| Literature DB >> 25408837 |
Manabu Watanabe1, Mai Kasai1, Hideyuki Tomizawa1, Masamitsu Aoki1, Kazuo Eiho1, Yoshiaki Isobe1, Shigehiro Asano2.
Abstract
Toll-like receptors (TLRs) play important roles in the innate immune system. In fact, recognition of endogenous immune complexes containing self-nucleic acids as pathogen- or damage-associated molecular patterns contributes to certain autoimmune diseases, and inhibition of these recognition signals is expected to have therapeutic value. We identified dihydropyrrolo[2,3-d]pyrimidines as novel selective TLR9 antagonists with high aqueous solubility. A structure-activity relationship study of a known TLR9 antagonist led to the promising compound 18, which showed potent TLR9 antagonistic activity, sufficient aqueous solubility for parenteral formulation, and druggable properties. Compound 18 suppressed the production of the proinflammatory cytokine IL-6 in CpG-induced mouse model. It is therefore believed that compound 18 has great potential in the treatment of TLR9-mediated systemic uncontrollable inflammatory response like sepsis.Entities:
Keywords: LLE; Toll-like receptor 9; autoimmune disease; dihydropyrrolo[2,3-d]pyrimidine; sepsis
Year: 2014 PMID: 25408837 PMCID: PMC4233361 DOI: 10.1021/ml5003184
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345