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查阅模式标本后发现Hypoestes pulgarense Elmer的花单生或少数花聚生于叶腋内,并且花药两室,下方一室具矩.这些特征与枪刀药属(Hypoestes)聚伞花序及单室花药的特征不符,而与爵床属(Justicia)一致.因此提出一新组合--菲律宾爵床(Justicia pulgarensis(Elmer)C.M.Gao & Y.F.Deng). 相似文献
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Antifungal diterpenes from Hypoestes serpens (Acanthaceae) 总被引:2,自引:0,他引:2
Rasoamiaranjanahary L Marston A Guilet D Schenk K Randimbivololona F Hostettmann K 《Phytochemistry》2003,62(3):333-337
Two new diterpenes, fusicoserpenol A and dolabeserpenoic acid A, with antifungal activity, were isolated from leaves of Hypoestes serpens (Acanthaceae). Their structures were elucidated by means of spectrometric methods including 1D and 2D NMR experiments and MS analysis. X-ray crystallographic analysis confirmed the structure of fusicoserpenol A and established the relative configuration. 相似文献
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Hypofolins A – L,ent‐Labdane Diterpenoids from the Roots of Hypoestes phyllostachya ‘Pink Splash’ 下载免费PDF全文
Bin Cheng Lin‐Fen Ding Tong Yan Zhang‐Qiao Xie Zhi‐jun Zhang Liu‐Dong Song Xing‐De Wu Qin‐Shi Zhao 《化学与生物多样性》2018,15(6)
Twelve new ent‐labdane diterpenoids, hypofolins A – F ( 1 – 6 ) and hypofolins G – L ( 7a / 7b , 8a / 8b , and 9a / 9b ), were isolated from the roots of Hypoestes phyllostachya ‘Pink Splash’. Their structures were elucidated by extensive 1D‐ and 2D‐NMR spectroscopic and HR‐MS data. The absolute configurations of 1 , 2 , 5 , and 7a / 7b were determined by single crystal X‐ray diffraction and ECD analysis, as well as chemical transformations. Compounds 7a / 7b , 8a / 8b , and 9a / 9b were isolated as three pairs of interconverting mixture of two isomers between ketone and hemiketal types. Compound 1 showed weak cytotoxicity against SMMC‐7721 cell line with IC50 value of 31.40 μm . 相似文献
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三花枪刀药化学成分研究 总被引:2,自引:0,他引:2
由爵床科枪刀药属植物三花枪刀药(Hypoestes triflora)的地上部分丙酮提取物中分离得到了6个化合物,通过波谱分析及晶体X射线分析确定为:尿囊素(allantoin)(1),β-谷甾醇(2),胡萝卜甙(3),硬脂酸(4),黄木灵(xanthoxylin)(5)和无机盐硝酸钾(6),这些成分均为首次由该种植物中分离得到。 相似文献
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Rasoamiaranjanahary L Guilet D Marston A Randimbivololona F Hostettmann K 《Phytochemistry》2003,64(2):543-548
Five isopimarane diterpenes (7beta-hydroxyisopimara-8,15-dien-14-one, 14alpha-hydroxyisopimara-7,15-dien-1-one, 1beta,14alpha-dihydroxyisopimara-7,15-diene, 7beta-hydroxyisopimara-8(14),15-dien-1-one and 7beta-acetoxyisopimara-8(14),15-dien-1-one) have been isolated from the leaves of Hypoestes serpens (Acanthaceae). All compounds exhibited antifungal activity against both the plant pathogenic fungus Cladosporium cucumerinum and the yeast Candida albicans; two of them also displayed an acetylcholinesterase inhibition. The structures of the compounds were determined by means of spectrometric methods, including 1D and 2D NMR experiments and MS analysis. 相似文献
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