- First-in-class, antimicrobially inactive anti-inflammatory macrolide for the treatment of neutrophil dominated chronic inflammatory lung diseases with once daily oral dosing
- Removal of antimicrobial activity with retention of anti-inflammatory activity and favourable PK properties, characteristic for azithromycin
- Design of screening cascade
- In order to completely suppress antibacterial activity, Fidelta’s scientists developed novel methods for modifications of the desosamine sugar of 14- and 15-membered antibacterial macrolides
- Included was annelation of N-substituted 2-imino-1,3-oxazolidine 1 and 1,3-oxazolidin-2-one 2 moiety to the 2’,3’-positions of desosamine
- The method is suitable for introduction of various R1 substituents and large scale synthesis of prospective drug candidates
Modifications that provide complete suppression of antibacterial activity with minor alterations to the macrolide structures and/or physico-chemical properties are of great interest.
- The screening cascade was designed to select compounds that inhibit IL-6 production without antibacterial activity and effects on THP-1 cell viability
- Pharmacokinetic studies in rodents revealed compounds with good oral bioavailability and a half-life that supports once-daily dosing in humans
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