Cladinose analogues of sixteen-membered macrolide antibiotics. VI. Synthesis of metabolically programmed, highly potent analogues of sixteen-membered macrolide antibiotics

Article abstract of DOI:10.7164/antibiotics.51.771

Five novel 3-hydroxyl derivatives of sixteen-membered macrolide possessing 4-O-acyl-α-L-cladinose as a neutral sugar moiety were synthesized by using a combination of structurally stable silyl acetal protection and selective hydrogenolysis of a 3'-methylthiomethyl ether to a 3'-OMe group. Several derivatives having n-butyryl, i-butyryl and n-valeryl substituent at the 4'-OH group exhibited significant antibacterial activity in vitro. One of them, 4'-O-n-butyryl-3'-O-methylleucomycin V, showed improved therapeutic effect in mice.