Sato M, Takemura M, Atarashi S, Higashi K, Nagahara T, Furukawa M, Ikeuchi T, Osada Y
Laboratory of Medicinal Chemistry, Daiichi Seiyaku Co., Ltd., Tokyo, Japan.
J Antibiot (Tokyo). 1987 Sep;40(9):1292-302. doi: 10.7164/antibiotics.40.1292.
Thienamycin derivatives (4) having a cyclic amidine moiety at the C-2 position were prepared. The susceptibility to renal dehydropeptidase-1 and the antimicrobial activity of these compounds were determined. Their structure-activity relationships are also discussed.
制备了在C-2位具有环脒部分的硫霉素衍生物(4)。测定了这些化合物对肾脱氢肽酶-1的敏感性和抗菌活性。还讨论了它们的构效关系。