OAK

Alkamides from the fruits of Piper longum and Piper nigrum displaying potent cell adhesion inhibition

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Author(s)
Lee, Seung WoongKim, Young KookKim, KoanhoiLee, Hyun SunChoi, Jung HoLee, Woo SongJun, Chang-DukPark, Jee HunLee, Jeong MinRho, Mun-Chual
Type
Article
Citation
Bioorganic and Medicinal Chemistry Letters, v.18, no.16, pp.4544 - 4546
Issued Date
2008-08
Abstract
Eight alkamides 1-8 were isolated by bioassay-guided isolation of EtOH extracts of the fruits of Piper longum and Piper nigum (Piperaceae). Their structures were elucidated by spectroscopic analysis ((1)H, (13)C NMR, and ESI-MS) as follows: guineensine (1), retrofracamide C (2), (2E,4Z,8E)-N-[9-(3,4-methylenedioxyphenyl)-2,4,8-nonatrienoyl]piperidine (3), pipernonaline (4), piperrolein B (5), piperchabamide D (6), pellitorin (7), and dehydropipernonaline (8). Their compounds 3-5, 7, and 8 inhibited potently the direct binding between sICAM-1 and LFA-1 of THP-1 cells in a dose-dependent manner, with IC(50) values of 10.7, 8.8, 13.4, 13.5, and 6.0 mu g/mL, respectively. (c) 2008 Elsevier Ltd. All rights reserved.
Publisher
Pergamon Press Ltd.
ISSN
0960-894X
DOI
10.1016/j.bmcl.2008.07.045
URI
https://scholar.gist.ac.kr/handle/local/17327
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