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Nat Prod Res ; 32(17): 2001-2007, 2018 Sep.
Article in English | MEDLINE | ID: mdl-28793804

ABSTRACT

Eight compounds were isolated from the leaves of Clerodendrum inerme, including one new rearranged abietane diterpene, crolerodendrum B (1). Their structures were determined by means of spectroscopic methods including one-dimensional and two-dimensional nuclear magnetic resonance (1-D and 2-DNMR), high-resolution electrospray ionisation mass spectrometry (HR-ESI-MS) and circular dichroism (CD). The DPPH radical scavenging and cytotoxic activities of isolated compounds against MCF7 (breast), HCT116 (colon) and B16F10 (melanoma) cancer cell lines were evaluated. Compounds 1, 3 and 4 exhibited strong DPPH radical-scavenging effects (ED50 values of 17.6 ± 2.1, 10.1 ± 0.8 and 11.3 ± 0.3 µM, respectively) and 4 showed strong cytotoxicity against the HCT116 cell line (IC50 = 3.46 ± 0.01 µM).


Subject(s)
Abietanes/chemistry , Abietanes/pharmacology , Clerodendrum/chemistry , Antioxidants/chemistry , Antioxidants/isolation & purification , Cell Line, Tumor , Cytotoxins/chemistry , Cytotoxins/isolation & purification , Cytotoxins/pharmacology , Free Radical Scavengers/chemistry , Free Radical Scavengers/pharmacology , HCT116 Cells , Humans , Lamiaceae/chemistry , MCF-7 Cells , Molecular Structure , Structure-Activity Relationship
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