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31.
Tan Yong Chia Chee Yuen Gan Vikneswaran Murugaiyah Syed F. Hashmi Tabinda Fatima Lazhari Ibrahim Mohammed H. Abdulla Farhan Khashim Alswailmi Edward James Johns Ashfaq Ahmad 《Molecules (Basel, Switzerland)》2022,27(1)
The application of natural products and supplements has expanded tremendously over the past few decades. Clinacanthus nutans (C. nutans), which is affiliated to the Acanthaceae family, has recently caught the interest of researchers from the countries of subtropical Asia due to its medicinal uses in alternative treatment for skin infection conditions due to insect bites, microorganism infections and cancer, as well as for health well-being. A number of bioactive compounds from this plant’s extract, namely phenolic compounds, sulphur containing compounds, sulphur containing glycosides compounds, terpens-tripenoids, terpens-phytosterols and chlorophyll-related compounds possess high antioxidant activities. This literature search yielded about one hundred articles which were then further documented, including the valuable data and findings obtained from all accessible electronic searches and library databases. The promising pharmacological activities from C. nutans leaves extract, including antioxidant, anti-cancer, anti-viral, anti-bacterial, anti-fungal, anti-venom, analgesic and anti-nociceptive properties were meticulously dissected. Moreover, the authors also discuss a few of the pharmacological aspect of C. nutans leaves extracts against anti-hyperlipidemia, vasorelaxation and renoprotective activities, which are seldom available from the previously discussed review papers. From the aspect of toxicological studies, controversial findings have been reported in both in-vitro and in-vivo experiments. Thus, further investigations on their phytochemical compounds and their mode of action showing pharmacological activities are required to fully grasp both traditional usage and their suitability for future drugs development. Data related to therapeutic activity and the constituents of C. nutans leaves were searched by using the search engines Google scholar, PubMed, Scopus and Science Direct, and accepting literature reported between 2010 to present. On the whole, this review paper compiles all the available contemporary data from this subtropical herb on its phytochemistry and pharmacological activities with a view towards garnering further interest in exploring its use in cardiovascular and renal diseases. 相似文献
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M. Heber Chr Liedtke H. Korte E. Hoffmann-Posorske A. Donella-Deana L. A. Pinna J. Perich E. Kitas R. B. Johns H. E. Meyer 《Chromatographia》1992,33(7-8):347-350
Summary Capillary electrophoresis is a novel technique in the non-radioactive determination of phosphoamino acids. The main advantage of the method presented is the high selectivity and the ability to separate all phosphoamino acid derivatives. Non-radioactive determination of PTH or dabsyl phosphoamino acids by capillary electrophoresis provides a fast and simple screening procedure for all O-phosphorylated amino acids in protein and peptides in the low picomolar range. 相似文献
33.
Lee J. Silverberg Tapas K. Mal Carlos N. Pacheco Megan L. Povelones Madeline F. Malfara Anthony F. Lagalante Mark A. Olsen Hemant P. Yennawar Hany F. Sobhi Kayla R. Baney Robin L. Bozeman Craig S. Eroh Michael J. Fleming Tracy L. Garcia Casey L. Gregory Julia E. Hahn Alyssa M. Hatter Lexi L. Johns Tianna L. Klinger Jennie J. Li Andrew J. Menig Grace C. Muench Melissa E. Ramirez Jordyn Reilly Nicole Sacco Alexandra M. Sheidy Marla M. Stoner Eric N. Thompson Soroush F. Yazdani 《Molecules (Basel, Switzerland)》2021,26(20)
A series of fourteen 2-aryl-3-phenyl-2,3-dihydro-4H-pyrido[3,2-e][1,3]thiazin-4-ones was prepared at room temperature by T3P-mediated cyclization of N-phenyl-C-aryl imines with thionicotinic acid, two difficult substrates. The reactions were operationally simple, did not require specialized equipment or anhydrous solvents, could be performed as either two or three component reactions, and gave moderate–good yields as high as 63%. This provides ready access to N-phenyl compounds in this family, which have been generally difficult to prepare. As part of the study, the first crystal structure of neutral thionicotinic acid is also reported, and showed the molecule to be in the form of the thione tautomer. Additionally, the synthesized compounds were tested against T. brucei, the causative agent of Human African Sleeping Sickness. Screening at 50 µM concentration showed that five of the compounds strongly inhibited growth and killed parasites. 相似文献
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Luk KB Diehl HT Duryea J Guglielmo G Heller K Ho PM James C Johns K Longo MJ Rameika R Teige S Thomson GB Zou Y 《Physical review letters》2000,85(23):4860-4863
A search for direct CP violation in the nonleptonic decays of hyperons has been performed. In comparing the product of the decay parameters, alpha(Xi)alpha(Lambda), in terms of an asymmetry parameter, A(XiLambda), between hyperons and antihyperons in the charged Xi-->Lambdapi and Lambda-->ppi decay sequence, we found no evidence of direct CP violation. The parameter A(XiLambda) was measured to be 0.012+/-0.014. 相似文献
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