Binding sites of anticancer drugs on human serum albumin (HSA): a review

P Molaei, H Mahaki, H Manoochehri… - Protein and peptide …, 2022 - ingentaconnect.com
Background: To recognize the action of pharmacologically approved anticancer drugs in
biological systems, information regarding its pharmacokinetics, such as its transport within …

Investigation on the binding behavior between BSA and lenvatinib with the help of various spectroscopic and in silico methods

BL Wang, SB Kou, ZY Lin, JH Shi - Journal of Molecular Structure, 2020 - Elsevier
Lenvatinib was a multi-tyrosine kinase inhibitor (TKI) used for treating advanced renal cell
carcinoma and differentiated thyroid cancer. Multiple fluorescence spectroscopy including …

[HTML][HTML] Intrinsically fluorescent anti-cancer drugs

ML Kabir, F Wang, AHA Clayton - Biology, 2022 - mdpi.com
Simple Summary Cancer is one of the biggest causes of death world-wide. The
development of anti-cancer drugs is important in combatting this disease. As good as these …

[HTML][HTML] Serum protein-hyaluronic acid complex nanocarriers: Structural characterisation and encapsulation possibilities

AN Kovács, N Varga, Á Juhász, E Csapó - Carbohydrate Polymers, 2021 - Elsevier
A protein-polysaccharide-based potential nanocarrier system have been developed via a
simple, one-step preparation protocol without the use of long-term heating and the utilization …

Improving the stability of EGFR inhibitor cobalt (III) prodrugs

M Mathuber, H Schueffl, O Dömötör… - Inorganic …, 2020 - ACS Publications
Although tyrosine kinase inhibitors (TKIs) have revolutionized cancer therapy in the past two
decades, severe drawbacks such as strong adverse effects and drug resistance limit their …

[HTML][HTML] Development and mechanistic insight into the enhanced cytotoxic potential of parvifloron D albumin nanoparticles in EGFR-overexpressing pancreatic cancer …

A Santos-Rebelo, P Kumar, V Pillay, YE Choonara… - Cancers, 2019 - mdpi.com
Pancreatic cancer is one of the most lethal cancers, with an extremely poor prognosis. The
development of more effective therapies is thus imperative. Natural origin compounds …

[HTML][HTML] Design, synthesis and biological evaluation of pyrazolo [3, 4-d] pyridazinone derivatives as covalent FGFR inhibitors

X Wu, M Dai, R Cui, Y Wang, C Li, X Peng… - … Pharmaceutica Sinica B, 2021 - Elsevier
Fibroblast growth factor receptors (FGFRs) have emerged as promising targets for
anticancer therapy. In this study, we synthesized and evaluated the biological activity of 66 …

[HTML][HTML] Investigating the effect of tyrosine kinase inhibitors on the interaction between human serum albumin by atomic force microscopy

Y Fu, J Wang, Y Wang, H Sun - Biomolecules, 2022 - mdpi.com
It is important for elucidating the regulation mechanism of life activities, as well as for the
prevention, diagnosis, and drug design of diseases, to study protein–protein interactions …

Theoretical and practical aspects of albumin esterase activity

DA Belinskaia, NV Goncharov - Russian Journal of Bioorganic Chemistry, 2020 - Springer
Unlike many other plasma proteins, albumin is barely glycosylated and plays an important
role in maintaining the colloidal osmotic blood pressure; it can bind and transport various …

Nanoparticle-based formulation of metallacarboranes with bovine serum albumin for application in cell cultures

B Schwarze, M Gozzi, C Zilberfain, J Rüdiger… - Journal of Nanoparticle …, 2020 - Springer
We report on the unique self-assembling properties of one molybdacarborane (1) and two
ruthenacarborane complexes (2 and 3) to spontaneously form nanoparticles alone or in …