posted on 2020-08-12, 15:35authored byChristopher
P. Mussari, Dharmpal S. Dodd, Ratna Kumar Sreekantha, Laxman Pasunoori, Honghe Wan, Shana L. Posy, David Critton, Stefan Ruepp, Murali Subramanian, Andrew Watson, Paul Davies, Gary L. Schieven, Luisa M. Salter-Cid, Ratika Srivastava, Debarati Mazumder Tagore, Shailesh Dudhgaonkar, Michael A. Poss, Percy H. Carter, Alaric J. Dyckman
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.