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81.
Hamdoon A. Mohammed Mohsen S. Al-Omar Salman A. A. Mohammed Ahmad H. Alhowail Hussein M. Eldeeb Mohammed S. M. Sajid Essam M. Abd-Elmoniem Osama A. Alghulayqeh Yasser I. Kandil Riaz A. Khan 《Molecules (Basel, Switzerland)》2021,26(8)
Salsola cyclophylla, an edible halophyte, is traditionally used for inflammation and pain. To confirm the claimed anti-inflammatory and analgesic properties, a detailed study on respective pharmacological actions was undertaken. The activities are contemplated to arise from its phytoconstituents. The LC-MS analysis of S. cyclophylla 95% aqueous-ethanolic extract revealed the presence of 52 compounds belonging to phenols, flavonoids, coumarins, and aliphatics class. A high concentration of Mn, Fe, and Zn was detected by atomic absorption spectroscopic analysis. The ethyl acetate extract showed the highest flavonoid contents (5.94 ± 0.04 mg/g, Quercetin Equivalents) and Fe2+-chelation (52%) potential with DPPH radicals-quenching IC50 at 1.35 ± 0.16 mg/mL, while the aqueous ethanolic extract exhibited maximum phenolics contents (136.08 ± 0.12 mg/g, gallic acid equivalents) with DPPH scavenging potential at IC50 0.615 ± 0.06 mg/mL. Aqueous ethanolic extract and standard quercetin DPPH radicals scavenging’s were equal potent at 10 mg/mL concentrations. The aqueous ethanolic extract showed highest analgesic effect with pain reduction rates 89.86% (p = 0.03), 87.50% (p < 0.01), and 99.66% (p = 0.0004) after 60, 90, and 120 min, respectively. Additionally, aqueous ethanolic extract exhibited the highest anti-inflammation capacity at 41.07% (p < 0.0001), 34.51% (p < 0.0001), and 24.82% (p < 0.0001) after 2, 3, and 6 h of extract’s administration, respectively. The phytochemical constituents, significant anti-oxidant potential, remarkable analgesic, and anti-inflammatory bioactivities of extracts supported the traditionally claimed anti-inflammatory and analgesic plant activities. 相似文献
82.
Salah E. M. Eltom Ahmed A. H. Abdellatif Hamzah Maswadeh Mohsen S. Al-Omar Atef A. Abdel-Hafez Hamdoon A. Mohammed Eiman ME. Agabein Ibrahim Alqasoomi Salem A. Alrashidi Mohammed S. M. Sajid Mugahid A. Mobark 《Molecules (Basel, Switzerland)》2021,26(12)
The ostrich oil of Struthio camelus (Ratite) found uses in folk medicine as an anti-inflammatory in eczema and contact dermatitis. The anti-inflammatory effect of a γ-lactone (5-hexyl-3H-furan-2-one) isolated from ostrich oil and its formulated nano-emulsion in formalin-induced paw edema was investigated in this study. Ostrich oil was saponified using a standard procedure; the aqueous residue was fractionated, purified, and characterized as γ-lactone (5-hexyl-3H-furan-2-one) through the interpretation of IR, NMR, and MS analyses. The γ-lactone was formulated as nano-emulsion using methylcellulose (MC) for oral solubilized form. The γ-lactone methylcellulose nanoparticles (γ-lactone-MC-NPs) were characterized for their size, shape, and encapsulation efficiency with a uniform size of 300 nm and 59.9% drug content. The γ-lactone was applied topically, while the formulated nanoparticles (NPs) were administered orally to rats. A non-steroidal anti-inflammatory drug (diclofenac gel) was used as a reference drug for topical use and ibuprofen suspension for oral administration. Edema was measured using the plethysmograph method. Both γ-lactone and γ-lactone-MC-NPs showed reduction of formalin-induced paw edema in rats and proved to be better than the reference drugs; diclofenac gel and ibuprofen emulsion. Histological examination of the skin tissue revealed increased skin thickness with subepidermal edema and mixed inflammatory cellular infiltration, which were significantly reduced by the γ-lactone compared to the positive control (p-value = 0.00013). Diuretic and toxicity studies of oral γ-lactone-MC-NPs were performed. No diuretic activity was observed. However, lethargy, drowsiness, and refusal to feeding observed may limit its oral administration. 相似文献
83.
