Structure-based design and evaluation of novel N-phenyl-1H-indol-2-amine derivatives for fat mass and obesity-associated (FTO) protein inhibition. (October 2016)

• Record Type: Journal Article
• Authors: Padariya, Monikaben; Kalathiya, Umesh
• Is Part Of: Computational biology and chemistry. Volume 64(2016)
• Page Start: 414
• Page End: 425
• Publication Date: 2016-10
• Subjects: FTO protein inhibitors -- Anti-obesity -- Molecular docking -- Binding affinity -- Molecular dynamics simulation; Chemistry -- Data processing -- Periodicals; Biology -- Data processing -- Periodicals; Biochemistry -- Data processing; Biology -- Data processing; Molecular biology -- Data processing; Periodicals; Electronic journals; 542.85
• DOI: 10.1016/j.compbiolchem.2016.09.008
• Languages: English
• ISSNs: 1476-9271

Abstract

Graphical abstract: Highlights: N -phenyl-1H-indol-2-amine was selected as a base for novel FTO protein inhibitors. Designed ligands were studied by molecular docking and dynamic simulation approach. Hydroxyl (OH) and carbonyl (CO) group of ligand played a key role in FTO inhibition. Abstract: Fat mass and obesity-associated (FTO) protein contributes to non-syndromic human obesity which refers to excessive fat accumulation in human body and results in health risk. FTO protein has become a promising target for anti-obesity medicines as there is an immense need for the rational design of potent inhibitors to treat obesity. In our study, a new scaffold N -phenyl-1H-indol-2-amine was selected as a base for FTO protein inhibitors by applying scaffold hopping approach. Using this novel scaffold, different derivatives were designed by extending scaffold structure with potential functional groups. Molecular docking simulations were carried out by using two different docking algorithm implemented in CDOCKER (flexible docking) and AutoDock programs (rigid docking). Analyzing results of rigid and flexible docking, compound MU06 was selected based on different properties and predicted binding affinities for further analysis. Molecular dynamics simulation of FTO/MU06 complex was performed to characterize structure rationale and binding stability. Certainly, Arg96 and His231 residue of FTO protein showed stable interaction with inhibitor MU06 throughout the production dynamics phase. Three residues of FTO protein (Arg96, Asp233, and His231) were found common in making H-bond interactions with MU06 during molecular dynamics simulation and CDOCKER docking.