A. Boumendjel

发表

A 3D linear solvation energy model to quantify the affinity of flavonoid derivatives toward P-glycoprotein.

P. Carrupt, S. Rudaz, F. Bajot, 2009, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Flavonoids as Anticancer Agents: Recent Progress and State of the Art?

A. Boumendjel, E. Nicolle, E. Genoux, 2011 .

Bioguidage search of active compounds from Waltheria indica L. (Malvaceae) used for asthma and inflammation treatment in Burkina Faso

A. Boumendjel, F. Zongo, C. Ribuot, 2014, Fundamental & clinical pharmacology.

Inhibitors of cancer cell multidrug resistance mediated by breast cancer resistance protein (BCRP/ABCG2)

A. di Pietro, S. Macalou, A. Boumendjel, 2006, Anti-cancer drugs.

Quantitative evaluation of the combination between cytotoxic drug and efflux transporter inhibitors based on a tumour growth inhibition model

J. Guitton, Myléne Honorat, P. Falson, 2014, Fundamental & clinical pharmacology.

A template model for studying anticancer drug efflux transporter inhibitors in vitro

J. Guitton, Myléne Honorat, P. Falson, 2013, Fundamental & clinical pharmacology.

MBL-II-141, a chromone derivative, enhances irinotecan (CPT-11) anticancer efficiency in ABCG2-positive xenografts

A. di Pietro, A. Puisieux, C. Rioufol, 2014, Oncotarget.

Cellular and molecular mechanisms activating the cell death processes by chalcones: Critical structural effects.

P. Champelovier, C. Garrel, A. Boumendjel, 2013, Toxicology in vitro : an international journal published in association with BIBRA.

New pseudodimeric aurones as palm pocket inhibitors of Hepatitis C virus RNA-dependent RNA polymerase.

J. Pawlotsky, Alessandra Nurisso, A. Boumendjel, 2016, European journal of medicinal chemistry.

2-Indolylmethylenebenzofuranones as first effective inhibitors of ABCC2.

L. Chow, P. Falson, A. Boumendjel, 2016, European journal of medicinal chemistry.

The acridone derivative MBLI-87 sensitizes breast cancer resistance protein-expressing xenografts to irinotecan.

S. Bates, A. di Pietro, E. Matera, 2011, European journal of cancer.

Two in one: bifonctional derivatives of trolox acting as antimalarial and antioxidant agents.

F. Souard, A. Boumendjel, E. Nicolle, 2020, Future medicinal chemistry.

Make azoles active again: chalcones as potent reversal agents of transporters-mediated resistance in Candida albicans.

R. Prasad, P. Falson, A. Pietro, 2018, Future medicinal chemistry.

Analogues of N-hydroxycinnamoylphenalkylamides as inhibitors of human melanocyte-tyrosinase.

E. Perrier, S. Bonnet, A. Boumendjel, 2006, Bioorganic & medicinal chemistry letters.

Recent Advances in the Discovery of Flavonoids and Analogues with High‐Affinity Binding to P‐Glycoprotein Responsible for Cancer Cell Multidrug Resistance

D. Barron, C. Dumontet, A. Pietro, 2002 .

Occurrences, biosynthesis and properties of aurones as high-end evolutionary products.

A. Boumendjel, Marine Peuchmaur, B. Boucherle, 2017, Phytochemistry.

The effect of flavonoid derivatives on doxorubicin transport and metabolism.

P. Stopka, P. Souček, R. Vaclavikova, 2008, Bioorganic & medicinal chemistry.

Chromones bearing amino acid residues: Easily accessible and potent inhibitors of the breast cancer resistance protein ABCG2.

C. Philouze, O. Renaudet, Aline Thomas, 2020, European journal of medicinal chemistry.

Investigation of Binding‐Site Homology between Mushroom and Bacterial Tyrosinases by Using Aurones as Effectors

E. Bergantino, L. Bubacco, A. Boumendjel, 2014, Chembiochem : a European journal of chemical biology.

Antimitotic activity of 5-hydroxy-7-methoxy-2-phenyl-4-quinolones.

