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Salan钛双齿配合物的Sonogashira合成后修饰反应研究 被引量:1
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作者 赵添堃 王鹏 +3 位作者 姬明宇 李善家 杨明俊 蒲秀瑛 《化学学报》 SCIE CAS CSCD 北大核心 2021年第11期1385-1393,共9页
报道了一种通过钯催化Sonogashira反应对具抗癌活性的ONNO型“Salan”、“2,6-吡啶二甲酸”双配位钛化合物进行高效后修饰的方法学研究.通过Sonogashira反应直接向两个配体引入不同炔烃功能基团,共制备了20个新型的钛配合物.进一步通过... 报道了一种通过钯催化Sonogashira反应对具抗癌活性的ONNO型“Salan”、“2,6-吡啶二甲酸”双配位钛化合物进行高效后修饰的方法学研究.通过Sonogashira反应直接向两个配体引入不同炔烃功能基团,共制备了20个新型的钛配合物.进一步通过该方法学向钛配合物引入三苯乙炔基及癌细胞靶向分子雌炔醇.通过1H NMR和13C NMR、HRMS、UV-vis和IR等手段对所有配合物进行了结构表征.多数炔基活化的钛配合物对HeLa S3和Hep G2癌细胞在微摩尔范围内表现出显著提升的抑制活性,其中配合物3j[Salan2,4-dimethylTi^((IV))Dipic4-(3-(dimethylamino)prop-1-yn-1-yl)]的IC_(50)值较顺铂提升约一个数量级,是本研究中活性最强的Salan钛双齿配合物[3j,HeLa S3:IC_(50)=(0.5±0.1)μmol/L,Hep G2:IC_(50)=(0.7±0.2)μmol/L;顺铂,HeLa S3:IC_(50)=(3.3±0.2)μmol/L,Hep G2:IC_(50)=(6.0±1.1)μmol/L].针对芳炔和脂肪炔取代不同配体的代表配合物2a、2f、3a和3j开展的稳定性研究表明,向2位无取代Salan引入的炔基可通过电负性改变配合物的水稳定性,2a和2f水解出无抗癌活性的炔基Salan配体1a*,半数水解时间(t1/2)分别为5和10 h.炔基功能化2,6-吡啶二甲酸的配合物3a和3j含有2位甲基取代的Salan配体,它们在水环境中保持稳定.此外,本文总结和阐释了这类新型炔基功能化钛配合物的“结构-活性”关系,并对后续开发此类钛配合物的前景和策略做出了分析与展望. 展开更多
关键词 SONOGASHIRA反应 [SalanTi^(IV)Dipic]配合物 抗癌活性 炔基功能化 水稳定性
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The Effect of Semen Ziziphi Spinosae Extract on the p38MAPK/NF-κB Signaling Pathway in Insomniac Rats 被引量:1
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作者 mingyu ji Wei Xiong +4 位作者 Zijing Xu Peipei Zhang Shuyu Li Qian Wang Dexian jia 《Chinese Medicine and Natural Products》 2024年第4期145-152,共8页
Objective The objective of the study was to explore whether Suanzaoren(Semen Ziziphi Spinosae,SZS)extract could improve insomnia by inhibiting the p38 mitogenactivated protein kinase(p38MAPK)/nuclear factor-κB(NF-κB... Objective The objective of the study was to explore whether Suanzaoren(Semen Ziziphi Spinosae,SZS)extract could improve insomnia by inhibiting the p38 mitogenactivated protein kinase(p38MAPK)/nuclear factor-κB(NF-κB)signaling pathway.Methods Forty SPF-grade Sprague-Dawley(SD)rats were included in the study,with 10 randomly selected rats serving as the control group.The remaining rats were injected intraperitoneally with p-chlorophenylalanine(PCPA)for 6 days to establish an insomnia model.After successful modeling,the rats were divided into the model group,SZS extract group(3.0 g/kg),and zopiclone group(1.25 g/kg).The rats in the SZS extract and zopiclone groups were administered with the corresponding drugs via gavage for 7 days,while the rats in the control and model groups received distilled water.Sleep latency and sleep duration were recorded,and behavioral changes were observed through elevated plusmaze and open field tests.The levels of oxidative stress markers and serum inflammatory factors were measured by enzyme-linked immunosorbent assay(ELISA).The expression levels of p38 MAPK,p-p38MAPK,p-NF-κBp65,and NF-κBp65 protein in the cerebral cortex were detected by Western blot.Neuronal structures in the cerebral cortex were observed under a transmission electron microscope.Results Compared with the control group,the model group exhibited abnormal appearances,significant body mass loss(p<0.001),prolonged sleep latency and shortened sleep duration(p<0.001).The SZS extract and zopiclone groups showed significant improvements in these parameters compared with the model group.Compared with the control group,the model group showed significant reduction in total movement distance(p<0.001),fewer entries into the central zone(p<0.01),and significant decrease in rearing frequency(p<0.001);the levels of glutathione peroxidase(GSH-Px)and catalase(CAT)in the hippocampus were significantly reduced(p<0.001);the serum levels of interleukin-1β(IL-1β),tumor necrosis factor-α(TNF-α),and the expression levels of p-p38MAPK and p-NF-κBp65 in the cerebral cortex were significantly increased(p<0.05).Compared with the model group,the SZS extract group showed significant increase in movement distance(p<0.01)and rearing frequency(p<0.001),significantly increased the GSH-Px and CAT levels(p<0.001),and decreased the IL-1βand TNF-αlevels(p<0.01);furthermore,the SZS extract group showed a significantly reduced p-p38MAPK and p-NF-κBp65 levels(p<0.05).The SZS extract group showed significant improvement in the neuronal structure compared with the model group.Conclusion SZS extract can inhibit the p38MAPK/NF-κB signaling pathway to improve insomnia. 展开更多
关键词 Semen Ziziphi Spinosae extract p38MAPK/NF-κB signaling pathway INSOMNIA oxidative stress inflammatory factors
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