Scaffold repurposing reveals new nanomolar phosphodiesterase type 5 (PDE5) inhibitors based on pyridopyrazinone scaffold : investigation of in vitro and in silico properties

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Amin, Kamelia M and El-Badry, Ossama M and Abdel Rahman, Doaa E and Abdellattif, Magda H and Abourehab, Mohammed A S and El-Maghrabey, Mahmoud H and Elsaid, Fahmy G and El Hamd, Mohamed A and Elkamhawy, Ahmed and Ammar, Usama M (2022) Scaffold repurposing reveals new nanomolar phosphodiesterase type 5 (PDE5) inhibitors based on pyridopyrazinone scaffold : investigation of in vitro and in silico properties. Pharmaceutics, 14 (9). 1954. ISSN 1999-4923 (https://doi.org/10.3390/pharmaceutics14091954)

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Abstract

Inhibition of PDE5 results in elevation of cGMP leading to vascular relaxation and reduction in the systemic blood pressure. Therefore, PDE5 inhibitors are used as antihypertensive and antianginal agents in addition to their major use as male erectile dysfunction treatments. Previously, we developed a novel series of 34 pyridopyrazinone derivatives as anticancer agents (series A–H). Herein, a multi-step in silico approach was preliminary conducted to evaluate the predicted PDE5 inhibitory activity, followed by an in vitro biological evaluation over the enzymatic level and a detailed SAR study. The designed 2D-QSAR model which was carried out to predict the IC 50 of the tested compounds revealed series B, D, E and G with nanomolar range of IC 50 values (6.00–81.56 nM). A further docking simulation model was performed to investigate the binding modes within the active site of PDE5. Interestingly, most of the tested compounds showed almost the same binding modes of that of reported PDE5 inhibitors. To validate the in silico results, an in vitro enzymatic assay over PDE5 enzyme was performed for a number of the promising candidates with different substitutions. Both series E and G exhibited a potent inhibitory activity (IC 50 = 18.13–41.41 nM). Compound 11b (series G, oxadiazole-based derivatives with terminal 4-NO 2 substituted phenyl ring and rigid linker) was the most potent analogue with IC 50 value of 18.13 nM. Structure–activity relationship (SAR) data attained for various substitutions were rationalized. Furthermore, a molecular dynamic simulation gave insights into the inhibitory activity of the most active compound (11b). Accordingly, this report presents a successful scaffold repurposing approach that reveals compound 11b as a highly potent nanomolar PDE5 inhibitor worthy of further investigation.

ORCID iDs

Amin, Kamelia M, El-Badry, Ossama M, Abdel Rahman, Doaa E, Abdellattif, Magda H, Abourehab, Mohammed A S, El-Maghrabey, Mahmoud H, Elsaid, Fahmy G, El Hamd, Mohamed A, Elkamhawy, Ahmed and Ammar, Usama M ORCID logoORCID: https://orcid.org/0000-0002-7218-641X;
CORE (COnnecting REpositories)