Isolation and structure elucidation of a new moenomycin antibiotic (A(
12), 1a) is reported that differs from moenomycin A by lack of the bra
nching methyl group and by the configuration at C-4 of unit F. The sma
llest antibiotically active degradation product of 1a is the trisaccha
ride derivative 3a. This observation is in contrast to structure activ
ity relations in the moenomycin A series where it was found that disac
charide 4b is fully active. An explanation is offered for this differe
nce.