Open AccessDiscovery of Potent and Orally Bioavailable Small Molecule Antagonists of Toll-like Receptors 7/8/9 (TLR7/8/9)
Author(s) -
Christopher P Mussari,
Dharmpal S. Dodd,
Ratna Kumar Sreekantha,
Laxman Pasunoori,
Honghe Wan,
Shana Posy,
David Critton,
Stefan Ruepp,
Murali Subramanian,
Andrew J. Watson,
Paul Davies,
Gary L. Schieven,
Luisa Salter–Cid,
Ratika Srivastava,
Debarati M. Tagore,
Shailesh Dudhgaonkar,
Michael A. Poss,
Percy H. Carter,
Alaric J. Dyckman
Publication year - 2020
Publication title -
acs medicinal chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.065
H-Index - 66
ISSN - 1948-5875
DOI - 10.1021/acsmedchemlett.0c00264
Subject(s) - tlr7 , autoimmunity , receptor , context (archaeology) , immunology , tlr9 , pharmacology , immune system , toll like receptor , medicine , innate immune system , biology , computational biology , biochemistry , gene , gene expression , paleontology , dna methylation
The toll-like receptor (TLR) family is an evolutionarily conserved component of the innate immune system, responsible for the early detection of foreign or endogenous threat signals. In the context of autoimmunity, the unintended recognition of self-motifs as foreign promotes initiation or propagation of disease. Overactivation of TLR7 and TLR9 have been implicated as factors contributing to autoimmune disorders such as psoriasis, arthritis, and lupus. In our search for small molecule antagonists of TLR7/9, 7f was identified as possessing excellent on-target potency for human TLR7/9 as well as for TLR8, with selectivity against other representative TLR family members. Good pharmacokinetic properties and a relatively balanced potency against TLR7 and TLR9 in mouse systems (systems which lack functional TLR8) made this an excellent in vivo tool compound, and efficacy from oral dosing in preclinical models of autoimmune disease was demonstrated.