C. Dumontet, N. Deka, A. Boumendjel, 2004, Journal of medicinal chemistry.

A novel chalcone derivative which acts as a microtubule depolymerising agent and an inhibitor of P-gp and BCRP in in-vitro and in-vivo glioblastoma models

F. Souard, M. Derouazi, Diane Allegro, 2009, BMC Cancer.

Flavonoids as RTK inhibitors and potential anticancer agents

X. Ronot, Florence Teillet, A. Boumendjel, 2008, Medicinal research reviews.

A Novel Platinum-Maurocalcine Conjugate Induces Apoptosis of Human Glioblastoma Cells by Acting through the ROS-ERK/AKT-p53 Pathway.

J. Muller, M. De Waard, A. Boumendjel, 2015, Molecular pharmaceutics.

Ovarian cancer cells cisplatin sensitization agents selected by mass cytometry target ABCC2 inhibition.

P. Falson, T. Andrieu, A. Boumendjel, 2018, Future medicinal chemistry.

Design, synthesis and biological evaluation of novel ring-opened cromakalim analogues with relaxant effects on vascular and respiratory smooth muscles and as stimulators of elastin synthesis.

A. Boumendjel, G. Faury, S. Khelili, 2018, European journal of medicinal chemistry.

Hesperitin Esters: Highly Stable Flavanones with Both Free Radical Scavenging and Anti-Elastase Activities

E. Perrier, A. Boumendjel, A. Boumendjel, 2003 .

Efficient synthesis of flavanone glucuronides.

D. Barron, G. Williamson, A. Boumendjel, 2009, Journal of agricultural and food chemistry.

Identification of Xanthones as Selective Killers of Cancer Cells Overexpressing the ABC Transporter MRP1

Doriane Lorendeau, A. Boumendjel, E. Nicolle, 2011, ChemMedChem.

AG11, a novel dichloroflavanone derivative with anti-mitotic activity towards human bladder cancer cells.

V. Martel-Frachet, X. Ronot, A. Guillot, 2013, Anticancer research.

ABCG2: recent discovery of potent and highly selective inhibitors.

A. di Pietro, Evelyn Winter, L. Payen, 2013, Future medicinal chemistry.

IPP51, a chalcone acting as a microtubule inhibitor with in vivo antitumor activity against bladder carcinoma

V. Martel-Frachet, X. Ronot, J. Coll, 2015, Oncotarget.

Anticancer multidrug resistance mediated by MRP1: Recent advances in the discovery of reversal agents

A. di Pietro, A. Boumendjel, H. Baubichon-Cortay, 2005, Medicinal research reviews.

Piperidinyl-embeded chalcones possessing anti PI3Kδ inhibitory properties exhibit anti-atopic properties in preclinical models.

E. Matera, C. Dumontet, A. Magnan, 2018, European journal of medicinal chemistry.

Antiproliferative activity, cell-cycle arrest, apoptotic induction and LC-HRMS/MS analyses of extracts from two Linum species

A. Broisat, C. Ghezzi, Z. Kabouche, 2022, Pharmaceutical biology.

A retro-biosynthetic approach to the prediction of biosynthetic pathways from position-specific isotope analysis as shown for tramadol

M. De Waard, G. Remaud, Virginie Silvestre, 2015, Proceedings of the National Academy of Sciences of the United States of America.

The first ADC bearing the ferroptosis inducer RSL3 as a payload with conservation of the fragile electrophilic warhead.

C. Dumontet, P. Falson, A. Boumendjel, 2022, European journal of medicinal chemistry.

SB 203580, a Mitogen-Activated Protein Kinase Inhibitor, Abolishes Resistance to Myocardial Infarction Induced by Heat Stress

D. Yellon, A. Boumendjel, C. Ribuot, 2000, Cardiovascular Drugs and Therapy.

2-Hydroxypyridine-N-oxide-Embedded Aurones as Potent Human Tyrosinase Inhibitors.

E. Bergantino, L. Bubacco, Elina Buitrago, 2017, ACS medicinal chemistry letters.

Arylthiosemicarbazones as antileishmanial agents.

F. Gamarro, A. Boumendjel, Marine Peuchmaur, 2016, European journal of medicinal chemistry.

Occurrence of the synthetic analgesic tramadol in an African medicinal plant.

A. Depaulis, V. Sinniger, B. Bonaz, 2013, Angewandte Chemie.

Optimization of the chromone scaffold through QSAR and docking studies: Identification of potent inhibitors of ABCG2.

