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Azoheteroarene-Modified Grapiprants Serving as Photoswitchable EP4 Antagonists.

Md. Akram Ali,S. Bera,Rajib Chakraborty,S. K. Mondal,Supriya Bhunia,T. Sardar,Sabyasachi Chakraborty,Subhas Samanta

Published 2025 in Chemistry

ABSTRACT

Photopharmacology offers a novel approach to eliminate side effects of chemotherapy treatment via site-specific activation of light-active anticancer agents, which are typically constructed by the installation of light-cleavable or light-switchable molecules onto known drugs or inhibitors. The light-switchable drugs being able to reversibly control biological activities are more advantageous, but the design of such compounds is very challenging. We synthesized a small series of photoswitchable S-arylsulfonylurea-based EP4 antagonists by substituting a core structural unit of a potent EP4 antagonist, grapiprant. In vitro cell-based EP4 activity studies revealed that all light-induced cis isomers of these compounds are more potent than their trans isomers. Compound 3, with an azopyrazole photoswitch and a para-methyl substitution in the S-phenyl ring, displayed the highest EP4 antagonism by its cis isomer and a considerably larger activity difference (ca. 1.8-fold) between trans and cis photoisomers. It showed (near) complete photoisomerization (∼95%-98%) upon 365 nm (forward) and 520 nm (reverse) light irradiations. The metastable cis isomers demonstrated high thermal stability (t1/2 = 1-3 days). All compounds were resistant to photobleaching and showed impressive stability for reduction with glutathione (10 mM). This study constitutes a proof-of-concept to design photoswitchable EP4 antagonists, and the structure-activity relationship revealed herein may help design more potent grapiprant derivatives.

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