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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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Marilines A-C: Novel phthalimidines from the sponge-derived fungus Stachylidium sp

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Autor
Almeida, C.; Hemberger, Y.; Schmitt, S. M.; Bouhired, S.; Natesan, L.; Kehraus, S.; Dimas, K.; Gütschow, M.; Bringmann, G.; König, G. M.
Datum
2012
DOI
10.1002/chem.201103278
Schlagwort
CD spectroscopy
human leukocyte elastase
marine fungus
phthalimidine
Stachylidium
Elastase
Biochemistry
Circular dichroism spectroscopy
Enantiomers
Quantum chemistry
Chemical compounds
leukocyte elastase
mariline A
mariline B
mariline C
phthalimide derivative
animal
article
Ascomycetes
chemical structure
chemistry
drug antagonism
human
isolation and purification
microbiology
nuclear magnetic resonance
sponge (Porifera)
Animals
Ascomycota
Humans
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Phthalimides
Porifera
Zur Langanzeige
Zusammenfassung
A marine-derived fungus of the genus Stachylidium was isolated from the sponge Callyspongia cf. C. flammea. Chemical investigation of the bioactive fungal extract led to the isolation of the novel phthalimidine derivatives marilines A 1 (1 a), A 2 (1 b), B (2), and C (3). The absolute configurations of the enantiomeric compounds 1 a and 1 b were assigned by a combination of experimental circular dichroism (CD) investigations and quantum chemical CD calculations. The skeleton of marilines is most unusual, and its biosynthesis is suggested to require uncommon biochemical reactions in fungal secondary metabolism. Both enantiomers, marilines A 1 (1 a) and A 2 (1 b), inhibited human leukocyte elastase (HLE) with an IC 50 value of 0.86 μM. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
URI
http://hdl.handle.net/11615/25477
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