O. Renaudet, P. Falson, A. Boumendjel, 2019, European journal of medicinal chemistry.

6‐Halogenochromones Bearing Tryptamine: One‐Step Access to Potent and Highly Selective Inhibitors of Breast Cancer Resistance Protein

R. Terreux, A. Boumendjel, G. Valdameri, 2012, ChemMedChem.

Synthesis and Anticancer Cytotoxicity of Azaaurones Overcoming Multidrug Resistance

G. Szakács, A. di Pietro, B. Sarkadi, 2020, Molecules.

Synthesis of an inhibitor of sphingosine-1-phosphate lyase

Stephen P. Miller, A. Boumendjel, 1994 .

A new synthesis of α,β-unsaturated aldehydes

J. Nuzillard, G. Massiot, A. Boumendjel, 1989 .

Antimitotic and antiproliferative activities of chalcones: forward structure-activity relationship.

P. Carrupt, E. Matera, C. Dumontet, 2008, Journal of medicinal chemistry.

Microwave mediated solvent-free acetylation of deactivated and hindered phenols

N. Deka, A. Boumendjel, A. Mariotte, 2001 .

Anticancer multidrug resistance mediated by MRP1: Recent advances in the discovery of reversal agents

A. di Pietro, A. Boumendjel, H. Baubichon-Cortay, 2005, Medicinal research reviews.

B-ring substituted 5,7-dihydroxyflavonols with high-affinity binding to P-glycoprotein responsible for cell multidrug resistance.

A. di Pietro, F. Bois, A. Boumendjel, 2001, Bioorganic & medicinal chemistry letters.

Discovery of benzylidenebenzofuran-3(2H)-one (aurones) as inhibitors of tyrosinase derived from human melanocytes.

E. Perrier, S. Bonnet, A. Boumendjel, 2006, Journal of medicinal chemistry.

Aurones: a subclass of flavones with promising biological potential.

A. Boumendjel, 2003, Current medicinal chemistry.

Exploring the interaction of N/S compounds with a dicopper center: tyrosinase inhibition and model studies.

C. Philouze, Elina Buitrago, A. Boumendjel, 2014, Inorganic chemistry.

ALKALOIDS FROM ALSTONIA UNDULIFOLIA

J. Nuzillard, B. David, G. Massiot, 1992 .

Halogenated chalcones with high-affinity binding to P-glycoprotein: potential modulators of multidrug resistance.

A. di Pietro, F. Bois, A. Boumendjel, 1998, Journal of medicinal chemistry.

Investigation of chalcones as selective inhibitors of the breast cancer resistance protein: critical role of methoxylation in both inhibition potency and cytotoxicity.

Raphaël Terreux, Xavier Ronot, A. di Pietro, 2012, Journal of medicinal chemistry.

Structural requirement of arylindolylpropenones as anti-bladder carcinoma cells agents.

Xavier Ronot, V. Martel-Frachet, X. Ronot, 2011, Bioorganic & medicinal chemistry.

Investigation of a new 1,3-diarylpropenone as a potential antimitotic agent targeting bladder carcinoma

V. Martel-Frachet, X. Ronot, B. Touquet, 2009, Anti-cancer drugs.

2-Arylidenedihydroindole-3-ones: design, synthesis, and biological activity on bladder carcinoma cell lines.

X. Ronot, P. Bringuier, P. Champelovier, 2007, Bioorganic & medicinal chemistry letters.

Exploiting HOPNO-dicopper center interaction to development of inhibitors for human tyrosinase.

E. Bergantino, C. Philouze, L. Bubacco, 2023, European journal of medicinal chemistry.

Targeting the Achilles Heel of Multidrug-Resistant Cancer by Exploiting the Fitness Cost of Resistance

M. Gottesman, G. Szakács, M. Hall, 2014, Chemical reviews.

Versatile Effects of Aurone Structure on Mushroom Tyrosinase Activity

M. Orio, A. Boumendjel, C. Belle, 2012, Chembiochem : a European journal of chemical biology.

Piperazinobenzopyranones and phenalkylaminobenzopyranones: potent inhibitors of breast cancer resistance protein (ABCG2).

X. Ronot, A. Boumendjel, E. Nicolle, 2005, Journal of medicinal chemistry.

Flavonoids as promising lead compounds in type 2 diabetes mellitus: molecules of interest and structure-activity relationship.

