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作 者:姜勇[1,2] 王乃利[1,2] 姚新生[1,2] 北中进[1,2]
机构地区:[1]沈阳药科大学天然药物化学教研室 [2]日本大学药学部生药教研室
出 处:《药学学报》1998年第5期355-361,共7页Acta Pharmaceutica Sinica
基 金:国家自然科学基金
摘 要:从百合科葱属植物薤(Aliumchinense)鳞茎的抗凝和抗癌活性部位中,分离得到了6个化合物。经过化学方法和光谱分析(IR,EIMS,1HNMR,13CNMR,1H1HCOSY,HMBC,HMQC和NOESY谱),鉴定它们的结构分别为(25R,S)5αspirostane3βol3O{βDglucopyranosyl(1→2)[βDglucopyranosyl(1→3)]βDglucopyranosyl(1→4)βDgalactopyranoside}(1),(25R,S)5αspirostane3βol3O{βDglucopyranosyl(1→2)[βDglucopyranosyl(1→3)](6acetylβDglucopyranosyl)(1→4)βDgalactopyranoside}(2),(25R,S)5αspirostane2α,3βdiol3O{βDglucopyranosyl(1→2)OβDglucopyranosyl(1→4)βDgalactopyranosi?Six compounds were isolated from the anticoagulation and anticancer fractions of the bulbs of Allium chinense G. Don. On the basis of chemical evidence and spectral analysis (IR, EIMS, 1HNMR, 13CNMR, 1H1H COSY, HMBC, HMQC and NOESY), their structures were established as (25R,S)5αspirostane3βol 3O{βDglucopyranosyl(1→2)[βDglucopyranosyl(1→3)]βDglucopyranosyl(1→4)βDgalactopyranoside} (1), (25R,S)5αspirostane3βol 3O{βDglucopyranosyl (1→2)[βDglucopyranosyl(1→3)](6acetylβDglucopyranosyl)(1→4)βDgalactopyranoside} (2), (25R,S)5αspirostane2α,3βdiol 3O{βDglucopyranosyl(1→2)OβDglucopyranosyl(1→4)βDgalactopyranoside} (3), (25S)24OβDglucopyranosyl3β,24βdihydroxy5αspirost3Oαarabinopyranosyl(1→6)βDglucopyranoside (4), chinenoside II (5) and 2,3,4,9tetrahydro1methyl1Hpyrido indole3carboxylic acid (6). 4 is a new steroidal saponin, named chinenoside VI. Compounds 1 to 3 are three pairs of steroidal saponin epimers. Among them, the 25S epimer of 2 is first reported, the 25R epimer of 2 and compound 6 were isolated from this title plant for the first time. The relative configuration of compound 6 was firstly determined by NOESY spectrum, and signals of C, H were assigned definitely.
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