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Urinary Concentrations of Hydroxyproline and 3-Methyl Histidine in Postpartum Cow 被引量:1
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作者 TIANWen-ru HEJian-bin 《Journal of Northeast Agricultural University(English Edition)》 CAS 2001年第1期23-29,共7页
The urinary concentrations of hydroxyproline (HYPRO)and 3 -methyl histidine (3 - MEHIS) were de- termined in 16 Chinese-Holstein cows. The objectives of the experiment were to find out thhe relationship between collag... The urinary concentrations of hydroxyproline (HYPRO)and 3 -methyl histidine (3 - MEHIS) were de- termined in 16 Chinese-Holstein cows. The objectives of the experiment were to find out thhe relationship between collagen and myosin ddegradation and uterine involution in the postpartum cow. The results in the experiment showed that the mean concentrations of HYPRO and 3-MEHIS were 138.32±22.99 and 37.09 ±3.90 nmol·mL-1,respectively,for the cows during the days between 60-90 postpartum,and for the cows immediately after calving the concentrations of HYPRO and 3 -MEHIS reduced from 284.30 and 65.48 nmol ·mL-1 on the day one after calving to the normal level of 109.18 and 33.51 nmol·mL^-1 on the day 50 post- partum,respectively. There was a good correlation between the urinary concentrations of both HYPRO and 3 -MEHIS and the diameters of the involuting uterus (r = 0. 79). 展开更多
关键词 COW 3-methyl histidine HYDROXYPROLINE uterine involution
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3-甲基芬太尼衍生物的合成及镇痛活性 被引量:1
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作者 朱国政 李云祥 颜松民 《药学学报》 CAS CSCD 北大核心 1990年第11期811-814,共4页
本文合成了6个1-取代-3-甲基芬太尼衍生物。初步的药理实验结果表明,它们均具有典型的吗啡样作用。某些1位β-取代乙烯基乙基衍生物有强镇痛活性。简要地讨论了其结构—活性关系。
关键词 吗啡 芬太尼 镇痛活性
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维生素K_3对芬太尼药理作用的实验研究
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作者 莫恃 谭至慈 +3 位作者 谭立清 钟正贤 周桂芬 韦保伟 《临床麻醉学杂志》 CAS CSCD 1998年第1期30-33,共4页
目的:研究维生素K3对芬太尼的药理作用。方法:用气相色谱法测定血浆芬太尼浓度。结果与结论:1.K3能拮抗芬太尼引起的血压下降和心率减慢作用。2.K3能拮抗芬太尼引起的呼吸抑制。3.K3能缩短试验动物的睡眠时间(P<0... 目的:研究维生素K3对芬太尼的药理作用。方法:用气相色谱法测定血浆芬太尼浓度。结果与结论:1.K3能拮抗芬太尼引起的血压下降和心率减慢作用。2.K3能拮抗芬太尼引起的呼吸抑制。3.K3能缩短试验动物的睡眠时间(P<0.05)。4.K3具有拮抗芬太尼对阿片受体的作用。5.用气相色谱法测定16个血样品均未检出芬太尼。 展开更多
关键词 维生素K3 芬太尼 气相色谱
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3-甲基-4-甲氧羰基芬太尼类似物的合成与镇痛活性 被引量:4
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作者 温素姐 杨玉龙 +3 位作者 邵华宙 杨志杰 刘林妮 陈冀胜 《中国药科大学学报》 CAS CSCD 北大核心 1992年第4期186-202,共17页
报道某些3-甲基-4-甲氧羰基芬太尼类似物的合成,顺反异构体的分离及其镇痛活性。实验结果表明,该类化合物具有与3-甲基芬太尼类和4-甲氧羰基芬太尼类相当的强效镇痛活性(活性最强的化合物18a镇痛强度为吗啡的2939倍),构效关系更类似于... 报道某些3-甲基-4-甲氧羰基芬太尼类似物的合成,顺反异构体的分离及其镇痛活性。实验结果表明,该类化合物具有与3-甲基芬太尼类和4-甲氧羰基芬太尼类相当的强效镇痛活性(活性最强的化合物18a镇痛强度为吗啡的2939倍),构效关系更类似于前者。顺式异构体的活性通常强于反式,且二者强度比较小,提示4-甲基羰基引入到3-甲基芬太尼类化合物分子中降低了3位甲基对阿片受体作用的选择性。 展开更多
关键词 镇痛作用 芬太尼 合成
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1-(4-甲基-3-戊烯基)-3-甲基-4-(N-丙酰苯胺基)哌啶立体异构体的合成及其镇痛作用
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作者 温素姐 李德金 +3 位作者 杨松林 杨玉龙 颜松民 陈冀胜 《中国医药工业杂志》 CAS CSCD 北大核心 1993年第5期202-204,共3页
合成了具有强效镇痛活性的3-甲基芬太尼衍生物1-(4-甲基-3-戊烯基)-3-甲基-4-(N-丙酰苯胺基)哌啶(1)及其顺(±)反-(±)-和顺-(+)-、顺-(-)-异构体。小白鼠热板试验结果表明,其异构体的构效关系类似于3-甲基芬太尼,但1-乙基的β... 合成了具有强效镇痛活性的3-甲基芬太尼衍生物1-(4-甲基-3-戊烯基)-3-甲基-4-(N-丙酰苯胺基)哌啶(1)及其顺(±)反-(±)-和顺-(+)-、顺-(-)-异构体。小白鼠热板试验结果表明,其异构体的构效关系类似于3-甲基芬太尼,但1-乙基的β-苯基被 Me_2C=CH 基取代后降低了分子对阿片受体作用的立体选择性。 展开更多
关键词 芬太尼 吗啡 合成 镇痛药 三甲基