F. Souard, P. Faure, A. Boumendjel, 2011, Current medicinal chemistry.

Substituted chromones as highly potent nontoxic inhibitors, specific for the breast cancer resistance protein.

Jérôme Guitton, Raphaël Terreux, A. di Pietro, 2012, Journal of medicinal chemistry.

Ferrocene-embedded flavonoids targeting the Achilles heel of multidrug-resistant cancer cells through collateral sensitivity.

A. di Pietro, A. Boumendjel, Malik Zarioh, 2017, European journal of medicinal chemistry.

Design and Asymmetric Synthesis of beta-Strand Peptidomimetics.

John C. Roberts, E. Hu, J. Rebek, 1996, The Journal of organic chemistry.

Modulation of P-glycoprotein-mediated multidrug resistance by flavonoid derivatives and analogues.

X. Ronot, A. Boumendjel, J. Boutonnat, 2003, Journal of medicinal chemistry.

2′-Amino-α-chloroacetophenone as a Valuable Tool for the Synthesis of Conveniently-Substituted α,β-Epoxychalcone Derivatives

A. Boumendjel, Sabrina Okombi, M. Blanc, 2005 .

3‐Aryl‐4‐methyl‐2‐quinolones Targeting Multiresistant Staphylococcus aureus Bacteria

Y. Wong, C. Dumontet, E. Bergeron, 2013, ChemMedChem.

New derivatives of azacoumarines presenting inhibitory activity of the mdr pump

Y. Wong, C. Dumontet, J. Freney, 2011 .

Breast cancer resistance protein (BCRP/ABCG2): new inhibitors and QSAR studies by a 3D linear solvation energy approach.

Julien Boccard, Pierre-Alain Carrupt, P. Carrupt, 2009, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Structure–Activity Relationships in the Development of Allosteric Hepatitis C Virus RNA‐Dependent RNA Polymerase Inhibitors: Ten Years of Research

J. Pawlotsky, A. Boumendjel, A. Ahmed-Belkacem, 2013, Medicinal research reviews.

Traditional uses, phytochemistry and pharmacological properties of African Nauclea species: A review.

A. Boumendjel, Marine Peuchmaur, B. Boucherle, 2018, Journal of ethnopharmacology.

Botany, traditional uses, phytochemistry and pharmacology of Waltheria indica L. (syn. Waltheria americana): a review.

A. Boumendjel, F. Zongo, C. Ribuot, 2013, Journal of ethnopharmacology.

Acridone derivatives: design, synthesis, and inhibition of breast cancer resistance protein ABCG2.

A. di Pietro, S. Macalou, A. Boumendjel, 2007, Bioorganic & medicinal chemistry.

Nauclea latifolia: biological activity and alkaloid phytochemistry of a West African tree.

J. Wolfender, M. De Waard, R. Robins, 2016, Natural product reports.

Biomimetic synthesis of Tramadol.

L. Marcourt, J. Wolfender, M. De Waard, 2015, Chemical communications.

Nauclea latifolia Smith (Rubiaceae) exerts antinociceptive effects in neuropathic pain induced by chronic constriction injury of the sciatic nerve.

V. Sinniger, B. Bonaz, M. De Waard, 2014, Journal of ethnopharmacology.

Energetic Bio-Activation of Some Organic Molecules and Their Antioxidant Activity in the Pulp of the Moroccan Argan Tree «Argania spinosa L.»

M. Mahrouz, M. Ouhammou, Nadia Hidar, 2022, Molecules.

Recombinant Tyrosinase from Polyporus arcularius: Overproduction in Escherichia coli, Characterization, and Use in a Study of Aurones as Tyrosinase Effectors.

E. Markova, P. Man, A. Boumendjel, 2016, Journal of agricultural and food chemistry.

Recent advances in the discovery of flavonoids and analogs with high‐affinity binding to P‐glycoprotein responsible for cancer cell multidrug resistance

A. di Pietro, D. Barron, C. Dumontet, 2002, Medicinal research reviews.

Discovery of naturally occurring aurones that are potent allosteric inhibitors of hepatitis C virus RNA-dependent RNA polymerase.

J. Pawlotsky, A. Boumendjel, E. Nicolle, 2011, Journal of medicinal chemistry.

Aurone derivatives as promising antibacterial agents against resistant Gram-positive pathogens.

