Chitin synthase targeting antifungal agents for Mucormycosis (Black fungus disease) caused by Rhizopus delemar - An in-silico study

Abstract

Mucormycosis, a severe fungal infection caused by Mucorales fungi, particularly Rhizopus delemar, has prompted the development of new and more potent antifungal drugs due to the emergence of drug-resistant strains. Currently used drugs are known to be toxic to human cells also, which is a major drawback in their administration. Antifungal drugs commercially under use and their structurally modified analogues along with 30 plants reported with antifungal activity from IMPPAT database, totalling 229 compounds, were screened against the best modelled structure of Chitin Synthase, a key target enzyme of Rhizopus delemar by in-silico molecular docking studies. Computerized methods to assess absorption, distribution, metabolism, excretion, and toxicity (ADMET) profiles was employed to further filter key lead drug candidates from among the docked ligands that could act as potential antifungal medications. Modified structures of Posaconazole, Nikkomycin and Isavuconazole were found to give better docking results than compared to the original drugs, though they failed to comply with ADMET parameters. Among the phytochemicals, 1-nonacosanol displayed binding affinity (highest LibDock score) greater than the synthetic drugs and their derivatives, though it too failed to comply with ADMET parameters. The phytochemical Dihydrocapsaicin was found to be the best compound that satisfied all the parameters such as ADMET, TOPKAT, Lipinskis and Vebers rule along with good binding affinity. All in all, this novel study paves a way to investigate the interaction of Chitin Synthase inhibitors at molecular level to achieve an alternative solution with less toxic effects to treat Mucormycosis.