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顺-3-甲基芬太尼的4-N-丙酰基结构类似物的合成与镇痛活性及构效关系的研究
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作者 陈晓盼 杨玉龙 +1 位作者 陈常英 商尔 《药学学报》 CAS CSCD 北大核心 1992年第7期503-509,共7页
以不同电性的基团取代顺-3-甲基芬太尼中4-N-丙酰基上的乙基,合成某些顺-3-甲基芬太尼的结构类似物。药理试验结果表明,所合成的化合物均有典型的吗啡样作用。化合物3的镇痛活性略强于顺-3-甲基芬太尼。应用半经验的INDO方法对4个代表... 以不同电性的基团取代顺-3-甲基芬太尼中4-N-丙酰基上的乙基,合成某些顺-3-甲基芬太尼的结构类似物。药理试验结果表明,所合成的化合物均有典型的吗啡样作用。化合物3的镇痛活性略强于顺-3-甲基芬太尼。应用半经验的INDO方法对4个代表化合物进行了量子化学计算,讨论了电子结构与镇痛活性间的关系,化合物3由于氯乙烯基的引入具有与顺-3-甲基芬太尼不同的电子结构特征,氯乙烯基可能作为电子接受体参与了与受体的作用。 展开更多
关键词 甲基芬太尼 镇痛活性 芬太尼
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芬太尼通过ILF3-AS1/miR-132对卵巢癌细胞生长和转移的影响
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作者 何含 刘群 +5 位作者 钟庆 翁艳 汪艳 黄凡 邬瑞刚 杨国仁 《安徽医药》 CAS 2022年第4期765-769,I0002,共6页
目的探讨芬太尼对卵巢癌细胞生长和转移的影响及分子机制。方法2018年8月至2019年10月,体外培养卵巢癌细胞A2780,用浓度分别为0、0.5、5、50、500 ng/mL的芬太尼处理,作为不同浓度芬太尼处理组。将过表达的白细胞介素增强结合因子3反义R... 目的探讨芬太尼对卵巢癌细胞生长和转移的影响及分子机制。方法2018年8月至2019年10月,体外培养卵巢癌细胞A2780,用浓度分别为0、0.5、5、50、500 ng/mL的芬太尼处理,作为不同浓度芬太尼处理组。将过表达的白细胞介素增强结合因子3反义RNA1(ILF3-AS1)(pcDNA3.1-ILF3-AS1、对照pcDNA3.1)、抑制微小RNA(miRNA/miR)-132表达(抗-miR-132、对照anti-miR-NC)的载体分别转染A2780细胞,并以500 ng/mL芬太尼处理,记为芬太尼500+pcDNA3.1-ILF3-AS1组、芬太尼500+pcDNA3.1组、芬太尼500+anti-miR-132组、芬太尼500+anti-miR-NC组。将pcDNA3.1、pcDNA3.1-ILF3-AS1、si-NC、si-ILF3-AS1转染至A2780细胞中,记为pcDNA3.1组、pcDNA3.1-ILF3-AS1组、si-NC组、si-ILF3-AS1组。四甲基偶氮唑盐比色法(MTT)检测细胞存活率;克隆形成实验检测细胞克隆形成数;Transwell检测细胞迁移和侵袭;实时荧光定量PCR(RT-qPCR)检测ILF3-AS1和miR-132的表达水平;荧光素酶报告实验检测ILF3-AS1和miR-132的靶向关系。结果与0 ng/mL芬太尼处理组相比,5、50、500 ng/mL的芬太尼处理的A2780中miR-132表达水平显著升高[(1.39±0.13)、(1.68±0.17)、(2.34±0.23)比(1.00±0.10)],细胞存活率[(86.14±8.25)%、(71.03±7.11)%、(43.26±4.34)%比(100.01±10.01)%]、克隆形成数、迁移、侵袭细胞数显著降低,ILF3-AS1表达水平显著降低[(0.78±0.08)、(0.54±0.05)、(0.30±0.03)比(1.01±0.10)](P<0.05)。过表达ILF3-AS1和抑制miR-132表达均逆转了芬太尼对A2780增殖、迁移、侵袭的抑制作用。且ILF3-AS1靶向调控miR-132的表达。结论芬太尼浓度大于5 ng/mL时可抑制卵巢癌细胞增殖、迁移和侵袭,其机制可能与ILF3-AS1及miR-132有关。 展开更多
关键词 芬太尼 白细胞介素增强结合因子3反义RNA1 微小RNA-132 卵巢癌
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Reactivity of 3-Cyanoacetylindole Derivatives: Synthesisof 3-Hydrazonopyrazolyl and 3-Thiadiazolyl Indole Derivatives
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作者 Hamdi M. Hassaneen Huwaida M. E. Hassaneen Zakaria Ahmed Gomaa 《International Journal of Organic Chemistry》 2011年第3期97-104,共8页
The coupling reaction of 3-cyanoacetyl-2-methylindole 1a with the aromatic diazonium salts gave the corresponding arylhydrazones 2a-e. Compounds 2 were used for synthesis of 4-aminopyrazole-5-carbonitrile 4a-e and 5-a... The coupling reaction of 3-cyanoacetyl-2-methylindole 1a with the aromatic diazonium salts gave the corresponding arylhydrazones 2a-e. Compounds 2 were used for synthesis of 4-aminopyrazole-5-carbonitrile 4a-e and 5-amino-4-arylazo-3-pyrazoles 5a-e derivatives. Also, treatment of 3-cyanoacetyl-2-phenylindole 1b with phenyl isothiocyanate gave the corresponding thioacetanilide 7. The later compound 7 was utilized as the key intermediate for the synthesis of some new thiadiazole derivatives 9a-r. The structures of all new compounds were elucidated on the basis of elemental analysis and spectral data. 展开更多
关键词 3-methyl INDOLE 3-Phenyl INDOLE PHENYL ISOTHIOCYANATE Cyanoacetic Acid
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Synthesis and Crystal Structure of(E)-Ethyl 2-(4-(2,4-dimethoxybenzylideneamino)-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazol-3-ylthio)acetate
