Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones
The minimum energy conformations of the four sterically reasonable SLex and SLea lactones were calculated using the molecular mechanics force-field MM2(91). The tetrasaccharide lactone involving the 3- and 2-position of the Gal moiety was found to be more stable than the 3,4-lactone both for SLex and SLea. © 1994.