全文获取类型
收费全文 | 172篇 |
免费 | 4篇 |
国内免费 | 3篇 |
专业分类
化学 | 138篇 |
力学 | 2篇 |
数学 | 4篇 |
物理学 | 35篇 |
出版年
2024年 | 3篇 |
2023年 | 3篇 |
2022年 | 20篇 |
2021年 | 16篇 |
2020年 | 8篇 |
2019年 | 3篇 |
2018年 | 7篇 |
2017年 | 8篇 |
2016年 | 5篇 |
2014年 | 10篇 |
2013年 | 15篇 |
2012年 | 8篇 |
2011年 | 14篇 |
2010年 | 8篇 |
2009年 | 5篇 |
2008年 | 4篇 |
2007年 | 1篇 |
2006年 | 2篇 |
2005年 | 4篇 |
2004年 | 11篇 |
2003年 | 6篇 |
2001年 | 3篇 |
1999年 | 2篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1991年 | 1篇 |
1990年 | 2篇 |
1989年 | 2篇 |
1987年 | 1篇 |
1982年 | 1篇 |
1981年 | 2篇 |
1971年 | 1篇 |
排序方式: 共有179条查询结果,搜索用时 15 毫秒
41.
Shoaib Khan Shahid Iqbal Mazloom Shah Wajid Rehman Rafaqat Hussain Liaqat Rasheed Hamad Alrbyawi Ayed A. Dera Mohammed Issa Alahmdi Rami Adel Pashameah Eman Alzahrani Abd-ElAziem Farouk 《Molecules (Basel, Switzerland)》2022,27(20)
A unique series of sulphonamide derivatives was attempted to be synthesized in this study using a new and effective method. All of the synthesized compounds were verified using several spectroscopic methods, including FTIR, 1H-NMR, 13C-NMR, and HREI-MS, and their binding interactions were studied using molecular docking. The enzymes urease and α-glucosidase were evaluated against each derivative (1–15). When compared to their respective standard drug such as acarbose and thiourea, almost all compounds were shown to have excellent activity. Among the screened series, analogs 5 (IC50 = 3.20 ± 0.40 and 2.10 ± 0.10 µM) and 6 (IC50 = 2.50 ± 0.40 and 5.30 ± 0.20 µM), emerged as potent molecules when compared to the standard drugs acarbose (IC50 = 8.24 ± 0.08 µM) and urease (IC50 = 7.80 ± 0.30). Moreover, an anti-microbial study also demonstrated that analogs 5 and 6 were found with minimum inhibitory concentrations (MICs) in the presence of standard drugs streptomycin and terinafine. 相似文献
42.
Sundas Mumtaz Shahid Iqbal Mazloom Shah Rafaqat Hussain Fazal Rahim Wajid Rehman Shoaib Khan Obaid-ur-Rahman Abid Liaqat Rasheed Ayed A. Dera Hanan A. Al-ghulikah Sana Kehili Eslam B. Elkaeed Hamad Alrbyawi Mohammed Issa Alahmdi 《Molecules (Basel, Switzerland)》2022,27(19)
Twenty-four analogs based on triazinoindole bearing benzimidazole/benzoxazole moieties (1–25) were synthesized. Utilizing a variety of spectroscopic methods, including 1H-, 13C-NMR, and HREI-MS, the newly afforded compounds (1–25) were analyzed. The synthesized analogs were tested against urease enzyme (in vitro) as compared to the standard thiourea drug. All triazinoindole-based benzimidazole/benzoxazole analogs (1–25) exhibited moderate to excellent inhibition profiles, having IC50 values of 0.20 ± 0.01 to 36.20 ± 0.70 μM when evaluated under the positive control of thiourea as a standard drug. To better understand the structure–activity relationship, the synthesized compounds were split into two groups, “A” and “B.” Among category “A” analogs, analogs 8 (bearing tri-hydroxy substitutions at the 2,4,6-position of aryl ring C) and 5 (bearing di-hydroxy substitutions at the 3,4-position of aryl ring C) emerged as the most potent inhibitors of urease enzyme and displayed many times more potency than a standard thiourea drug. Besides that, analog 22 (which holds di-hydroxy substitutions at the 2,3-position of the aryl ring) and analog 23 (bearing ortho-fluoro substitution) showed ten-fold-enhanced inhibitory potential compared to standard thiourea among category “B” analogs. Molecular docking studies on the active analogs of each category were performed; the results obtained revealed that the presence of hydroxy and fluoro-substitutions on different positions of aryl ring C play a pivotal role in binding interactions with the active site of the targeted urease enzyme. 相似文献
43.
Anam Iqbal Syed Ali Raza Naqvi Rashid Rasheed Asim Mansha Matloob Ahmad Ameer Fawad Zahoor 《Applied biochemistry and biotechnology》2018,185(1):127-139
Bacterial infection poses life-threatening challenge to humanity and stimulates to the researchers for developing better diagnostic and therapeutic agents complying with existing theranostic techniques. Nuclear medicine technique helps to visualize hard-to-diagnose deep-seated bacterial infections using radionuclide-labeled tracer agents. Metronidazole is an antiprotozoal antibiotic that serves as a preeminent anaerobic chemotherapeutic agent. The aim of this study was to develop technetium-99m-labeled metronidazole radiotracer for the detection of deep-seated bacterial infections. Radiosynthesis of 99mTc-metronidazole was carried by reacting reduced technetium-99m and metronidazole at neutral pH for 30 min. The stannous chloride dihydrate was used as the reducing agent. At optimum radiolabeling conditions, ~ 94% radiochemical was obtained. Quality control analysis was carried out with a chromatographic paper and instant thin-layer chromatographic analysis. The biodistribution study of radiochemical was performed using Escherichia coli bacterial infection-induced rat model. The scintigraphic study was performed using E. coli bacterial infection-induced rabbit model. The results showed promising accumulation at the site of infection and its rapid clearance from the body. The tracer showed target-to-non-target ratio 5.57 ± 0.04 at 1 h post-injection. The results showed that 99mTc-MNZ has promising potential to accumulate at E. coli bacterial infection that can be used for E. coli infection imaging. 相似文献
44.
