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141.
Hijazi Abu Ali Israel Goldberg Morris Srebnik 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(6):770-771
The B atoms in the title compound, C8H16B2Br4N2, bridge between the two monomeric moieties, forming a (BN)2 four‐membered ring with partial bond orders of the B—N bonds. 相似文献
142.
Crystals of ammonium tetrachlorozincate (AZC) undoped and doped with Sr2+ or Mn2+ in different concentrations were grown by the slow evaporation method from an aqueous solution. The crystal morphology changed considerably by doping. The dopant concentration in the crystals was measured by the atomic absorption technique. Slight changes in the unit cell parameters of AZC after doping with Sr2+‐ or Mn2+ have been detected. Optical absorption measurements indicated strong influence of Sr2+ and Mn2+ doping. The optical energy gap at room temperature decreased continuously with increasing Sr2+ and Mn2+ concentration but with two different rates. The dc conductivity was also measured as a function of temperature for the undoped and two samples doped with 0.144 Sr2+ and 0.191 Mn2+ and the results were compared. Positions possibly occupied by Sr2+ and Mn2+ cations in AZC lattice have been identified. (© 2005 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
143.
Tarfah Al-Warhi Adil Aldhahrani Fayez Althobaiti Eman Fayad Ola A. Abu Ali Sarah Albogami Ali H. Abu Almaaty Amgad I. M. Khedr Syed Nasir Abbas Bukhari Islam Zaki 《Molecules (Basel, Switzerland)》2022,27(12)
A novel series of amides based TMP moiety was designed, synthesized and evaluated for their antiproliferative as well as enzyme inhibition activity. Compounds 6a and 6b showed remarkable cytotoxic activity against HepG2 cells with IC50 values 0.65 and 0.92 μM, respectively compared with SAHA and CA-4 as reference compounds. In addition, compound 6a demonstrated good HDAC-tubulin dual inhibition activity as it showed better HDAC activity as well as anti-tubulin activity. Moreover, compound 6a exhibited G2/M phase arrest and pre-G1 apoptosis as demonstrated by cell cycle analysis and Annexin V assays. Further apoptosis studies demonstrated that compound 6a boosted the level of caspase 3/7. Caspase 3/7 activation and apoptosis induction were evidenced by decrease in mitochondrial permeability suggesting that activation of caspase 3/7 may occur via mitochondrial apoptotic pathway. 相似文献
144.
Shafia Shafiq Ronok Zahan Samina Yesmin Alam Khan Md. Sabbir Mahmud Md Abu Reza Sarah M. Albogami Mohammed Alorabi Michel De Waard Hebatallah M. Saad Jean-Marc Sabatier Tarannum Naz Gaber El-Saber Batiha 《Molecules (Basel, Switzerland)》2022,27(20)
Litsea glutinosa (L. glutinosa) is considered an evidence-based medicinal plant for the treatment of cancer, the leading cause of death worldwide. In our study, the in vitro antioxidant and in vivo anticancer properties of an essential ethno-medicinal plant, L. glutinosa, were examined using non-toxic doses and a phytochemical analysis was executed using gas-chromatography–mass-spectrometry. The in vitro antioxidant study of the L. glutinosa methanolic extract (LGBME) revealed a concentration-dependent antioxidant property. The bark extract showed promising antioxidant effects in the 2,2-diphenyl-1-picryl-hydrazyl (DPPH) assay. The strongest antioxidant activity was demonstrated at the maximum concentration (50 µg/mL). The IC50 values of the LGBME and BHT were 5.51 and 5.01 µg/mL, respectively. At the same concentration, the total antioxidant capacity of the LGBME was 0.161 µg/mL and the ferric reducing antioxidant power assay result of the LGBME was 1.783 µg/mL. In the cytotoxicity study, the LD50 of the LGBME and gallic acid were 24.93 µg/mL and 7.23 µg/mL, respectively. In the in vivo anticancer-activity studies, the LGBME, particularly at a dose of 150 mg/kg/bw, showed significant cell-growth inhibition, decreased tumor weight, increased mean survival rate, and upregulated the reduced hematological parameters in EAC (Ehrlich’s ascites carcinoma)-induced Swiss albino mice. The highest cell-growth inhibition, 85.76%, was observed with the dose of 150 mg/kg/bw. Furthermore, the upregulation of pro-apoptotic genes (p53, Bax) and the downregulation of anti-apoptotic Bcl-2 were observed. In conclusion, LGBME extract has several bioactive phytoconstituents, which confirms the antioxidant and anticancer properties of L. glutinosa. 相似文献
145.
