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Meglumine: A Novel and Efficient Catalyst for One-Pot, Three-Component Combinatorial Synthesis of Functionalized 2‑Amino‑4H‑pyrans

ACS combinatorial science, 2013-11, Vol.15 (11), p.557-563

2013

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A facile one-pot green synthesis and antibacterial activity of 2-amino-4H-pyrans and 2-amino-5-oxo-5,6,7,8-tetrahydro-4H-chromenes

European journal of medicinal chemistry, 2009-09, Vol.44 (9), p.3805-3809

2009

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Salinomycin: a novel anti-cancer agent with known anti-coccidial activities

Current medicinal chemistry, 2013-11, Vol.20 (33), p.4095-4101

2013

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Genomics-Guided Discovery of Thailanstatins A, B, and C As Pre-mRNA Splicing Inhibitors and Antiproliferative Agents from Burkholderia thailandensis MSMB43

Journal of natural products (Washington, D.C.), 2013-04, Vol.76 (4), p.685-693

2013

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Discovery of Chromane-6-Sulfonamide Derivative as a Potent, Selective, and Orally Available Novel Retinoic Acid Receptor-Related Orphan Receptor γt Inverse Agonist

Journal of medicinal chemistry, 2021-11, Vol.64 (21), p.16106-16131

2021

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Ecofriendly synthesis of pyrano[2,3‐d]pyrimidine derivatives and related heterocycles with anti‐inflammatory activities

Archiv der Pharmazie (Weinheim), 2020-09, Vol.353 (9), p.e2000084-n/a

2020

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Synthesis, screening and docking of fused pyrano[3,2-d]pyrimidine derivatives as xanthine oxidase inhibitor

European journal of medicinal chemistry, 2017-05, Vol.131, p.14-28

2017

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Evaluation of the Pharmacophoric Role of the O–O Bond in Synthetic Antileishmanial Compounds: Comparison between 1,2-Dioxanes and Tetrahydropyrans

Journal of medicinal chemistry, 2020-11, Vol.63 (21), p.13140-13158

2020

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A peptide-salinomycin conjugate with a bystander effect reduces the stemness characteristics of ovarian cancer cells and enhances drug sensitivity

European journal of medicinal chemistry, 2024-10, Vol.276, p.116701, Article 116701

2024

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Design and Development of Highly Potent HIV‑1 Protease Inhibitors with a Crown-Like Oxotricyclic Core as the P2-Ligand To Combat Multidrug-Resistant HIV Variants

Journal of medicinal chemistry, 2017-05, Vol.60 (10), p.4267-4278

2017

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Cytotoxic Spliceostatins from Burkholderia sp. and Their Semisynthetic Analogues

Journal of natural products (Washington, D.C.), 2014-08, Vol.77 (8), p.1864-1870

2014

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Design, synthesis and biological evaluation of 2-substituted 3-hydroxy-6-methyl-4H-pyran-4-one derivatives as Pseudomonas aeruginosa biofilm inhibitors

European journal of medicinal chemistry, 2018-10, Vol.158, p.753-766

2018

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Synthesis, cytotoxicity and antibacterial activity of new esters of polyether antibiotic – salinomycin

European journal of medicinal chemistry, 2014-04, Vol.76, p.435-444

2014

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Structure–activity relationships of a novel pyranopyridine series of Gram-negative bacterial efflux pump inhibitors

Bioorganic & medicinal chemistry, 2015-05, Vol.23 (9), p.2024-2034

2015

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Synthesis of biscoumarin and dihydropyran derivatives with promising antitumor and antibacterial activities

Bioorganic & medicinal chemistry letters, 2015-12, Vol.25 (23), p.5520-5523

2015

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Caspase-Dependent Apoptosis in Prostate Cancer Cells and Zebrafish by Corchorusoside C from Streptocaulon juventas

Journal of natural products (Washington, D.C.), 2019-06, Vol.82 (6), p.1645-1655

2019

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The fungus Colletotrichum as a source for bioactive secondary metabolites

Archives of Pharmacal Research, 2019, 42(9), , pp.735-753

2019

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Antitumor activities of biscoumarin and dihydropyran derivatives

Bioorganic & medicinal chemistry letters, 2016-08, Vol.26 (16), p.3876-3880

2016

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Chemodiversity of Ladder-Frame Prymnesin Polyethers in Prymnesium parvum

Journal of natural products (Washington, D.C.), 2016-09, Vol.79 (9), p.2250-2256

2016

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Discovery of 4-(((4-(5-chloro-2-(((1s,4s)-4-((2-methoxyethyl)amino)cyclohexyl)amino)pyridin-4-yl)thiazol-2-yl)amino)methyl)tetrahydro-2H-pyran-4-carbonitrile (JSH-150) as a novel highly selective and potent CDK9 kinase inhibitor

