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Barbara Kaproń

Medical University of Lublin

H指数:16

被引数:790

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The new thiazolidine-2,4-dione-based hybrids with promising antimycobacterial activity: design, synthesis, biological evaluation, and drug interaction analysis

具有良好抗分枝杆菌活性的新型thiazolidine-2，基于4-二酮的杂种: 设计，合成，生物学评估和药物相互作用分析

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY

IF5.4

2025-01-030

OAAI

In Vitro and In Silico of Cholinesterases Inhibition and In Vitro and In Vivo Anti-Melanoma Activity Investigations of Extracts Obtained from Selected Berberis Species

IF4.6

2024-02-283

OAAI

Effect of Linker Elongation on the VGSC Affinity and Anticonvulsant Activity among 4-Alkyl-5-aryl-1,2,4-triazole-3-thione Derivatives

IF4.6

2023-07-072

OAAI

Determination of Some Isoquinoline Alkaloids in Extracts Obtained from Selected Plants of the Ranunculaceae, Papaveraceae and Fumarioideae Families by Liquid Chromatography and In Vitro and In Vivo Investigations of Their Cytotoxic Activity

IF4.6

2023-04-168

OAAI

Identification of the first-in-class dual inhibitors of human DNA topoisomerase IIα and indoleamine-2,3-dioxygenase 1 (IDO 1) with strong anticancer properties

具有强抗癌特性的人类DNA拓扑异构酶ii α 和indoleamine-2，3-双加氧酶1 (IDO 1) 的一流双重抑制剂的鉴定

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY

IF5.4

2022-11-085

OAAI

Inhibition of Toxoplasma gondii by 1,2,4-triazole-based compounds: marked improvement in selectivity relative to the standard therapy pyrimethamine and sulfadiazine

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY

IF5.4

2022-09-279

OAAI

Design, Synthesis, and Characterization of Novel Coordination Compounds of Benzimidazole Derivatives with Cadmium

IF5.5

2022-08-037

OA

Aloe arborescens: In Vitro Screening of Genotoxicity, Effective Inhibition of Enzyme Characteristics for Disease Etiology, and Microbiological Activity

IF4.6

2022-04-037

OAAI

Lichen-Derived Compounds and Extracts as Biologically Active Substances with Anticancer and Neuroprotective Properties

PHARMACEUTICALS

IF4.8

2021-12-1032

OAAI

Determination of Cytotoxic Activity of Sanguinaria canadensis Extracts against Human Melanoma Cells and Comparison of Their Cytotoxicity with Cytotoxicity of Some Anticancer Drugs

IF4.6

2021-03-2013

OAAI

Determination of Cytotoxic Activity of Selected Isoquinoline Alkaloids and Plant Extracts Obtained from Various Parts of Mahonia aquifolium Collected in Various Vegetation Seasons

IF4.6

2021-02-048

OAAI

Hydrogel Delivery System ContainingCalendulae flosLyophilized Extract with Chitosan as a Supporting Strategy for Wound Healing Applications

IF5.5

2020-07-0720

OAAI

1,2,4-Triazole-based anticonvulsant agents with additional ROS scavenging activity are effective in a model of pharmacoresistant epilepsy

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY

IF5.4

2020-04-0741

OAAI

Determination of Selected Isoquinoline Alkaloids from Mahonia aquifolia; Meconopsis cambrica; Corydalis lutea; Dicentra spectabilis; Fumaria officinalis; Macleaya cordata Extracts by HPLC-DAD and Comparison of Their Cytotoxic Activity

IF4

2019-10-0234

OAAI

Development of the 1,2,4-triazole-based anticonvulsant drug candidates acting on the voltage-gated sodium channels. Insights from in-vivo, in-vitro, and in-silico studies

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES

IF4.7

2019-03-0153

PREAI

Molecular mechanism of action and safety of 5-(3-chlorophenyl)-4-hexyl-2,4-dihydro-3H-1,2,4-triazole-3-thione - a novel anticonvulsant drug candidate

INTERNATIONAL JOURNAL OF MEDICAL SCIENCES

IF3.2

2017-01-0118

OAAI

Search for factors affecting antibacterial activity and toxicity of 1,2,4-triazole-ciprofloxacin hybrids

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2015-06-0165

PREAI

Design, synthesis and biological evaluation of 4-benzoyl-1-dichlorobenzoylthiosemicarbazides as potent Gram-positive antibacterial agents

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY

IF5.4

2015-04-217

PREAI

Determination of the Primary Molecular Target of 1,2,4-Triazole-Ciprofloxacin Hybrids

IF4.6

2015-04-0930

OAAI

Search for human DNA topoisomerase II poisons in the group of 2,5-disubstituted-1,3,4-thiadiazoles

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY

IF5.4

2015-03-2015

OAAI