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作者 YOU Wen-Wei ZHAO Pei—Liang +1 位作者 DUAN An-Na WU Shu-Guang 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2011年第4期600-603,共4页
The crystal structure of the title compound(E)-ethyl 2-(4-(2,4-dimethoxy benzylide-neamino)-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazol-3-ylthio)acetate(4,C_(24)H_(28)N_(4)O_(7)S,Mr=516.17)was synthesized and determin... The crystal structure of the title compound(E)-ethyl 2-(4-(2,4-dimethoxy benzylide-neamino)-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazol-3-ylthio)acetate(4,C_(24)H_(28)N_(4)O_(7)S,Mr=516.17)was synthesized and determined by X-ray single-crystal diffraction.The crystal belongs to the monoclinic system,space group P2_(1)/n with a=13.162(2),b=8.4506(13),c=22.602(4)Å,β=99.888(3)°,μ=0.183 mm^(-1),V=2476.5(7)Å^(3),Z=4,D_(c)=1.385 g/cm^(3),F(000)=1088,T=110(2)K,R=0.0426 and wR=0.1216 for 3859 observed reflections with I 2σ(Ⅰ). 展开更多
关键词 synthesis crystal structure (Z)-methyl 3-methoxy-2-{2-[(4-(E-3-p-tolylacryloyl)-phenoxy)methyl]phenyl}acrylate
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Determination of 8,2′-diprenylquercetin 3-methyl ether in plasma by UPLC-MS-MS and its pharmacokinetic application in rats
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作者 刘焕 范珊珊 +6 位作者 张雯 张驿帆 李腾 尚明英 刘广学 徐风 蔡少青 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2017年第10期747-753,共7页
8,2'-Diprenylquercetin 3-methyl ether with significant anti-breast cancer activity is the main constituent of Tibetan medicine Sinopodophylli Fructus. In the present study, we developed and validated a rapid and sens... 8,2'-Diprenylquercetin 3-methyl ether with significant anti-breast cancer activity is the main constituent of Tibetan medicine Sinopodophylli Fructus. In the present study, we developed and validated a rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the determination of 8,2'-diprenylquercetin 3-methyl ether in rat plasma. 8-Prenylkaempferol was used as the internal standard. The separation was carried out using Waters ACQUITY UPLC BEH C18 column (2.1 mm×100 ram, 1.7 μm) with a mobile phase consisting of acetonitrile and 0.1% formic acid in water on a gradient program at a flow rate of 0.4 mL'min-1 and temperature of 30 ℃. Triple quadrupole mass spectrometric detection in negative ion mode was used for multiple-reaction monitoring of the transitions at m/z 451.30→177.25 and m/z 353.25→298.15 for 8,2'-diprenylquercetin 3-methyl ether and 8-prenylkaempferol, respectively. The calibration curves were linear within the concentration range 0.1-2000 ng/mL (r = 0.9954). The recoveries were 103%-115%, and the results were consistent across low, middle and high concentration levels. The intra- and inter-day precisions were within 15%, and the bias was between --6%-15%. This method was simple, rapid and sensitive, which could be applied to the determination of 8,2'-diprenylquercetin 3-methyl ether in plasma and pharmacokinetic study in rats. Pharmacokinetic test indicated that the peak plasma concentration occurred in 2 h after the female rats were intragastrically administered with 8,2'-diprenylquercetin 3-methyl ether at the dose of 100 mg/kg, and the biological half-life was 6.79 h. The blood drug concentration maintained equal amount for 20 h, which was conducive to the in vivo effects of drugs. 展开更多
