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Merck
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  • Prenylflavonoids and prenyl/alkyl-phloroacetophenones: synthesis and antitumour biological evaluation.

Prenylflavonoids and prenyl/alkyl-phloroacetophenones: synthesis and antitumour biological evaluation.

European journal of medicinal chemistry (2010-07-14)
P Basabe, M de Román, I S Marcos, D Diez, A Blanco, O Bodero, F Mollinedo, B G Sierra, J G Urones
摘要

Several prenylflavonoids have been synthesised and tested against human tumour cell lines. The prenyl unit has been geranyl or a labdane diterpene. These labdane-flavonoids have been synthesised for the first time. The antitumour activity increase with the prenylation at C-8 position. Twenty-three C and O-prenylated acylphloroglucinols have been synthesised as well. In this case the C-alkylation products have resulted, in general, more active.

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Sigma-Aldrich
山柰酚, ≥97.0% (HPLC)
Sigma-Aldrich
山柰酚, ≥90% (HPLC), powder
Sigma-Aldrich
柯因, ≥96.5%