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Galina Karabanovich

faculty of pharmacy in hradec kralove
H指数:13
被引数:685

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Discovery and Pharmacological Profiling of Quinoline- and Quinoxaline-Based Phenoxypropanoic Acid Derivatives as Multitarget Modulators of PPARα, FXR, and LXRα receptors

喹啉基和喹喔啉基苯氧基丙酸衍生物的发现及其作为PPARα、FXR和LXRα受体多靶点调节剂的药理学表征

2026-10-270
OAAI
Topobexin targets the Topoisomerase II ATPase domain for beta isoform-selective inhibition and anthracycline cardioprotection

Topobexin靶向Topoisomerase II ATPase结构域,以实现β异构体选择性抑制和蒽环类心脏保护。

2025-05-280
OA
Both Nitro Groups Are Essential for High Antitubercular Activity of 3,5-Dinitrobenzylsulfanyl Tetrazoles and 1,3,4-Oxadiazoles through the Deazaflavin-Dependent Nitroreductase Activation Pathway
2023-12-291
OAAI
Cardioprotective Effects Of Dexrazoxane Derivatives Against Chronic Anthracycline Cardiotoxicity Depend On Topoisomerase II Beta Inhibition And Prevention Of DNA Damage Signaling In The Heart

右雷佐生衍生物对慢性蒽环类药物心脏毒性的心脏保护作用取决于拓扑异构酶II β 的抑制作用和心脏DNA损伤信号的预防

2022-08-050
PRE
Clinically Translatable Prevention of Anthracycline Cardiotoxicity by Dexrazoxane Is Mediated by Topoisomerase II Beta and Not Metal Chelation

右雷佐生对蒽环类药物心脏毒性的临床上可翻译的预防是由拓扑异构酶II β 介导的,而不是金属螯合

2021-11-0139
OA
Structure-Activity Relationship Study of Dexrazoxane Analogues Reveals ICRF-193 as the Most Potent Bisdioxopiperazine against Anthracycline Toxicity to Cardiomyocytes Due to Its Strong Topoisomerase IIβ Interactions
2021-03-2216
OAAI
Investigation of Structure-Activity Relationships of Dexrazoxane Analogs Reveals Topoisomerase IIβ Interaction as a Prerequisite for Effective Protection against Anthracycline Cardiotoxicity
2020-06-0114
OAAI
Development of 3,5-Dinitrophenyl-Containing 1,2,4-Triazoles and Their Trifluoromethyl Analogues as Highly Efficient Antitubercular Agents Inhibiting Decaprenylphosphoryl-β-D-ribofuranose 2′-Oxidase
2019-08-0841
PREAI
EFFECTIVE CARDIOPROTECTION AGAINST ANTHRACYCLINE CARDIOTOXICITY IN ISOLATED CARDIOMYOCYTES AND RABBITS IS BASED ON DEXRAZOXANE INTERACTION WITH TOPOISOMERASE II BETA INSTEAD OF IRON CHELATION BY ITS METABOLITE ADR-925
HEART
IF4.4
2019-05-010
OAAI
S-substituted 3,5-dinitrophenyl 1,3,4-oxadiazole-2-thiols and tetrazole-5-thiols as highly efficient antitubercular agents

S-取代的3,5-二硝基苯基1,3,4-恶二唑-2-硫醇和tetrazole-5-thiols作为高效抗结核药

2017-01-0154
PREAI
Development of 3,5-Dinitrobenzylsulfanyl-1,3,4-oxadiazoles and Thiadiazoles as Selective Antitubercular Agents Active Against Replicating and Nonreplicating Mycobacterium tuberculosis
2016-03-1595
PREAI
1-Substituted-5-[(3,5-dinitrobenzyl)sulfanyl]-1H-tetrazoles and their isosteric analogs: A new class of selective antitubercular agents active against drug-susceptible and multidrug-resistant mycobacteria

1-取代-5-[(3,5-二硝基苄基) 硫烷基]-1h-四唑及其等排类似物: 一类新的选择性抗结核药,对药物敏感和多重耐药分枝杆菌具有活性

2014-07-0150
PREAI