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秦岭冷杉茎叶的化学成分研究
引用本文:赵倩倩,肖琴,苗宇,王静. 秦岭冷杉茎叶的化学成分研究[J]. 中草药, 2020, 51(6): 1491-1497
作者姓名:赵倩倩  肖琴  苗宇  王静
作者单位:陕西科技大学食品与生物工程学院, 陕西 西安 710000
基金项目:陕西省科技厅基金资助项目(2019JQ-252);陕西省科技厅基金资助项目(2019JQ-453)
摘    要:目的研究秦岭冷杉Abies chensiensis茎叶的化学成分。方法利用大孔吸附树脂、葡聚糖凝胶、硅胶柱色谱、半制备高效液相色谱等多种色谱方法分离纯化,根据理化性质及波谱数据对化合物进行结构鉴定。结果从秦岭冷杉95%乙醇提取物中分离得到24个化合物,分别鉴定为7,14,24-mariesatrien-26,23-olide-3α,23-diol(1)、(23R)-3α-hydroxy-9,19-cyclo-9β-lanost-24-en-26,23-olide(2)、7-oxocallitrisicacid(3)、23-hydroxy-3-oxomariesia-8(9),14,24-trien-26,23-olide(4)、紫果冷杉三萜E(5)、3-oxo-9β-lanosta-7,24-dien-26,23R-olide(6)、7,14,22Z,24-mariesatetraen-26,23-olide-3-one(7)、(+)-rel-3α-hydroxy-23-oxocycloart-25 (27)-en-26-oic acid(8)、cycloart-25-en-3β,24-diol(9)、紫果冷杉三萜H(10)、3-oxo-24,25,26,27-tetranolanost-8-en-23-oic acid(11)、abiesadine C(12)、13β-epidioxy-8(14)-abieten-18-oic acid(13)、dehydroabietic acid(14)、15-hydroxydehydroabietic acid(15)、methyl 18-methoxydehydroabietate(16)、7β-hydroxy dehydroabietic acid(17)、dehydroabietan-18-ol(18)、centdaroic acid(19)、abietic acid(20)、6,8,11,13-abi-etatrien-18-oic acid(21)、abiesadine B(22)、abiesadine N(23)、12β-hydroxyabietic acid(24)。结论所有化合物均为首次从该植物中分离得到,其中化合物11为属内首次分离得到。

关 键 词:秦岭冷杉  三萜类化合物  二萜类化合物  紫果冷杉三萜E  紫果冷杉三萜H
收稿时间:2019-08-23

Study on chemical constituents of Abies chensiensis
ZHAO Qian-qian,XIAO Qin,MIAO Yu,WANG Jing. Study on chemical constituents of Abies chensiensis[J]. Chinese Traditional and Herbal Drugs, 2020, 51(6): 1491-1497
Authors:ZHAO Qian-qian  XIAO Qin  MIAO Yu  WANG Jing
Affiliation:College of Food and Biological Engineering, Shaanxi University of Science and Technology, Xi''an 710000, China
Abstract:Objective To study the chemical constituents of the sterns and leaves parts of Abies chensiensis. Methods The isolation and purification were carried out by HP-20 macroporous resin, Sephadex LH-20, silica gel column chromatography, semi-preparative HPLC. Their structures were elucidated on the basis of physicochemical properties and spectroscopic data. Results Twenty-four compounds were isolated and elucidated from the sterns and leaves parts of A. chensiensis, their structures were identified as 7,14,24-mariesatrien-26,23-olide-3α,23-diol(1),(23 R)-3α-hydroxy-9,19-cyclo-9β-lanost-24-en-26,23-olide(2), 7-oxocallitrisic acid(3), 23-hydroxy-3-oxomariesia-8(9),14,24-trien-26,23-olide(4), neoabiestrine E(5), 3-oxo-9β-lanosta-7,24-dien-26,23 R-olide(6), 7,14,22 Z,24-mariesatetraen-26,23-olide-3-one(7),(+)-rel-3α-hydroxy-23-oxocycloart-25(27)-en-26-oic acid(8), cycloart-25-en-3β,24-diol(9), neoabiestrine H(10), 3-oxo-24,25,26,27-tetranolanost-8-en-23-oic acid(11), abiesadine C(12), 13β-epidioxy-8(14)-abieten-18-oic acid(13), dehydroabietic acid(14), 15-hydroxydehydroabietic acid(15), methyl 18-methoxydehydroabietate(16), 7β-hydroxy dehydroabietic acid(17), dehydroabietan-18-ol(18), centdaroic acid(19), abietic acid(20), 6,8,11,13-abi-etatrien-18-oic acid(21), abiesadine B(22), abiesadine N(23), 12β-hydroxyabietic acid(24). Conclusion All compounds are isolated from the plants of A. chensiensis for the first time, and compound 11 is isolated from the Abies genus for the first time.
Keywords:Abies chensiensis Tiegh.  triperpenoids  diterpenoids  neoabiestrine E  neoabiestrine H
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