyo). 2009 Nov;57(11):1227-30. | | The constituents and their bioactivities of Houttuynia cordata.[Pubmed: 19881272] |
METHODS AND RESULTS:
Chemical investigation on the whole plant of Houttuynia cordata has resulted in the isolation of two new compounds, named as houttuynoside A (1) and houttuynamide A (2), together with thirty-eight known compounds. The structures of 1 and 2 were elucidated on the basis of spectroscopic analysis. In the inhibitory effects on herpes simplex virus type 1 (HSV-1) assay, Norcepharadione B (10) showed good inhibitory activity against the replication of HSV-1. In addition, the antioxidant and antityrosinase activities of some isolated compounds were also evaluated.
CONCLUSIONS:
Among these compounds, quercitrin (25) and quercetin-3-O-beta-D-galactopyranoside (26) showed excellent 2,2-diphenyl-1-picrylhydrazyl radical-scavenging property with IC50 values of 31 and 63 microM, respectively. Cepharadione B (9) exhibited strong tyrosinase inhibitory activity with an IC50 value of 170 microM. | | Arch Pharm Res. 2001 Dec;24(6):518-21. | | Cytotoxic alkaloids from Houttuynia cordata.[Pubmed: 11794526] |
METHODS AND RESULTS:
Six bioactive alkaloids, aristolactam B(1), piperolactam A(2), aristolactam A(3), Norcepharadione B(4), cepharadione B(5) and splendidine(6) were isolated by bioactivity-guided fractionation of a methanolic extract of the aerial part of Houttuynia cordata.
CONCLUSIONS:
Several of them exhibited significant cytotoxicity against five human tumor cell lines (A-549, SK-OV-3, SK-MEL-2, XF-498 and HCT-15) in vitro. | | Chinese Journal of Natural Medicines, 2011, 9(6):425-8. | | Alkaloids from Houttuynia cordata and Their Antiplatelet Aggregation Activities.[Reference: WebLink] | | To study the chemical constituents from Houttuynia cordata and to test their antiplatelet aggregation activities.Methods The chemical constituents were isolated and purified by silica gel column chromatography and their structures were elucidated on the basis of spectral analysis. The antiplatelet aggregation activities were evaluated by Born's method, using rat PRP induced by ADP and thrombin.ResultsNine alkaloids were isolated and their structures were identified as Norcepharadione B (1), 4, 5-dioxodehydroasimilobine (2), cepharadione B (3), aristololactam B II (4), aristololactam A II (5), sauristolactam (6), piperolactam A (7), splendidine (8), and aristololactam F II (9). Antiplatelet aggregation test indicated significant inhibitory activities of compounds 1, 2, 4–7, 9 induced by ADP and 1, 2, 4, 7 induced by thrombin.Conclusion Compounds 2, 6, 7, 9 were isolated from the genus Houttuynia for the first time. Compounds 1, 2, 4, 7 showed significant inhibitory effects on both ADP-induced and thrombin-induced platelet aggregation. |
|
Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.IF=36.216(2019)
Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.IF=22.415(2019)
Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.IF=14.548(2019)
ACS Nano. 2018 Apr 24;12(4): 3385-3396. doi: 10.1021/acsnano.7b08969.IF=13.903(2019)
Nature Plants. 2016 Dec 22;3: 16206. doi: 10.1038/nplants.2016.205.IF=13.297(2019)
Sci Adv. 2018 Oct 24;4(10): eaat6994. doi: 10.1126/sciadv.aat6994.IF=12.804(2019)