关键词 8 2'-Diprenylquercetin 3-methyl ether UPLC-MS/MS Blood concentration Anti-breast cancer PHARMACOKINETIC
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Impact of CYP3A4*1G Polymorphism on Fentanyl Analgesia Assessed by Analgesia Nociception Index in Chinese Patients Undergoing Hysteroscopy 被引量:9
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作者 Qi Yan Yi Su +6 位作者 Lan Gao Nan Ding Hong-Ying Zhang Wen E Yue Wang Yi Feng Hai-Yan An 《Chinese Medical Journal》 SCIE CAS CSCD 2018年第22期2693-2698,共6页
Background:The clinical efficacy of fentanyl for pain control differs greatly across individuals.The purpose of this study was to investigate the impact of CYP3A4*1G polymorphism including wild-type homozygote (CYP3A4... Background:The clinical efficacy of fentanyl for pain control differs greatly across individuals.The purpose of this study was to investigate the impact of CYP3A4*1G polymorphism including wild-type homozygote (CYP3A4*1/*1,GG),mutant heterozygote (CYP3A4*1/*1G,GA),and mutant homozygote (CYP3A4*1G/*1G,AA)on fentanyl analgesia in Chinese patients undergoing hysteroscopy by the assessment of analgesia nociception index (ANI). Methods:A total of 200 gynecologic patients scheduled for elective hysteroscopy under general anesthesia at Peking University People's Hospital from May to December in 2017 were enrolled in this study.Venous blood was withdrawn for genotyping of CYP3A4*1G before operation.Fentanyl 1μg/kg was administered preoperatively followed by target-controlled infusion of propofol for induction and maintenance.Intraoperative analgesic efficacy of fentanyl was assessed by ANI monitoring at T0(entering room),T1(cervical dilation), T2(start of cervical aspiration),and T3(end of cervical aspiration)time points.The duration of propofol infusion and total dosage of propofol were recorded as well. Results:The patients were divided into three groups according to CYP3A4*1G polymorphism,including 143 in GG group,47in GA group, and 10 in AA group.There was no significant difference in clinical demographics among three groups.The frequency of CYP3A4*1G variant alleles accounted for 16.8%and the distribution of variant alleles was consistent with Hardy-Weinberg equilibrium.Using a multilevel model,ANI values at T1(63.81±19.61),T2(63.63±17.82),and T3(65.68±17.79)were significantly lower than that at T0 (77.16±12.93)in the study population (F =23.50,P <0.001),suggesting that higher levels of pain at T 1,T2,and T3 than T0.Patients with GG genotype showed significantly lower ANI than those with GA or AA genotypes during hysteroscopy under the same dose of fentanyl. Conclusion:CYP3A4*1G polymorphism associated with the analgesic efficacy of intraoperative fentanyl in the patients undergoing hysteroscopy under general anesthesia. 展开更多
关键词 ANALGESIA CYP3A4 fentanyl Genetic POLYMORPHISM
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Global hypomethylation in hepatocellular carcinoma and its relationship to aflatoxin B_1 exposure 被引量:5
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作者 Hulya Yazici Ming-Whei Yu +1 位作者 Po-Huang Lee Regina M Santella 《World Journal of Hepatology》 CAS 2012年第5期169-175,共7页
