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Total Synthesis and Stereochemical Assignment of Nostosin B.

Authors :
Wang X
Feng J
Xu Z
Ye T
Meng Y
Zhang Z
Source :
Marine drugs [Mar Drugs] 2017 Feb 27; Vol. 15 (3). Date of Electronic Publication: 2017 Feb 27.
Publication Year :
2017

Abstract

Nostosins A and B were isolated from a hydrophilic extract of Nostoc sp. strain from Iran, which exhibits excellent tryps inhibitory activity. Nostosin A was the most potent natural tripeptide aldehyde as trypsin inhibitor up to now. Both R- and S-2-hydroxy-4-(4-hydroxy-phenyl) butanoic acid (Hhpba) were prepared and incorporated into the total synthesis of nostosin B, respectively. Careful comparison of the NMR spectra and optical rotation data of synthetic nostosin B (1a and 1b) with the natural product led to the unambiguous identification of the R-configuration of the Hhpba fragment, which was further confirmed by co-injection with the authentic sample on HPLC using both reversed phase column and the chiral AD-RH column.

Details

Language :
English
ISSN :
1660-3397
Volume :
15
Issue :
3
Database :
MEDLINE
Journal :
Marine drugs
Publication Type :
Academic Journal
Accession number :
28264450
Full Text :
https://doi.org/10.3390/md15030058