Phytochemical investigation of the MeOH extract of twigs and leaves of Baeckea frutescens led to the isolation of seven new polymethylated phloroglucinol meroterpenoids(PPMs),named baeckfrutones M-S(1-7).Their structu...Phytochemical investigation of the MeOH extract of twigs and leaves of Baeckea frutescens led to the isolation of seven new polymethylated phloroglucinol meroterpenoids(PPMs),named baeckfrutones M-S(1-7).Their structures and absolute configurations were determined by spectroscopic analyses,chiral-phase HPLC analysis,and electronic circular dichroism(ECD)calculations.PPM 1 is a novel meroterpenoid possessing a 6/6/5/3 tetracyclic skeleton in PPMs,whereas 3 and 4 are the first hydroxytasmanone type phloroglucinol-monoterpene hybrids.(+)-2 and 7 displayed potent antiinflammatory activity with IC50 values of 20.86±0.60 and 36.21±1.18 lL,respectively.展开更多
Callisalignenes G–I(1–3),three new meroterpenoids of b-triketone and monoterpene,along with two known analogues(4 and 5),were isolated from Callistemon salignus.Their structures and absolute configurations were unam...Callisalignenes G–I(1–3),three new meroterpenoids of b-triketone and monoterpene,along with two known analogues(4 and 5),were isolated from Callistemon salignus.Their structures and absolute configurations were unambiguously established by a combination of NMR and MS analysis and electronic circular dichroism(ECD)evidence.Callisalignenes H(2)and I(3)have a rare sec-butyl moiety at C-7.Meroterpenoids 1–3 exhibited cytotoxicity against HCT116 cells with IC50 values of 8.51±1.8,9.12±0.3,and 16.33±3.3 lM,respectively.展开更多
Correction to:Natural Products and Bioprospecting(2018)8:431–439 https://doi.org/10.1007/s13659-018-0189-3 In the original publication,two errors have occurred.The corrected texts are provided below:1.The author,Xu-J...Correction to:Natural Products and Bioprospecting(2018)8:431–439 https://doi.org/10.1007/s13659-018-0189-3 In the original publication,two errors have occurred.The corrected texts are provided below:1.The author,Xu-Jie Qi,should read as Xu-Jie Qin among the author group.2.The reference 9 should be cited as X.J.Qin,Y.E.Zhi,H.Yan,Y.Zhang,H.Liu,Q.Yu,S.Wang,Q.Zhao,L.He,X.Ma,L.K.An,H.Y.Liu,Tetrahedron 74,6658–6666(2018).展开更多
基金This work was financially supported by the National Natural Science Foundation of China(Nos.31570363 and 31770391)Key Research and Development Plan of Yunnan Province–Special Project of Science and Technology in Yunnan Province(2017IB007)+2 种基金Major Biomedical Project of Yunnan Province(2018ZF005)Innovation Team of the Ministry of Education(No.IRT-17R49)the Foundation of State Key Laboratory of Phytochemistry and Plant Resources in West China(P2017-ZZ04 and P2017-KF06),Kunming Institute of Botany,Chinese Academy of Sciences.
文摘Phytochemical investigation of the MeOH extract of twigs and leaves of Baeckea frutescens led to the isolation of seven new polymethylated phloroglucinol meroterpenoids(PPMs),named baeckfrutones M-S(1-7).Their structures and absolute configurations were determined by spectroscopic analyses,chiral-phase HPLC analysis,and electronic circular dichroism(ECD)calculations.PPM 1 is a novel meroterpenoid possessing a 6/6/5/3 tetracyclic skeleton in PPMs,whereas 3 and 4 are the first hydroxytasmanone type phloroglucinol-monoterpene hybrids.(+)-2 and 7 displayed potent antiinflammatory activity with IC50 values of 20.86±0.60 and 36.21±1.18 lL,respectively.
基金National Natural Science Foundation of China(Nos.31600283 and 31570363)fund of State Key Laboratory of Phytochemistry and Plant Resources in West China(No.P2017-ZZ04)from Kunming Institute of Botany,Chinese Academy of Sciences.
文摘Callisalignenes G–I(1–3),three new meroterpenoids of b-triketone and monoterpene,along with two known analogues(4 and 5),were isolated from Callistemon salignus.Their structures and absolute configurations were unambiguously established by a combination of NMR and MS analysis and electronic circular dichroism(ECD)evidence.Callisalignenes H(2)and I(3)have a rare sec-butyl moiety at C-7.Meroterpenoids 1–3 exhibited cytotoxicity against HCT116 cells with IC50 values of 8.51±1.8,9.12±0.3,and 16.33±3.3 lM,respectively.
文摘Correction to:Natural Products and Bioprospecting(2018)8:431–439 https://doi.org/10.1007/s13659-018-0189-3 In the original publication,two errors have occurred.The corrected texts are provided below:1.The author,Xu-Jie Qi,should read as Xu-Jie Qin among the author group.2.The reference 9 should be cited as X.J.Qin,Y.E.Zhi,H.Yan,Y.Zhang,H.Liu,Q.Yu,S.Wang,Q.Zhao,L.He,X.Ma,L.K.An,H.Y.Liu,Tetrahedron 74,6658–6666(2018).
