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Merck
  • Synthesis, cytotoxicity, and antioxidative activity of minor prenylated chalcones from Humulus lupulus.

Synthesis, cytotoxicity, and antioxidative activity of minor prenylated chalcones from Humulus lupulus.

Journal of natural products (2008-07-10)
Susanne Vogel, Jörg Heilmann
要旨

The minor hop ( Humulus lupulus) chalcones 3'-geranylchalconaringenin (3), 5'-prenylxanthohumol (4), flavokawin (5), xanthohumol H (8), xanthohumol C (9), and 1'',2''-dihydroxanthohumol C (10) were synthesized. The non-natural chalcones 3'-geranyl-6'-O-methylchalconaringenin (2), 3'-methylflavokawin (6), and 2'-O-methyl-3'-prenylchalconaringenin (7) were also synthesized. Cytotoxicity was investigated in HeLa cells, and these compounds all had IC 50 values comparable to xanthohumol (8.2-19.2 microM). The ORAC-fluorescein assay revealed potent antioxidative activity for 7 and 8 with 5.2 and 4.8 Trolox equivalents, respectively.

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製品内容

Sigma-Aldrich
カフェイン酸, ≥98.0% (HPLC)
Sigma-Aldrich
trans-フェルラ酸, 99%
Sigma-Aldrich
trans-フェルラ酸, ≥99%
Sigma-Aldrich
キサントフモール ホップ(Humulus lupulus)由来, ≥96% (HPLC)
Supelco
trans-フェルラ酸, matrix substance for MALDI-MS, ≥99.0% (HPLC)
Supelco
カフェイン酸, matrix substance for MALDI-MS, ≥99.0% (HPLC)
Supelco
trans-フェルラ酸, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
Supelco
カフェイン酸, matrix substance for MALDI-MS, ≥99.0% (HPLC), powder, light beige