E. Baydoun, J. Raymond, M. Maresca, 2019, European journal of medicinal chemistry.

Are Human Tyrosinase and Related Proteins Suitable Targets for Melanoma Therapy?

L. Bubacco, Elina Buitrago, A. Boumendjel, 2016, Current topics in medicinal chemistry.

Recent advances in the medicinal chemistry of aurones.

A. Boumendjel, R. Haudecoeur, Romain Haudecoeur, 2012, Current medicinal chemistry.

1-Azaaurones derived from the naturally occurring aurones as potential antimalarial drugs.

F. Souard, S. Chevalley, A. Boumendjel, 2010, Bioorganic & medicinal chemistry.

Disruption of Fibers from the Tau Model AcPHF6 by Naturally Occurring Aurones and Synthetic Analogues.

S. Chierici, A. Boumendjel, H. Bonnet, 2016, ACS chemical neuroscience.

B-ring modified aurones as promising allosteric inhibitors of hepatitis C virus RNA-dependent RNA polymerase.

J. Pawlotsky, A. Boumendjel, A. Ahmed-Belkacem, 2014, European journal of medicinal chemistry.

Modulation of paclitaxel transport by flavonoid derivatives in human breast cancer cells. Is there a correlation between binding affinity to NBD of P-gp and modulation of transport?

R. Vaclavikova, M. Ehrlichová, I. Gut, 2006, Bioorganic & medicinal chemistry.

Refinement of arylthiosemicarbazone pharmacophore in inhibition of mushroom tyrosinase.

Huacan Song, A. Boumendjel, C. Belle, 2011, European journal of medicinal chemistry.

4-Hydroxy-6-methoxyaurones with high-affinity binding to cytosolic domain of P-glycoprotein.

A. di Pietro, N. Deka, A. Boumendjel, 2002, Chemical & pharmaceutical bulletin.

A one-step synthesis of 2-Alkyl-5-hydroxychromones and 3-Alkoyl-2-alkyl-5-hydroxychromones.

E. Perrier, A. Boumendjel, A. Mariotte, 2005, Chemical & pharmaceutical bulletin.

An Efficient Synthesis of 4,6-Dimethoxyaurones

A. Boumendjel, A. Mariotte, C. Beney, 2001 .

High-content imaging assay to evaluate Toxoplasma gondii infection and proliferation: A multiparametric assay to screen new compounds

B. Touquet, D. Aldebert, A. Boumendjel, 2018, PloS one.

Use of derivatives for-coumaric acid or para-hydroxyC inamico in cosmetic or dermatological compositions.

E. Perrier, A. Boumendjel, A. Mariotte, 2006 .

Cytotoxicity of chalcone derivatives towards glioblastoma.

M. Mininno, P. Champelovier, A. Boumendjel, 2011, Anticancer research.

Chalcones derivatives acting as cell cycle blockers: potential anti cancer drugs?

X. Ronot, A. Boumendjel, J. Boutonnat, 2009, Current drug targets.

A One-Step Synthesis of 5-Hydroxyflavones

F. Bois, A. Boumendjel, A. Mariotte, 1999 .

Structure-activity relationships of chromone derivatives toward the mechanism of interaction with and inhibition of breast cancer resistance protein ABCG2.

G. Szakács, A. di Pietro, Evelyn Winter, 2013, Journal of medicinal chemistry.

GENISTEIN AND FLUORINATED ANALOGS SUPPRESS AGONIST-INDUCED AIRWAY SMOOTH MUSCLE CONTRACTION

P. Devillier, G. Bessard, F. Bois, 1997 .

Molecular analysis of the massive GSH transport mechanism mediated by the human Multidrug Resistant Protein 1/ABCC1

J. Cortay, V. Chaptal, P. Falson, 2020, Scientific Reports.

Dicer-Mediated Upregulation of BCRP Confers Tamoxifen Resistance in Human Breast Cancer Cells

S. Fuqua, I. Barone, S. Andò, 2011, Clinical Cancer Research.

Involvement of Tetrahymena pyriformis and selected fungi in the elimination of anthracene, and toxicity assessment of the biotransformation products.

J. Bonnet, P. Guiraud, J. Bohatier, 2008, Ecotoxicology and environmental safety.

New, highly potent and non-toxic, chromone inhibitors of the human breast cancer resistance protein ABCG2.

