Статті в журналах з теми "Amide function"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Amide function".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Asahara, Haruyasu, Keita Arikiyo, and Nagatoshi Nishiwaki. "Development of variously functionalized nitrile oxides." Beilstein Journal of Organic Chemistry 11 (July 23, 2015): 1241–45. http://dx.doi.org/10.3762/bjoc.11.138.
Повний текст джерелаZHANG, JIA-XIANG, LEI-YANG ZHANG, NAI-XING WANG, YUE-HUA WU, ZHAN YAN, and DUMITRA LUCAN. "NMR studies of rotamers with multi-substituted amides." Journal of Engineering Sciences and Innovation 6, no. 4 (November 17, 2021): 373–80. http://dx.doi.org/10.56958/jesi.2021.6.4.2.
Повний текст джерелаZhou, Xueer, Petra Vasko, Jamie Hicks, M. Ángeles Fuentes, Andreas Heilmann, Eugene L. Kolychev, and Simon Aldridge. "Cooperative N–H bond activation by amido-Ge(ii) cations." Dalton Transactions 49, no. 27 (2020): 9495–504. http://dx.doi.org/10.1039/d0dt01960g.
Повний текст джерелаZhang, Bengang, Xinyi Chen, Antonio Pizzi, Mathieu Petrissans, Stephane Dumarcay, Anelie Petrissans, Xiaojian Zhou, Guanben Du, Baptiste Colin, and Xuedong Xi. "Highly Branched Tannin-Tris(2-aminoethyl)amine-Urea Wood Adhesives." Polymers 15, no. 4 (February 10, 2023): 890. http://dx.doi.org/10.3390/polym15040890.
Повний текст джерелаSun, Chang-Liang, Xiao-Nan Jiang, and Chang-Sheng Wang. "An analytic potential energy function for the amide-amide and amide-water intermolecular hydrogen bonds in peptides." Journal of Computational Chemistry 30, no. 15 (November 30, 2009): 2567–75. http://dx.doi.org/10.1002/jcc.21266.
Повний текст джерелаPandita, Sangeeta, and Rohit Ishpujani. "AN ENVIRONMENTALLY FRIENDLY, EFFICIENT, AND FACILE METHODOLOGY FOR THE NITRATION OF AROMATIC COMPOUNDS USING UREA NITRATE." RASAYAN Journal of Chemistry 15, no. 04 (2022): 2933–37. http://dx.doi.org/10.31788/rjc.2022.1548002.
Повний текст джерелаImhof, Wolfgang. "N-Phenyl-2-(phenyliminomethyl)pyrrole-1-carboxamide." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (October 5, 2007): o4265. http://dx.doi.org/10.1107/s1600536807048416.
Повний текст джерелаMcKinney, Michele K., and Benjamin F. Cravatt. "STRUCTURE AND FUNCTION OF FATTY ACID AMIDE HYDROLASE." Annual Review of Biochemistry 74, no. 1 (June 2005): 411–32. http://dx.doi.org/10.1146/annurev.biochem.74.082803.133450.
Повний текст джерелаMcguire, Edward J., Robert H. Gray, and Felix A. De La Iglesia. "Chemical Structure-Activity Relationships: Peroxisome Proliferation and Lipid Regulation in Rats." Journal of the American College of Toxicology 11, no. 3 (May 1992): 353–61. http://dx.doi.org/10.3109/10915819209141875.
Повний текст джерелаSchmidtler, J., W. Schepp, I. Janczewska, N. Weigert, C. Furlinger, V. Schusdziarra, and M. Classen. "GLP-1-(7-36) amide, -(1-37), and -(1-36) amide: potent cAMP-dependent stimuli of rat parietal cell function." American Journal of Physiology-Gastrointestinal and Liver Physiology 260, no. 6 (June 1, 1991): G940—G950. http://dx.doi.org/10.1152/ajpgi.1991.260.6.g940.
