Zhang Y Z, Sun X, Zeckner D J, Sachs R K, Current W L, Chen S H
Lilly Research Laboratories, A Division of Eli Lilly and Company, Lillly Corporate Center, Indianapolis, IN 46285, USA.
Bioorg Med Chem Lett. 2001 Jan 22;11(2):123-6. doi: 10.1016/s0960-894x(00)00606-5.
During the course of a structure-activity relationship (SAR) study on novel depsinonapeptide pseudomycin B, we synthesized a total of 12 8-amidopseudomycin analogues via standard two-step sequence from either ZPSB 2 or AllocPSB 3. A number of these amides exhibited good in vitro antifungal activities.
在对新型去甲伪霉素B进行构效关系(SAR)研究的过程中,我们通过标准的两步序列从ZPSB 2或AllocPSB 3总共合成了12种8-氨基伪霉素类似物。其中一些酰胺表现出良好的体外抗真菌活性。