Histamine H 3 receptor ligands by hybrid virtual screening, docking, molecular dynamics simulations, and investigation of their biological effects

• Published in: Chemical biology & drug design 2019-05, Vol.93 (5), p.832-843
• Main Authors: Ghamari, Nakisa, Zarei, Omid, Reiner, David, Dastmalchi, Siavoush, Stark, Holger, Hamzeh-Mivehroud, Maryam
• Format: Article
• Language: English
• Subjects: Binding Sites; Humans; Hydrogen Bonding; Ligands; Molecular Docking Simulation; Molecular Dynamics Simulation; Protein Structure, Tertiary; Receptors, Histamine H3 - chemistry; Receptors, Histamine H3 - metabolism; Thermodynamics
• ISSN: 1747-0277; 1747-0285
• DOI: 10.1111/cbdd.13471

Histamine H receptors (H R), belonging to G-protein coupled receptors (GPCR) class A superfamily, are responsible for modulating the release of histamine as well as of other neurotransmitters by a negative feedback mechanism mainly in the central nervous system (CNS). These receptors have gained increased attention as therapeutic target for several CNS related neurological diseases. In the current study, we aimed to identify novel H R ligands using in silico virtual screening methods. To this end, a combination of ligand- and structure-based approaches was utilized for screening of ZINC database on the homology model of human H R. Structural similarity- and pharmacophore-based approaches were employed to generate compound libraries. Various molecular modeling methodologies such as molecular docking and dynamics simulation along with different drug likeness filtering criteria were applied to select anti-H R ligands as promising candidate molecules based on different known parent lead compounds. In vitro binding assays of the selected molecules demonstrated three of them being active within the micromolar and submicromolar K range. The current integrated computational and experimental methods used in this work can provide new general insights for systematic hit identification for novel anti-H R agents from large compound libraries.