Статті в журналах з теми "Biomolecular and medicinal chemistry, n.e.c"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Biomolecular and medicinal chemistry, n.e.c".
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Jin, Bong-Suk, Won-Kyu Lee, Kwangseog Ahn, Myung Kyu Lee, and Yeon Gyu Yu. "High-Throughput Screening Method of Inhibitors that Block the Interaction between 2 Helical Regions of HIV-1 gp41." Journal of Biomolecular Screening 10, no. 1 (February 2005): 13–19. http://dx.doi.org/10.1177/1087057104269726.
Повний текст джерелаSauermann, Mamatha, Florian Hahne, Christian Schmidt, Meher Majety, Heiko Rosenfelder, Stephanie Bechtel, Wolfgang Huber, Annemarie Poustka, Dorit Arlt, and Stefan Wiemann. "High-Throughput Flow Cytometry–Based Assay to Identify Apoptosis-Inducing Proteins." Journal of Biomolecular Screening 12, no. 4 (March 22, 2007): 510–20. http://dx.doi.org/10.1177/1087057107301271.
Повний текст джерелаTodorov, Petar, Stela Georgieva, Desislava Staneva, Petia Peneva, Petar Grozdanov, Ivanka Nikolova, Evgenia Vasileva-Tonkova, and Ivo Grabchev. "Study of Novel Peptides for Antimicrobial Protection in Solution and on Cotton Fabric." Molecules 27, no. 15 (July 26, 2022): 4770. http://dx.doi.org/10.3390/molecules27154770.
Повний текст джерелаDams, Géry, Koen Van Acker, Emmanuel Gustin, Inge Vereycken, Lieve Bunkens, Pascale Holemans, Liesbet Smeulders, Reginald Clayton, Asa Ohagen, and Kurt Hertogs. "A Time-Resolved Fluorescence Assay to Identify Small-Molecule Inhibitors of HIV-1 Fusion." Journal of Biomolecular Screening 12, no. 6 (May 21, 2007): 865–74. http://dx.doi.org/10.1177/1087057107304645.
Повний текст джерелаWang, Zhongyang, Ge Sun, Mrinmay Mandal, Paul Kohl, Juan de Pablo, Shrayesh N. Patel, and Paul F. Nealey. "Role of Water Molecules in Enabling Site Hopping and Vehicular Transport Mechanisms in Polynorbornene-Based Anion Exchange Membrane." ECS Meeting Abstracts MA2022-02, no. 41 (October 9, 2022): 1536. http://dx.doi.org/10.1149/ma2022-02411536mtgabs.
Повний текст джерелаFrey, Johanna, Sabine Choppin, Françoise Colobert, and Joanna Wencel-Delord. "Towards Atropoenantiopure N–C Axially Chiral Compounds via Stereoselective C–N Bond Formation." CHIMIA International Journal for Chemistry 74, no. 11 (November 25, 2020): 883–89. http://dx.doi.org/10.2533/chimia.2020.883.
Повний текст джерелаSun, Kai, Fengji Ma, Lulu Liu, Jingjing Sun, Xin Liu, Yachao Wang, Zhiguo Zhang, and Guisheng Zhang. "Iodine-mediated regioselective C–N and C–I bond formation of alkenes." RSC Advances 5, no. 100 (2015): 82492–95. http://dx.doi.org/10.1039/c5ra14407h.
Повний текст джерелаZhang, Ming, Qiuhong Wang, Yiyuan Peng, Zhiyuan Chen, Changfeng Wan, Junmin Chen, Yongli Zhao, Rongli Zhang, and Ai Qin Zhang. "Transition metal-catalyzed sp3 C–H activation and intramolecular C–N coupling to construct nitrogen heterocyclic scaffolds." Chemical Communications 55, no. 87 (2019): 13048–65. http://dx.doi.org/10.1039/c9cc06609h.
Повний текст джерелаDar’in, Dmitry, Mikhail Krasavin, Anton V. Budeev, and Grigory Kantin. "Continued Exploration of Trifunctional Alkyl 4-Chloro-2-diazo-3-oxobutanoates: Streamlined Entry into [1,2,3]Triazolo[5,1-c][1,4]benzoxazines and [1,2,3]Triazolo[5,1-c][1,4]benzoxazepines." Synthesis 53, no. 12 (January 8, 2021): 2155–66. http://dx.doi.org/10.1055/a-1348-9031.
