J. Boustie

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Lichens—a promising source of bioactive secondary metabolites

M. Grube, J. Boustie, 2005, Plant Genetic Resources.

Bioactive lichen metabolites: alpine habitats as an untapped source

M. Grube, J. Boustie, S. Tomasi, 2011, Phytochemistry Reviews.

Halotolerance in Lichens: Symbiotic Coalition Against Salt Stress

M. Grube, P. Labrousse, J. Boustie, 2013 .

Cytotoxic activity of some lichen extracts on murine and human cancer cell lines.

J. Boustie, S. Tomasi, C. Bézivin, 2003, Phytomedicine : international journal of phytotherapy and phytopharmacology.

Photoprotective capacities of lichen metabolites: a joint theoretical and experimental study.

P. Trouillas, F. Di Meo, J. Boustie, 2012, Journal of photochemistry and photobiology. B, Biology.

NMR spectral data of salazinic acid isolated from some species of Parmotrema

E. Schenkel, V. Eifler-Lima, J. Boustie, 2000 .

Chemotaxonomic discrimination of lichen species using an infrared chalcogenide fibre optic sensor: a useful tool for on-field biosourcing

O. Sire, F. Charpentier, B. Bureau, 2016 .

ASAP‐MS and DART‐MS as ancillary tools for direct analysis of the lichen metabolome

J. Boustie, P. Jéhan, S. Ollivier, 2022, Phytochemical analysis : PCA.

Salazinic Acid-Derived Depsidones and Diphenylethers with α-Glucosidase Inhibitory Activity from the Lichen Parmotrema dilatatum

M. Beniddir, W. Chavasiri, J. Boustie, 2020, Planta Medica.

The inherent matrix properties of lichen metabolites in matrix-assisted laser desorption ionization time-of-flight mass spectrometry.

Antoine Denis, J. Boustie, P. Richomme, 2017, Rapid communications in mass spectrometry : RCM.

The inherent matrix properties of lichen metabolites in matrix-assisted laser desorption ionization time-of-flight mass spectrometry.

Antoine Denis, J. Boustie, P. Richomme, 2017, Rapid communications in mass spectrometry : RCM.

Chemical diversity of five coastal Roccella species from mainland France, the Scattered Islands, and São Tomé and Príncipe

J. Boustie, R. Poncet, Olivier Berry, 2020, Plant and Fungal Systematics.

Synthesis of an Exhaustive Library of Naturally Occurring Galf-Manp and Galp-Manp Disaccharides. Toward Fingerprinting According to Ring Size by Advanced Mass Spectrometry-Based IM-MS and IRMPD.

H. Rogniaux, V. Ferrières, J. Guégan, 2021, The Journal of organic chemistry.

Gas chromatographic analysis to compare the fatty acid composition of fifteen lichen species, with a focus on Stereocaulon

P. Legrand, J. Boustie, D. Delmail, 2016, The Lichenologist.

Protolichesterinic acid derivatives: α-methylene-γ-lactones as potent dual activators of PPARγ and Nrf2 transcriptional factors.

H. Authier, J. Boustie, B. Pipy, 2014, Bioorganic & medicinal chemistry letters.

Minor Pyranonaphthoquinones from the Apothecia of the Lichen Ophioparma ventosa.

D. Jacquemin, J. Boustie, J. Graton, 2016, Journal of natural products.

Ionic liquids based microwave-assisted extraction of lichen compounds with quantitative spectrophotodensitometry analysis.

