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Merck
CN

ACAT inhibition of alkamides identified in the fruits of Piper nigrum.

Phytochemistry (2006-12-26)
Mun-Chual Rho, Seung Woong Lee, Hye Ran Park, Jung-Ho Choi, Ji Yun Kang, Koanhoi Kim, Hyun Sun Lee, Young Kook Kim
摘要

In this study, via a bioactivity-guided fractionation of MeOH extracts of the fruits of Piper nigrum, alkamide (5) and five previously-identified alkamides were isolated. Their structures were elucidated via spectroscopic analysis ((1)H, (13)C NMR and ESI-MS), as follows: retrofractamide A (1), pipercide (2), piperchabamide D (3), pellitorin (4), dehydroretrofractamide C (5) and dehydropipernonaline (6). The IC(50) values determined for the compounds were 24.5 (1), 3.7 (2), 13.5 (3), 40.5 (4), 60 (5) and 90 microM (6), according to the results of an ACAT enzyme assay system using rat liver microsomes. These compounds all inhibited cholesterol esterification in HepG2 cells.

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Sigma-Aldrich
胆固醇油酸酯, ≥98% (HPLC; detection at 205 nm)