M. Shahid Rafique M. Khaleeq-ur-Rahman Aziz-ul-Rehman Khurram Siraj M. Fiaz Khan 《Laser Physics》2007,17(3):282-285
Investigations were performed on laser-assisted ion emission when a copper target was irradiated with a Nd:YAG laser (1.064 μm 10 mJ and 1.1 MW). Charge states present in the ion core emitted from plasma were determined employing Faraday cup arrangement using a four-channel 500 MHz Digital Storage Oscilloscope YOKOGAWA DL 1740. The Thomson parabola scattering (TPS) technique was used to measure the energy of ions emitted from plasma. Singly charged positive ions were found to be in excessive amount. For the energy analysis, the ion beam was collimated using a pinhole arrangement. The collimated beam was then made to pass through a uniform magnetic field of 0.4 T. A solid-state nuclear track detector PM-355 was used to register the ion tracks. The energy of ions, found to be in the range of 9–50 keV. The ion energy spectra d 2 N/dEdΩ show a decreasing trend with increasing ion energy. The empirical relation dN/dE ∞ E ?n fits well with the experimental data at higher values of energy, i.e., greater than 20 keV. 相似文献
84.
Javid Hussain Hidayatullah Khan Liaqat Ali Abdul Latif Khan Najeeb Ur Rehman Sajid Jahangir Ahmed Al‐Harrasi 《Helvetica chimica acta》2015,98(5):719-723
The phytochemical investigations on Cleome droserifolia resulted in the isolation and characterization of a new indole alkaloid, 5‐hydroxy‐2‐methoxy‐1‐methyl‐1H‐indole‐3‐carbaldehyde ( 1 ). The structure elucidation was carried out on the basis of 1D‐ and 2D‐NMR techniques. In addition to 1 , two known aromatic derivatives, veratrol ( 2 ) and 2‐methoxy‐4‐methylacetophenone ( 3 ), were also obtained. All these compounds were purified by repeated column chromatography of the CH2Cl2 fraction obtained from MeOH extract of Cleome droserifolia. The structure of the new compound 1 was finally confirmed by the combined 1D (1H‐ and 13C‐) and 2D (H? C correlations; HMBC and HSQC) NMR and IR spectroscopy, mass spectrometry (MS), and UV absorption spectroscopy techniques. The comparison of the physical and spectroscopic data with those in the literature provided evidence for the structure confirmation of known compounds. All the purified compounds were subjected to urease and α‐glucosidase enzymes inhibition. The results showed that compound 1 was more potent with an IC50 value 11.97±2.067 μg/ml towards urease inhibition, while the activity of α‐glucosidase enzyme was marginal. 相似文献
85.
Naveed Akhtar Shad Muhammad Munir Sajid Yasir Javed Nasir Amin Muhammad Ikram Kanwal Akhtar Gulzar Ahmad Faisal Ali Aamir Razaq 《中国化学会会志》2020,67(6):1045-1053
Zinc oxide (ZnO) nanostructures were synthesized via a one-step solid-state reaction approach in ammonia (NH3) gas environment with different temperature ramp rates. The so-formed nanostructures were characterized using X-ray diffraction (XRD) for phase identification, where the typical wurtzite hexagonal structure was observed. Scanning electron microscopy (SEM) confirmed the particle size to be in the range 45–50 nm, the same as calculated by the XRD pattern for the ramp rate of 10 °C/min. Energy dispersive X-ray (EDX) spectroscopy and X-ray photoelectron spectroscopy (XPS) confirmed the chemical purity of the samples. The photoluminescence (PL) spectrum indicated multiple near-band-edge emissions and energy-band emissions. Then, these ZnO nanomaterials were used for the degradation of crystal violet (CV) dye under UV light irradiation. The CV solution was completely degraded in 2 hr. The initial photocatalyst and dye amounts of 0.2 g/100 ml and 0.5 mg/L, respectively, were found to be the optimum values for maximum degradation efficiency. The ZnO-based photocatalyst was stable up to three cycles of reuse. These results indicate that the high surface area and porosity of the nanomaterials are responsible for the high efficiency, which was confirmed by specific surface area analysis. 相似文献
86.
In the present paper, we study warped product CR-submanifolds of cosymplectic manifolds. It is shown that the warped product of the type ${N_\perp\times{_f}N_T}$ is trivial and obtain a characterization result for the warped product of the type ${N_T\times{_f}N_\perp}$ , where N T and ${N_\perp}$ are invariant and anti-invariant submanifolds of a cosymplectic manifold ${\bar M}$ , respectively. 相似文献
87.