D. Carrie, J. Boustie, S. Tomasi, 2011, Analytica chimica acta.

Isolation, semi-synthesis, free-radicals scavenging, and advanced glycation end products formation inhibitory constituents from Parmotrema tinctorum

A. Tiwari, J. Boustie, A. Anand, 2020, Journal of Asian natural products research.

Chemotype variations among lichen ecotypes of Umbilicaria aprina as revealed by LC-ESI-MS/MS: a survey of antioxidant phenolics

M. Gholami, J. Boustie, M. Sohrabi, 2020, Environmental Science and Pollution Research.

New insights into the Van Krevelen diagram: Automated molecular formula determination from HRMS for a large chemical profiling of lichen extracts

J. Boustie, P. Jéhan, S. Ollivier, 2022, Phytochemical analysis : PCA.

Mass spectrometry as a versatile ancillary technique for the rapid in situ identification of lichen metabolites directly from TLC plates

D. Ertz, J. Boustie, P. Le Pogam, 2017, The Lichenologist.

Matrix-Free UV-Laser Desorption Ionization Mass Spectrometry as a Versatile Approach for Accelerating Dereplication Studies on Lichens.

J. Boustie, P. Richomme, A. Schinkovitz, 2015, Analytical chemistry.

Stictic acid derivatives from the lichen Usnea articulata and their antioxidant activities.

J. Elix, P. Uriac, J. Boustie, 2007, Journal of natural products.

NMR reassignment of stictic acid isolated from a Sumatran lichen Stereocaulon montagneanum (Stereocaulaceae) with superoxide anion scavenging activities

J. Boustie, A. Bakhtiar, F. Ismed, 2016, Zeitschrift fur Naturforschung. C, Journal of biosciences.

Spatial mapping of lichen specialized metabolites using LDI-MSI: chemical ecology issues for Ophioparma ventosa

H. Rogniaux, J. Boustie, A. Geairon, 2016, Scientific Reports.

UPLC–MS/MS quantitative analysis and structural fragmentation study of five Parmotrema lichens from the Eastern Ghats

N. R. Rao, A. Tiwari, J. Boustie, 2018, Journal of pharmaceutical and biomedical analysis.

Anti-herpes virus activity of aporphine alkaloids.

J. Boustie, J. Montanha, L. Girre, 1995, Planta medica.

Xanthones of Lichen Source: A 2016 Update

J. Boustie, P. Le Pogam, 2016, Molecules.

Components and Antioxidant Activity of Hypericum tomentosum L. (Clusiaceae)

Z. Kabouche, O. Touafek, C. Bruneau, 2012 .

Comprehensive Analysis of Secondary Metabolites in Usnea longissima (Lichenized Ascomycetes, Parmeliaceae) Using UPLC-ESI-QTOF-MS/MS and Pro-Apoptotic Activity of Barbatic Acid

A. Tiwari, B. Sridhar, J. Boustie, 2019, Molecules.

Eumitrins C-E: Structurally diverse xanthone dimers from the vietnamese lichen Usnea baileyi.

G. Genta‐Jouve, J. Gallard, M. Beniddir, 2019, Fitoterapia.

Mycosporine-Like Amino Acids (MAAs) in Time-Series of Lichen Specimens from Natural History Collections

H. Thüs, J. Boustie, Thi Thu Tram Nguyen, 2019, Molecules.

Comparison of the anti-herpes simplex virus activities of propolis and 3-methyl-but-2-enyl caffeate.

J. Boustie, F. Sauvager, M. Cormier, 1994, Journal of natural products.

Axenic culture and biosynthesis of secondary compounds in lichen symbiotic fungi, the Parmeliaceae

J. C. Zamora, C. Ruibal, A. Crespo, 2020, Symbiosis.

Imbricaric Acid and Perlatolic Acid: Multi-Targeting Anti-Inflammatory Depsides from Cetrelia monachorum

O. Werz, A. Atanasov, E. Heiss, 2013, PloS one.

A degraded limonoid from Fagaropsis glabra

J. Gleye, J. Boustie, I. Fourasté, 1990 .

Separation of a mixture of paraconic acids from Cetraria islandica (L.) Ach. employing a fluorous tag—catch and release strategy

P. Uriac, J. Boustie, David Horhant, 2007 .

Further terpenoids from Euphorbia tirucalli.

