全文获取类型
收费全文 | 49580篇 |
免费 | 8683篇 |
国内免费 | 11121篇 |
专业分类
化学 | 37351篇 |
晶体学 | 1368篇 |
力学 | 2828篇 |
综合类 | 946篇 |
数学 | 6213篇 |
物理学 | 20678篇 |
出版年
2024年 | 56篇 |
2023年 | 716篇 |
2022年 | 1360篇 |
2021年 | 1642篇 |
2020年 | 1909篇 |
2019年 | 2008篇 |
2018年 | 1673篇 |
2017年 | 2023篇 |
2016年 | 2189篇 |
2015年 | 2568篇 |
2014年 | 3156篇 |
2013年 | 3944篇 |
2012年 | 4423篇 |
2011年 | 4765篇 |
2010年 | 4061篇 |
2009年 | 3997篇 |
2008年 | 4299篇 |
2007年 | 3832篇 |
2006年 | 3668篇 |
2005年 | 2987篇 |
2004年 | 2232篇 |
2003年 | 1700篇 |
2002年 | 1518篇 |
2001年 | 1469篇 |
2000年 | 1391篇 |
1999年 | 979篇 |
1998年 | 650篇 |
1997年 | 545篇 |
1996年 | 501篇 |
1995年 | 469篇 |
1994年 | 440篇 |
1993年 | 361篇 |
1992年 | 359篇 |
1991年 | 234篇 |
1990年 | 240篇 |
1989年 | 173篇 |
1988年 | 183篇 |
1987年 | 126篇 |
1986年 | 120篇 |
1985年 | 107篇 |
1984年 | 64篇 |
1983年 | 69篇 |
1982年 | 38篇 |
1981年 | 30篇 |
1980年 | 16篇 |
1979年 | 38篇 |
1978年 | 8篇 |
1971年 | 8篇 |
1959年 | 7篇 |
1936年 | 7篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
81.
82.
Jihua Liu Huizhu Gan Ting Li Jia Wang Guangguang Du Yang An Xiaojing Yan Cong Geng 《Biomedical chromatography : BMC》2020,34(8):e4856
Ocotillol, pseudo-ginsenoside RT5 (RT5), and pseudo-ginsenoside F11 (PF11) are ocotillol-type saponins that have the same aglycone structure but with different numbers of glucose at the C-6 position. In this study, the metabolites of ocotillol, RT5, and PF11 in rat plasma, stomach, intestine, urine, and feces after oral administration were investigated by ultra-performance liquid chromatography coupled with time-of-flight mass spectrometry. The results showed that RT5 was easily biotransformed into metabolites in vivo, whereas PF11 and RT5 were difficult to be biotransformed. Hydrogenation, dehydrogenation, dehydration, deglycosylation, deoxygenation, hydration, phosphorylation, deoxidation, glucuronidation, and reactions combining amino acid were speculated to be involved in the biotransformation of ocotillol, RT5, and PF11. Based on the structural analysis of metabolites, it was deduced that hydrogenation, dehydration, deoxidation, and reactions combining amino acid occurred on the aglycone structure, whereas deglycosylation, hydration, and phosphorylation occurred on the glycosyl chain. Further, metabolites in plasma, urine, feces, and tissues were different: First, glucuronidation products were found in urine, stomach, intestine, and feces, but not in plasma. Second, the ocotillol prototype was not identified in urine samples. Third, the RT5 prototype was found in stomach, intestine, feces, and urine, but not in plasma. 相似文献
83.
