摘要
通过活性追踪的方法,从一株来源于药用红树尖瓣海莲的内生真菌Phomopsis longicolla HL-2232中分离鉴定了5个生物碱类化合物、1个色原酮类化合物以及4个甾醇类化合物,分别鉴定为:6-氨基嘌呤-9-羧酸甲酯(1),腺嘌呤核苷(2),尿嘧啶核苷(3),N,N'-二苯基尿素(4),(2S,2'R,3R,4E,8E,3'E)-2-(2'-羟基-3'-十八碳烯酰胺)-9-甲基-4,8-十八碳二烯-1,3-二醇(5),2-(2'S-羟丙基)-5-甲基-7-羟基对氧萘酮(6),fortisterol(7),(22E)-5α,8α-表二氧麦角甾-6,22-二烯-3β-醇(8),啤酒甾醇(9),β-谷甾醇亚油酸酯(10).其中化合物1为新化合物,化合物5为新天然产物,其碳谱数据至今未曾报道.细胞毒活性表明化合物1-3对肿瘤细胞A549,B16F10,HL-60,MCF-7具有不同程度的抑制活性.其中新化合物1对乳腺癌细胞(MCF-7)的IC50值为14.9μmol·L-1、化合物3对肺癌细胞(A549)的IC50值为8.6μmol·L-1,两者活性强于阳性对照药顺铂.
Under the guidance of bioassay, five alkaloids, one chromone and four steroids were isolated from the Phomopsis longicolla HL-2232, a fungus isolated from a mangrove Bruguiera sexangula var. Rhynchopetala. Their structures were identified as 6-aminopurine-9-carboxylic acid methyl ester(1), adenine riboside(2), uridine(3), N,N'-diphenyl urea(4),(2S,2'R,3R,4E,8E,3'E)-2-(2'-hydroxy-3'-octadecenoylamino)-9-methyl-4,8-octadecadiene-l,3-diol(5), 2-(2'S-hydroxypropyl)-5-methyl-7-hydroxychromone(6), fortisterol(7),(22E)-5α,8α-epidioxyergosta-6,22-dien-3β-ol(8), cerevisterol(9) andβ-sitosteryl linoleate(10). Among them, compound 1 was a new compound. Compound 5 was a new natural product, and its13 C NMR spectroscopic data has not reported until now. Compounds 1-3 showed inhibitory activities against B16F10, A549, HL-60 and MCF-7. Compounds 1 and 3 exhibited the higher inhibitory activities against MCF-7 and A549 than positive control cisplatin with IC50 values of 14.9 and 8.6 μmol·L-1, respectively.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2015年第10期2102-2107,共6页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(Nos.21462015,21362009,31360069)
海南省自然科学基金(Nos.20152037,20152034)
海南师范大学科研启动基金(No.QN1434)资助项目~~