共查询到20条相似文献,搜索用时 125 毫秒
1.
罂粟花粉十七肽类似物和片段的合成及其抗肿瘤活性研究 总被引:7,自引:0,他引:7
以从罂粟花粉中分离得到的具有促免疫和抗肿瘤活性的十七肽为先导化合物,设计了4个类似物和3个片段,并用固相法合成,通过CD谱测定了它们在溶液中的初级二级结构,同时测定了它们对人胃癌和人膀胱癌肿瘤细胞的抑制活性,初步讨论了构效关系. 相似文献
2.
罂栗花粉中水溶性肽的分离纯化、序列测定和合成的研究 总被引:4,自引:0,他引:4
从罂栗花粉中分离得到含21, 17, 13和16个氨基酸残基的四种肽PSPP1~4, 测定了它们的序列。用固相法合成了PSPP2~4, 经HPLC和电泳法对比, 确定了分离肽的一级结构。用FT-IR、CD谱初步讨论了它们在固态和溶液中的二级结构。通过T-淋巴细胞转化实验等生理活性测定方法表明它们具有一定的促免疫活性。 相似文献
3.
从罂栗花粉中分离得到含21, 17, 13和16个氨基酸残基的四种肽PSPP1~4, 测定了它们的序列。用固相法合成了PSPP2~4, 经HPLC和电泳法对比, 确定了分离肽的一级结构。用FT-IR、CD谱初步讨论了它们在固态和溶液中的二级结构。通过T-淋巴细胞转化实验等生理活性测定方法表明它们具有一定的促免疫活性。 相似文献
4.
油菜花粉十二肽和类似物的合成及性质的研究 总被引:6,自引:1,他引:6
用固相法合成了首次从油菜花粉中提取的十二肽,为进一步研究其结构与活性的关系,设计并合成了它的7个肽片段和5个类似物,并通过FTIR和CD谱的测定与分析,初步讨论了它们在固体状态和不同溶剂中的结构问题,同进,用肿瘤坏死因子TNF实验,T-淋巴细胞转化实验和E-玫瑰花结实验测定了它们的生理活性,结果提示该十二肽和它的某些片段具有增强TNF抗肿瘤细胞和在体外能促进猪胸腺细胞成熟的作用。 相似文献
5.
合成了21个混合三烃基锡羧酸酯。利用红外光谱、核磁共振谱(^1H,^13C,^119Sn)和质谱表征了化合物的结构。对取代苯甲酸酯化合物,锡原子的化学位移δ(^119Sn)与苯环上取代基的Hammett常数有很好的线性关系。化合物的生物活性测定结果表明,它们具有高效杀螨活性。 相似文献
6.
7.
采用“一锅法”设计合成了9个N-硝基脲衍生物,收率50.2%-76.8%。通过红外光谱、核磁共振谱及元素分析等测试技术确证了它们的结构。初步杀菌活性测试表明,当浓度为50mg/L时,部分化合物对水稻纹枯菌具有较好的抑菌活性。 相似文献
8.
9.
10.
烷基磷酰二氯分别与4-(喹Wu啉-2-氧基)苯酚钠和仲胺在极性有机溶剂中亲核取代反应合成了8种新的标题化合物,其结构用元素分析,红外光谱,核磁区振谱及质进行了表征,并测定它们的除草活性。 相似文献
11.
XU Liang zhong ** ZHANG Shu sheng LI Hui jing JIAO Kui *** Institute of Chemical Molecular Technology Qingdao University of Science Technology Qingdao P. R. China 《高等学校化学研究》2002,18(3):284-286
IntroductionTriazole compounds have attracted muchattention having been used as high efficient andwide spectrum fungicide and plant growthregulator[1— 4] .The triazole compounds containtintg1 ,3- dioxolane have the remarkable prevention ofthe control over plant diseases[5] .Propiconazol anddifenoconazole are two important representatives.But the necessary intermediate for synthesizingpropiconazol depends on imports,which leads tothe cost of production and application too high.According to th… 相似文献
12.
