Статті в журналах з теми "Biological Active Molecules"
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Freeman, Amihay, Yael Dror, Carmit Ophir Porat, Noa Hadar, and Yossi Shacham Diamand. "Silver-Coated Biologically Active Protein Hybrids: Antimicrobial Applications." Applied Mechanics and Materials 749 (April 2015): 453–56. http://dx.doi.org/10.4028/www.scientific.net/amm.749.453.
Повний текст джерелаRana, Aniruddhasinh M., Kishor R. Desai, and Smita Jauhari. "Rhodanine-based biologically active molecules: synthesis, characterization, and biological evaluation." Research on Chemical Intermediates 40, no. 2 (January 22, 2013): 761–77. http://dx.doi.org/10.1007/s11164-012-1001-3.
Повний текст джерелаInsuasty, Daniel, Juan Castillo, Diana Becerra, Hugo Rojas, and Rodrigo Abonia. "Synthesis of Biologically Active Molecules through Multicomponent Reactions." Molecules 25, no. 3 (January 24, 2020): 505. http://dx.doi.org/10.3390/molecules25030505.
Повний текст джерелаKarolak-Wojciechowska, J., and A. Fruzinski. "Spacer conformation in biologically active molecules." Pure and Applied Chemistry 76, no. 5 (January 1, 2004): 959–64. http://dx.doi.org/10.1351/pac200476050959.
Повний текст джерелаLIU, Yan, and Rong GUO. "Interaction between organized assemblies of amphiphilic molecules and biological active molecules." Chinese Science Bulletin 62, no. 6 (November 14, 2016): 486–97. http://dx.doi.org/10.1360/n972016-00426.
Повний текст джерелаSmith, David P. "Active learning in the lecture theatre using 3D printed objects." F1000Research 5 (June 3, 2016): 61. http://dx.doi.org/10.12688/f1000research.7632.2.
Повний текст джерелаStan, Adina Dora, Codruta Birle, and Dana Slavoaca. "Biological molecules in clinical stroke trials." Romanian Journal of Neurology 12, no. 4 (December 31, 2013): 175–79. http://dx.doi.org/10.37897/rjn.2013.4.2.
Повний текст джерелаPushpanathan, Muthuirulan, Paramasamy Gunasekaran, and Jeyaprakash Rajendhran. "Antimicrobial Peptides: Versatile Biological Properties." International Journal of Peptides 2013 (June 26, 2013): 1–15. http://dx.doi.org/10.1155/2013/675391.
Повний текст джерелаCyphert, Jaime M., Carol S. Trempus, and Stavros Garantziotis. "Size Matters: Molecular Weight Specificity of Hyaluronan Effects in Cell Biology." International Journal of Cell Biology 2015 (2015): 1–8. http://dx.doi.org/10.1155/2015/563818.
Повний текст джерелаFotopoulos, Ioannis, and Dimitra Hadjipavlou-Litina. "Hybrids of Coumarin Derivatives as Potent and Multifunctional Bioactive Agents: A Review." Medicinal Chemistry 16, no. 3 (April 17, 2020): 272–306. http://dx.doi.org/10.2174/1573406415666190416121448.
Повний текст джерелаZatloukalová, Martina. "3D Lipidic Matrix for Incorporation and Stabilization of Biologically Active Molecules." Chemické listy 116, no. 3 (March 15, 2022): 172–79. http://dx.doi.org/10.54779/chl20220172.
Повний текст джерелаLi, L., and P. K. Moore. "An overview of the biological significance of endogenous gases: new roles for old molecules." Biochemical Society Transactions 35, no. 5 (October 25, 2007): 1138–41. http://dx.doi.org/10.1042/bst0351138.
Повний текст джерелаОглобліна, М. В., І. В. Бушуєва, and В. В. Парченко. "Review of the research on the influence of different functional substituents of new 1,2,4-triazole derivatives on the compounds biological properties." Farmatsevtychnyi zhurnal, no. 5 (October 29, 2022): 74–80. http://dx.doi.org/10.32352/0367-3057.5.22.08.
Повний текст джерелаKottalanka, Ravi K., Eswar Pagadala, Shiva K. Loke, S. Rex Jeya Rajkumar, Venkatesan Srinivasadesikan, and Balajee Ramchandran. "Biological Evolution of Titanium(IV) Complex [{(NNO)2Ti}3O3] Bearing Bidentate Heteroditopic Schiff Base Ligand: Synthesis, Structure and Biological Studies." Asian Journal of Chemistry 32, no. 2 (December 30, 2019): 441–50. http://dx.doi.org/10.14233/ajchem.2020.22464.
