| Literature DB >> 29932031 |
Abstract
Rational drug design is accomplished through the complementary use of structural biology and computational biology of biological macromolecules involved in disease pathology. Most of the known theoretical approaches for drug design are based on knowledge of the biological targets to which the drug binds. This approach can be used to design drug molecules that restore the balance of the signaling pathway by inhibiting or stimulating biological targets by molecular modeling procedures as well as by molecular dynamics simulations. Type III receptor tyrosine kinase affects most of the fundamental cellular processes including cell cycle, cell migration, cell metabolism, and survival, as well as cell proliferation and differentiation. Many inhibitors of successful rational drug design show that some computational techniques can be combined to achieve synergistic effects. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Keywords: CSF1R; FLT3; PDGFR; Type III receptor tyrosine kinase; c-KIT; computer-aidedzzm321990drug design; docking simulation; molecular dynamics; molecular modeling; rational drug design.
Year: 2019 PMID: 29932031 DOI: 10.2174/0929867325666180622143548
Source DB: PubMed Journal: Curr Med Chem ISSN: 0929-8673 Impact factor: 4.530