Yangang Cheng Yan Liu Jinyan Tan Yanping Sun Wei Guan Yuan Liu Bingyou Yang Haixue Kuang 《Biomedical chromatography : BMC》2020,34(9):e4881
Our previous work demonstrated that total withanolides of Datura metel L. leaves (TWD) exhibited excellent therapeutic effects on psoriasis. However, current knowledge of its mechanisms is incomplete. In this study, integrated spleen and thymus untargeted metabolomics were used to analyze the changes in endogenous metabolites underlying the immunosuppressive activity of TWD on psoriasis animal models induced by imiquimod. The results suggested that TWD treatment markedly attenuated imiquimod-induced psoriasis and showed significant immunosuppressive activity as evidenced by decreased elevation index of spleen and thymus. Meanwhile, TWD significantly reversed the elevation of immunoregulatory factors, including IL-10, IL-17, IL-22 and IL-23. Multivariate trajectory analysis revealed that TWD treatment could restore the psoriasis-disturbed spleen and thymus metabolite profiles towards the normal metabolic status. A total of 25 and 27 metabolites associated with the immunomodulatory effects for which levels changed markedly upon treatment have been identified in spleen and thymus, respectively. These differential metabolites were mainly involved in amino acid metabolism, nucleotide metabolism, fatty acid metabolism and lipid metabolism. Our investigation provided a holistic view of TWD for intervention in psoriasis through immunoregulation and provided further scientific information in vivo about a clinical value of TWD for psoriasis. 相似文献
84.
利用共价自组装的方法,将刚性组装基元与柔性链在一定条件下进行横向交联,可以方便地制备出单层高分子纳米胶囊.相比于传统的非共价超分子囊泡,这种新型的共价纳米胶囊具有结构稳定、尺度可控且分散性优异等诸多优点.因此,如何利用化学合成的手段来制备新型的纳米胶囊,并进一步实现对其结构调控和性能的探究具有十分重要的意义.针对这些问题,分别发展了功能化的柱[5]芳烃、四苯乙烯、卟啉、三嗪、苯硼酸酐等不同类型构筑基元,并使之与两端具有活性位点的柔性烷基链在适当的溶剂中进行聚合反应,最终获得了一系列的共价纳米胶囊.通过对其结构的修饰和调控,发现这些功能化的高分子纳米胶囊在光捕获、人工酶、抗菌材料以及药物载体等领域具有诸多潜在应用价值.未来,新型共价高分子纳米胶囊的开发、功能化以及应用有望得到进一步的拓展. 相似文献
85.
Meng Xia Wang Lizhen Zhai Yunge Duan Hongdong 《Research on Chemical Intermediates》2020,46(12):5517-5533
Research on Chemical Intermediates - Two novel Schiff-base fluorescent probes bearing different substituents were synthesized by the reaction of indole derivatives with 4-aminoantipyrine. The... 相似文献
86.
以二水氯化铜(CuCl2·2H2O)、硅酸钠(Na2SiO3)、钼酸钠(Na2 MoO4)和2,6-二甲基-3,5-二(吡唑-3-基)吡啶(简写为H2L)为原料,通过水热反应,成功地合成了一个一维链状Keggin型多酸基杂化化合物[Cu2(H3L)2](SiMo12O40).通过X-射线单晶衍射、TGA、IR以及元素分析对该化合物的结构进行表征.测试结果表明,该化合物属于三斜晶系,P-1空间群,晶胞参数a=1.1689(5) nm,b=1.2157(5) nm,c=1.2233(5) nm,α=62.066(5)°,β=62.833(5)°,γ =74.789(5)°,V=1.363 8(10) nm3,Z=2,R1=0.082 4,wR2=0.174 5.电化学分析结果表明该化合物对亚硝酸盐的还原具有良好的电催化效果. 相似文献
87.
88.
Abstract Gastrodigenin, also known as 4-hydroxybenzyl alcohol (HBA), is one of the main components of Gastrodia elata, which is a perfect lead compound of natural products. In order to get new active compounds, we modified the structure of HBA through esterification with carboxylic acid, and got a series of derivatives in which 4-hydroxybenzyl alcohol 2-naphthoate (NHBA) showed stronger antidepressant activity than HBA. In this paper, we firstly evaluated the antidepressant activity of NHBA by tail suspension test (TST) and forced swimming test (FST). Then, we carried out the biochemical assay and western blot to determine its mechanism. The results displayed that NHBA could increase the content of serotonin, dopamine, norepinephrine, γ-aminobutyric acid, brain-derived neurotrophic factor (BDNF) and tropomyosin receptor kinase B (TrkB) in mice brain. It suggested that NHBA exhibited an antidepressant-like effect through monoaminergic system, GABAergic system and BDNF/TrkB signaling pathways. 相似文献
89.
90.