Design, Synthesis, and Characterization of Prodrugs of Sulfonamide TLR4 Signaling Inhibitor TAK-242 (Resatorvid)
We have previously reported two prodrug designs for the delivery of the potent TLR4 inhibitor TAK-242. Our initial design was used to covalently link TAK-242 to pancreatic islets using a linker to afford sustained delivery of the active drug after transplant. Those drug-eluting islets provided local inhibition of TLR4-linked inflammation and improved islet graft survival. Here, we describe a third family of TAK-242 prodrugs featuring two rate modulating sites, a self-immolative aniline-stabilized methylene spacer bonded directly to the sulfonamide nitrogen, an alcohol tether for bioconjugation, and a β-eliminative aryl-sulfone “trigger”. These prodrugs rapidly release TAK-242 after activation by β-elimination and a rapid subsequent 1,2-elimination, cleanly releasing the drug without detectable intermediates. This manuscript reports the preparation and characterization of a series of methylene-linked TAK-242 prodrugs, evaluating the impact of various modifications on drug release kinetics.
Authors
- Avery T. Lallande
- Chloë A. Sells (ORCID: https://orcid.org/0000-0002-9895-0949)
- Jessica H. Kostyo (ORCID: https://orcid.org/0000-0001-7004-2159)
- Robert R. Kane (ORCID: https://orcid.org/0000-0003-0459-7505)
- Maheen I. Kara
- Rahul N. Gaykar
Institutions
- Baylor University (US)
- Institute of Biomedical Science (GB)
Publication Details
- Journal
- ACS Medicinal Chemistry Letters
- Published
- 2026-03-16
- DOI
- https://doi.org/10.1021/acsmedchemlett.6c00026
- Primary Topic
- Phosphodiesterase function and regulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00