Повний текст джерелаOH, Jong-Eun, and Keun-Hyeung LEE. "Characterization of the unique function of a reduced amide bond in a cytolytic peptide that acts on phospholipid membranes." Biochemical Journal 352, no. 3 (December 8, 2000): 659–66. http://dx.doi.org/10.1042/bj3520659.
Повний текст джерелаWang, Haopei, and Zachary T. Ball. "A photochemical C=C cleavage process: toward access to backbone N-formyl peptides." Beilstein Journal of Organic Chemistry 17 (December 15, 2021): 2932–38. http://dx.doi.org/10.3762/bjoc.17.202.
Повний текст джерелаGoormaghtigh, Erik, Harmen H. J. de Jongh, and Jean-Marie Ruysschaert. "Relevance of Protein Thin Films Prepared for Attenuated Total Reflection Fourier Transform Infrared Spectroscopy: Significance of the pH." Applied Spectroscopy 50, no. 12 (December 1996): 1519–27. http://dx.doi.org/10.1366/0003702963904610.
Повний текст джерелаBurkhart, Brandon J., Christopher J. Schwalen, Greg Mann, James H. Naismith, and Douglas A. Mitchell. "YcaO-Dependent Posttranslational Amide Activation: Biosynthesis, Structure, and Function." Chemical Reviews 117, no. 8 (March 3, 2017): 5389–456. http://dx.doi.org/10.1021/acs.chemrev.6b00623.
Повний текст джерелаMoskvina, V. S., O. V. Shablykina, V. V. Ishchenko, and V. P. Khilya. "Efficient preparative synthesis of isoflavones with the amide function." Reports of the National Academy of Sciences of Ukraine, no. 9 (September 20, 2015): 79–83. http://dx.doi.org/10.15407/dopovidi2015.09.079.
Повний текст джерелаSami El-banna, Fatma, Magdy Elsayed Mahfouz, Stefano Leporatti, Maged El-Kemary, and Nemany A. N. Hanafy. "Chitosan as a Natural Copolymer with Unique Properties for the Development of Hydrogels." Applied Sciences 9, no. 11 (May 29, 2019): 2193. http://dx.doi.org/10.3390/app9112193.
Повний текст джерелаMöhrle, Hans, та Georg Keller. "α-Dicarbonylmonoxime als Nucleophile und Nachbargruppen / α-Dicarbonylmonoximes as Nucleophiles and Neighbour Groups". Zeitschrift für Naturforschung B 54, № 5 (1 травня 1999): 632–42. http://dx.doi.org/10.1515/znb-1999-0511.
Повний текст джерелаUkena, Kazuyoshi, and Kazuyoshi Tsutsui. "A new member of the hypothalamic RF-amide peptide family, LPXRF-amide peptides: Structure, localization, and function." Mass Spectrometry Reviews 24, no. 4 (July 12, 2004): 469–86. http://dx.doi.org/10.1002/mas.20031.
Повний текст джерелаIp, Wilfred, Weijuan Shao, Yu-ting Alex Chiang, and Tianru Jin. "GLP-1-derived nonapeptide GLP-1(28–36)amide represses hepatic gluconeogenic gene expression and improves pyruvate tolerance in high-fat diet-fed mice." American Journal of Physiology-Endocrinology and Metabolism 305, no. 11 (December 1, 2013): E1348—E1358. http://dx.doi.org/10.1152/ajpendo.00376.2013.
Повний текст джерелаFang, Jun-Jia, Jian Lan, Gang Yang, Gao-Qing Yuan, Hai-Yang Liu, and Li-Ping Si. "Synthesis of cobalt A2B triaryl corroles bearing aldehyde and amide pyridyl groups and their performance in electrocatalytic hydrogen evolution." New Journal of Chemistry 45, no. 11 (2021): 5127–36. http://dx.doi.org/10.1039/d0nj04953k.