Повний текст джерелаZiarani, Ghodsi M., Fatemeh Mohajer, Razieh Moradi, and Parisa Mofatehnia. "The Molecular Diversity Scope of Urazole in the Synthesis of Organic Compounds." Current Organic Synthesis 16, no. 7 (December 26, 2019): 953–67. http://dx.doi.org/10.2174/1570179416666190925162215.
Повний текст джерелаHansen, Poul Erik. "Structural Studies of β-Diketones and Their Implications on Biological Effects". Pharmaceuticals 14, № 11 (20 листопада 2021): 1189. http://dx.doi.org/10.3390/ph14111189.
Повний текст джерелаPatel, Geetika, and Subhash Banerjee. "Review on Synthesis of Bio-active Coumarin-fused Heterocyclic Molecules." Current Organic Chemistry 24, no. 22 (December 18, 2020): 2566–87. http://dx.doi.org/10.2174/1385272824999200709125717.
Повний текст джерелаSrivastava, Ambrish Kumar, and Neeraj Misra. "A comparative theoretical study on the biological activity, chemical reactivity, and coordination ability of dichloro-substituted (1,3-thiazol-2-yl)acetamides." Canadian Journal of Chemistry 92, no. 3 (March 2014): 234–39. http://dx.doi.org/10.1139/cjc-2013-0335.
Повний текст джерелаSandhya, P. V., K. V. Satheesh Kumar, and K. R. Haridas. "Synthesis, Molecular Docking and DFT Studies of Biologically Active N-((3-(4-Nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)aniline Derivatives." Asian Journal of Chemistry 34, no. 2 (2022): 297–304. http://dx.doi.org/10.14233/ajchem.2022.23500.
Повний текст джерелаde Oliveira Costa, Bruna, and Octávio Luiz Franco. "Cryptic Host Defense Peptides: Multifaceted Activity and Prospects for Medicinal Chemistry." Current Topics in Medicinal Chemistry 20, no. 14 (June 11, 2020): 1274–90. http://dx.doi.org/10.2174/1568026620666200325112425.
Повний текст джерелаBelyakova, L. A., A. M. Varvarin, D. Yu Lyashenko, and O. V. Khora. "Designing Adsorption Centres for Biological Active Molecules on a Silica Surface." Adsorption Science & Technology 23, no. 9 (November 2005): 703–19. http://dx.doi.org/10.1260/026361705776316596.
Повний текст джерелаPolat, M. Fatih. "Synthesis of Asebogenin and Balsacone A Precursor by a Novel Synthetic Strategy: Recent Opportunities for and Challenges of Total Synthesis of Balsacone A." Molecules 27, no. 11 (May 30, 2022): 3523. http://dx.doi.org/10.3390/molecules27113523.
Повний текст джерелаDumpis, Marina A., Dmitrii N. Nikolayev, Elena V. Litasova, Viktor V. Iljin, Mariya A. Brusina, and Levon B. Piotrovsky. "Biological activity of fullerenes - reality and prospects." Reviews on Clinical Pharmacology and Drug Therapy 16, no. 1 (March 15, 2018): 4–20. http://dx.doi.org/10.17816/rcf1614-20.
Повний текст джерелаBisha, Ina, and Alessandra Magistrato. "The molecular mechanism of secondary sodium symporters elucidated through the lens of the computational microscope." RSC Advances 6, no. 12 (2016): 9522–40. http://dx.doi.org/10.1039/c5ra22131e.
Повний текст джерелаSkoreński, Marcin, and Marcin Sieńczyk. "The Fellowship of Privileged Scaffolds—One Structure to Inhibit Them All." Pharmaceuticals 14, no. 11 (November 16, 2021): 1164. http://dx.doi.org/10.3390/ph14111164.
Повний текст джерелаMaestro, Aitor, Xabier del Corte, Adrián López-Francés, Edorta Martínez de Marigorta, Francisco Palacios та Javier Vicario. "Asymmetric Synthesis of Tetrasubstituted α-Aminophosphonic Acid Derivatives". Molecules 26, № 11 (27 травня 2021): 3202. http://dx.doi.org/10.3390/molecules26113202.
Повний текст джерелаLee, Alpha A., Qingyi Yang, Asser Bassyouni, Christopher R. Butler, Xinjun Hou, Stephen Jenkinson, and David A. Price. "Ligand biological activity predicted by cleaning positive and negative chemical correlations." Proceedings of the National Academy of Sciences 116, no. 9 (February 11, 2019): 3373–78. http://dx.doi.org/10.1073/pnas.1810847116.
