In Vitro and in Silico Binding Studies of Chromeno-Pyrimidine Derivatives With Biological Important Protein-Part III

In this study, in vitro and in silico interactions of bovine serum albumin with chromeno-pyrimidine derivatives (CP), 5-(7- bromo-2,4-dioxo-1,3,4,5-tetrahydro-2H-chromeno-[2,3-d]pyrimidin-5-yl)pyrimidine2,4,6(1H,3H,5H)-tri-one (CP1) and 8,9-dihydroxy-2H-chromeno[2,3-d] pyrimidine <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">$2,4(3 H)$</tex> dione (CP-2), are investigated. The high value of in vitro obtained binding constants are the result of good binding of the investigated compounds to BSA. Molecular docking results explain the interactions of BSA to the tested compounds and it is consistent with the experimentally obtained results.

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Published
2024-11-27
DOI
https://doi.org/10.1109/bibe63649.2024.10820495
Primary Topic
Synthesis and Characterization of Heterocyclic Compounds
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article
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article

In Vitro and in Silico Binding Studies of Chromeno-Pyrimidine Derivatives With Biological Important Protein-Part III

Edina Avdović, Dušica Simijonović, Danijela Lj. Stojković, Sandra Jovičić Milić et al.
Synthesis and Characterization of Heterocyclic Compounds
article

In Vitro and in Silico Binding Studies of Chromeno-Pyrimidine Derivatives With Biological Important Protein-Part III

Edina Avdović, Dušica Simijonović, Danijela Lj. Stojković, Sandra Jovičić Milić, Zoran Marković, Tamara M. Mladenović
article en

Abstract

In this study, in vitro and in silico interactions of bovine serum albumin with chromeno-pyrimidine derivatives (CP), 5-(7- bromo-2,4-dioxo-1,3,4,5-tetrahydro-2H-chromeno-[2,3-d]pyrimidin-5-yl)pyrimidine2,4,6(1H,3H,5H)-tri-one (CP1) and 8,9-dihydroxy-2H-chromeno[2,3-d] pyrimidine <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">$2,4(3 H)$</tex> dione (CP-2), are investigated. The high value of in vitro obtained binding constants are the result of good binding of the investigated compounds to BSA. Molecular docking results explain the interactions of BSA to the tested compounds and it is consistent with the experimentally obtained results.

University of Kragujevac (RS), State University of Novi Pazar (RS)
Openalex Percentile: Top 82%
Synthesis and Characterization of Heterocyclic Compounds
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