Al-Ayed AS Ali MS Al-Lohedan HA Al-Sulaim AM Issa ZA Kabir-ud-Din 《Journal of colloid and interface science》2011,357(2):393-399
Herein we have investigated the hydrolysis of 1H-indol-2,3-dione (isatin, I) and its derivatives of different hydrophobicities, viz. N-dimethylaminomethyl indol-2,3-dione (II), N-morpholinomethyl indol-2,3-dione (III), N-pipridinomethyl indol-2,3-dione (IV), N-heptylaminomethyl indol-2,3-dione (V), N-dodecylaminomethyl indol-2,3-dione (VI), N-hexylanilinomethyl indol-2,3-dione (VII), N-decylanilinomethyl indol-2,3-dione (VIII), and N-hexadecylanilinomethyl indol-2,3-dione (IX), in the presence of an excess amount of sodium hydroxide. All the isatin derivatives were synthesized in the laboratory. The progress of the reactions was studied by exploiting UV-visible spectrophotometry. The observed rate constant, k(w), increases linearly on increasing the hydroxide ion concentration, indicating first-order dependence on [OH(-)]. The effects of surfactants, cationic (cetyltrimethylammonium chloride, CTACl), and anionic (sodium dodecyl sulfate, SDS) were also investigated. The rate of reaction increased on increasing the concentration of CTACl and, after reaching a maximum, it started decreasing. Conversely, anionic micelles of SDS inhibited the rate of hydrolysis of isatin and its derivatives. The results of the effect of CTACl were analyzed using a pseudophase ion-exchange model while the inhibition by SDS was analyzed using a simple Menger-Portnoy model. The effects of added salts, such as NaBr, NaCl, and (CH(3))(4)NBr, were also seen on the isatin hydrolysis. It was found that the addition of salts decreased the rate enhancement efficiency of the CTACl. 相似文献
88.
Soybean hulls were subjected to thermo-mechanical extrusion pretreatment at various in-barrel moisture contents and screw
speeds. Extrusion degraded the lignocellulosic structure and enhanced enzymatic hydrolysis of soybean hulls, with up to 155%
increase in glucose yield as compared to untreated substrate. Greater glucose yields were observed at higher in-barrel moistures
(45% and 50%) and lower screw speed (280 and 350 rpm). Maximum 74% cellulose to glucose conversion resulted from using a two-enzyme
cocktail consisting of cellulase and β-glucosidase. Conversion increased to 87% when a three-enzyme cocktail having a cell
wall degrading enzyme complex was used for hydrolysis. Fermentation inhibitors, such as furfural, 5-(hydroxymethyl)-2-furaldehyde
(HMF), and acetic acid, were found in the extrusion pretreated soybean hulls and hydrolysate. However, their concentrations
were below the known thresholds for inhibition. Fermentation of hydrolysate by Saccharomyces cerevisiae led to high yields of ethanol, with concentration ranging from 13.04 to 15.44 g/L. 相似文献
89.
A new bulky biarylphosphine ligand (L8) has been developed that allows the Pd-catalyzed C-O cross-coupling of a wide range of aryl halides and phenols under milder conditions than previously possible. A direct correlation between the size of the ligand substituents in the 2', 4', and 6' positions of the nonphosphine containing ring and the reactivity of the derived catalyst system was observed. Specifically, the rate of coupling increased with the size of these substituents. 相似文献
90.
SU Siyi LI Xiaoyu GUO Xu ZHOU Ruiming LI Manman MING Pengfei HUANG Yingying Sajid Ur RAHMAN DING Hongyan FENG Shibin LI Jinchun WANG Xichun LI Yu WU Jinjie 《高等学校化学研究》2019,35(6):1105-1110
The anti-inflammatory activity of tea polyphenols(TPs) in RAW264.7 macrophages stimulated by lipopolysaccharide(LPS) was investigated in this paper. RAW264.7 macrophages were treated with different concentrations of TP(0, 12.5, 25, 50, 100, and 200 μg/mL) and then stimulated by LPS. Another blank control group was set up. The expression of pro-inflammatory cytokines associated with the nuclear factor-kappa B(NF-κB) signaling pathway was investigated before and after TP treatment. Pretreatment of RAW264.7 cells with TP decreased the expression of tumor necrosis factor-α(TNF-α), interleukin-6(IL-6) and interleukin 1 beta(IL-1β) pro-inflammatory cytokines. In addition, TP inhibited the phosphorylation of p65 and IκB by blocking the phosphorylation and the degradation of NF-κB inhibitor protein. In conclusion, TP exerts anti-inflammatory effects by regulating the release of inflammatory mediators via the NF-κB signaling pathway. 相似文献