5 research outputs found
Four New Anthraquinones with Histone Deacetylase Inhibitory Activity from Ventilago denticulata Roots
Chromatographic separation of the crude extracts from the roots of Ventilago denticulata led to the isolation of four new anthraquinones, ventilanones L–O (1–4), together with eight known anthraquinones (5–12). Their structures were elucidated by spectroscopic methods (UV, IR, 1H NMR, 13C NMR, and 2D NMR) and mass spectrometry (MS), as well as comparison of their spectroscopic data with those reported in the literature. HDACs inhibitory activity evaluation resulted that compound 2 exhibited moderate antiproliferative activity against HeLa and A549 cell lines but nontoxic to normal cell. Molecular docking indicated the phenolic functionality of 2 plays crucial interactions with class II HDAC4 enzyme
Cytotoxic Aporphine Alkaloids from Leaves and Twigs of Pseuduvaria trimera (Craib)
From ethyl acetate-methanol extracts of leaves and twigs of Pseuduvaria trimera a new aporphine alkaloid; 8-hydroxy-1,4,5-trimethoxy-7-oxoaporphine or 8-hydroxyartabonatine C (1) was isolated, together with the known 1,2,3-trimethoxy-4,5-dioxo-6a,7-dehydroaporphine (ouregidione, 2). Their structures were elucidated by a combination of spectral methods; mainly 2D NMR; IR and MS. Compounds 1 and 2 exhibited cytotoxic activity with IC50 values of 26.36 ± 5.18 μM and 12.88 ± 2.49 μM, respectively, for human hepatocellular carcinoma HepG2 cells, and 64.75 ± 4.45 and 67.06 ± 3.5 μM, respectively, for human breast cancer MDA-MB231 cells. Both compounds displayed anti-cancer activity but less than that of doxorubicin; a conventional chemotherapeutic drug, the IC50 levels of which were 2.21 ± 1.72 and 1.83 ± 0.09 μM for HepG2 and MDA-MB231 cells, respectively
Terpenoids from the Root Bark of <i>Pterolobium macropterum</i>
Five new compounds, including pteroloterins
A–C (<b>1</b>, <b>3</b>, and <b>4</b>), 1β-acetoxytaepeenin
C (<b>2</b>), and 8aα-hydroxycadinenal (<b>5</b>), and 11 known compounds were isolated from the root bark of <i>Pterolobium macropterum</i>. All compounds were evaluated for
cytotoxicity against the cholangiocarcinoma cell lines. Compound <b>9</b> showed weak cytotoxicity against the KKU-M139 cell line
with an IC<sub>50</sub> value of 23.24 ± 0.18 μM and showed
no activity against normal cells