G. Genta‐Jouve, M. Beniddir, W. Chavasiri, 2019, Fitoterapia.

Analysis of Lichen Metabolites, a Variety of Approaches

G. Herbette, J. Boustie, Pierre Le Pogam, 2015 .

Synthesis and Anti-HSV-1 Activity of New 3-Amino-3-Arylpropionic Acid Esters

S. Rault, J. Boustie, P. Dallemagne, 1996 .

DP4-Assisted Structure Elucidation of Isodemethylchodatin, a New Norlichexanthone Derivative Meager in H-Atoms, from the Lichen Parmotrema tsavoense

M. Beniddir, W. Chavasiri, J. Boustie, 2019, Molecules.

New erythritol derivatives from the fertile form of Roccella montagnei.

P. Hansen, H. Thüs, W. Chavasiri, 2017, Phytochemistry.

Which Specialized Metabolites Does the Native Subantarctic Gastropod Notodiscus hookeri Extract from the Consumption of the Lichens Usnea taylorii and Pseudocyphellaria crocata?

J. Boustie, M. Charrier, P. Le Pogam, 2017, Molecules.

Synthesis and cytotoxic activities of usnic acid derivatives.

J. Delcros, P. Uriac, J. Boustie, 2008, Bioorganic & medicinal chemistry.

Antiviral and cytotoxic activities of some Indonesian plants.

J. Boustie, C. Bézivin, A. Bakhtiar, 2002, Fitoterapia.

Cytotoxic activity of compounds from the lichen: Cladonia convoluta.

J. Delcros, J. Boustie, S. Tomasi, 2004, Planta medica.

Specialized Metabolites of the Lichen Vulpicida pinastri Act as Photoprotective Agents

M. Bertrand, J. Boustie, P. Le Pogam, 2017, Molecules.

A New Long-Chain Unsaturated Ester and Other Constituents of Hypericum tomentosum

Z. Kabouche, O. Touafek, C. Bruneau, 2012, Natural product communications.

Mycosporine‐Like Amino Acids (MAAs) in Biological Photosystems

S. Barre, C. Roullier, J. Boustie, 2014 .

Solamargine: The Main Glycoalkaloid from the Fruits of Solanum paludosum.

J. Boustie, M. Henry, H. E. Badaoui, 1993, Planta medica.

Antiviral Activity of Homobasidiomycetes: Evaluation of 121 Basidiomycetes Extracts on Four Viruses

J. Boustie, M. Amorós, V. Hervé, 1997 .

Secondary metabolites from lichen as potent inhibitors of advanced glycation end products and vasodilative agents.

M. Zehl, H. Stuppner, D. Henrion, 2018, Fitoterapia.

Lichenic extracts and metabolites as UV filters.

J. Boustie, C. Couteau, L. Coiffard, 2013, Journal of photochemistry and photobiology. B, Biology.

New seco-limonoids from Cipadessa baccifera: Isolation, structure determination, synthesis and their antiproliferative activities.

N. Jain, J. Boustie, P. Usha Rani, 2017, Fitoterapia.

A database of high-resolution MS/MS spectra for lichen metabolites

R. Lücking, H. Sipman, J. Wolfender, 2019, Scientific Data.

Lichen-derived compounds show potential for central nervous system therapeutics.

J. Boustie, S. Chakravarty, S. Tomasi, 2016, Phytomedicine : international journal of phytotherapy and phytopharmacology.

Depsides: Lichen Metabolites Active against Hepatitis C Virus

J. Boustie, M. Samson, J. Le Seyec, 2015, PloS one.

Discovery of Depsides and Depsidones from Lichen as Potent Inhibitors of Microsomal Prostaglandin E2 Synthase‐1 Using Pharmacophore Models

O. Werz, S. Noha, D. Schuster, 2012, ChemMedChem.

New meta-depsidones and diphenyl ethers from the lichen Parmotrema tsavoense (Krog & Swinscow) Krog & Swinscow, Parmeliaceae

W. Chavasiri, J. Boustie, T. Duong, 2015 .

Lobarin from the Sumatran lichen, Stereocaulon halei.

