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Org Lett ; 21(4): 1078-1081, 2019 02 15.
Article in English | MEDLINE | ID: mdl-30730149

ABSTRACT

A pair of enantiomeric norsesquiterpenoids, (+)- and (-)-preuisolactone A (1) [(+)-1 and (-)-1)] featuring an unprecedented tricyclo[4.4.01,6.02,8]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.


Subject(s)
Anti-Bacterial Agents/pharmacology , Ascomycota/chemistry , Heterocyclic Compounds/pharmacology , Micrococcus luteus/drug effects , Sesquiterpenes/pharmacology , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/isolation & purification , Heterocyclic Compounds/chemistry , Heterocyclic Compounds/isolation & purification , Microbial Sensitivity Tests , Molecular Conformation , Sesquiterpenes/chemistry , Sesquiterpenes/isolation & purification , Stereoisomerism
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