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排序方式: 共有188条查询结果,搜索用时 250 毫秒
1.
A phytochemical investigation of secondary metabolites from Micromelum integerrimum was reported. Two new prenylated coumarins named as hydramicromelin D (1) and integerrimelin (2) were isolated along with 9 known coumarin derivatives. The chemical structures as well as relative stereochemistries of those coumarins were confirmed on the basis of extensive spectroscopic data interpretation and comparison with those previously published data. 相似文献
2.
S. N. Kovalenko S. G. Stepanian V. P. Chuev M. M. Asimov V. M. Nikitchenko V. P. Chernykh 《Molecular Engineering》1992,2(2):153-163
In order to improve the generating and photochemical properties of coumarin laser dyes, the following active media were synthesized: inclusion complexes of -cyclodextrin (-CD) and 7-amino-4-methylcoumarins (COU1, COU102, COU120). Complex formation processes were studied, and the structure of the inclusion complexes was estimated using the method of MM2 molecular mechanics. The data obtained suggest the reasons underlying the complex structure effects on their spectral, luminescent and generating characteristics. 相似文献
3.
骨缘当归的化学成分 总被引:2,自引:0,他引:2
骨缘当归Angellica cartilaginomarginata var.foliata Yuan et Shen,别名:山藁本、野芹菜(江苏),仅分布于江苏和浙江。在江苏镇江等地用干燥全草作山藁本入药,其化学成分未见报道。 样品采自江苏省句容县。将干根磨粉,提取物经中性氧化铝层析,根据色谱及光谱鉴定为两种脂肪酸、四种已知香豆素和一种植物甾醇即:正葵酸(n-capric acid)、月桂酸(lauric acid)、骨缘当归素(cartilaginomarginadin)、蝉翼素(pteryxin)、白花前胡素F(praeruptorin F)、佛手柑内酯(bergapten)及β-谷甾醇(β-sitosterol)。 相似文献
4.
从崖椒(Zanthoxglum schinifolutm Sieb.et Zucc.)茎的石油醚、二氯甲烷提取物中分离得到8个化合物。经物理常数测定及光谱(UV,IR,MS,NMR)分析鉴定其为(1)白鲜碱(dictamning),(2)茵芋碱(skimmianine),(3)滨蒿内酯(scoparone),(4)崖椒内酯(schinifolin),(5)莨菪亭(scopoletin),(6)7-羟基-8-甲氧基香豆素(7-hydroxy-8-methoxycoumarin),(7)N-甲基弗林辛(N-methylflindersine),(8)β-谷甾醇(β-sitosterol),其中化合物(5)、(6)和(7)为首次从该植物中分离。 相似文献
5.
中药前胡核磁共振氢谱法鉴定 总被引:1,自引:1,他引:0
使用^1H-NMR法对19种前胡乙醚提取物进行了测试和解析,其中9种前胡的化学成分未见报道。根据主要化学成分香豆素的类型,将含角型二氢吡喃香豆素的10种前胡归入白花前胡类;含线型二氢吡喃香豆素或线型二氢呋喃香豆素的8种前胡归秋紫花前胡类。研究结果表明,^1H-NMR法是鉴别中药前胡的快速、简便而可靠的检测方法。 相似文献
6.
Three new coumarin glycosides isolated from roots of Seseli montanum were shown to be the 3′-O-,2′-O-, and the 7-O-β-D-glucopyranosides respectively of 2′(R)-6-(2′,3′-dihydroxy-3′-methylbutyl)-7-hydroxy-coumarin. The structures were elucidated by spectroscopic and chemical methods. (R)-Configuration was assigned to the aglycone, also known as ( + )-peucedanol, and to its 7-methyl ether, ( + )-ulopterol, by chemical correlation. Additionally, apterin was obtained and characterized. 相似文献
7.
Four coumarins and seven isoprenoid compounds have been identified in potato tubers infected with Phoma exigua var. foveata. Among these were the 7-O-β-D-glucopyranoside of 7-hydroxy-6,8-dimethoxycoumarin (isofraxidin) and the sesquiterpene 2-(11,12-dihydroxy-11-methylethyl)-6,10-dimethyl-spiro[4,5]dec-6-en-8-one and its 12-O-β-D-glucopyranoside, which apparently have not been previously identified in potato tubers. At least two diastereoisomers of the latter glucoside were present. Analysis of eight fluorescent compounds in different parts of infected potatoes was performed by an improved HPLC technique. 相似文献
8.
9.
A water-soluble root extract of Angelica archangelica subsp. litoralis afforded, in addition to adenosine, coniferin and the two known dihydrofurocoumarin glycosides, apterin and 1′-O-β-d-glycopyranosyl-(S)-marmesin (marmesinin), two new dihydrofuranocoumarin glycosides, 1′-O-β-d-glucopyranosyl-(2S, 3R)-3-hydroxymarmesin, and 2′-β-d-glucopyranosyloxymarmesin. For the latter a 2S-configuration was demonstrated, the stereochemistry at position 1′ remaining undefined. Roots of A. silvestris similarly afforded 1′-O-β-d-glucopyranosyl-(2S, 3R)-3-hydroxymarmesin. By correlation with the aglycone 2S,3R)-3-hydroxymarmesin obtained in this work, the absolute configurations (2S,3R) were established for the known dihydrofurocoumarin diesters smirniorin and smirnioridin. 相似文献
10.
Hybrid molecules have attracted attention for their improved biological activity, selectivity and lesser side effects profile, distinct from their individual components. In the quest for novel anticancer drug entities, three series of indole–coumarin hybrids – 3-(1-benzyl-1H-indol-2-yl)-2H-chromen-2-ones, 2-(2-oxo-2H-chromen-3-yl)-1H-indole-3-carbaldehydes and 2-(2-oxo-2H-chromen-3-yl)-1H-indole-3-carboxylic acids were synthesized. All the synthesized compounds were characterized by spectral techniques like IR, 1H NMR, 13C NMR, mass spectrometry and elemental analysis. In silico docking studies of synthesized molecules with apoptosis related gene Bcl-2 that is recognized to play an important role in tumerogenesis were carried out. Dose-dependent cytotoxic effect of the compounds in human breast adenocarcinoma (MCF-7) and normal cell lines were assessed using MTT assay and compared with that of the standard marketed drug, Vincristine. Compound 4c had a highly lipophilic bromine substituent capable of forming halogen bond and was identified as a potent molecule both in docking as well as cytotoxicity studies. Flow cytometric cell cycle analysis of 4c exhibited apoptotic mode of cell death due to cell cycle arrest in G2/M phase. Structure activity relationship of these hybrid molecules was also studied to determine the effect of steric and electronic properties of the substituents on cell viability. 相似文献