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bursera hollickii/antikancerogena
Veza se sprema u međuspremnik
9 rezultati
Antitumor activity of Bursera schlechtendalii (burseraceae): isolation and structure determination of two new lignans.
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Antitumor agents from Bursera microphylla (Burseraceae). 3. Synthesis of burseran.
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Antitumor agents from Bursera microphylla (Burseraceae). II. Isolation of a new lignan-burseran.
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Antitumor agents from Bursera fagaroides (Burseraceae). (Beta-peltatin-A-methylether and 5'-desemethoxy-beta-peltatin-A-methylether).
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Antitumor agents from Bursera microphylla (Burseraceae) I. Isolation and characterization of deoxypodophyllotoxin.
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Cytotoxic podophyllotoxin type-lignans from the steam bark of Bursera fagaroides var. fagaroides.
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The hydroalcoholic extract of the steam bark of B. fagaroides var. fagaroides displayed potent cytotoxic activity against four cancer cell lines, namely KB (ED50 = 9.6 × 10(-2) μg/mL), PC-3 (ED50 = 2.5 × 10(-1) μg/mL), MCF-7 (ED50 = 6.6 μg/mL), and HF-6 (ED50 = 7.1 × 10(-3) μg/mL). This extract also
Cytotoxic activity and triterpenes content of nine Mexican species of Bursera.
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The genus Bursera (Burseraceae) is considered an interesting source of antitumour compounds. This study aimed to evaluate the cytotoxic activity of the dichloromethane-soluble extracts from the bark of nine Mexican Bursera species. The chemical components of the extracts were
An Ethnopharmacological, Phytochemical and Pharmacological Review on Lignans from Mexican Bursera spp.
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The genus Bursera belongs to the family Burseraceae and has been used in traditional Mexican medicine for treating various pathophysiological disorders. The most representative phytochemicals isolated from this genus are terpenoids and lignans. Lignans are phenolic metabolites known for their
Absolute configuration of phomactatriene diterpenoids obtained by Wagner-Meerwein rearrangement of epimeric verticillols.
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The epimeric diterpenes (+)-(1S,3E,7E,11S,12S)-verticilla-3,7-dien-12-ol (1), isolated from Bursera suntui, and (+)-(1S,3E,7E,11S,12R)-verticilla-3,7-dien-12-ol (2), isolated from Bursera kerberi, gave the same Wagner-Meerwein rearrangement product (-)-(1E,4Z,8Z,11S,12R)-phomacta-1,(15)4,8-triene
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