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Synthesis and characterization of new metal complexes containing Triazino[5,6-b]indole moiety: In vitro DNA and HSA binding studies
被引:11
|作者:
Alanazi, Reem L. B.
[1
]
Zaki, Mehvash
[1
]
Bawazir, Wafa A.
[1
]
机构:
[1] King Abdulaziz Univ, Dept Chem, POB 80203, Jeddah, Saudi Arabia
关键词:
Triazino[5,6-b]indole;
Cu(II)/Ni(II) metal complexes;
In vitro DNA binding;
HSA binding;
FRET;
Molecular docking;
HUMAN SERUM-ALBUMIN;
COPPER(II) COMPLEXES;
BIOLOGICAL-ACTIVITY;
SCHIFF-BASE;
SPECTROSCOPIC CHARACTERIZATION;
MOLECULAR DOCKING;
CRYSTAL-STRUCTURE;
PROTEIN-BINDING;
ANTIPROLIFERATIVE ACTIVITY;
LIGAND HYDROPHOBICITY;
D O I:
10.1016/j.molstruc.2021.131203
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The present study reports the synthesis, structural characterization of Ni(II) (1,3) and Cu(II) (2,4) metal complexes of Schiff-base (L) derived from 5H-[1,2,4]triazino[5,6-b]indol-3-amine and salicylaldehyde moiety. The coordination sphere of Cu(II)/Ni(II) was completed by tethering secondary ligand 2,2'-Bipyridine and 1,10 phenanthroline to obtain the final complexes 1-4 , respectively. The spectral analysis of complexes 1 and 3 suggested square planar geometry while complexes 2 and 4 acquire the octahedral geometry around the metal centers. In vitro DNA binding profiles of the newly synthesized metal complexes 1-4 with calf thymus DNA (CT DNA) were explored by employing electronic absorption titrations and fluorescence spectral studies. The results revealed that complexes 1-4 bind to DNA through electrostatic surface binding mode along with partial intercalation in the minor groove. Moreover, complexes 3 and 4 have stronger DNA binding propensity with higher intrinsic binding constant K-b values of 1.9 x 10(4) and 4.8 x 10(4) M-1 , respectively. Additionally, HSA binding studies of ligand L and metal complexes 1-4 support the static quenching mechanism and alterations in the microenvironment around Trp-214 residues causing conformational distortions in the HSA secondary structure. Furthermore, molecular docking studies of complexes 3 and 4 with DNA and HSA confirms that both specifically binds in G-C rich regions of the DNA minor groove and subdomain IIA pocket of HSA near the Trp-214 residue. (C) 2021 Elsevier B.V. All rights reserved.
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页数:19
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