Повний текст джерелаKakou Yao, Rita, Jules Abodou Tenon, and Akoun Abou. "Bioactive molecules modelised by numerical simulation:molecules against Escherichia Coli." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1008. http://dx.doi.org/10.1107/s2053273314089918.
Повний текст джерелаRydel-Ciszek, Katarzyna, Tomasz Pacześniak, Izabela Zaborniak, Paweł Błoniarz, Karolina Surmacz, Andrzej Sobkowiak, and Paweł Chmielarz. "Iron-Based Catalytically Active Complexes in Preparation of Functional Materials." Processes 8, no. 12 (December 20, 2020): 1683. http://dx.doi.org/10.3390/pr8121683.
Повний текст джерелаCetin, Adnan, and Havva Kurt. "Synthesis, Antibacterial Activity and Molecular Docking Studies of New Pyrazole Derivatives." Letters in Drug Design & Discovery 17, no. 6 (June 29, 2020): 745–56. http://dx.doi.org/10.2174/1570180816666190905155510.
Повний текст джерелаCoelho, Simao, Jongho Baek, Matthew S. Graus, James M. Halstead, Philip R. Nicovich, Kristen Feher, Hetvi Gandhi, J. Justin Gooding, and Katharina Gaus. "Ultraprecise single-molecule localization microscopy enables in situ distance measurements in intact cells." Science Advances 6, no. 16 (April 2020): eaay8271. http://dx.doi.org/10.1126/sciadv.aay8271.
Повний текст джерелаMontuori, Nunzia, Valeria Visconte, Guido Rossi, and Pia Ragno. "Soluble and cleaved forms of the urokinase-receptor: degradation products or active molecules?" Thrombosis and Haemostasis 93, no. 02 (2005): 192–98. http://dx.doi.org/10.1160/th04-09-0580.
Повний текст джерелаKatsuyama, Isamu. "Synthesis of Trifluoromethyl-Containing Pyridines and Their Applications to Biological Active Molecules." Journal of Synthetic Organic Chemistry, Japan 67, no. 10 (2009): 992–1000. http://dx.doi.org/10.5059/yukigoseikyokaishi.67.992.
Повний текст джерелаFlood, P. M., C. Waltenbaugh, T. Tada, B. Chue, and D. B. Murphy. "Serologic heterogeneity in I-J determinants associated with functionally distinct T cell regulatory factors." Journal of Immunology 137, no. 7 (October 1, 1986): 2237–44. http://dx.doi.org/10.4049/jimmunol.137.7.2237.
Повний текст джерелаKalasariya, Haresh S., Virendra Kumar Yadav, Krishna Kumar Yadav, Vineet Tirth, Ali Algahtani, Saiful Islam, Neha Gupta, and Byong-Hun Jeon. "Seaweed-Based Molecules and Their Potential Biological Activities: An Eco-Sustainable Cosmetics." Molecules 26, no. 17 (September 1, 2021): 5313. http://dx.doi.org/10.3390/molecules26175313.
Повний текст джерелаHegedüs, Imre, Kitti Andreidesz, József L. Szentpéteri, Zoltán Kaleta, László Szabó, Krisztián Szigeti, Balázs Gulyás, Parasuraman Padmanabhan, Ferenc Budan, and Domokos Máthé. "The Utilization of Physiologically Active Molecular Components of Grape Seeds and Grape Marc." International Journal of Molecular Sciences 23, no. 19 (September 22, 2022): 11165. http://dx.doi.org/10.3390/ijms231911165.
Повний текст джерелаLuo, Huiqing, Na Li, Liyan Liu, Huaqiao Wang, and Feng He. "Synthesis of New AIEE-Active Chalcones for Imaging of Mitochondria in Living Cells and Zebrafish In Vivo." International Journal of Molecular Sciences 22, no. 16 (August 19, 2021): 8949. http://dx.doi.org/10.3390/ijms22168949.
Повний текст джерелаMorozkina, Svetlana N., Thi Hong Nhung Vu, Yuliya E. Generalova, Petr P. Snetkov, and Mayya V. Uspenskaya. "Mangiferin as New Potential Anti-Cancer Agent and Mangiferin-Integrated Polymer Systems—A Novel Research Direction." Biomolecules 11, no. 1 (January 9, 2021): 79. http://dx.doi.org/10.3390/biom11010079.
