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Total Synthesis and Stereochemical Assignment of Nostosin B.
- 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