School of Pharmaceutical Sciences , South-Central University for Nationalities , Wuhan 430074 , People's Republic of China.
Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences , Chongqing University , Chongqing 401331 , People's Republic of China.
Org Lett. 2019 Feb 15;21(4):1078-1081. doi: 10.1021/acs.orglett.8b04123. Epub 2019 Feb 7.
A pair of enantiomeric norsesquiterpenoids, (+)- and (-)-preuisolactone A (1) [(+)-1 and (-)-1)] featuring an unprecedented tricyclo[4.4.0.0]decane carbon scaffold were isolated from Preussia isomera. Their structures were determined by spectroscopic and computed methods and X-ray crystallography. Compounds (+)-1 and (-)-1 are two rare naturally occurring sesquiterpenoidal enantiomers. A plausible biosynthetic pathway for 1 is proposed. Additionally, (±)-1 exhibited remarkable antibacterial activity against Micrococcus luteus with an MIC value of 10.2 μM.
一对对映体的非环倍半萜,(+)-和(-)-普雷乌异内酯 A(1)[(+)-1 和(-)-1)],从 Preussia isomera 中分离出来,具有前所未有的三环[4.4.0.0]癸烷碳支架。它们的结构通过光谱和计算方法以及 X 射线晶体学确定。化合物(+)-1 和(-)-1 是两种罕见的天然存在的倍半萜对映异构体。提出了 1 的可能生物合成途径。此外,(±)-1 对微球菌显示出显著的抗菌活性,MIC 值为 10.2 μM。