European journal of medicinal chemistry, 2018-10, Vol.158, p.896-916

2018

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Singly and doubly modified analogues of C20-epi-salinomycin: A new group of antiparasitic agents against Trypanosoma brucei

European journal of medicinal chemistry, 2021-01, Vol.209, p.112900-112900, Article 112900

2021

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Antifungal compounds from cyanobacteria

Marine drugs, 2015-04, Vol.13 (4), p.2124-2140

2015

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Biologically active perspective synthesis of heteroannulated 8-nitroquinolines with green chemistry approach

Bioorganic & medicinal chemistry letters, 2017-04, Vol.27 (7), p.1538-1546

2017

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Pyranodipyran Derivatives with Tyrosyl DNA Phosphodiesterase 1 Inhibitory Activities and Fluorescent Properties from Aspergillus sp. EGF 15-0-3

Marine drugs, 2022-03, Vol.20 (3), p.211

2022

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Design, synthesis and biological studies of a library of NK1-Receptor Ligands Based on a 5-arylthiosubstituted 2-amino-4,6-diaryl-3-cyano-4H-pyran core: Switch from antagonist to agonist effect by chemical modification

European journal of medicinal chemistry, 2017-09, Vol.138, p.644-660

2017

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Meglumine: A Novel and Efficient Catalyst for One-Pot, Three-Component Combinatorial Synthesis of Functionalized 2‑Amino‑4H‑pyrans

A facile one-pot green synthesis and antibacterial activity of 2-amino-4H-pyrans and 2-amino-5-oxo-5,6,7,8-tetrahydro-4H-chromenes

Salinomycin: a novel anti-cancer agent with known anti-coccidial activities

Genomics-Guided Discovery of Thailanstatins A, B, and C As Pre-mRNA Splicing Inhibitors and Antiproliferative Agents from Burkholderia thailandensis MSMB43

Discovery of Chromane-6-Sulfonamide Derivative as a Potent, Selective, and Orally Available Novel Retinoic Acid Receptor-Related Orphan Receptor γt Inverse Agonist

Ecofriendly synthesis of pyrano[2,3‐d]pyrimidine derivatives and related heterocycles with anti‐inflammatory activities

Synthesis, screening and docking of fused pyrano[3,2-d]pyrimidine derivatives as xanthine oxidase inhibitor

Evaluation of the Pharmacophoric Role of the O–O Bond in Synthetic Antileishmanial Compounds: Comparison between 1,2-Dioxanes and Tetrahydropyrans

A peptide-salinomycin conjugate with a bystander effect reduces the stemness characteristics of ovarian cancer cells and enhances drug sensitivity

Design and Development of Highly Potent HIV‑1 Protease Inhibitors with a Crown-Like Oxotricyclic Core as the P2-Ligand To Combat Multidrug-Resistant HIV Variants

Cytotoxic Spliceostatins from Burkholderia sp. and Their Semisynthetic Analogues

Design, synthesis and biological evaluation of 2-substituted 3-hydroxy-6-methyl-4H-pyran-4-one derivatives as Pseudomonas aeruginosa biofilm inhibitors

Synthesis, cytotoxicity and antibacterial activity of new esters of polyether antibiotic – salinomycin

Structure–activity relationships of a novel pyranopyridine series of Gram-negative bacterial efflux pump inhibitors

Synthesis of biscoumarin and dihydropyran derivatives with promising antitumor and antibacterial activities

Caspase-Dependent Apoptosis in Prostate Cancer Cells and Zebrafish by Corchorusoside C from Streptocaulon juventas

The fungus Colletotrichum as a source for bioactive secondary metabolites

Antitumor activities of biscoumarin and dihydropyran derivatives

Chemodiversity of Ladder-Frame Prymnesin Polyethers in Prymnesium parvum

Discovery of 4-(((4-(5-chloro-2-(((1s,4s)-4-((2-methoxyethyl)amino)cyclohexyl)amino)pyridin-4-yl)thiazol-2-yl)amino)methyl)tetrahydro-2H-pyran-4-carbonitrile (JSH-150) as a novel highly selective and potent CDK9 kinase inhibitor

Singly and doubly modified analogues of C20-epi-salinomycin: A new group of antiparasitic agents against Trypanosoma brucei

Antifungal compounds from cyanobacteria

Biologically active perspective synthesis of heteroannulated 8-nitroquinolines with green chemistry approach

Pyranodipyran Derivatives with Tyrosyl DNA Phosphodiesterase 1 Inhibitory Activities and Fluorescent Properties from Aspergillus sp. EGF 15-0-3

Design, synthesis and biological studies of a library of NK1-Receptor Ligands Based on a 5-arylthiosubstituted 2-amino-4,6-diaryl-3-cyano-4H-pyran core: Switch from antagonist to agonist effect by chemical modification

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