A. di Pietro, Evelyn Winter, A. Boumendjel, 2016, European journal of medicinal chemistry.

Collateral sensitivity of resistant MRP1-overexpressing cells to flavonoids and derivatives through GSH efflux.

P. Carrupt, A. di Pietro, R. Terreux, 2014, Biochemical pharmacology.

Inhibitors of ABCG2-mediated multidrug resistance: Lead generation through computer-aided drug design.

L. Goracci, V. Chaptal, P. Falson, 2023, European journal of medicinal chemistry.

Substrate-bound and substrate-free outward-facing structures of a multidrug ABC exporter

G. Schoehn, Juliette Martin, L. Monticelli, 2022, Science advances.

Drug-bound and -free outward-facing structures of a multidrug ABC exporter point to a swing mechanism

Juliette Martin, L. Monticelli, M. Högbom, 2021, bioRxiv.

Diversity-Oriented Synthesis: Amino Acetophenones as Building Blocks for the Synthesis of Natural Product Analogs

A. Boumendjel, Mathias Eymery, V. Tran-Nguyen, 2021, Pharmaceuticals.

Alkylation of 2-phenyl-4-quinolones: synthetic and structural studies.

A. Boumendjel, A. Mariotte, M. Hadjeri, 2001, Chemical & pharmaceutical bulletin.

Modulation by flavonoids of cell multidrug resistance mediated by P-glycoprotein and related ABC transporters

A. Goffeau, J. M. Pérez-Victoria, A. di Pietro, 2002, Cellular and Molecular Life Sciences CMLS.

Synthesis and biological activity of 4-alkoxy chalcones: potential hydrophobic modulators of P-glycoprotein-mediated multidrug resistance.

F. Bois, A. Boumendjel, G. Conseil, 1999, Bioorganic & medicinal chemistry.

A convenient method for the synthesis of 3,5,7-trimethoxy-2-phenyl-4-quinolones

A. Boumendjel, A. Mariotte, M. Hadjeri, 2000 .

Phytochemical and Biological Investigation of Helianthemum nummularium, a High-Altitude Growing Alpine Plant Overrepresented in Ungulates Diets

L. Marcourt, B. Gao, J. Wolfender, 2020, Planta Medica.

Identification of specific reversal agents for Leishmania ABCI4-mediated antimony resistance by flavonoid and trolox derivative screening.

A. di Pietro, S. Castanys, F. Gamarro, 2014, The Journal of antimicrobial chemotherapy.

New model system for testing effects of flavonoids on doxorubicin-related formation of hydroxyl radicals

P. Stopka, P. Souček, I. Gut, 2011, Anti-cancer drugs.

Focus on the high therapeutic potentials of quercetin and its derivatives

P. Gasque, P. Guiraud, A. Boumendjel, 2022, Phytomedicine Plus.

Biodriven investigation of the wild edible mushroom Pleurotus eryngii revealing unique properties as functional food

B. Gao, J. McCord, A. Boumendjel, 2022, Journal of Functional Foods.

A SHORT METHOD FOR THE SYNTHESIS OF 4,6-DIMETHOXY-1-AZAAURONES

A. Boumendjel, A. Mariotte, Martin A. Lawson, 2003 .

A synthetic chalcone as a potent inducer of glutathione biosynthesis.

A. di Pietro, B. Day, A. Boumendjel, 2012, Journal of medicinal chemistry.

Chemical composition of the pods of Albizia polyphylla

A. Boumendjel, C. Rajemiarimoelisoa, H. Randrianarivo, 2016, Natural product research.

Electronic Reprint Synchrotron Radiation Chalcone Jai-51 Improves Efficacy of Synchrotron Microbeam Radiation Therapy of Brain Tumors

J. Laissue, E. Khalil, R. Serduc, 2012 .

A One‐Step Synthesis of 5‐Hydroxyflavones.

F. Bois, A. Boumendjel, A. Mariotte, 1999 .

Characterization of Potent ABCG2 Inhibitor Derived from Chromone: From the Mechanism of Inhibition to Human Extracellular Vesicles for Drug Delivery

A. Poso, T. Kronenberger, S. Ambudkar, 2023, Pharmaceutics.

Chemically Modified Extracellular Vesicles and Applications in Radiolabeling and Drug Delivery

C. Ghezzi, A. Boumendjel, N. S. Orefice, 2022, Pharmaceutics.

Deacetylation of Activated Acetophenones with Tin(IV) Chloride †

A. Boumendjel, A. Mariotte, M. Hadjeri, 2002 .

Synthesis of sphingosine-1-phosphate and dihydrosphingosine-1-phosphate.

