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Assessing the Dual Activity of a Chalcone–Phthalocyanine Conjugate: Design, Synthesis, and Antivascular and Photodynamic Properties

Molecular pharmaceutics, 2013-10, Vol.10 (10), p.3706-3716

2013

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Perspectives on the Two-Pore Domain Potassium Channel TREK-1 (TWIK-Related K+ Channel 1). A Novel Therapeutic Target?

Journal of medicinal chemistry, 2016-06, Vol.59, p.5149-5157

2016

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Safe laboratory practices & procedures introduced to the students through an augmented reality application

Proceedings of the 4th International Conference on Smart City Applications, 2019, p.1-7

2019

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Perspectives on the Two-Pore Domain Potassium Channel TREK‑1 (TWIK-Related K+ Channel 1). A Novel Therapeutic Target?: Miniperspective

Journal of medicinal chemistry, 2016-06, Vol.59 (11), p.5149-5157

2016

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Design, synthesis and biological evaluation of conformationnally-restricted analogues of E7010 as inhibitors of tubulin assembly (ITA) and vascular disrupting agents (VDA)

European journal of medicinal chemistry, 2022-12, Vol.244, p.114809-114809, Article 114809

2022

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Development of the First Two-Pore Domain Potassium Channel TWIK-Related K+ Channel 1‑Selective Agonist Possessing in Vivo Antinociceptive Activity

Journal of medicinal chemistry, 2017-02, Vol.60 (3), p.1076-1088

2017

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Analgesic molecules interleaved between layered double hydroxide: Exchange versus in situ reaction and release properties

Journal of solid state chemistry, 2018-12, Vol.268, p.159-167

2018

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Optimization of the synthesis of a key intermediate for the preparation of glucocorticoids

Steroids, 2018-09, Vol.137, p.14-21

2018

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Synthesis and structure–activity relationship study of substituted caffeate esters as antinociceptive agents modulating the TREK-1 channel

European journal of medicinal chemistry, 2014-03, Vol.75, p.391-402

2014

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Perspectives on the Two-Pore Domain Potassium Channel TREK-1 (TWIK-Related K(+) Channel 1). A Novel Therapeutic Target?

Journal of medicinal chemistry, 2016-06, Vol.59 (11), p.5149-5157

2016

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Synthesis and structure-activity relationship study of substituted caffeateesters as antinociceptive agents modulating the TREK-1 channel

European journal of medicinal chemistry, 2014, Vol.75, p.391-402

2014

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Correction to “Assessing the Dual Activity of a Chalcone–Phthalocyanine Conjugate: Design, Synthesis, and Antivascular and Photodynamic Properties”

Molecular pharmaceutics, 2015-02, Vol.12 (2), p.663-663

2015

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Phthalocyanine-chalcone conjugates

Journal of porphyrins and phthalocyanines, 2016-01, Vol.20 (1n04), p.497-504

2016

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Synthesis and Glycosidase Inhibitory Study of New Polyhydroxylated Indolizidines

European Journal of Organic Chemistry, 2008-11, Vol.2008 (31), p.5289-5300

2008

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A simple and efficient synthesis of new cyclic ureas

Tetrahedron letters, 2007-11, Vol.48 (47), p.8363-8365

2007

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Chemoenzymatic synthesis of thio-nod factor intermediates Enzymatic transfer of glucosamine on thiochitobiose derivatives

Canadian journal of chemistry, 2006-04, Vol.84 (4), p.587-596

2006

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Synthesis of S-linked thiooligosaccharide analogues of Nod factors: synthesis of new protected thiodisaccharide and thiotrisaccharide intermediates

Carbohydrate research, 2003-06, Vol.338 (13), p.1369-1379

2003

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Synthesis of Enantiomerically Pure Heterocycles: Access to Hydroxylated Piperidines from a Sugar Lactone

Synthesis (Stuttgart), 1997-02, Vol.1997 (2), p.191-194

1997

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Diastereoselective elaboration of 2,3,4-substituted piperidines using diene iron tricarbonyl complexes. Total synthesis of (±)-dienomycin C and (±)-4-epi-dienomycin C

Tetrahedron letters, 1996-06, Vol.37 (23), p.3991-3992

1996

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A new route to some enantiomerically pure substituted morpholines from d-ribono- and d-gulono-1,4-lactones

