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Two New Steroidal Glycosides from Ophiopogon japonicus 被引量:4
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作者 Hao Fu DAI Jun ZHOU +2 位作者 Zhong Tao DING Jiang XIONG Ning Hua TAN 《Chinese Chemical Letters》 SCIE CAS CSCD 2000年第10期901-904,共4页
Two new C-27 steroidal: glycosides, named ophiopojaponin A(1)and B(2), were isolated from the tubers of famous traditional Chinese herb-Ophiopogon japonicus. The spectroscopic and chemical evidences revealed their str... Two new C-27 steroidal: glycosides, named ophiopojaponin A(1)and B(2), were isolated from the tubers of famous traditional Chinese herb-Ophiopogon japonicus. The spectroscopic and chemical evidences revealed their structures to be Pennogenin 3-O-[2'-O-acetyl-alpha-L-rhamnopyranosyl (1-->2)]-beta-D-xylopyranosyl (1-->3)-beta-D-glucopyranoside (1) and 26-O-beta-D-glucopyranosyl-(22 xi, 25R)-3 beta, 14 alpha, 22 xi, 26-tetrahydroxyfurost-5-ene 3-O-alpha-L-rhamnopyranosyl (1-->2)-beta-D-glucopyranoside (2), respectively. 展开更多
关键词 LILIACEAE Ophiopogon jappnicus c-27 steroidal glycosides ophiopojaponin A and B
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新鲜黄山药中C_(27)甾体皂苷的化学成分的研究 被引量:12
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作者 耿勇 谭宁华 +1 位作者 周俊 孔令义 《中国天然药物》 SCIE CAS CSCD 2004年第1期25-27,共3页
目的 :研究黄山药 (DioscoreapanthaicaPrainetBurkill)的化学成分 ,寻找新的活性物质。结果 :分离鉴定了 3个C2 7甾体皂苷 ,其结构分别鉴定为 2 6 O β D 吡喃葡萄糖基 (2 5R) 呋甾烷 5 烯 3β,2 2 ξ ,2 6 三醇 3 O α L 吡喃鼠... 目的 :研究黄山药 (DioscoreapanthaicaPrainetBurkill)的化学成分 ,寻找新的活性物质。结果 :分离鉴定了 3个C2 7甾体皂苷 ,其结构分别鉴定为 2 6 O β D 吡喃葡萄糖基 (2 5R) 呋甾烷 5 烯 3β,2 2 ξ ,2 6 三醇 3 O α L 吡喃鼠李糖基 (1→ 2 ) β D 吡喃葡萄糖苷 (protobiosideⅠ ) ,2 6 O β D 吡喃葡萄糖基 (2 5R) 呋甾烷 5 烯 3β ,2 2 ξ ,2 6 三醇 3 O β D 吡喃葡萄糖基 (1→ 4 ) [α L 吡喃鼠李糖基 (1→ 2 ) ] β D 吡喃葡萄糖苷 (deltosideⅡ ) ,2 6 O β D 吡喃葡萄糖基 (2 5R) 呋甾烷 5 烯 3β ,2 2 ξ ,2 6 三醇 3 O β D 吡喃葡萄糖基 (1→ 3) β D 吡喃葡萄糖基 (1→ 4 ) [α L 吡喃鼠李糖基 (1→ 2 ) ] β D 吡喃葡萄糖苷 (Ⅲ )。 结论 :以上化合物均为首次从该植物中分到。与文献报道的从该植物中分到的化合物进行比较 ,认为文献报道的化合物可能为药材久放后的酶解产物或提取分离过程中的人工产物。 展开更多
关键词 黄山药 C27甾体皂苷 化学成分 中药
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Chemical Constituents from Leaves of Camellia nitidissima and Their Potential Cytotoxicity on SGC7901 Cells 被引量:24
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作者 Jing Qi Ruo-fu Shi +5 位作者 Jian-ming Yu Yi Li Sheng-tao Yuan Ji-zhu Yang Jiang-miao Hu Ai-qun Jia 《Chinese Herbal Medicines》 CAS 2016年第1期80-84,共5页
Objective To isolate and identify the bioactive phytochemicals from the leaves of Camellia nitidissima. Methods The chemical constituents were isolated and purified by repeated silica gel, Sephadex LH-20, MCI gel colu... Objective To isolate and identify the bioactive phytochemicals from the leaves of Camellia nitidissima. Methods The chemical constituents were isolated and purified by repeated silica gel, Sephadex LH-20, MCI gel columns, recrystallization, and semi-preparative HPLC techniques. The chemicl structures of these compounds were identified on the basis of spectral data including NMR and MS. Then quorum sensing inhibition (QSI) activities of these compounds were tested using Chromobacterium violaceum CV026 as the bioindicator strain. The antitumor activities of these compounds were measured using SGC7901 as cell proliferation and cytotoxicity. Results cx-Spinasteryl-I^-D-glucopyranoside (1), stigmasta-7,22-diene-3-O-[c^-L-arabinopyranosyl (1 -2)]-β-D-galactopyranoside (2), kaempferol 3-O-[2-O-(trans-p-coumaroyl)-3-O-α -D-glucopyranosyl]-α-D-glucopyranoside (3), aromadendrin (4), catechin (5), phlorizin 4'-O-β-D-glucopyranoside (6), (3R,6R,7Lg-3-hydroxy-4,7-megastigmadien- 9-one (7), dodecanoic acid (8), 3α-acetoxy-20-1upanol (9), and 3β,6α- trihydroxyolean- 7-one (1 0) were successively isolated from the leaves of C. nitidissima. Unfortunately, these compounds had no QSI activity. Based on Cell Counting Kit-8 (CCK-8) assay, compound 10 showed the best anti-tumor activity or all compounds (ICs0 = 91.7 μg/mL). Conclusion Apart from compounds 4 and 5, other eight compounds are reported in this plant for the first time. All compounds show no QSI activity, compound 10 shows potential cytotoxic activity on SGC7901 cells in vitro. 展开更多
关键词 ANTITUMOR Camellia nitidissima c-27 steroidal saponins FLAVONOIDS quorum sensinginhibitors SGC7901 triterpenes
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