(+)-Magoilgomer A[(±)-1]and magoilgomer B(2)were identified from the bark of Magnolia officinalis var.biloba.(+)-1 and(-)-1 were a pair of novel biphenyl derivatives featuring three C6-C3 subunits.2 was an unprec...(+)-Magoilgomer A[(±)-1]and magoilgomer B(2)were identified from the bark of Magnolia officinalis var.biloba.(+)-1 and(-)-1 were a pair of novel biphenyl derivatives featuring three C6-C3 subunits.2 was an unprecedented adduct containing magnolol and honokiol.These three oligomers possessed new parallel mode which should be biosynthesized from the coupling of three or four C6-C3 subunits.The structures of(±)-1 and 2 were elucidated based on the spectroscopic data analyses and electronic circular dichroism(ECD)calculations.2 exhibited neuroprotective effects of oxygen glucose deprivation-induced SK-N-SH cell injury.展开更多
Two unprecedented polycyclic spirooliganones C and D(1 and 2)with a novel spiro[bicyclo[2.2.2]octane-2,2′-bicyclo[3.1.0]hexane]carbon skeleton,one known dimeric prenylated C_(6)single bondC_(3)compound(3),and a pair ...Two unprecedented polycyclic spirooliganones C and D(1 and 2)with a novel spiro[bicyclo[2.2.2]octane-2,2′-bicyclo[3.1.0]hexane]carbon skeleton,one known dimeric prenylated C_(6)single bondC_(3)compound(3),and a pair of new enantiomeric prenylated C_(6)single bondC_(3)compounds(+)-5 and(−)-5 together with their direct precursors(+)-4 and(−)-4 were isolated from the roots of Illicium oligandrum.Their structures and absolute configurations were elucidated by spectroscopic analysis,single crystal X-ray diffraction data,and electronic circular dichroism calculations.A possible biosynthetic pathway for compounds 1 and 2 involving the Diels-Alder reaction between(−)-sabinene and cyclic prenylated tetrahydropyrano-type C_(6)single bondC_(3)compounds was proposed.The characteristic prenylated C_(6)single bondC_(3)compounds(+)-4 and(−)-4 were separated on a chiral stationary phase and their absolute configurations were determined by calculated ECD for the first time.In the antiviral bioassays,compounds 1 and(+)-5 exhibited significant inhibitory activity against CVB3 with IC_(50)values of 11.11μmol/L and 1.11μmol/L,respectively.Compounds 1 and 2 also showed moderate inhibition against influenza A(H1N1)virus.展开更多
基金supported by the National Natural Science Foundation of China(No.81730093)the CAMS Innovation Fund for Medical Sciences(No.2017-I2M-3-010)In Dependent Project of State Key Laboratory of Bioactive Substance and Function of Natural Medicines(No.GTZA201803)。
文摘(+)-Magoilgomer A[(±)-1]and magoilgomer B(2)were identified from the bark of Magnolia officinalis var.biloba.(+)-1 and(-)-1 were a pair of novel biphenyl derivatives featuring three C6-C3 subunits.2 was an unprecedented adduct containing magnolol and honokiol.These three oligomers possessed new parallel mode which should be biosynthesized from the coupling of three or four C6-C3 subunits.The structures of(±)-1 and 2 were elucidated based on the spectroscopic data analyses and electronic circular dichroism(ECD)calculations.2 exhibited neuroprotective effects of oxygen glucose deprivation-induced SK-N-SH cell injury.
基金supported by grants from the National Natural Science Foundation of China(Nos.21732008 and 22177135)。
文摘Two unprecedented polycyclic spirooliganones C and D(1 and 2)with a novel spiro[bicyclo[2.2.2]octane-2,2′-bicyclo[3.1.0]hexane]carbon skeleton,one known dimeric prenylated C_(6)single bondC_(3)compound(3),and a pair of new enantiomeric prenylated C_(6)single bondC_(3)compounds(+)-5 and(−)-5 together with their direct precursors(+)-4 and(−)-4 were isolated from the roots of Illicium oligandrum.Their structures and absolute configurations were elucidated by spectroscopic analysis,single crystal X-ray diffraction data,and electronic circular dichroism calculations.A possible biosynthetic pathway for compounds 1 and 2 involving the Diels-Alder reaction between(−)-sabinene and cyclic prenylated tetrahydropyrano-type C_(6)single bondC_(3)compounds was proposed.The characteristic prenylated C_(6)single bondC_(3)compounds(+)-4 and(−)-4 were separated on a chiral stationary phase and their absolute configurations were determined by calculated ECD for the first time.In the antiviral bioassays,compounds 1 and(+)-5 exhibited significant inhibitory activity against CVB3 with IC_(50)values of 11.11μmol/L and 1.11μmol/L,respectively.Compounds 1 and 2 also showed moderate inhibition against influenza A(H1N1)virus.