Synthetic Analogues of Aminoadamantane as Influenza Viral Inhibitors - In Vitro, In Silico and QSAR Studies
Abstract
A series of nineteen amino acid analogues of amantadine (Amt) and rimantadine (Rim) were synthesized and their antiviral activity was evaluated against influenza virus A (H3N2). Among these analogues, the conjugation of rimantadine with glycine illustrated high antiviral activity combined with low cytotoxicity.
Moreover, this compound presented a profoundly high stability after in vitro incubation in human plasma for 24 h. Its thermal stability was established using differential and gravimetric thermal analysis.
The crystal structure of glycyl-rimantadine revealed that it crystallizes in the orthorhombicPbcaspace group. The structure-activity relationship for this class of compounds was established, with CoMFA (Comparative Molecular Field Analysis) 3D-Quantitative Structure Activity Relationships (3D-QSAR) studies predicting the activities of synthetic molecules.
In addition, molecular docking studies were conducted, revealing the structural requirements for the activity of the synthetic molecules.