Повний текст джерелаNaro, Yuta, Meryl Thomas, Matthew D. Stephens, Colleen M. Connelly, and Alexander Deiters. "Aryl amide small-molecule inhibitors of microRNA miR-21 function." Bioorganic & Medicinal Chemistry Letters 25, no. 21 (November 2015): 4793–96. http://dx.doi.org/10.1016/j.bmcl.2015.07.016.
Повний текст джерелаChang, Jung C., Geoff M. Gurr, Murray J. Fletcher, and Robert G. Gilbert. "Structure - Property and Structure - Function Relations of Leafhopper (Kahaono montana) Silk." Australian Journal of Chemistry 59, no. 8 (2006): 579. http://dx.doi.org/10.1071/ch06179.
Повний текст джерелаRodriguez, Jean, and Adrien Quintard. "Acyl Transfer Strategies as Transient Activations for Enantioselective Synthesis." Synthesis 51, no. 09 (March 14, 2019): 1923–34. http://dx.doi.org/10.1055/s-0037-1611743.
Повний текст джерелаSoong, Chee-Leong, Jun Ogawa, Michinari Honda, and Sakayu Shimizu. "Cyclic-Imide-Hydrolyzing Activity ofd-Hydantoinase from Blastobacter sp. Strain A17p-4." Applied and Environmental Microbiology 65, no. 4 (April 1, 1999): 1459–62. http://dx.doi.org/10.1128/aem.65.4.1459-1462.1999.
Повний текст джерелаWackerbarth, Ines, Ni Nyoman Agnes Tri Widhyadnyani, Simon Schmitz, Kathrin Stirnat, Katharina Butsch, Ingo Pantenburg, Gerd Meyer, and Axel Klein. "CuII Complexes and Coordination Polymers with Pyridine or Pyrazine Amides and Amino Benzamides—Structures and EPR Patterns." Inorganics 8, no. 12 (December 1, 2020): 65. http://dx.doi.org/10.3390/inorganics8120065.
Повний текст джерелаVarney, Michelle L., Daniel B. Goetz, David F. Wiemer, and Sarah A. Holstein. "Isoprenoid Amide Bisphosphonates As a Novel Class of Geranylgeranyl Diphosphate Synthase Inhibitors." Blood 132, Supplement 1 (November 29, 2018): 4679. http://dx.doi.org/10.1182/blood-2018-99-112965.
Повний текст джерелаHeo, Nam Jung, Ju Hyun Oh, Jeong Tae Lee, Qing He, Jonathan L. Sessler, and Sung Kuk Kim. "Phenanthroline-strapped calix[4]pyrroles: anion receptors displaying affinity reversal as a function of solvent polarity." Organic Chemistry Frontiers 7, no. 3 (2020): 548–56. http://dx.doi.org/10.1039/c9qo01377f.
Повний текст джерелаReibnegger, Gilbert, Brian J. Denny, and Helmut Wachter. "Ab Initio Quantum Chemical Calculations on the Stability of Different Tautomers of 6- and 7-Phenacetyl Pterin." Pteridines 4, no. 1 (February 1993): 23–26. http://dx.doi.org/10.1515/pteridines.1993.4.1.23.
Повний текст джерелаSchmidtler, J., K. Dehne, S. Offermanns, W. Rosenthal, M. Classen, and W. Schepp. "Stimulation of rat parietal cell function by histamine and GLP-1-(7-36) amide is mediated by Gs alpha." American Journal of Physiology-Gastrointestinal and Liver Physiology 266, no. 5 (May 1, 1994): G775—G782. http://dx.doi.org/10.1152/ajpgi.1994.266.5.g775.
Повний текст джерелаCaroff, Martine, and Alexey Novikov. "Lipopolysaccharides: structure, function and bacterial identification." OCL 27 (2020): 31. http://dx.doi.org/10.1051/ocl/2020025.
