A new artifact bisbenzylisoquinoline,2,2′-N,N-dichloromethyltetrandrine(1),has been ob- tained from the root of Stephania tetrandra and its structure has been advanced on the basis of spectroscopic and chemical evide...A new artifact bisbenzylisoquinoline,2,2′-N,N-dichloromethyltetrandrine(1),has been ob- tained from the root of Stephania tetrandra and its structure has been advanced on the basis of spectroscopic and chemical evidence.展开更多
One new bisbenzylisoquinoline alkaloid, neferine N-oxide （1）, along with three known compounds, neferine （2）, liensinine （3）, and isoliensinine （4）, were isolated from Plumulanelumbinis - the embryo of the see...One new bisbenzylisoquinoline alkaloid, neferine N-oxide （1）, along with three known compounds, neferine （2）, liensinine （3）, and isoliensinine （4）, were isolated from Plumulanelumbinis - the embryo of the seed of Nelumbonucifera. Their structures were elucidated by extensive spectroscopic analysis （MS, UV, IR, NMR）, and the absolute configurations were determined by experimental circulardichroism （CD） spectra. Compound 1 is a new naturally occurring bisbenzylisoquinoline alkaloid with an N-oxide functionality, and the CD spectrum of （1R, 1＇R） neferine is first reported. The antioxidant activities of compounds 1-4 were evaluated using the ORAC assay, which illustrated that all these compounds showed the different levels of oxygen radical absorbance capacity.展开更多
(+)/(-)-Yanhusuosines A(1) and B(2), two pairs of trace benzylisoquinoline-protoberberine atropoenantiomeric homodimers featuring an unprecedented 6/7/6/6/6/6 hexacyclic skeleton, were isolated from the tubers of Cory...(+)/(-)-Yanhusuosines A(1) and B(2), two pairs of trace benzylisoquinoline-protoberberine atropoenantiomeric homodimers featuring an unprecedented 6/7/6/6/6/6 hexacyclic skeleton, were isolated from the tubers of Corydalis yanhusuo. The structures of(+)/(-)-1 and(+)/(-)-2 were elucidated using spectroscopic and quantum-chemical calculation approaches.(+)/(-)-Yanhusuosines A(1) and B(2)represent a new class of alkaloid dimers biogenetically constructed by a molecule of benzylisoquinoline with a unit of protoberberine via an intermolecular [4 + 3] cycloaddition. Their plausible biosynthetic pathways are discussed, and compound 2 exerted moderate inhibitory activity of NO formation in LPS induced RAW264.7 macrophages.展开更多
文摘A new artifact bisbenzylisoquinoline,2,2′-N,N-dichloromethyltetrandrine(1),has been ob- tained from the root of Stephania tetrandra and its structure has been advanced on the basis of spectroscopic and chemical evidence.
基金financially supported by 12th Five-Year Plan Major New Drug Discovery Science and Technology Projects for support of this research (No.2014ZX09304307-002)
文摘One new bisbenzylisoquinoline alkaloid, neferine N-oxide （1）, along with three known compounds, neferine （2）, liensinine （3）, and isoliensinine （4）, were isolated from Plumulanelumbinis - the embryo of the seed of Nelumbonucifera. Their structures were elucidated by extensive spectroscopic analysis （MS, UV, IR, NMR）, and the absolute configurations were determined by experimental circulardichroism （CD） spectra. Compound 1 is a new naturally occurring bisbenzylisoquinoline alkaloid with an N-oxide functionality, and the CD spectrum of （1R, 1＇R） neferine is first reported. The antioxidant activities of compounds 1-4 were evaluated using the ORAC assay, which illustrated that all these compounds showed the different levels of oxygen radical absorbance capacity.
基金supported by the National Natural Science Foundation of China (No. 82073978)the Fundamental Research Funds for the Central Universities (No. 2022-JYB-JBZR-015)Beijing Natural Science Foundation (No. JQ18026)。
文摘(+)/(-)-Yanhusuosines A(1) and B(2), two pairs of trace benzylisoquinoline-protoberberine atropoenantiomeric homodimers featuring an unprecedented 6/7/6/6/6/6 hexacyclic skeleton, were isolated from the tubers of Corydalis yanhusuo. The structures of(+)/(-)-1 and(+)/(-)-2 were elucidated using spectroscopic and quantum-chemical calculation approaches.(+)/(-)-Yanhusuosines A(1) and B(2)represent a new class of alkaloid dimers biogenetically constructed by a molecule of benzylisoquinoline with a unit of protoberberine via an intermolecular [4 + 3] cycloaddition. Their plausible biosynthetic pathways are discussed, and compound 2 exerted moderate inhibitory activity of NO formation in LPS induced RAW264.7 macrophages.
