Annelise Lobstein

Prof. Annelise Lobstein


Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 February 2013 in Marine Drugs
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Journal Article
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JGJean-Baptiste Gallé
Jean-Baptiste Gallé
BABarthélémy Attioua
Barthélémy Attioua
MKMarcel Kaiser
Marcel Kaiser
ARAnne-Marie Rusig
Anne-Marie Rusig
ALAnnelise Lobstein
Annelise Lobstein
CVCatherine Vonthron-Senecheau
Catherine Vonthron-Senecheau
Organic extracts of 20 species of French seaweed have been screened against Trypanosoma brucei rhodesiense trypomastigotes, the parasite responsible for sleeping sickness. These extracts have previously shown potent antiprotozoal activities in vitro against Plasmodium falciparum and Leishmania donovani. The selectivity of the extracts was also evaluated by testing cytotoxicity on a mammalian L6 cell line. The ethyl acetate extract of the brown seaweed, Bifurcaria bifurcata, showed strong trypanocidal activity with a mild selectivity index (IC50 = 0.53 µg/mL; selectivity index (SI) = 11.6). Bio-guided fractionation led to the isolation of eleganolone, the main diterpenoid isolated from this species. Eleganolone contributes only mildly to the trypanocidal activity of the ethyl acetate extract (IC50 = 45.0 µM, SI = 4.0). However, a selective activity against P. falciparum erythrocytic stages in vitro has been highlighted (IC50 = 7.9 µM, SI = 21.6).

27 October 2016 in Molecules
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FAFlorence Auberon
Florence Auberon
Opeyemi Joshua OlatunjiOpeyemi Joshua Olatunji
Opeyemi Joshua Olatunji
SKStephanie Krisa
Stephanie Krisa
CACyril Antheaume
Cyril Antheaume
HGHERBETTE Gaëtan
HERBETTE Gaëtan
ALAnnelise Lobstein
Annelise Lobstein
Two new phenanthrene derivatives, a phenanthrenequinone named arundiquinone (1) and a 9,10-dihydrophenanthrene named arundigramin (2) together with a known lignin dimer (3) and seven known stilbenoids (4–10) were isolated from the aerial parts of the Asian orchid Arundina graminifolia. The structures of the isolated compounds were elucidated by spectroscopic methods, including extensive 1D, 2D NMR (heteronuclear single quantum coherence (HSQC), heteronuclear multiple-bond correlation spectroscopy (HMBC), and HR-ESI-MS techniques, as well as comparison with respective literature reports. The cytoprotective activity of the isolated compounds were evaluated for their ability to reduce beta amyloid induced toxicity on undifferentiated PC12 cells. Compound 8 showed moderate cytoprotective activity at 0.5 µmol/L (71% of cell viability) while the other compounds showed no significant activity at the highest concentration tested.

6 August 2014 in Phytochemical Analysis
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VCVeronika Cakova
Veronika Cakova
AUAurélie Urbain
Aurélie Urbain
CACyril Antheaume
Cyril Antheaume
NRNicole Rimlinger
Nicole Rimlinger
PWPatrick Wehrung
Patrick Wehrung
ALAnnelise Lobstein
Annelise Lobstein

24 October 2016 in Molecules
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Journal Article
Open access
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FAFlorence Auberon
Florence Auberon
Opeyemi Joshua OlatunjiOpeyemi Joshua Olatunji
Opeyemi Joshua Olatunji
HGHERBETTE Gaëtan
HERBETTE Gaëtan
DRDiamondra Raminoson
Diamondra Raminoson
CACyril Antheaume
Cyril Antheaume
ALAnnelise Lobstein
Annelise Lobstein
We report the first phytochemical study of the neotropical orchid Cyrtopodium paniculatum. Eight new compounds, including one phenanthrene 1, one 9,10-dihydro-phenanthrene 2, one hydroxybenzylphenanthrene 3, two biphenanthrenes 4–5, and three 9,10 dihydrophenanthrofurans 6–8, together with 28 known phenolic compounds, mostly stilbenoids, were isolated from the CH2Cl2 extract of its leaves and pseudobulbs. The structures of the new compounds were established on the basis of extensive spectroscopic methods.

21 August 2014
Verified
Journal Article
Closed access
ALAnnelise Lobstein
Annelise Lobstein
FMFrançoise Marinier
Françoise Marinier

1 January 2014
Verified
Journal Article
Closed access
FBFrédéric Bonté
Frédéric Bonté
BKBernard Kuballa
Bernard Kuballa
ALAnnelise Lobstein
Annelise Lobstein