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authFullName_s : Marylene Chollet-Krugler
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Lichen butyrolactone derivatives disrupt oral bacterial membrane

Alaa Sweidan , Imen Smida , Marylene Chollet-Krugler , Aurélie Sauvager , Julien Vallet et al.
Fitoterapia, 2019, 137, pp.104274. ⟨10.1016/j.fitote.2019.104274⟩
Journal articles hal-02280840v1

Lichesterinic acid and its derivatives as pigmentation inhibitors

Joël Boustié , Marie-Dominique Galibert-Anne , Françoise Lohézic-Le Dévéhat , Marylene Chollet-Krugler , Sophie Tomasi et al.
France, Patent n° : WO 2013156738. 2013
Patents hal-01116115v1
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Two New Retigerane-Type Sesterterpenoids from the Lichen Leprocaulon microscopicum

Marion Millot , Marie Martin-De-Lassalle , Marylene Chollet-Krugler , Yves Champavier , Lengo Angèle Mambu et al.
Helvetica Chimica Acta, 2016, 99 (2), pp.169--173. ⟨10.1002/hlca.201500225⟩
Journal articles hal-01274108v1

Characterization and identification of mycosporines-like compounds in cyanolichens. Isolation of mycosporine hydroxyglutamicol from Nephroma laevigatum Ach.

Catherine Roullier , Marylene Chollet-Krugler , Eva-Maria Pferschy-Wenzig , Anne Maillard , Gerald N Rechberger et al.
Phytochemistry, 2011, 72 (11-12), pp.1348-57. ⟨10.1016/j.phytochem.2011.04.002⟩
Journal articles istex hal-00843484v1

Mycosporine-Like Compounds in Chlorolichens: Isolation from Dermatocarpon luridum and Dermatocarpon miniatum, and their Photoprotective Properties

Thi Thu Tram Nguyen , Marylene Chollet-Krugler , Françoise Lohézic-Le Dévéhat , Isabelle Rouaud , Joël Boustie et al.
Planta Medica Letters, 2015, 2 (01), pp.e1-e5. ⟨10.1055/s-0034-1396321⟩
Journal articles hal-01470074v1
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Mycosporine-Like Amino Acids (MAAs) in Time-Series of Lichen Specimens from Natural History Collections

Marylene Chollet-Krugler , Thi Thu Tram Nguyen , Aurélie Sauvager , Holger Thüs , Joël Boustie et al.
Molecules, 2019, 24 (6), pp.1070. ⟨10.3390/molecules24061070⟩
Journal articles hal-02087812v1
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New erythritol derivatives from the fertile form of Roccella montagnei

Thuc Huy Duong , Bui Linh Chi Huynh , Warinthorn Chavasiri , Marylene Chollet-Krugler , van Kieu Nguyen et al.
Phytochemistry, 2017, 137, pp.156-164. ⟨10.1016/j.phytochem.2017.02.012⟩
Journal articles hal-01501264v1

Multiple dual-mode centrifugal partition chromatography as an efficient method for the purification of a mycosporine from a crude methanolic extract of Lichina pygmaea

Catherine Roullier , Marylene Chollet-Krugler , Aurélie Bernard , Joël Boustie
Journal of Chromatography B Biomedical Sciences and Applications, 2009, 877 (22), pp.2067-2073. ⟨10.1016/j.jchromb.2009.05.040⟩
Journal articles hal-03015797v1

UV-protectant metabolites from lichens and their symbiotic partners.

Khanh-Hung Nguyen , Marylene Chollet-Krugler , Nicolas Gouault , Sophie Tomasi
Natural Product Reports, 2013, 30, pp.1490--1508. ⟨10.1039/c3np70064j⟩
Journal articles hal-01069965v1

A novel aryl-hydrazide from the marine lichen Lichina pygmaea: isolation, synthesis of derivatives, and cytotoxicity assays.

Catherine Roullier , Marylene Chollet-Krugler , Pierre van de Weghe , Françoise Lohézic-Le Dévéhat , Joël Boustie et al.
Bioorganic and Medicinal Chemistry Letters, 2010, 20 (15), pp.4582-6. ⟨10.1016/j.bmcl.2010.06.013⟩
Journal articles istex hal-00844454v1

Antibacterial activities of natural lichen compounds against Streptococcus gordonii and Porphyromonas gingivalis

Alaa Sweidan , Marylene Chollet-Krugler , Aurélie Sauvager , Pierre van de Weghe , Ali Chokr et al.
Fitoterapia, 2017, 121, pp.164-169. ⟨10.1016/j.fitote.2017.07.011⟩
Journal articles hal-01579650v1

Chemical constituents of the lichen Dermatocarpon luridum (With.) J.R.Laundon.

Thu Tram Nguyen , Marylene Chollet-Krugler , Aurélie Sauvager , Joël Boustie
Journées internationales AFERP & STOLON, May 2013, Bruxelles, Belgium
Conference papers hal-00873172v1
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A database of high-resolution MS/MS spectra for lichen metabolites

Damien Olivier-Jimenez , Marylene Chollet-Krugler , David Rondeau , Mehdi A Beniddir , Solenn Ferron et al.
Scientific Data , 2019, 6 (1), pp.294. ⟨10.1038/s41597-019-0305-1⟩
Journal articles hal-02397308v1

Acide lichestérinique et ses dérivés comme inhibiteurs de la pigmentation.

Joël Boustie , Marie-Dominique Galibert-Anne , Françoise Lohézic-Le Dévéhat , Marylene Chollet-Krugler , Sophie Tomasi et al.
France, N° de brevet: FR 12.53585 18 04 2012. 2012
Patents hal-00868403v1