TY - JOUR
T1 - A new furan carboxamide and two potential precursors from a terrestrial streptomycete
AU - Naureen, Humaira
AU - Tala, Michel Feussi
AU - Shaaban, Khaled A.
AU - Shaaban, Mohamed
AU - Schüffler, Anja
AU - Laatsch, Hartmut
PY - 2017
Y1 - 2017
N2 - Three new bioactive metabolites, 1,6-dihydroxy-2-methyl-heptan-4-one (1), 4-hydroxy-1-(2-methyl-oxiranyl)-pentan-2-one (2), and 2-(2-hydroxy-propyl)-4-methylfuran-3-carboxylic acid amide (3) were isolated from the terrestrial Streptomyces sp. isolate ANK245, along with the new microbial constituent p-vinylanisol (4a) and the known metabolites p-vinyl-phenol (4b) and phenethyl alcohol. Analysis of the nonpolar part of the extract by gas chromatography/mass spectrometry (GC-MS) provided further evidence for tetradecanoic acid, 9-octadecenoic acid, hexadecanoic acid, 2-methoxy-4-vinylphenol (4c), 4-hydroxy-3-methoxy-benzaldehyde, o-hydroxybiphenyl, and 1,5,9-trimethyl-4,8,13-cyclotetradecatrien-1,3-diol (5). Structures 1-3 of the new compounds were elucidated by nuclear magnetic resonance (NMR) and NMR spectroscopy, but mass spectrometry (MS) techniques and their absolute configuration were determined by density functional theory (DFT) calculations and Mosher derivatisation. Their antimicrobial and cytotoxic activities were evaluated in comparison with the crude bacterial extract.
AB - Three new bioactive metabolites, 1,6-dihydroxy-2-methyl-heptan-4-one (1), 4-hydroxy-1-(2-methyl-oxiranyl)-pentan-2-one (2), and 2-(2-hydroxy-propyl)-4-methylfuran-3-carboxylic acid amide (3) were isolated from the terrestrial Streptomyces sp. isolate ANK245, along with the new microbial constituent p-vinylanisol (4a) and the known metabolites p-vinyl-phenol (4b) and phenethyl alcohol. Analysis of the nonpolar part of the extract by gas chromatography/mass spectrometry (GC-MS) provided further evidence for tetradecanoic acid, 9-octadecenoic acid, hexadecanoic acid, 2-methoxy-4-vinylphenol (4c), 4-hydroxy-3-methoxy-benzaldehyde, o-hydroxybiphenyl, and 1,5,9-trimethyl-4,8,13-cyclotetradecatrien-1,3-diol (5). Structures 1-3 of the new compounds were elucidated by nuclear magnetic resonance (NMR) and NMR spectroscopy, but mass spectrometry (MS) techniques and their absolute configuration were determined by density functional theory (DFT) calculations and Mosher derivatisation. Their antimicrobial and cytotoxic activities were evaluated in comparison with the crude bacterial extract.
KW - Cd calculations
KW - Furan carboxamide
KW - Terrestrial Streptomyces sp
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U2 - 10.1515/znb-2016-0202
DO - 10.1515/znb-2016-0202
M3 - Article
AN - SCOPUS:85018574647
SN - 0932-0776
VL - 72
SP - 175
EP - 182
JO - Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences
JF - Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences
IS - 3
ER -