O. Delalande, J. Boustie, S. Sinbandhit, 2012, Fitoterapia.

Phytochemical investigation of Tephromela atra: NMR studies of collatolic acid derivatives

J. Boustie, S. Tomasi, S. Sinbandhit, 2008 .

Sesquiterpene lactones from Centaurea tougourensis

Z. Kabouche, J. Boustie, P. Richomme, 2012 .

A New Cryptic Lineage in Parmeliaceae (Ascomycota) with Pharmacological Properties

P. Divakar, J. Boustie, E. González-Burgos, 2022, Journal of fungi.

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

C. Roullier, J. Boustie, A. Bernard, 2009, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

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

R. Bauer, Eva-Maria Pferschy-Wenzig, C. Roullier, 2011, Phytochemistry.

Cytotoxic constituents of the lichen Diploicia canescens.

J. Boustie, S. Tomasi, M. Millot, 2009, Journal of natural products.

Metabolites from the Lichen Ochrolechia parella growing under two different heliotropic conditions.

J. Boustie, S. Tomasi, M. Millot, 2007, Journal of natural products.

In situ DART-MS as a Versatile and Rapid Dereplication Tool in Lichenology: Chemical Fingerprinting of Ophioparma ventosa.

J. Boustie, D. Rondeau, David Rondeau, 2016, Phytochemical analysis : PCA.

Aglycone flavonoids of Centaurea tougourensis from Algeria

Z. Kabouche, R. Touzani, J. Boustie, 2006, Chemistry of Natural Compounds.

In vitro antiviral activity of thirty-six plants from La Réunion Island.

J. Boustie, F. Lohézic-Le Dévéhat, H. Fortin, 2002, Fitoterapia.

In Vivo Antitumor Activity of Clitocine, an Exocyclic Amino Nucleoside Isolated from Lepista inversa

J. Bansard, J. Delcros, J. Boustie, 2006, ChemMedChem.

Cytotoxic Activity of Tricholomatales determined with Murine and Human Cancer Cell Lines

J. Boustie, P. Sauleau, C. Bézivin, 2002 .

In vivo Antitumor Activity of Clitocine (I), an Exocyclic Amino Nucleoside Isolated from Lepista inversa.

J. Bansard, J. Delcros, J. Boustie, 2006 .

Toxicity and Antitumor Activity of a Crude Extract from Lepista inversa (Scop.:Fr.) Pat. (Agaricomycetideae): A Preliminary Study

J. Delcros, J. Boustie, C. Bézivin, 2003 .

Notes: Flavonols from Scurrula ferruginea Danser (Loranthaceae)

J. Boustie, S. Tomasi, F. L. Dévéhat, 2002, Zeitschrift für Naturforschung C - A Journal of Biosciences.

Cytotoxic activity of methanol extracts from Basidiomycete mushrooms on murine cancer cell lines.

J. Boustie, P. Sauleau, S. Tomasi, 2004, Die Pharmazie.

Phytochemical review of the lichen genus Stereocaulon (Fam. Stereocaulaceae) and related pharmacological activities highlighted by a focus on nine species

A. Guiller, J. Boustie, A. Bakhtiar, 2018, Phytochemistry Reviews.

Two novel diterpenes from the roots of Phyllanthus acidus (L.) Skeel

W. Chavasiri, J. Boustie, T. Duong, 2017 .

Sulfonic Acid-Containing Flavonoids from the Roots of Phyllanthus acidus.

J. Gallard, M. Beniddir, W. Chavasiri, 2018, Journal of natural products.

Tsavoenones A-C: unprecedented polyketides with a 1,7-dioxadispiro[4.0.4.4]tetradecane core from the lichen Parmotrema tsavoense.

