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Editorial for the Special Issue "Advances in the Development of Anticancer Drugs"

International journal of molecular sciences, 2024-01, Vol.25 (1), p.641

Fotie, Jean

2024

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Inosine 5'-Monophosphate Dehydrogenase (IMPDH) as a Potential Target for the Development of a New Generation of Antiprotozoan Agents

Mini reviews in medicinal chemistry, 2018-01, Vol.18 (8), p.656

Fotie, Jean

2018

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Silicon switch: Carbon–silicon Bioisosteric replacement as a strategy to modulate the selectivity, physicochemical, and drug‐like properties in anticancer pharmacophores

Chemical biology & drug design, 2023-08, Vol.102 (2), p.235-254

2023

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The Fundamental Role of Oxime and Oxime Ether Moieties in Improving the Physicochemical and Anticancer Properties of Structurally Diverse Scaffolds

International journal of molecular sciences, 2023-12, Vol.24 (23), p.16854

2023

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Palladium(II) acetate catalyzed acylative cleavage of cyclic and acyclic ethers under neat conditions

Tetrahedron letters, 2017-12, Vol.58 (49), p.4648-4651

2017

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Tandem CuI – Zinc dust as a sustainable catalyst for the preparation of propargylamine derivatives via an A3 coupling reaction, under neat conditions

Tetrahedron Green Chem, 2023-12, Vol.2, p.100027, Article 100027

2023

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Silver(I)-mediated regioselective oxidative cross-coupling of phenol and aniline derivatives resulting in 2′-aminobiphenyl-2-ols

Tetrahedron letters, 2016-04, Vol.57 (14), p.1613-1618

2016

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Identification of new fisetin analogs as kinase inhibitors: Data on synthesis and anti-skin cancer activities evaluation

Data in brief, 2021-04, Vol.35, p.106858-106858, Article 106858

2021

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Two new indolic and quinolinic alkaloids and other secondary metabolites from Mostuea thomsonii (Loganiaceae)

Phytochemistry letters, 2018-08, Vol.26, p.154-158

2018

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Synthesis and antitrypanosomal evaluation of derivatives of N-benzyl-1,2-dihydroquinolin-6-ols: Effect of core substitutions and salt formation

Bioorganic & medicinal chemistry, 2011-01, Vol.19 (1), p.513-523

2011

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Depsipeptides from microorganisms: a new class of antimalarials

Mini reviews in medicinal chemistry, 2008-10, Vol.8 (11), p.1088

2008

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Pt-catalyzed O-silylation of oximes by tri-substituted organosilanes

Tetrahedron letters, 2019-06, Vol.60 (25), p.1636-1639

2019

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Dichloro(ethylenediamine)platinum(II), a water-soluble analog of the antitumor cisplatin, as a heterogeneous catalyst for a stereoselective hydrosilylation of alkynes under neat conditions

Tetrahedron letters, 2020-09, Vol.61 (36), p.152300, Article 152300

2020

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Nano-dispersed platinum(0) in organically modified silicate matrices as sustainable catalysts for a regioselective hydrosilylation of alkenes and alkynesElectronic supplementary information (ESI) available: 1H NMR, 13C NMR, HRMS (ESI/Q-TOF) and GC-MS. See DOI: 10.1039/c8nj01889h

2018-07

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Multifaceted approach toward mapping out the anticancer properties of small molecules via in vitro evaluation on melanoma and nonmelanoma skin cancer cells, and in silico target fishing

Chemical biology & drug design, 2024-01, Vol.103 (1), p.e14418-n/a

2024

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Synthesis, inverse docking-assisted identification and in vitro biological characterization of Flavonol-based analogs of fisetin as c-Kit, CDK2 and mTOR inhibitors against melanoma and non-melanoma skin cancers

Bioorganic chemistry, 2021-02, Vol.107, p.104595, Article 104595

2021

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4-(8-Eth-oxy-2,3-dihydro-1H-cyclo-penta-[c]quinolin-4-yl)butane-1-peroxol

Acta crystallographica. Section E, Structure reports online, 2010-06, Vol.66 (Pt 7), p.o1660-o1660

2010

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Nano-dispersed platinum(0) in organically modified silicate matrices as sustainable catalysts for a regioselective hydrosilylation of alkenes and alkynes

New journal of chemistry, 2018, Vol.42 (14), p.11782-11795

2018

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Antibacterial flavonoids from the fruits of Macaranga hurifolia

Journal of asian natural products research, 2022-11, Vol.24 (11), p.1041-1051

2022

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Antitrypanosomal Activity of 1,2-Dihydroquinolin-6-ols and Their Ester Derivatives