Повний текст джерелаHromádková, Zdenka, Anna Malovíková, Štefan Mozeš, Iva Sroková, and Anna Ebringerová. "Hydrophobically modified pectates as novel functional polymers in food and non-food applications." BioResources 3, no. 1 (December 8, 2007): 71–78. http://dx.doi.org/10.15376/biores.3.1.71-78.
Повний текст джерелаSheng, Guozhu, and Wei Zhang. "New Advances of the Methods of Amide Function Group for Construction." Chinese Journal of Organic Chemistry 33, no. 11 (2013): 2271. http://dx.doi.org/10.6023/cjoc201305048.
Повний текст джерелаEndsley, Michael P., Rebecca Thill, Iffat Choudhry, Carol L. Williams, Andre Kajdacsy‐Balla, William B. Campbell, and Kasem Nithipatikom. "Expression and function of fatty acid amide hydrolase in prostate cancer." International Journal of Cancer 123, no. 6 (September 15, 2008): 1318–26. http://dx.doi.org/10.1002/ijc.23674.
Повний текст джерелаPalermo, Giulia, Ursula Rothlisberger, Andrea Cavalli, and Marco De Vivo. "Computational insights into function and inhibition of fatty acid amide hydrolase." European Journal of Medicinal Chemistry 91 (February 2015): 15–26. http://dx.doi.org/10.1016/j.ejmech.2014.09.037.
Повний текст джерелаPirotte, Bernard, Pascal De Tullio, Bernard Masereel, Marc Schynts, Jacques Delarge, Léon Dupont, and Léopold Thunus. "4-Acylamino-4H-1,2,4-triazoles and related structures: new investigations of their chemical and physicochemical properties associated with their particular exocyclic amide function." Canadian Journal of Chemistry 71, no. 11 (November 1, 1993): 1857–66. http://dx.doi.org/10.1139/v93-233.
Повний текст джерелаJensen, Elisa P., Sophie Møller, Aleksander Vauvert Hviid, Simon Veedfald, Jens J. Holst, Jens Pedersen, Cathrine Ørskov, and Charlotte M. Sorensen. "GLP-1-induced renal vasodilation in rodents depends exclusively on the known GLP-1 receptor and is lost in prehypertensive rats." American Journal of Physiology-Renal Physiology 318, no. 6 (June 1, 2020): F1409—F1417. http://dx.doi.org/10.1152/ajprenal.00579.2019.
Повний текст джерелаMercer, Frank W. "Synthesis and characterization of aromatic poly(ether ketone amide)s." High Performance Polymers 5, no. 3 (June 1993): 187–96. http://dx.doi.org/10.1088/0954-0083/5/3/002.
Повний текст джерелаYadav, Samanta, Paranthaman Vijayan, Sunil Yadav, and Rajeev Gupta. "Ruthenium complexes of phosphine–amide based ligands as efficient catalysts for transfer hydrogenation reactions." Dalton Transactions 50, no. 9 (2021): 3269–79. http://dx.doi.org/10.1039/d0dt04401f.
Повний текст джерелаZaleskaya, Marta, Damian Jagleniec, and Jan Romański. "Macrocyclic squaramides as ion pair receptors and fluorescent sensors selective towards sulfates." Dalton Transactions 50, no. 11 (2021): 3904–15. http://dx.doi.org/10.1039/d0dt04273k.
Повний текст джерелаBansal, Deepak, Gulshan Kumar, Geeta Hundal, and Rajeev Gupta. "Mononuclear complexes of amide-based ligands containing appended functional groups: role of secondary coordination spheres on catalysis." Dalton Trans. 43, no. 39 (2014): 14865–75. http://dx.doi.org/10.1039/c4dt02079k.
Повний текст джерелаShojai Nasab, Sajad, and Saeed Zahmatkesh. "Preparation, structural characterization, and gas separation properties of functionalized zinc oxide particle filled poly(ether-amide) nanocomposite films." Journal of Plastic Film & Sheeting 33, no. 1 (August 1, 2016): 92–113. http://dx.doi.org/10.1177/8756087916638120.
