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T

Tamás Jernei

eotvos lorand university

H指数:6

被引数:128

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Comparative Study of Ferrocene- and Indene-Based Tamoxifen Derivatives of Different Molecular Flexibility on High-Mortality Cancer Cell Lines

基于不同分子柔韧性的二茂铁基和茚基他莫昔芬衍生物对高死亡率癌细胞系的比较研究

Pharmaceuticals

IF4.8

2026-03-030

OAAI

Fragment-based structure-activity relationship analysis of CK-571 reveals non-interacting groups drive smooth muscle myosin selectivity

CK-571的基于片段的结构-活性关系分析揭示了非相互作用基团驱动平滑肌肌球蛋白的选择性

European Journal of Medicinal Chemistry

IF5.9

2025-12-160

PRE

CuAAC-Based Synthesis, Copper-Catalyzed Aldehyde-Forming Hydrolytic Fission and Antiproliferative Evaluation of Novel Ferrocenoylamino-Substituted Triazole-Tethered Quinine-Chalcone Hybrids

基于CuAAC的合成，铜催化的形成醛的水解裂变和新型二茂铁酰基氨基取代的三唑束缚的奎宁-查耳酮杂化物的抗增殖评估

IF4.6

2024-01-110

OAAI

Synthesis and SAR Analysis of Novel 4-Hydroxytamoxifen Analogues Based on Their Cytotoxic Activity and Electron-Donor Character

IF4.6

2022-10-104

OAAI

Investigation of the Antitumor Effects of Tamoxifen and Its Ferrocene-Linked Derivatives on Pancreatic and Breast Cancer Cell Lines

PHARMACEUTICALS

IF4.8

2022-03-058

OAAI

Protoflavone-Chalcone Hybrids Exhibit Enhanced Antitumor Action through Modulating Redox Balance, Depolarizing the Mitochondrial Membrane, and Inhibiting ATR-Dependent Signaling

IF6.6

2020-06-1217

OAAI

Novel Polycondensed Partly Saturated β-Carbolines Including Ferrocene Derivatives: Synthesis, DFT-Supported Structural Analysis, Mechanism of Some Diastereoselective Transformations and a Preliminary Study of their In Vitro Antiproliferative Effects

IF4.6

2020-03-311

OAAI

Synthesis, Structure and In Vitro Cytotoxic Activity of Novel Cinchona-Chalcone Hybrids with 1,4-Disubstituted- and 1,5-Disubstituted 1,2,3-Triazole Linkers

IF4.6

2019-11-1112

OAAI