S. P. Miller, A. Boumendjel, 1994, Journal of lipid research.

Glycosyl-Substituted Dicarboxylates as Detergents for the Extraction, Overstabilization, and Crystallization of Membrane Proteins.

A. Jawhari, V. Chaptal, P. Falson, 2018, Angewandte Chemie.

Evaluation of antiproliferative activity, apoptotic induction and LC-HRMS/MS analyses of the VLC fractions of L. numidicum

A. Broisat, C. Ghezzi, Z. Kabouche, 2022, Natural product research.

Exploring the structure-activity relationship of benzylidene-2,3-dihydro-1H-inden-1-one compared to benzofuran-3(2H)-one derivatives as inhibitors of tau amyloid fibers.

S. Chierici, A. Boumendjel, H. Bonnet, 2022, European journal of medicinal chemistry.

A straightforward conversion of aurones to 2-benzoylbenzofurans: transformation of one class of natural products into another

A. Boumendjel, Marine Peuchmaur, S. Yahiaoui, 2011 .

A Straightforward Conversion of Aurones to 2‐Benzoylbenzofurans: Transformation of One Class of Natural Products into Another.

A. Boumendjel, Marine Peuchmaur, S. Yahiaoui, 2012 .

Structure, function, and inhibition of catalytically asymmetric ABC transporters: Lessons from the PDR subfamily.

R. V. Prasad, V. Chaptal, P. Falson, 2023, Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy.

Drug candidates targeting multidrug resistance in cancer and infections

P. Falson, A. Boumendjel, M. Le Borgne, 2023, European Journal of Medicinal Chemistry.

Modulators of the Efflux Pump Cdr1p of Candida albicans: Mechanisms of Action and Chemical Features.

R. Prasad, P. Falson, A. Boumendjel, 2017, Current medicinal chemistry.

Disruption of Fibers from the Tau Model AcPHF6 by Naturally Occurring Aurones and Synthetic Analogues.

S. Chierici, A. Boumendjel, H. Bonnet, 2016, ACS chemical neuroscience.

Modulation by flavonoids of cell multidrug resistance mediated by P-glycoprotein and related ABC transporters

A. Goffeau, J. M. Pérez-Victoria, D. Barron, 2002, Cellular and Molecular Life Sciences CMLS.

Synthesis of tritium labelled 2-vinyl dihydrosphingosine-1-phosphate

Stephen P. Miller, A. Boumendjel, 1995 .

Glycosyl-Substituted Dicarboxylates as Detergents for the Extraction, Overstabilization, and Crystallization of Membrane Proteins.

A. Jawhari, V. Chaptal, P. Falson, 2018, Angewandte Chemie.

Discovery of potent chromone-based autotaxin inhibitors inspired by cannabinoids.

A. Boumendjel, Mathias C. Eymery, Kim-Anh Nguyen, 2023, European journal of medicinal chemistry.

QSAR analysis and molecular modeling of ABCG2-specific inhibitors.

P. Carrupt, S. Macalou, A. Boumendjel, 2009, Advanced drug delivery reviews.

New coumarin derivatives accessible in short and eco-friendly conditions with antifungal activity.

D. Villemin, A. Boumendjel, N. Cheikh, 2023, Future medicinal chemistry.

Purification and characterization of Cdr1, the drug-efflux pump conferring azole resistance in Candida species.

V. Chaptal, P. Falson, A. Boumendjel, 2023, Biochimie.

A novel quinone biosynthetic pathway illuminates the evolution of aerobic metabolism

J. Leadbetter, S. Abby, E. Spieck, 2024, bioRxiv.

Molecular analysis of the massive GSH transport mechanism mediated by the human Multidrug Resistant Protein 1/ABCC1

J. Cortay, V. Chaptal, P. Falson, 2020, Scientific Reports.

Elaboration of New Monoterpenoid Indole Alkaloids Containing a Dihydrofuran Unit

J. Nuzillard, G. Massiot, A. Boumendjel, 2001 .