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Two New Phenolic Amides from the Seeds of Pharbitis nil

Authors
Kim, KH[Kim, Ki Hyun]Choi, SU[Choi, Sang Un]Son, MW[Son, Mi Won]Lee, KR[Lee, Kang Ro]
Issue Date
Nov-2010
Publisher
PHARMACEUTICAL SOC JAPAN
Keywords
Pharbitis nil; Convolvulaceae; phenolic amide; pharnilatin A; pharnilatin B; cytotoxicity
Citation
CHEMICAL & PHARMACEUTICAL BULLETIN, v.58, no.11, pp.1532 - 1535
Indexed
SCIE
SCOPUS
Journal Title
CHEMICAL & PHARMACEUTICAL BULLETIN
Volume
58
Number
11
Start Page
1532
End Page
1535
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/73021
ISSN
0009-2363
Abstract
Two new phenolic amides, pharnilatins A (1) and B (2), were isolated from the seeds of Pharbitis nil. These new compounds possess a p-coumaroyl unit with a structurally unique side chain, (2S,3S)-2,3-dihydroxyputrescine. The chemical structures and absolute stereochemistries of the new compounds were determined on the basis of spectroscopic analyses including 1D- and 2D-NMR experiments and chemical reactions. Compounds 1 and 2 exhibited cytotoxicity against A549, SK-OV-3, SK-MEL-2, and HCT-15 human tumor cells. However, none of the compounds inhibited nitric oxide (NO) production in lipopolysaccharide (LPS)-activated microglia cells.
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