Повний текст джерелаMorozkina, Svetlana N., Thi Hong Nhung Vu, Yuliya E. Generalova, Petr P. Snetkov, and Mayya V. Uspenskaya. "Mangiferin as New Potential Anti-Cancer Agent and Mangiferin-Integrated Polymer Systems—A Novel Research Direction." Biomolecules 11, no. 1 (January 9, 2021): 79. http://dx.doi.org/10.3390/biom11010079.
Повний текст джерелаDunkel, Petra. "Photoremovable Protecting Groups." Encyclopedia 2, no. 3 (July 1, 2022): 1225–36. http://dx.doi.org/10.3390/encyclopedia2030082.
Повний текст джерелаBerlaga, Alex, and Anatoly B. Kolomeisky. "Theoretical study of active secondary transport: Unexpected differences in molecular mechanisms for antiporters and symporters." Journal of Chemical Physics 156, no. 8 (February 28, 2022): 085102. http://dx.doi.org/10.1063/5.0082589.
Повний текст джерелаAsif, Mohammad. "Chemical Characteristics, Synthetic Methods, and Biological Potential of Quinazoline and Quinazolinone Derivatives." International Journal of Medicinal Chemistry 2014 (November 13, 2014): 1–27. http://dx.doi.org/10.1155/2014/395637.
Повний текст джерелаNurkenov, O. A., S. D. Fazylov, G. K. Mukusheva, Ye V. Minayeva, I. V. Kulakov, Zh S. Nurmaganbetov, A. S. Kishkentaeva, and A. R. Zhasymbekova. "HYBRID MOLECULES BASED ON ALKALOIDS." Chemical Journal of Kazakhstan 3 (September 30, 2021): 67–82. http://dx.doi.org/10.51580/2021-1/2710-1185.40.
Повний текст джерелаPagel, Mareen, and Annette G. Beck-Sickinger. "Multifunctional biomaterial coatings: synthetic challenges and biological activity." Biological Chemistry 398, no. 1 (January 1, 2017): 3–22. http://dx.doi.org/10.1515/hsz-2016-0204.
Повний текст джерелаHansma, H. G., A. L. Weisenhorn, A. B. Edmundson, H. E. Gaub, and P. K. Hansma. "Atomic force microscopy: seeing molecules of lipid and immunoglobulin." Clinical Chemistry 37, no. 9 (September 1, 1991): 1497–501. http://dx.doi.org/10.1093/clinchem/37.9.1497.
Повний текст джерелаBian, Yuemin, and Xiang-Qun Xie. "Artificial Intelligent Deep Learning Molecular Generative Modeling of Scaffold-Focused and Cannabinoid CB2 Target-Specific Small-Molecule Sublibraries." Cells 11, no. 5 (March 7, 2022): 915. http://dx.doi.org/10.3390/cells11050915.
Повний текст джерелаMikhailov, Alexander S., and Raymond Kapral. "Hydrodynamic collective effects of active protein machines in solution and lipid bilayers." Proceedings of the National Academy of Sciences 112, no. 28 (June 29, 2015): E3639—E3644. http://dx.doi.org/10.1073/pnas.1506825112.
Повний текст джерелаCaporali, Sabrina, Alessandro De Stefano, Cinzia Calabrese, Alfredo Giovannelli, Massimo Pieri, Isabella Savini, Manfredi Tesauro, Sergio Bernardini, Marilena Minieri, and Alessandro Terrinoni. "Anti-Inflammatory and Active Biological Properties of the Plant-Derived Bioactive Compounds Luteolin and Luteolin 7-Glucoside." Nutrients 14, no. 6 (March 9, 2022): 1155. http://dx.doi.org/10.3390/nu14061155.
Повний текст джерелаVanguru, Mahathy, Ramchander Merugu, Swetha Garimella, and Laxminarayana E. "A REVIEW ON THE SYNTHETIC METHODOLOGIES OF CHROMONES." Asian Journal of Pharmaceutical and Clinical Research 11, no. 12 (December 7, 2018): 9. http://dx.doi.org/10.22159/ajpcr.2018.v11i12.27960.
Повний текст джерелаHatchell, Tashi, Kasci Hutchenson, Gibin George, Zhiping Luo, and Shubo Han. "Morphological and Compositional Characterization of Electrochemically Active Perovskite Oxides for Sensing Biological Molecules." Microscopy and Microanalysis 26, S2 (July 30, 2020): 2664–65. http://dx.doi.org/10.1017/s1431927620022369.
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