Повний текст джерелаRečnik, Lisa-Maria, Wolfgang Kandioller, and Thomas L. Mindt. "1,4-Disubstituted 1,2,3-Triazoles as Amide Bond Surrogates for the Stabilisation of Linear Peptides with Biological Activity." Molecules 25, no. 16 (August 6, 2020): 3576. http://dx.doi.org/10.3390/molecules25163576.
Повний текст джерелаDarme, Pierre, Manuel Dauchez, Arnaud Renard, Laurence Voutquenne-Nazabadioko, Dominique Aubert, Sandie Escotte-Binet, Jean-Hugues Renault, Isabelle Villena, Luiz-Angelo Steffenel, and Stéphanie Baud. "AMIDE v2: High-Throughput Screening Based on AutoDock-GPU and Improved Workflow Leading to Better Performance and Reliability." International Journal of Molecular Sciences 22, no. 14 (July 13, 2021): 7489. http://dx.doi.org/10.3390/ijms22147489.
Повний текст джерелаTakahashi, Yo-ta, Shin-ichi J. Takayama, Shin-ichi Mikami, Hajime Mita, Yoshihiro Sambongi, and Yasuhiko Yamamoto. "Influence of a Single Amide Group on the Redox Function ofPseudomonas aeruginosaCytochromec551." Chemistry Letters 35, no. 5 (May 2006): 528–29. http://dx.doi.org/10.1246/cl.2006.528.
Повний текст джерелаDas, Jayanta, Sabyasachi Ta, Noor Salam, Sudipta Das, Subhasis Ghosh, and Debasis Das. "Polymeric copper(ii) and dimeric oxovanadium(v) complexes of amide–imine conjugate: bilirubin recognition and green catalysis." RSC Advances 13, no. 19 (2023): 13195–205. http://dx.doi.org/10.1039/d3ra00702b.
Повний текст джерелаNuamsrinuan, Nisakorn, Noppadon Suttisiri, Ekachai Hoonnivathana, Pichet Limsuwan, and Kittisakchai Naemchanthara. "Effect of Fish Scales Gelatin and Mixing Ratio on Chemical and Mechanical Characteristics of Gelatin/Chitosan Films." Applied Mechanics and Materials 866 (June 2017): 8–11. http://dx.doi.org/10.4028/www.scientific.net/amm.866.8.
Повний текст джерелаZahn, Dirk. "On the solvation of metal ions in liquid ammonia: a molecular simulation study of M(NH2)x(NH3)ycomplexes as a function of pH." RSC Advances 7, no. 85 (2017): 54063–67. http://dx.doi.org/10.1039/c7ra11462a.
Повний текст джерелаGHOSH, MADHUBRATA, and GANESH S. ANAND. "PROTEIN DYNAMICS IN PHOSPHORYLATION-MEDIATED ALLOSTERY PROBED BY AMIDE EXCHANGE MASS SPECTROMETRY." COSMOS 09, no. 01 (December 2013): 19–27. http://dx.doi.org/10.1142/s0219607713300014.
Повний текст джерелаBrosa, Carme, Ismael Zamora, Emma Terricabras, and Ladislav Kohout. "The Effect of Electrostatic Properties and Abibility to Form Hydrogen-Bonds on the Activity of Brassinosteroid Side-Chain Analogs." Collection of Czechoslovak Chemical Communications 63, no. 10 (1998): 1635–45. http://dx.doi.org/10.1135/cccc19981635.
Повний текст джерелаStenclova, Pavla, Simon Freisinger, Holger Barth, Alexander Kromka, and Boris Mizaikoff. "Cyclic Changes in the Amide Bands Within Escherichia coli Biofilms Monitored Using Real-Time Infrared Attenuated Total Reflection Spectroscopy (IR-ATR)." Applied Spectroscopy 73, no. 4 (February 20, 2019): 424–32. http://dx.doi.org/10.1177/0003702819829081.
Повний текст джерела