G. Genta‐Jouve, M. Beniddir, W. Chavasiri, 2018, Organic and biomolecular chemistry.

Sanctis A–C: Three Racemic Procyanidin Analogues from The Lichen Parmotrema sancti‐angelii

G. Genta‐Jouve, M. Beniddir, W. Chavasiri, 2018 .

Antipoliovirus structure-activity relationships of some aporphine alkaloids.

J. Stigliani, J. Boustie, M. Payard,, 1998, Journal of Natural Products.

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

J. Boustie, Thi Thu Tram Nguyen, I. Rouaud, 2015 .

A chemotaxonomic study of the Xanthoparmelia pulla group in Algeria

P. Uriac, J. Boustie, P. Jéhan, 2019, Herzogia.

Mass Spectrometry Imaging of Specialized Metabolites for Predicting Lichen Fitness and Snail Foraging

H. Rogniaux, M. Fanuel, J. Boustie, 2020, Plants.

Synthesis of Novel Cyclic Nitrones with gem ‐Difluoroalkyl Side Chains Through Cascade Reactions

A. Hachem, T. Roisnel, R. Grée, 2020 .

Antiviral activity of carrageenans from marine red algae

J. Boustie, N. Bourgougnon, J. Montanha, 2009 .

From mass spectral features to molecules in molecular networks: a novel workflow for untargeted metabolomics

J. Wolfender, J. V. D. van der Hooft, J. Boustie, 2021, bioRxiv.

Tridepsides as potential bioactives: a review on their chemistry and the global distribution of their lichenic and non-lichenic natural sources

M. Yousefi, J. Boustie, M. Sohrabi, 2023, Frontiers in Fungal Biology.

Analysis of the cyanolichen Lichina pygmaea metabolites using in situ DART-MS: from detection to thermochemistry of mycosporine serinol.

J. Boustie, D. Rondeau, P. Le Pogam, 2015, Journal of mass spectrometry : JMS.

A prenyloxycoumarin from Psiadia dentata.

J. Boustie, S. Tomasi, P. Jaccard, 2001, Chemical and pharmaceutical bulletin.

In-vitro Antiherpetic Activity of Erythroxylon laurifolium (Erythroxylaceae)

J. Boustie, L. Girre, M. Amoros, 1999 .

Overcoming deterrent metabolites by gaining essential nutrients: A lichen/snail case study.

H. Rogniaux, M. Fanuel, P. Clerc, 2019, Phytochemistry.

Optimization of a microwave-assisted extraction of secondary metabolites from crustose lichens with quantitative spectrophotodensitometry analysis.

E. Hitti, J. Boustie, S. Tomasi, 2009, Journal of chromatography. A.

Intrathalline Metabolite Profiles in the Lichen Argopsis friesiana Shape Gastropod Grazing Patterns

D. Ertz, J. Boustie, M. Charrier, 2018, Journal of Chemical Ecology.

Solid-phase synthesis of polyfunctionalized natural products: application to usnic acid, a bioactive lichen compound.

C. Lainé, P. Uriac, S. Picard, 2006, Journal of combinatorial chemistry.

Synthesis and Antiviral Effect against Herpes Simplex Type 1 of 12-substituted Benzo[c]phenanthridinium Salts

J. Boustie, R. Waigh, M. Lynch, 2004, Journal of enzyme inhibition and medicinal chemistry.

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

J. Boustie, I. Rouaud, F. Lohézic-Le Dévéhat, 2015, Planta Medica Letters.

Synthesis of New γ-Lactams with gem-Difluorinated Side Chains

A. Hachem, T. Roisnel, R. Grée, 2019, Synlett.

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

P. D. Weghe, C. Roullier, J. Boustie, 2010, Bioorganic & medicinal chemistry letters.

Lichen or Associated Micro-Organism Compounds Are Active against Human Coronaviruses

S. Belouzard, Y. Rouillé, K. Séron, 2023, Viruses.