Journal of medicinal chemistry, 2010-02, Vol.53 (3), p.966-982

2010

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Unexpected 5,6,7,8,9,10-Hexahydro-6,6-pentamethylenephenanthridines and 2,3,4,5-Tetrahydro-4,4-tetramethylene-1 H -cyclopenta[ c ]quinolines from Skraup–Doebner–Von Miller Quinoline Synthesis and Their Implications for the Mechanism of That Reaction

Journal of organic chemistry, 2012-03, Vol.77 (6), p.2784-2790

2012

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The antiprotozoan potential of flavonoids

Pharmacognosy reviews, 2008-01, Vol.2 (3), p.6

Fotie, Jean

2008

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Iodine-catalyzed cycloalkenylation of dihydroquinolines and arylamines through a reaction with cyclic ketones under neat conditions

Tetrahedron letters, 2013-12, Vol.54 (51), p.7069-7073

2013

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Trypanocidal and Antileishmanial Dihydrochelerythrine Derivatives from Garcinia lucida

Journal of natural products (Washington, D.C.), 2007-10, Vol.70 (10), p.1650-1653

2007

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Editorial for the Special Issue "Advances in the Development of Anticancer Drugs"

Inosine 5'-Monophosphate Dehydrogenase (IMPDH) as a Potential Target for the Development of a New Generation of Antiprotozoan Agents

Silicon switch: Carbon–silicon Bioisosteric replacement as a strategy to modulate the selectivity, physicochemical, and drug‐like properties in anticancer pharmacophores

The Fundamental Role of Oxime and Oxime Ether Moieties in Improving the Physicochemical and Anticancer Properties of Structurally Diverse Scaffolds

Palladium(II) acetate catalyzed acylative cleavage of cyclic and acyclic ethers under neat conditions

Tandem CuI – Zinc dust as a sustainable catalyst for the preparation of propargylamine derivatives via an A3 coupling reaction, under neat conditions

Silver(I)-mediated regioselective oxidative cross-coupling of phenol and aniline derivatives resulting in 2′-aminobiphenyl-2-ols

Identification of new fisetin analogs as kinase inhibitors: Data on synthesis and anti-skin cancer activities evaluation

Two new indolic and quinolinic alkaloids and other secondary metabolites from Mostuea thomsonii (Loganiaceae)

Synthesis and antitrypanosomal evaluation of derivatives of N-benzyl-1,2-dihydroquinolin-6-ols: Effect of core substitutions and salt formation

Depsipeptides from microorganisms: a new class of antimalarials

Pt-catalyzed O-silylation of oximes by tri-substituted organosilanes

Dichloro(ethylenediamine)platinum(II), a water-soluble analog of the antitumor cisplatin, as a heterogeneous catalyst for a stereoselective hydrosilylation of alkynes under neat conditions

Nano-dispersed platinum(0) in organically modified silicate matrices as sustainable catalysts for a regioselective hydrosilylation of alkenes and alkynesElectronic supplementary information (ESI) available: 1H NMR, 13C NMR, HRMS (ESI/Q-TOF) and GC-MS. See DOI: 10.1039/c8nj01889h

Multifaceted approach toward mapping out the anticancer properties of small molecules via in vitro evaluation on melanoma and nonmelanoma skin cancer cells, and in silico target fishing

Synthesis, inverse docking-assisted identification and in vitro biological characterization of Flavonol-based analogs of fisetin as c-Kit, CDK2 and mTOR inhibitors against melanoma and non-melanoma skin cancers

4-(8-Eth-oxy-2,3-dihydro-1H-cyclo-penta-[c]quinolin-4-yl)butane-1-peroxol

Nano-dispersed platinum(0) in organically modified silicate matrices as sustainable catalysts for a regioselective hydrosilylation of alkenes and alkynes

Antibacterial flavonoids from the fruits of Macaranga hurifolia

Antitrypanosomal Activity of 1,2-Dihydroquinolin-6-ols and Their Ester Derivatives

Unexpected 5,6,7,8,9,10-Hexahydro-6,6-pentamethylenephenanthridines and 2,3,4,5-Tetrahydro-4,4-tetramethylene-1 H -cyclopenta[ c ]quinolines from Skraup–Doebner–Von Miller Quinoline Synthesis and Their Implications for the Mechanism of That Reaction

Synthesis, Inverse Docking-Assisted Identification and in vitro Biological Characterization of Flavonol-based Analogs of Fisetin as c-Kit, CDK2 and mTOR Inhibitors against Melanoma and Non-melanoma Skin Cancer

The antiprotozoan potential of flavonoids

Iodine-catalyzed cycloalkenylation of dihydroquinolines and arylamines through a reaction with cyclic ketones under neat conditions

Trypanocidal and Antileishmanial Dihydrochelerythrine Derivatives from Garcinia lucida

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