Abstract Microluside A 4 (19-para-hydroxy benzoyloxy-O-β-d-cellobiosyl), 5 (30-para-hydroxy benzoyloxy-O-β-d-glucopyranosyl) xanthone (1) is a unique O-glycosylated disubstituted xanthone isolated from the broth culture of Micrococcus sp. \EG45\ cultivated from the Red Sea sponge Spheciospongia vagabunda. The structure of microluside A was determined by 1D- and 2D-NMR techniques as well as high resolution tandem mass spectrometry. The antimicrobial activity evaluation showed that 1 exhibited antibacterial potential against Enterococcus faecalis \JH212\ and Staphylococcus aureus \NCTC\ 8325 with \MIC\ values of 10 and 13 μM, respectively.
%0 Journal Article
%1 Eltamany20144939
%A Eltamany, Enas E.
%A Abdelmohsen, Usama Ramadan
%A Ibrahim, Amany K.
%A Hassanean, Hashim A.
%A Hentschel, Ute
%A Ahmed, Safwat A.
%D 2014
%J Bioorganic & Medicinal Chemistry Letters
%K myown
%N 21
%P 4939 - 4942
%R http://dx.doi.org/10.1016/j.bmcl.2014.09.040
%T New antibacterial xanthone from the marine sponge-derived Micrococcus sp. \EG45\
%U http://www.sciencedirect.com/science/article/pii/S0960894X14009822
%V 24
%X Abstract Microluside A 4 (19-para-hydroxy benzoyloxy-O-β-d-cellobiosyl), 5 (30-para-hydroxy benzoyloxy-O-β-d-glucopyranosyl) xanthone (1) is a unique O-glycosylated disubstituted xanthone isolated from the broth culture of Micrococcus sp. \EG45\ cultivated from the Red Sea sponge Spheciospongia vagabunda. The structure of microluside A was determined by 1D- and 2D-NMR techniques as well as high resolution tandem mass spectrometry. The antimicrobial activity evaluation showed that 1 exhibited antibacterial potential against Enterococcus faecalis \JH212\ and Staphylococcus aureus \NCTC\ 8325 with \MIC\ values of 10 and 13 μM, respectively.
@article{Eltamany20144939,
abstract = {Abstract Microluside A [4 (19-para-hydroxy benzoyloxy-O-β-d-cellobiosyl), 5 (30-para-hydroxy benzoyloxy-O-β-d-glucopyranosyl) xanthone (1)] is a unique O-glycosylated disubstituted xanthone isolated from the broth culture of Micrococcus sp. \{EG45\} cultivated from the Red Sea sponge Spheciospongia vagabunda. The structure of microluside A was determined by 1D- and 2D-NMR techniques as well as high resolution tandem mass spectrometry. The antimicrobial activity evaluation showed that 1 exhibited antibacterial potential against Enterococcus faecalis \{JH212\} and Staphylococcus aureus \{NCTC\} 8325 with \{MIC\} values of 10 and 13 μM, respectively. },
added-at = {2015-04-30T14:02:44.000+0200},
author = {Eltamany, Enas E. and Abdelmohsen, Usama Ramadan and Ibrahim, Amany K. and Hassanean, Hashim A. and Hentschel, Ute and Ahmed, Safwat A.},
biburl = {https://www.bibsonomy.org/bibtex/270b6a0d69856113a73b57789061b3bf2/abdelmohsen},
doi = {http://dx.doi.org/10.1016/j.bmcl.2014.09.040},
interhash = {6131fd5b9eade4a19314e558d37dff46},
intrahash = {70b6a0d69856113a73b57789061b3bf2},
issn = {0960-894X},
journal = {Bioorganic & Medicinal Chemistry Letters },
keywords = {myown},
number = 21,
pages = {4939 - 4942},
timestamp = {2015-04-30T14:02:44.000+0200},
title = {New antibacterial xanthone from the marine sponge-derived Micrococcus sp. \{EG45\} },
url = {http://www.sciencedirect.com/science/article/pii/S0960894X14009822},
volume = 24,
year = 2014
}