取代罗丹明B酰胺基硫脲类荧光探针化合物合成和应用

来源 :河南省化学会2016年学术年会 | 被引量 : 0次 | 上传用户：liyunfeng890406

【摘要】

：

汞是造成环境污染的主要重金属离子之一，在浓度很低时对生物体就表现出极强的生理毒性。且汞易经生物富集作用最终转移到人类体内，且无法通过自身代谢作用排出体外，严重危害人类的身体健康。因此，对生物体和环境中汞的分析检测一直是人们非常关注的问题，建立快速、高效的汞离子检测方法在生命科学、医学、环境保护等领域中具有重大意义。

【作者】

：

时蕾鹿泽华徐晶晶董燕平

【机构】

：

河南师范大学化学化工学院,河南省新乡市建设东路46号,453007

【出处】

：

河南省化学会2016年学术年会

【发表日期】

：

2016年10期

下载到本地 , 更方便阅读

下载此文赞助VIP

声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架

论文部分内容阅读

其他文献

Synthesis of Chromeno[4',3':4,5]imidazo[1,2-a]pyridin-6-ones via Cascade Reactions of 2-(2

Imidazopyridine compounds are important nitrogen-containing heterocycles existing widely in natural products,pharmaceuticals,pesticides,and dyes.In another aspect,chromenone derivatives are found to b

会议

Imidazo[12-a]pyridinesChromenoneCascade reactionCarbonylation

Synthesis of 2,2'-biphenols through Direct C(sp2)-H Hydroxylation of [1,1'-Biphenyl]-2-ols

The 2,2-biphenol framework is frequently found in natural products,pharmaceuticals and functional materials.Moreover,2,2-biphenol and its derivatives are also acting as efficient ligands in numerous m

会议

C(sp2)-H hydroxylation22'-Biphenoltert-Butyl hydroperoxide

Synthesis of Chiral Acyclic Nucleoside Analogues via the Ring-Opening Reaction of Chiral Epoxides

Many chiral acyclic nucleoside analogues exhibit outstanding anti-virus and anti-cancer activities.Thus,developing efficient synthesis methods to construct chiral acyclic nucleoside analogues have att

会议

Chiral acyclic Nucleoside AnaloguesRing-opening reaction

1,3-氧氮天然生物碱化合物骨架合成研究

1,3-氧氮天然生物碱Chinese Bittersweet Alkaloid(1)和(2)是一类具有全新骨架的生物活性化合物[1]。作为生物活性的研究,经过美国NCI癌症研究中心筛选,该类化合物中化合物(2)在筛选的9个细胞系的60个癌细胞株中对非小细胞肺癌HOP-92细胞株展现出良好的抑制活性。

会议

含氟抗菌剂苯甘氨酸氟甲酯的合成

本课题组前期从五谷虫[1,2]的70％的甲醇提取液中提取得到了微量的活性氟化合物苯甘氨酸氟甲酯(1)。初步药理筛选结果显示化合物1具有较强的抗枯草杆菌活性,较青霉素作用更加显著 [3]。

会议

A Straightforward Entry to Chiral Cyclopropyl Carbocyclic Purine Nucleosides via Asymmetric Intramol

Chiral carbocyclic purine nucleosides have been the focus of much attention in the search for new antiviral and antitumor therapeutic agents.Cyclopentyl carbocyclic guanosine nucleoside Carbovir has b

会议

CyclopropanationCyclopropyl carbocyclic Nucleaside Analogues

Synthesis of Chiral Cyclopropyl Pyrimidine Carbocyclic Nucleosides via Asymmetric Intermolecular Cyc

Chiral nucleosides and their derivatives have shown significant antivirus and antitumor activities.Sofosbuvir is a novel anti-HCV agent that has displayed impressively excellent treatment effect that

会议

CyclopropanationCyclopropyl carbocyclic Nucleoside AnaloguesN1 vinyl pyrimidin

Monofluoromethylation of Purin-9-yl Allenes with FBSM

Monofluoromethylation has attracted substantial attention in organic synthesis,owing to the increasing important application of selectively fluorinated organics in medicinal chemistry and materials sc

会议

MonofluoromethylationAcyclic Nucleaside Analogues

Highly efficient synthesis of a series of N-fused heterocyclic compounds via copper-catalyzed cascad

N-Fused heterocycles have attracted much interest since they are widely present in naturally occurring alkaloids and synthetic compounds with a broad spectrum of biological activities.

会议

Copper-catalyzedCascade reactionAqueous ammoniaN-fused heterocycles

Synthesis of 9-(β-D-glucopyranosyl)adenine

Natural products that target RNA include the macrolides(e.g.,erythromycin,clarythromycin,and azithromycin)and the aminoglycosides(e.g.,tobramycin and gentamicin).

会议

9-(β-D-glucopyranosyl)adeninemicrowave assistedpyranosyl rings

取代罗丹明B酰胺基硫脲类荧光探针化合物合成和应用

其他学术论文