Salma Eldesouki Rama Qadri Rashid Abu Helwa Hiba Barqawi Yasser Bustanji Eman Abu-Gharbieh Waseem El-Huneidi 《Molecules (Basel, Switzerland)》2022,27(21)
Kahweol and cafestol are two diterpenes extracted from Coffea arabica beans that have distinct biological activities. Recent research describes their potential activities, which include anti-inflammatory, anti-diabetic, and anti-cancer properties, among others. The two diterpenes have been shown to have anticancer effects in various in vitro and in vivo cancer models. This review aims to shed light on the recent developments regarding the potential effects of kahweol and cafestol on various cancers. A systematic literature search through Google Scholar and PubMed was performed between February and May 2022 to collect updates about the potential effects of cafestol and kahweol on different cancers in in vitro and in vivo models. The search terms “Kahweol and Cancer” and “Cafestol and Cancer” were used in this literature review as keywords; the findings demonstrated that kahweol and cafestol exhibit diverse effects on different cancers in in vitro and in vivo models, showing pro-apoptotic, cytotoxic, anti-proliferative, and anti-migratory properties. In conclusion, the diterpenes kahweol and cafestol display significant anticancer effects, while remarkably unaffecting normal cells. Our results show that both kahweol and cafestol exert their actions on various cancers via inducing apoptosis and inhibiting cell growth. Additionally, kahweol acts by inhibiting cell migration. 相似文献
146.
147.
Khalid M. Abed Adeeb Hayyan Amal A. M. Elgharbawy Hanee F. Hizaddin Mohd Ali Hashim Hassimi Abu Hasan Mahar Diana Hamid Fathiah M. Zuki Jehad Saleh Ahmad GH Aldaihani 《Molecules (Basel, Switzerland)》2022,27(24)
This study concerns the role of activated carbon (AC) from palm raceme as a support material for the enhancement of lipase-catalyzed reactions in an aqueous solution, with deep eutectic solvent (DES) as a co-solvent. The effects of carbonization temperature, impregnation ratio, and carbonization time on lipase activity were studied. The activities of Amano lipase from Burkholderia cepacia (AML) and lipase from the porcine pancreas (PPL) were used to investigate the optimum conditions for AC preparation. The results showed that AC has more interaction with PPL and effectively provides greater enzymatic activity compared with AML. The optimum treatment conditions of AC samples that yield the highest enzymatic activity were 0.5 (NaOH (g)/palm raceme (g)), 150 min, and a carbonization temperature of 400 °C. DES was prepared from alanine/sodium hydroxide and used with AC for the further enhancement of enzymatic activity. Kinetic studies demonstrated that the activity of PPL was enhanced with the immobilization of AC in a DES medium. 相似文献
148.
Thiosemicarbazide copper (II) complexes; [Cu2(HL1)2(H2O)2Cl2].H2O (1) and [Cu2(HL2)2(H2O)2Cl2].2H2O (2) (where H2L1 = 2-picolinoyl-N-(pyridin-2-yl)hydrazine-1-carbothioamide and H2L2 = 2-(2-(2-aminothiazol-4-yl)acetyl)-N-(pyridin-2-yl)hydrazine-1-carbothioamide) have been synthesized and characterized. Analytical and spectroscopic data revealed that ligands behaves as monobasic tetradentate with octahedral geometry. In addition, the optimized geometry of the ligands and their complexes was approved with the Jaguar 9.1 program in the Schrödinger set using DFT (density functional theory) to predict chemical processes and to estimate the properties of the material made by the hybrid functional density system B3LYP. Furthermore, the thermal degradation curves of complexes were discussed in order to determine the kinetic and thermodynamic parameters by various approaches. Additionally, the antioxidant (using the DPPH and SOD methods) and the antibacterial potency of the compounds were examined. Also, docking study of ligands and their complexes was carried out against Staphylococcus aureus gram +ve, gram -ve bacterial strains of Escherichia coli and Candida albicans using the XP glide protocol of Schrödinger suite. 相似文献
149.
Abu Yousuf Hossin Masashi Inafuku Kensaku Takara Ruwani N. Nugara Hirosuke Oku 《Molecules (Basel, Switzerland)》2021,26(6)
Cirsium brevicaule A. GRAY is a wild perennial herb, and its roots (CbR) have traditionally been used as both food and medicine on the Japanese islands of Okinawa and Amami. The present study evaluated the antiadipogenic effect of CbR using mouse embryonic fibroblast cell line 3T3-L1 from JCRB cell bank. Dried CbR powder was serially extracted with solvents of various polarities, and these crude extracts were tested for antiadipogenic activity. Treatment with the methanol extract of CbR showed a significant suppression of lipid accumulation in 3T3-L1 cells. Methanol extract of CbR was then fractionated and subjected to further activity analyses. The phenylpropanoid glycosidic molecule syringin was identified as an active compound. Syringin dose dependently suppressed lipid accumulation of 3T3-L1 cells without cytotoxicity, and significantly reduced the expressions of peroxisome proliferator-activated receptor gamma, the master regulator of adipogenesis, and other differentiation markers. It was demonstrated that syringin effectively enhanced the phosphorylation of the AMP-activated protein kinase and acetyl-CoA carboxylase. These results indicate that syringin attenuates adipocyte differentiation, adipogenesis, and promotes lipid metabolism; thus, syringin may potentially serve as a therapeutic candidate for treatment of obesity. 相似文献
150.
Chromatographia - Ivermectin injectable product is widely used as a parasiticide for the treatment and control of internal and external parasites of cattle and swine. A reversed-phase high... 相似文献