2022
DOI: 10.1080/07391102.2022.2036238
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Molecular interactions of esculin with bovine serum albumin and recognition of binding sites with spectroscopy and molecular docking

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Cited by 10 publications
(1 citation statement)
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“…In the development of new drugs, pharmacokinetics research and pharmacodynamics research are equally important, and have become an important part of drug preclinical research and clinical research (Li et al, 2019). Molecular docking simulation showed that esculin could bind to bovine serum albumin, and Lys‐294, Tyr‐340, Val‐342, Ser‐343, and Trp‐213 were the major residues of bovine serum albumin that formed a binding pocket for esculin (Qureshi, Akbar, Amir, & Javed, 2022). Xu et al used molecular docking simulation to explore the interaction of esculin and human serum albumin.…”
Section: Pharmacokinetics Of Esculinmentioning
confidence: 99%
“…In the development of new drugs, pharmacokinetics research and pharmacodynamics research are equally important, and have become an important part of drug preclinical research and clinical research (Li et al, 2019). Molecular docking simulation showed that esculin could bind to bovine serum albumin, and Lys‐294, Tyr‐340, Val‐342, Ser‐343, and Trp‐213 were the major residues of bovine serum albumin that formed a binding pocket for esculin (Qureshi, Akbar, Amir, & Javed, 2022). Xu et al used molecular docking simulation to explore the interaction of esculin and human serum albumin.…”
Section: Pharmacokinetics Of Esculinmentioning
confidence: 99%