13.
α-(1H-1,2,4-三唑-1-基)-β-芳硫基取代苯酮的合成及生物活性研究 总被引:1,自引:0,他引:1
利用 2 (1H 1,2 ,4 三唑 1 基 ) 2 丙烯 1 酮 (2 )与取代硫酚或含巯基的杂环化合物进行 1,4 亲核加成 ,得到目标化合物 3,其结构经元素分析、核磁和红外光谱所证实 ,并对其进行了生物活性的测试 ,发现大部分化合物具有很好的抑菌活性 .结构与活性的关系表明不同的R1取代对其生物活性有较大的影响 ,当R1=(CH3 ) 3 C时 ,对小麦锈病的抑制活性要高于R1=Ar的活性 ,而Ar上不同的取代基对其活性影响不大 相似文献
14.
15.
Synthesis of Novel 2-(Pyridin-2-yl) Pyrimidine Derivatives and Study of Their Anti-Fibrosis Activity
Yi-Fei Gu Yue Zhang Feng-li Yue Shao-tong Li Zhuo-qi Zhang Jing Li Xu Bai 《Molecules (Basel, Switzerland)》2020,25(22)
A pyrimidine moiety exhibiting a wide range of pharmacological activities has been employed in the design of privileged structures in medicinal chemistry. To prepare libraries of novel heterocyclic compounds with potential biological activities, a series of novel 2-(pyridin-2-yl) pyrimidine derivatives were designed, synthesized and their biological activities were evaluated against immortalized rat hepatic stellate cells (HSC-T6). Fourteen compounds were found to present better anti-fibrotic activities than Pirfenidone and Bipy55′DC. Among them, compounds ethyl 6-(5-(p-tolylcarbamoyl)pyrimidin-2-yl)nicotinate (12m) and ethyl 6-(5-((3,4-difluorophenyl)carbamoyl)pyrimidin-2-yl)nicotinate (12q) show the best activities with IC50 values of 45.69 μM and 45.81 μM, respectively. Furthermore, the study of anti-fibrosis activity was evaluated by Picro-Sirius red staining, hydroxyproline assay and ELISA detection of Collagen type I alpha 1 (COL1A1) protein expression. Our study showed that compounds 12m and 12q effectively inhibited the expression of collagen, and the content of hydroxyproline in cell culture medium in vitro, indicating that compounds 12m and 12q might be developed the novel anti-fibrotic drugs. 相似文献
16.
17.
XULiang-zhong ZHANGShu-sheng CHENXiao JIAOKui 《高等学校化学研究》2003,19(3):306-309
Sixteen new triazole organic phosphorus compounds were synthesized. Their structures were confirmed with IR, IH NMR, elemental analysis and MS. The primary biological tests show that the titled compounds have the fungicidal activities, which are influenced by R groups and the substituents attached to the P atom. 相似文献
18.
Eighteen novel triazole compounds containing 1,3,4-oxadiazole groups were synthesized from 2-(1H-1,2,4-triazol-1-yl)acetohydrazide and carbon disulfide by several step reactions. The target compounds were characterized by elemental analysis, 1H NMR, 13C NMR, IR, MS, and X-ray crystallography. The results of preliminary biological tests show that all the compounds exhibit certain fungicidal activities. 相似文献
19.
20.
XU Liang-zhong LI Wei-hua YU Guan-ping QIN Yong-qi YANG Shuang-hua HOU Bao-rong 《高等学校化学研究》2005,21(5):528-530
In order to find leading compounds with an excellent fungicidal activity, the title compound 2-( 1,3-dithiolan-2- yl-idene)-1-phenyl-2-( 1,2,4-tfiazol-1-yl) ethanone was synthesized according to the biological isosterism and its structure was confirmed by means of IR, MS, ^1 H NMR and elemental analysis. The single crystal structure of the title compound was determined by X-ray diffraction. The preliminary biological test shows that the synthesized compound exhibits some biological activities. 相似文献