Through several waves of technological research and un-matched innovation strategies, bio-catalysis has been widely used at the industrial level. Because of the value of enzymes, methods for producing value-added compounds and industrially-relevant fine chemicals through biological methods have been developed. A broad spectrum of numerous biochemical pathways is catalyzed by enzymes, including enzymes that have not been identified. However, low catalytic efficacy, low stability, inhibition by non-cognate substrates, and intolerance to the harsh reaction conditions required for some chemical processes are considered as major limitations in applied bio-catalysis. Thus, the development of green catalysts with multi-catalytic features along with higher efficacy and induced stability are important for bio-catalysis. Implementation of computational science with metabolic engineering, synthetic biology, and machine learning routes offers novel alternatives for engineering novel catalysts. Here, we describe the role of synthetic biology and metabolic engineering in catalysis. Machine learning algorithms for catalysis and the choice of an algorithm for predicting protein-ligand interactions are discussed. The importance of molecular docking in predicting binding and catalytic functions is reviewed. Finally, we describe future challenges and perspectives. 相似文献
45.
Fathi M. A. M. Aqra Shakeel A. Shah Sartaj Tabassum Rasheed M. A. Q. Jamhour Khwaja S. Siddiqi Osama Al-Jowder Fawzia Al-Saleh 《Transition Metal Chemistry》1995,20(2):123-125
Summary New ionic bimetallic complexes of the type [Cu(en)2]-[MCl4], where M = CuII, ZnII, CdII and HgII, were prepared by reacting bis(ethylenediamine)copper(II) dichloride (1 mol) with copper, zinc, cadmium and mercury dichlorides (1 mol) in absolute alcohol. Elemental analyses, conductivity and magnetic susceptibility measurements, and spectroscopic data (such as i.r., u.v.-vis. and e.p.r.) confirm that the compounds are 22 electrolytes in MeOH and that the copper(II) ion is paramagnetic, maintaining its square-planar geometry, while metal ions in the anionic moiety of the complexes achieve their usual tetrahedral environment. An augmented magnetic moment has been observed in the [Cu(en)2] [CuCl4] complex, which is attributed to the ferromagnetic effect and TIP.Author to whom all correspondence should be directed. 相似文献
46.
47.
The aminocarbonylation of various alkenyl and (hetero)aryl iodides was carried out using tropane-based amines of biological importance, such as 8-azabicyclo[3.2.1]octan-3-one (nortropinone) and 3α-hydroxy-8-azabicyclo[3.2.1]octane (nortropine) as N-nucleophile. Using iodoalkenes, the two nucleophiles were selectively converted to the corresponding amide in the presence of Pd(OAc)2/2 PPh3 catalysts. In the presence of several iodo(hetero)arenes, the application of the bidentate Xantphos was necessary to produce the target compounds selectively. The new carboxamides of varied structure, formed in palladium-catalyzed aminocarbonylation reactions, were isolated and fully characterized. In this way, a novel synthetic method has been developed for the producing of N-acylnortropane derivatives of biological importance. 相似文献
48.
The vibrational frequencies for diphenyl selenide, diphenyl telluride, diphenyl diselenide, diphenyl ditelluride, diphenyl disulfide mercury and diphenyl diselenide mercury have been assigned and were consistent with the vibrational assignments for diphenyl ether, diphenyl sulfide and diphenyl disulfide previously reported. The vibrational assignments for diphenyl telluride confirmed the linearity of the Gordy Rule plot for the t-vibration of Group VI A elements. 相似文献
49.
Emergence of classicality from quantum mechanics, a hotly debated topic, has had no satisfactory resolution so far. Various approaches including decoherence and gravitational interactions have been suggested. In the present work, the Schrödinger–Newton model is used to study the role of semi-classical self-gravity in the evolution of massive spin-1/2 particles in a Stern-Gerlach experiment. For small mass, evolution of the initial wavepacket in a spin superposition shows a splitting in the magnetic field gradient into two trajectories as in the standard Stern–Gerlach experiment. For larger mass, the deviations from the central path are less than in the standard Stern–Gerlach case, while for high enough mass, the wavepacket does not split, and instead follows the classical trajectory for a magnetic moment in inhomogeneous magnetic field. This indicates the emergence of classicality due to self-gravitational interaction when the mass is increased. In contrast, decoherence which is a strong contender for emergence of classicality, leads to a mixed state of two trajectories corresponding to the spin-up and spin-down states, and not the classically expected path. The classically expected path of the particle probably cannot be explained even in the many-worlds interpretation of quantum mechanics. Stern–Gerlach experiments in the macroscopic domain are needed to settle this question. 相似文献
50.
Rasheed M. S. Mahmood 《Mediterranean Journal of Mathematics》2009,6(1):87-103
In this paper we show that if G is a group acting on a graph X with inversions such that G has a presentation induced by a fundamental domain for the action of G on X, then X is a tree.
Received: January 3, 2007., Revised: August 10, 2007 and May 3, 2008., Accepted: October 17, 2008. 相似文献