| 摘要 |
The present invention provides a process for synthesizing a glycopeptide having structure (I), wherein R1, R2, R3, R4, R5, R6, R7 and R8 are each independently H, OH, OR<i>, NH2, NHCOR<i>, F, CH2OH, CH2OR<i>, or a substituted or unsubstituted linear or branched chain alkyl, arylalkyl or aryl group, where R<i> is H, CHO, CO2R<ii>, a linear or branched chain alkyl, arylalkyl or aryl group, or an oligosaccharide moiety, etc., wherein R0 is H, a linear or branched chain alkyl, arylalkyl or aryl group; wherein R10 is a substituted or unsubstituted linear or branched chain acyl, arylacyl or aroyl group; wherein R11[X] represents X amino acid side-chains, and denotes position from the N-terminus, and R13[Y] represents Y amino acid side-chains, and denotes position from the C-terminus, wherein a, b, c, h, i, j, r, s and t are each independently an integer between about 0 and about 3; wherein m and n are each independently an integer between about 0 and about 5; and wherein x, x'(N), y and y'(N) are each independently an integer between about 0 and about 25; such glycopeptides being useful as a vaccine for inducing antibodies to human breast cancer cells in an adjuvant therapy therefor.
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