AIM:To determine global DNA methylation in paired hepatocellular carcinoma(HCC) samples using several different assays and explore the correlations between hypomethylation and clinical parameters and biomarkers,includ... AIM:To determine global DNA methylation in paired hepatocellular carcinoma(HCC) samples using several different assays and explore the correlations between hypomethylation and clinical parameters and biomarkers,including that of aflatoxin B 1 exposure.METHODS:Using the radio labeled methyl acceptance assay as a measure of global hypomethylation,as well as two repetitive elements,including satellite 2(Sat2) by MethyLight and long interspersed nucleotide elements(LINE1),by pyrosequencing.RESULTS:By all three assays,mean methylation levels in tumor tissues were significantly lower than that in adjacent tissues.Methyl acceptance assay log(mean ± SD) disintegrations/min/ng DNA are 70.0 ± 54.8 and 32.4 ± 15.6,respectively,P = 0.040;percent methylation of Sat2 42.2 ± 55.1 and 117.9 ± 88.8,respectively,P < 0.0001 and percent methylation LINE1 48.6 ± 14.8 and 71.7 ± 1.4,respectively,P < 0.0001.Aflatoxin B 1 albumin(AFB 1-Alb) adducts,a measure of exposure to this dietary carcinogen,were inversely correlated with LINE1 methylation(r =-0.36,P = 0.034).CONCLUSION:Consistent hypomethylation in tumor compared to adjacent tissue was found by the three different methods.AFB 1 exposure is associated with DNA global hypomethylation,suggesting that chemical carcinogens may influence epigenetic changes in humans. 展开更多
关键词 Hepatocellular carcinoma EPIGENETICS HYPOMETHYLATION [3 H]-methyl acceptance assay Satellite 2 Long interspersed nucleotide element-1 Aflatoxin B_1
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Even-carbon predominance of Monomethyl branched alkanes in Humic coal from Junggar Basin,NW China 被引量:1
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作者 Qingsong Cheng Min Zhang Guanghui Huang 《Acta Geochimica》 EI CAS CSCD 2020年第3期434-444,共11页
A series of Monomethyl branched alkanes compounds were detected between nC14-nC36,in immature and low maturity Jurassic humic coal,Junggar basin.2-methyl alkanes and 3-methyl alkanes accounted for the vast majority of... A series of Monomethyl branched alkanes compounds were detected between nC14-nC36,in immature and low maturity Jurassic humic coal,Junggar basin.2-methyl alkanes and 3-methyl alkanes accounted for the vast majority of the compounds.It is worth noting that the2-methyl alkanes in the humic coal samples show an obvious distribution of even carbon predominances rarely reported in the literature.The results show that with the increase of Pr/Ph(pristane/phytane),the even carbon dominance of 2-methyl alkanes is more obvious,while the odd carbon number distribution of 3-methyl alkanes is weakened.As Pr/Ph increases in the humic coal,the relative content of the hopanes increased,while the relative content of 2-methyl alkanes and 3-methyl alkanes increases first and then decreases. 展开更多
关键词 Junggar basin Humic coal Even carbon predominance 2-methyl alkanes 3-methyl alkanes
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Indole Alkaloids from the Roots of Ervatamia hainanensis 被引量:4
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作者 Jian Peng HUANG Zi Ming FENG +2 位作者 Chong Fei ZHENG Pei Cheng ZHANG Yang Min MA 《Chinese Chemical Letters》 SCIE CAS CSCD 2006年第6期779-782,共4页
