Characterizing the binding interaction between erlotinib and calf thymus DNA in vitro using multi‐spectroscopic methodologies and viscosity measurement combined …
XJ Chen, BL Wang, KL Zhou, YY Lou, SB Kou… - …, 2019 - Wiley Online Library
The binding interaction between erlotinib (ELTN) and calf thymus DNA (ct‐DNA) was
characterized with the help of multi‐spectroscopic approaches, viscosity measurement and …
characterized with the help of multi‐spectroscopic approaches, viscosity measurement and …
Electrochemical and theoretical study on interaction between erlotinib and DNA
M Jovanović, K Nikolic, M Čarapić… - Journal of Pharmaceutical …, 2023 - Elsevier
A comprehensive investigation of tyrosine kinase inhibitor erlotinib (ERL) electrochemical
behavior and interaction with DNA was performed with the aim to clarify its redox …
behavior and interaction with DNA was performed with the aim to clarify its redox …
Assessment on the binding characteristics of dasatinib, a tyrosine kinase inhibitor to calf thymus DNA: Insights from multi-spectroscopic methodologies and molecular …
YJ Luo, BL Wang, SB Kou, ZY Lin, KL Zhou… - Journal of …, 2020 - Taylor & Francis
The binding characteristics of calf thymus DNA (ct-DNA) with dasatinib (DSTN), a tyrosine
kinase inhibitor was assessed through multi-spectroscopic methodologies and viscosity …
kinase inhibitor was assessed through multi-spectroscopic methodologies and viscosity …
[HTML][HTML] Characterization of interaction of calf thymus DNA with gefitinib: Spectroscopic methods and molecular docking
JH Shi, TT Liu, M Jiang, J Chen, Q Wang - Journal of Photochemistry and …, 2015 - Elsevier
The binding interaction of gefitinib with calf thymus DNA (ct-DNA) under the simulated
physiological pH condition was studied employing UV absorption, fluorescence, circular …
physiological pH condition was studied employing UV absorption, fluorescence, circular …
Study of the binding interaction of salmon sperm DNA with nintedanib, a tyrosine kinase inhibitor using multi-spectroscopic, thermodynamic, and in silico approaches
The study of the intermolecular binding interaction of small molecules with DNA can guide
the rational drug design with greater efficacy and improved or more selective activity. In the …
the rational drug design with greater efficacy and improved or more selective activity. In the …
Kinetic and thermodynamic insights into interaction of erlotinib with epidermal growth factor receptor: Surface plasmon resonance and molecular docking approaches
S Mohammadzadeh-Asl, A Aghanejad, R Yekta… - International Journal of …, 2020 - Elsevier
Epidermal growth factor receptor (EGFR) plays an important role in cell proliferation at non-
small cell lung cancer (NSCLC). Therefore, targeted therapy of cancer via this kind of …
small cell lung cancer (NSCLC). Therefore, targeted therapy of cancer via this kind of …
The use of molecular docking and spectroscopic methods for investigation of the interaction between regorafenib with human serum albumin (HSA) and calf thymus …
H Tanzadehpanah, H Mahaki, M Moradi… - Protein and Peptide …, 2021 - ingentaconnect.com
Background: Interactions of drugs with DNA and proteins may modify their biological
activities and conformations, which effect transport and biological metabolism of drugs …
activities and conformations, which effect transport and biological metabolism of drugs …
Binding study of florfenicol with DNA by multi-spectroscopy and molecular docking techniques
X Li, Y Yuan, Y Wang, F Zhang, R Zhao, D Shao… - Process …, 2021 - Elsevier
The investigation on the binding interaction mechanism of florfenicol with DNA in vitro was
reported via multi-spectroscopy measurements and molecular docking approach in the …
reported via multi-spectroscopy measurements and molecular docking approach in the …
Exploring the binding interaction of calf thymus DNA with lapatinib, a tyrosine kinase inhibitor: Multi-spectroscopic techniques combined with molecular docking
KY Chen, KL Zhou, YY Lou, JH Shi - Journal of Biomolecular …, 2019 - Taylor & Francis
Lapatinib, a double-target receptor tyrosine kinase inhibitor, is an oral-targeted anticancer
drug developed by GlaxoSmithKline (GSK). It mainly acts on epidermal growth factor …
drug developed by GlaxoSmithKline (GSK). It mainly acts on epidermal growth factor …
Elucidation of binding interactions and mechanism of Fludarabine with dsDNA via multispectroscopic and molecular docking studies
Fludarabine is a purine derivative, anti-neoplastic drug and is still being used in the
treatments of chronic lymphocytic leukemia, small lymphocytic lymphoma, acute myeloid …
treatments of chronic lymphocytic leukemia, small lymphocytic lymphoma, acute myeloid …
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