Carbohydrate research, 1994-11, Vol.264 (1), p.33-44

1994

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Synthesis from lactose of new enantiomerically pure polyhydroxylated pyrrolidines with branched structures

Carbohydrate research, 1995-12, Vol.279, p.307-314

1995

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ChemInform Abstract: A Simple and Efficient Synthesis of New Cyclic Ureas

ChemInform, 2008-03, Vol.39 (11), p.no-no

2008

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Synthesis of S-linked thiooligosaccharide analogues of Nod factors. Part 1: selectively N-protected 4-thiochitobiose precursors

Journal of the Chemical Society, Perkin Transactions 1, 1998-11 (21), p.3629-3636

1998

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Design, Synthesis and Biological Evaluation of Conformationnally-Restricted Analogues of E7010 as Inhibitors of Tubulin Assembly (ITA) and Vascular Disrupting Agents (VDA)

SSRN Electronic Journal

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ChemInform Abstract: Synthesis of S-Linked Thiooligosaccharide Analogues of Nod Factors. Part 1. Selectively N-Protected 4-Thiochitobiose Precursors

ChemInform, 1999-04, Vol.30 (15), p.no-no

1999

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Assessing the Dual Activity of a Chalcone–Phthalocyanine Conjugate: Design, Synthesis, and Antivascular and Photodynamic Properties

Perspectives on the Two-Pore Domain Potassium Channel TREK-1 (TWIK-Related K+ Channel 1). A Novel Therapeutic Target?

Safe laboratory practices & procedures introduced to the students through an augmented reality application

Perspectives on the Two-Pore Domain Potassium Channel TREK‑1 (TWIK-Related K+ Channel 1). A Novel Therapeutic Target?: Miniperspective

Design, synthesis and biological evaluation of conformationnally-restricted analogues of E7010 as inhibitors of tubulin assembly (ITA) and vascular disrupting agents (VDA)

Development of the First Two-Pore Domain Potassium Channel TWIK-Related K+ Channel 1‑Selective Agonist Possessing in Vivo Antinociceptive Activity

Analgesic molecules interleaved between layered double hydroxide: Exchange versus in situ reaction and release properties

Optimization of the synthesis of a key intermediate for the preparation of glucocorticoids

Synthesis and structure–activity relationship study of substituted caffeate esters as antinociceptive agents modulating the TREK-1 channel

Perspectives on the Two-Pore Domain Potassium Channel TREK-1 (TWIK-Related K(+) Channel 1). A Novel Therapeutic Target?

Synthesis and structure-activity relationship study of substituted caffeateesters as antinociceptive agents modulating the TREK-1 channel

Correction to “Assessing the Dual Activity of a Chalcone–Phthalocyanine Conjugate: Design, Synthesis, and Antivascular and Photodynamic Properties”

Phthalocyanine-chalcone conjugates

Synthesis and Glycosidase Inhibitory Study of New Polyhydroxylated Indolizidines

A simple and efficient synthesis of new cyclic ureas

Chemoenzymatic synthesis of thio-nod factor intermediates Enzymatic transfer of glucosamine on thiochitobiose derivatives

Synthesis of S-linked thiooligosaccharide analogues of Nod factors: synthesis of new protected thiodisaccharide and thiotrisaccharide intermediates

Synthesis of Enantiomerically Pure Heterocycles: Access to Hydroxylated Piperidines from a Sugar Lactone

Diastereoselective elaboration of 2,3,4-substituted piperidines using diene iron tricarbonyl complexes. Total synthesis of (±)-dienomycin C and (±)-4-epi-dienomycin C

A new route to some enantiomerically pure substituted morpholines from d-ribono- and d-gulono-1,4-lactones

Synthesis from lactose of new enantiomerically pure polyhydroxylated pyrrolidines with branched structures

ChemInform Abstract: A Simple and Efficient Synthesis of New Cyclic Ureas

Synthesis of S-linked thiooligosaccharide analogues of Nod factors. Part 1: selectively N-protected 4-thiochitobiose precursors

Design, Synthesis and Biological Evaluation of Conformationnally-Restricted Analogues of E7010 as Inhibitors of Tubulin Assembly (ITA) and Vascular Disrupting Agents (VDA)

ChemInform Abstract: Synthesis of S-Linked Thiooligosaccharide Analogues of Nod Factors. Part 1. Selectively N-Protected 4-Thiochitobiose Precursors

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