Two new indole alkaloids, named ibogamine-18-carboxylic acid, 3, 4-didehydro-7, 8-dioxo-methyl ester 1, ibogamine-18-carboxylic acid, 16, 17-didehydro-9, 17-dihydro-9-hydroxy (2-oxopropyl)-methyl ester 2, were isola... Two new indole alkaloids, named ibogamine-18-carboxylic acid, 3, 4-didehydro-7, 8-dioxo-methyl ester 1, ibogamine-18-carboxylic acid, 16, 17-didehydro-9, 17-dihydro-9-hydroxy (2-oxopropyl)-methyl ester 2, were isolated from Ervatamia hainanensis. Their structures were elucidated on the basis of spectroscopic methods. 展开更多
关键词 Ervatamia hainanensis indole alkaloid ibogamine-18-carboxylic acid 3 4-didehydro-7 8-dioxo-methyl ester ibogamine- 18-carboxylic acid 16 17-didehydro-9 17-dihydro-9-hydroxy-(2-oxopropyl)-methyl ester.
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Effect of Chemical Doping and Ion Implantation on Cond uctivity of Poly(p-phenylene vinylene) Derivatives 被引量:1
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作者 LI Bao-ming WU Hong-cai LIU Xiao-zeng LI Xiao-qi GAO Chao 《Semiconductor Photonics and Technology》 CAS 2005年第3期188-191,共4页
The surface conductivity of poly [ 2-methoxy-5-(3'-methyl) butoxy]-p-phenylene vinylene (PMOMBOPV) films doped with FeCl3 and H2SO4 by chemical method and implanted by N^+ ions was studied and the comparison of ... The surface conductivity of poly [ 2-methoxy-5-(3'-methyl) butoxy]-p-phenylene vinylene (PMOMBOPV) films doped with FeCl3 and H2SO4 by chemical method and implanted by N^+ ions was studied and the comparison of environmental stability of conductive behavior was also investigated. The energy and dose of N^+ ions were in the rang 15~35 keV and 3. 8×10^15~9. 6×10^16 ions/cm^2, respectively. The conductivity of PMOMBOPV film was enhanced remarkably with the increases of the energy and dose of N^+ ions. For example, the conductivity of PMOMBOPV film was 3. 2×10^-2S/cm when ion implantation was performed with an energy of 35 keV at a dose of 9. 6 × 10^14 ions/cm^2 , which was almost seven orders of magnitude higher than that of film unimplanted. The environmental stability of conductive behavior for ionimplanted film was much better than that of chemical doped films. Moreover, the conductive activation energy of ion-implanted films was measured to be about 0.17 eV. 展开更多
关键词 Ion implantation Chemical doping Poly[2-methoxy-5-(3-methyl)butoxy]-p-phenylene vinylene Surface conductivity Conductive activation energy
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Screening of chemokine receptor CCR4 antagonists by capillary zone electrophoresis 被引量:1
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作者 Zhe Sun Lin-Jie Tian +3 位作者 Qian Lin Xiao-Mei Ling Jun-Hai Xiao Ying Wang 《Journal of Pharmaceutical Analysis》 SCIE CAS 2011年第4期264-269,共6页
CC chemokine receptor 4(CCR4)is a kind of G-protein-coupled receptor,which plays a pivotal role in allergic inflammation.The interaction between 2-(2-(4-chloro-phenyl)-5-{[(naphthalen-1-ylmethyl)-carbamlyl]-methyl-4-o... CC chemokine receptor 4(CCR4)is a kind of G-protein-coupled receptor,which plays a pivotal role in allergic inflammation.The interaction between 2-(2-(4-chloro-phenyl)-5-{[(naphthalen-1-ylmethyl)-carbamlyl]-methyl-4-oxo-thiazolidin-3-yl)-N-(3-morpholin-4-yl-propyi)-acetamide(S009)and the N-terminal extracellular tail(ML40)of CCR4 has been validated to be high affinity by capillary zone electrophoresis(CZE).The S009 is a known CCR4 antagonist.Now,a series of new thiourea derivatives have been synthesized.Compared with positive control S009,they were screened using ML40 as target by CZE