Title: Synthesis, crystallographic study, in silico and in vitro investigation of novel flavonol-amino acid conjugate as an anti-proliferative agent
| dc.contributor.author | Prerna Kumari | |
| dc.contributor.author | Pradeep Harish Kumar | |
| dc.contributor.author | Rakesh Kumar Gupta | |
| dc.contributor.author | Anima Tripathi | |
| dc.contributor.author | Pawan Kumar Dubey | |
| dc.contributor.author | Anuradha Ambasta | |
| dc.contributor.author | Jayhind Kumar Chauhan | |
| dc.contributor.author | Joydeb Goura | |
| dc.contributor.author | Abhijeet Kumar | |
| dc.contributor.author | Garima Tripathi | |
| dc.date.accessioned | 2026-02-19T06:59:36Z | |
| dc.date.issued | 2025 | |
| dc.description.abstract | In this article, a flavonol-Aib conjugate; {(4-oxo-2-phenyl-4-H-chromen-3-yl-2-((start-butoxy-carbonyl) amino)-2-methyl-propanoate) (3A)} has been synthesized, purified and characterized through 1H and 13C NMR, mass spectrometry and X-ray crystallography. X-ray crystallography of these molecules revealed that this is a flavonol-Aib conjugate; there is no intramolecular hydrogen bond, while two intermolecular H-bonds occur between two molecules of flavonol-Aib conjugate, between O2 of C=O (flavonol ring) and H1 (Aib NH) is 2.183Å. This intermolecular interaction generates a stacked two-dimensional (2-D) structure. There are weak interactions between H3 of the flavonol-benzene ring and H18B of the tertiary Butyl-CH<inf>3</inf> is 2.804Å., and the same H3 interaction with other molecules' H14 of phenyl of substituted flavonol is 2.332Å. The distance between O2 of C=O (flavonol ring) and H11 (other phenyl-substituted flavonol rings) is 2.610Å, giving a specific molecular conformation. A complete molecular structure investigation of the molecule shows that several inter- and intramolecular weak to strong interactions lead to a peculiar array of molecules in two and three dimensions. In silico studies, molecular docking via Auto doc vina reveals that flavonol with 2-aminoisobutyric acid conjugate, among conjugates of different amino acids (glycine, alanine, valine, leucine, Isoleucine), Aib conjugate shows highest binding affinity with CDC42 (-7.7), BCL2L1 (-8.9), GSK3B (-6.8), MAPK1 (-8.8), PPARG (-7.4), ICAM1 (-7.8), MMP9 (8.0), BCL2 (-8.9), ERBB2 (-9,0), HSP90A1 (9.5) gene. The result of in vitro studies exhibits remarkable inhibitory ability with IC<inf>50</inf> values of 400 µg/ml. The overall outcome indicates that flavonol conjugated with 2-aminoisobutyric acid (Aib) can inhibit the growth of the MCF-7 cancer cell line by targeting multiple biological pathways. © 2025 | |
| dc.identifier.doi | 10.1016/j.molstruc.2025.142768 | |
| dc.identifier.issn | 222860 | |
| dc.identifier.uri | https://doi.org/10.1016/j.molstruc.2025.142768 | |
| dc.identifier.uri | https://dl.bhu.ac.in/bhuir/handle/123456789/63337 | |
| dc.publisher | Elsevier B.V. | |
| dc.subject | Breast cancer | |
| dc.subject | Conjugate chemistry | |
| dc.subject | Flavonol | |
| dc.subject | In silico studies | |
| dc.subject | In vitro studies | |
| dc.subject | Molecular docking | |
| dc.title | Synthesis, crystallographic study, in silico and in vitro investigation of novel flavonol-amino acid conjugate as an anti-proliferative agent | |
| dc.type | Publication | |
| dspace.entity.type | Article |
