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Eur J Med Chem ; 46(1): 175-82, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21130542

ABSTRACT

Three new diterpenes Amijiol acetate (3), dolabellane, Dolabellatrienol (4), and dolastane, Amijiol-7, 10-diacetate (9) were isolated together with the previously described Pachydictyol A (1), Isopachydictyol A (2), 8ß-hydroxypachydictyol A (5), Amijiol (6), Isodictyohemiacetal (7) and Dictyol C (8) from the Red Sea brown alga Dictyota dichotoma var. implexa. The structures and relative stereochemistry of the new diterpenoids were proposed on the basis of their spectral data. Compounds 3 and 9 have potent activity against DNA damage, cytotoxicity against WI-38, HepG2, and MCF-7 cell lines, and antioxidant using ABTS and erythrocytes hemolysis.


Subject(s)
Antineoplastic Agents/pharmacology , Antioxidants/pharmacology , DNA Damage , Diterpenes/pharmacology , Phaeophyceae/chemistry , Animals , Antineoplastic Agents/chemistry , Antineoplastic Agents/isolation & purification , Antineoplastic Agents/toxicity , Antioxidants/chemistry , Antioxidants/isolation & purification , Antioxidants/toxicity , Benzothiazoles/pharmacology , Cell Line, Tumor , Cell Survival/drug effects , Chlorocebus aethiops , Diterpenes/chemistry , Diterpenes/isolation & purification , Diterpenes/toxicity , Erythrocytes/drug effects , Erythrocytes/immunology , Hemolysis/drug effects , Humans , Sulfonic Acids/pharmacology , Vero Cells
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