to find some new drugs for allergic inflammation diseases.The synthesized compounds XJH-5,XJH-4,XJH-17 and XJH-1 displayed the interaction with ML40,but XJH-9,XJH-10,XJH-I 1,XJH-12,XJH-13,XJH-14,XJH-3,XJH-8,XJH-6,XJH-7,XJH-15,XJH-16 and XJH-2 did not bind to ML40.Both qualification and quantification characterizations of the binding were determined.The affinity of the four compounds was valued by the binding constant,which was similar with the results of chemotactic experiments.The established CEZ method is capable of sensitive and fast screening for a series of lactam analogs in the drug discovery for allergic inflammation diseases. 展开更多
关键词 Capillary zone electrophoresis CCR4 antagonist 2-(2-(4-chloro-phenyl)-5-{[(naphthalen-1-ylmethyl)-carbamoyl]-methyl}-4-oxo-thiazoli-din-3-yl)-N-(3-morpho-lin-4-yl-propyl)-aceta-mide Interactions Structural modification
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Talachalasins A-C,Undescribed Cytochalasans with a 16β-Methyl or 2-Oxabicyclo[3.3.1]nonan-3-one unit from the Deep-Sea-Derived Fungus Talaromyces muroii sp.SCSIO 40439
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作者 Xuemin Ding Weixia Ye +12 位作者 Bin Tan Qiaoyun Song Yuchan Chen Wei Liu Lili Sun Wei Tang Yulei Qiao Qingbo Zhang Haibo Zhang Ying Wang Weimin Zhang Changsheng Zhang Wenjun Zhang 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2023年第8期915-923,共9页
Comprehensive Summary Talachalasins A-C(1-3),three new cytochalasans(CYTs),were isolated from deep-sea-derived fungus Talaromyces muroii sp.SCSIO 40439.The structures of 1-3,including absolute configurations,were dete... Comprehensive Summary Talachalasins A-C(1-3),three new cytochalasans(CYTs),were isolated from deep-sea-derived fungus Talaromyces muroii sp.SCSIO 40439.The structures of 1-3,including absolute configurations,were determined based on HRESIMS,NMR spectroscopic data,ECD comparison,and single crystal X-ray diffraction analysis.Talachalasins A-C(1-3)represented the first examples of cytochalasans possessing a unique 16β-methyl group,distinct from>500 reported CYTs.Talachalasin C(3)was an unprecedented 20,21-seco-cytochalasans characterized by a 2-oxabicyclo[3.3.1]nonan-3-one unit.Talachalasin A(1)displayed moderate cytotoxic activity against four tumor cell lines(IC_(50)3.40-10.02μM).Talachalasin B(2)showed comparable anti-RSV and HSV-1 activities(IC5012.5μM or IC5020.0μM). 展开更多
关键词 Cytochalasans 166-methyl group 20 21-seco-Cytochalasans 2-Oxabicyclo-[3.3.1]nonan-3-one unit Cytotoxic activity
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A New 10-Hydroxyl Anthrone Glycoside from Cassia siamea Lam
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作者 TaiShengLUE YangHuaYI 《Chinese Chemical Letters》 SCIE CAS CSCD 2002年第8期731-733,共3页
A new 10-hydroxyl anthrone glycoside, 1, 8, 10 - trihydroxyl-1ObDglucopyrano- syl-3-methyl-10- C (S) b D- glucopyranosyl-anthrone-9 1 was isolated from the stem of Cassia siamea Lam. The structure was elucidated by... A new 10-hydroxyl anthrone glycoside, 1, 8, 10 - trihydroxyl-1ObDglucopyrano- syl-3-methyl-10- C (S) b D- glucopyranosyl-anthrone-9 1 was isolated from the stem of Cassia siamea Lam. The structure was elucidated by spectral evidences, especially by 2 D techniques. 展开更多
关键词 Cassia siamea ANTHRONE 1 8 10 -trihydroxyl-1-O-b-D-glucopyranosyl-3-methyl 10-C (S) -b-D- glucopyranosyl-anthrone-9 1.
