Isolation, Characterization and Antiproliferative Activity of New Metabolites from the South African Endemic Red Algal Species Laurencia alfredensis

被引:12
作者
Dziwornu, Godwin A. [1 ]
Caira, Mino R. [1 ]
de la Mare, Jo-Anne [2 ]
Edkins, Adrienne L. [2 ]
Bolton, John J. [3 ,4 ]
Beukes, Denzil R. [5 ]
Sunassee, Suthananda N. [1 ,4 ,6 ]
机构
[1] Univ Cape Town, Dept Chem, ZA-7701 Rondebosch, South Africa
[2] Rhodes Univ, Dept Biochem & Microbiol, Biomed Biotechnol Res Unit, ZA-6140 Grahamstown, South Africa
[3] Univ Cape Town, Dept Biol Sci, ZA-7701 Rondebosch, South Africa
[4] Univ Cape Town, Marine Res Ma Re Inst, ZA-7701 Rondebosch, South Africa
[5] Univ Western Cape, Dept Pharmaceut Chem, Sch Pharm, ZA-7535 Bellville, South Africa
[6] Univ Cape Town, South African Med Res Council, Drug Discovery & Dev Res Unit, ZA-7701 Rondebosch, South Africa
来源
MOLECULES | 2017年 / 22卷 / 04期
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
labdane-type diterpenes; polyether triterpenes; cholestane-type ecdysteroids; glycolipid; antiproliferative activity; Rhodomelaceae; SULFUR-CONTAINING POLYBROMOINDOLES; MARINE NATURAL-PRODUCTS; BROMINATED INDOLES; ORGANIC-MOLECULES; IN-VITRO; BRONGNIARTII; RHODOMELACEAE; CONFIGURATION; DITERPENOIDS; SIMILIS;
D O I
10.3390/molecules22040513
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The marine red algae of the genus Laurencia have been widely studied for their structurally diverse and biologically active secondary metabolites. We report here the natural product investigation of the organic extract of a newly identified South African endemic species, Laurencia alfredensis. A sequence of column chromatography, preparative TLC and normal phase HPLC resulted in the isolation of eleven compounds comprising three labdane-type diterpenes (1-3), four polyether triterpenes (4-7), three cholestane-type ecdysteroids (8-10) and a glycolipid (11). Compounds 1-3, 5-8 and 10 have not previously been reported, while compound 9 is reported here for the first time from a natural source and the known compound 11 isolated for the first time from the genus Laurencia. The structural elucidation and the relative configuration assignments of the compounds were accomplished by extensive use of 1D- and 2D-NMR, HR-ESI-MS, UV and IR spectroscopic techniques, while the absolute configuration of compound 1 was determined by single-crystal X-ray diffraction analysis. All compounds were evaluated against the MDA-MB-231 breast and HeLa cervical cancer cell lines. Compound 2 exhibited low micromolar antiproliferative activity (IC50 = 9.3 mu M) against the triple negative breast carcinoma and compound 7 was similarly active (IC50 = 8.8 mu M) against the cervical cancer cell line.
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页数:16
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