Thiol-Activated 1,2,4-Thiadiazolidin-3,5-diones Release Hydrogen Sulfide through a Carbonyl-Sulfide-Dependent Pathway
Haley M. Smith, Michael D. Pluth
Abstract
Haley M. Smith, Michael D. Pluth
Abstract
Recent efforts have expanded the development of small molecule donors that release the important biological signaling molecule hydrogen sulfide (H 2 S). Previous work on 1,2,4-thiadiazolidin-3,5-diones (TDZNs) reported that these compounds release H 2 S directly, albeit inefficiently. However, TDZNs showed promising efficacy in H 2 S-mediated relaxation in ex vivo aortic ring relaxation models. Here, we show that TDZNs release carbonyl sulfide (COS) efficiently, which can be converted to H 2 S by the enzyme carbonic anhydrase (CA) rather than releasing H 2 S directly as previously reported.
OpenAlex reports 5 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Recent efforts have expanded the development of small molecule donors that release the important biological signaling molecule hydrogen sulfide (H 2 S). Previous work on 1,2,4-thiadiazolidin-3,5-diones (TDZNs) reported that these compounds release H 2 S directly, albeit inefficiently. However, TDZNs showed promising efficacy in H 2 S-mediated relaxation in ex vivo aortic ring relaxation models. Here, we show that TDZNs release carbonyl sulfide (COS) efficiently, which can be converted to H 2 S by the enzyme carbonic anhydrase (CA) rather than releasing H 2 S directly as previously reported.
Key concepts: Chemistry, Carbonyl sulfide, Hydrogen sulfide, Carbonic anhydrase, Sulfide, Thiol, Ex vivo, Small molecule