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A New Sesquiterpene-substituted Benzoic Acid from the Brown Alga Dictyopteris divaricata
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作者 FuHangSONG XiaoFAN +3 位作者 XiuLiXU JieLuZHAO LiJunHAN JianGongSHI 《Chinese Chemical Letters》 SCIE CAS CSCD 2004年第3期316-318,共3页
A new sesquiterpene-substituted benzoic acid has been isolated from the brown Alga Dictyopteris divaricata Okam.. Its structure was elucidated as 3-[(2-hydroxy-2,5,5,8a-tetra- methyldecahydro-1-naphthalenyl)methyl]-4... A new sesquiterpene-substituted benzoic acid has been isolated from the brown Alga Dictyopteris divaricata Okam.. Its structure was elucidated as 3-[(2-hydroxy-2,5,5,8a-tetra- methyldecahydro-1-naphthalenyl)methyl]-4-hydroxybenzoic acid, named dictyvaric acid on the basis of spectroscopic methods including IR, HRFABMS, 1D and 2D NMR techniques. 展开更多
关键词 Brown alga Dictyopteris divaricata 3-[(2-hydroxy-2 5 5 8a-tetramethyl-decahydro-1- naphthalenyl)-methyl]-4-hydroxybenzoic acid dictyvaric acid.
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Tribological Properties of Functionalized Ionic Liquids Containing Ester-group as Lubricants for Steel-Steel System
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作者 Zhu Liye Chen Ligong +2 位作者 Xiang Shuo Chen Guoxu Yang Xin 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2012年第2期60-65,共6页
A series of functionalized ionic liquids (ILs) containing ester-group were synthesized and their tribological prop- erties as lubricants for steel-steel contact were studied and compared with a non-functionalized io... A series of functionalized ionic liquids (ILs) containing ester-group were synthesized and their tribological prop- erties as lubricants for steel-steel contact were studied and compared with a non-functionalized ionic liquid and perfluo- ropolyethers (PFPE). The morphology and chemical composition of the worn scars were analyzed by scanning electron mi- croscopy and X-ray photoelectron spectroscopy, respectively, and the possible lubrication mechanism of ILs was discussed. As a result, all ILs demonstrated a better lubricity and a much higher load-carrying capacity than PFPE used as lubricants for the steel-steel tribomates system. The functionalized ILs with ester-group showed slightly worse friction reducing abil- ity than their nonfunctionalized counterparts at relatively lower loads owing to their higher viscosity, but then exhibited better antiwear ability because the ester group they contained had not only physical but also strong chemical reactions with the freshly exposed steel surface and formed chemical adsorption boundary films on the worn surface during friction pro- cess. Under high loads, some triboehemical reactions took place between the active elements, such as fluorine which were released from the ILs, and fresh metal surfaces of rubbing pairs to form the admixture reaction films, which were mainly composed of ferric fluoride mixed with ferric oxide, leading to lower friction coefficients and good wear resistance. 展开更多
关键词 functionalized ionic liquid 1-ethoxycarbonylmethyl-3-methyl bis(trifluoromethylsulfonyl)imide tribological behavior LUBRICANT
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