Insignin A, a new C21-steroidal aglycone having the rare 15,16-seco pregnane skeleton was isolated from the acidic hydrolysis part of the 95% EtOH extract of Biondia insignis. It's structure was identified to be ...Insignin A, a new C21-steroidal aglycone having the rare 15,16-seco pregnane skeleton was isolated from the acidic hydrolysis part of the 95% EtOH extract of Biondia insignis. It's structure was identified to be 15R,16-epoxy-3?,14?,16?-trihydroxy-15,16-secopregn-5-ene-20-one based on the spectral data.展开更多
A new C21-steroidal glycoside with two known compounds were isolated from the root of Cynanchum Stauntonii. Based on the spectral analysis, including MS, 1H NMR, 13C NMR, DEPT, 1H-1H COSY, 13C-1H COSY, HMQC and HMBC, ...A new C21-steroidal glycoside with two known compounds were isolated from the root of Cynanchum Stauntonii. Based on the spectral analysis, including MS, 1H NMR, 13C NMR, DEPT, 1H-1H COSY, 13C-1H COSY, HMQC and HMBC, their chemical structures were determinated as glaucogenin-C 3-O-α-L-cymaropyranosyl-（1→ 4）-β-o-digitoxopyranosyl-（1→4）-β-D-canaropyranoside （1）, stigmasterol （2） and ursolic acid （3）.展开更多
文摘Insignin A, a new C21-steroidal aglycone having the rare 15,16-seco pregnane skeleton was isolated from the acidic hydrolysis part of the 95% EtOH extract of Biondia insignis. It's structure was identified to be 15R,16-epoxy-3?,14?,16?-trihydroxy-15,16-secopregn-5-ene-20-one based on the spectral data.
文摘A new C21-steroidal glycoside with two known compounds were isolated from the root of Cynanchum Stauntonii. Based on the spectral analysis, including MS, 1H NMR, 13C NMR, DEPT, 1H-1H COSY, 13C-1H COSY, HMQC and HMBC, their chemical structures were determinated as glaucogenin-C 3-O-α-L-cymaropyranosyl-（1→ 4）-β-o-digitoxopyranosyl-（1→4）-β-D-canaropyranoside （1）, stigmasterol （2） and ursolic acid （3）.