Повний текст джерелаCucu (Diaconu), Dumitrela, and Violeta Mangalagiu. "Pyridine-Imidazlolium Salts: Oxidatively Cleavage of N-C Bond via Nitration." Molbank 2019, no. 4 (November 23, 2019): M1095. http://dx.doi.org/10.3390/m1095.
Повний текст джерелаMcMurray, Lindsay, Thomas M. McGuire, and Rachel L. Howells. "Recent Advances in Photocatalytic Decarboxylative Coupling Reactions in Medicinal Chemistry." Synthesis 52, no. 12 (March 9, 2020): 1719–37. http://dx.doi.org/10.1055/s-0039-1690843.
Повний текст джерелаTian, Lifang, Yahui Wang, Yue Zheng, Xiaoqing Shao, and Velayudham Ramadoss. "Recent Developments in Photochemical and Electrochemical Decarboxylative C(sp3)–N Bond Formation." Synthesis 52, no. 09 (March 2, 2020): 1357–68. http://dx.doi.org/10.1055/s-0039-1690839.
Повний текст джерелаKnipe, Peter C., and Jamie S. Sweet. "Catalytic Enantioselective Synthesis of C–N Atropisomeric Heterobiaryls." Synthesis 54, no. 09 (February 23, 2022): 2119–32. http://dx.doi.org/10.1055/s-0040-1719896.
Повний текст джерелаSurendra Reddy, G., A. Suresh Kumar, and Dhevalapally B. Ramachary. "Organocatalytic enone-azide [3 + 2]-cycloaddition: synthesis of functionally rich C/N-double vinyl 1,2,3-triazoles." Organic & Biomolecular Chemistry 18, no. 23 (2020): 4470–78. http://dx.doi.org/10.1039/d0ob00848f.
Повний текст джерелаQiu, Mengyu, Xuegang Fu, Peng Fu, and Jianhui Huang. "Construction of aziridine, azetidine, indole and quinoline-like heterocycles via Pd-mediated C–H activation/annulation strategies." Organic & Biomolecular Chemistry 20, no. 7 (2022): 1339–59. http://dx.doi.org/10.1039/d1ob02146j.
Повний текст джерелаGagné, Michel, and Brandon Moyer. "Taming Silylium Ions for Synthesis: N-Heterocycle Synthesis via Stereoselective C–C Bond Formation." Synlett 28, no. 18 (August 16, 2017): 2429–34. http://dx.doi.org/10.1055/s-0036-1590967.
Повний текст джерелаBöser, Richard, Lars Denker, and René Frank. "N-Heterocyclic Carbene Adducts of Alkynyl Functionalized 1,3,2-Dithioborolanes." Molecules 24, no. 9 (April 30, 2019): 1690. http://dx.doi.org/10.3390/molecules24091690.
Повний текст джерелаZhang, Yitao, Balaram S. Takale, Fabrice Gallou, John Reilly, and Bruce H. Lipshutz. "Sustainable ppm level palladium-catalyzed aminations in nanoreactors under mild, aqueous conditions." Chemical Science 10, no. 45 (2019): 10556–61. http://dx.doi.org/10.1039/c9sc03710a.
Повний текст джерелаBatalha, Pedro N., Luana da S. M. Forezi, Maria Clara R. Freitas, Nathalia M. de C. Tolentino, Ednilsom Orestes, José Walkimar de M. Carneiro, Fernanda da C. S. Boechat, and Maria Cecília B. V. de Souza. "Study on the regioselectivity of the N-ethylation reaction of N-benzyl-4-oxo-1,4-dihydroquinoline-3-carboxamide." Beilstein Journal of Organic Chemistry 15 (February 12, 2019): 388–400. http://dx.doi.org/10.3762/bjoc.15.35.
Повний текст джерелаAssefa Sisay, Melaku, Estifanos Ele Yaya, and Wendimagegn Mammo. "Essential oil and smoke components of Carissa spinarum." Bulletin of the Chemical Society of Ethiopia 36, no. 3 (July 15, 2022): 641–49. http://dx.doi.org/10.4314/bcse.v36i3.13.
Повний текст джерелаEngeloch, Caroline, Ulrich Schopfer, Ingo Muckenschnabel, Francois Le Goff, Hervé Mees, Karoline Boesch, and Maxim Popov. "Stability of Screening Compounds in Wet DMSO." Journal of Biomolecular Screening 13, no. 10 (November 21, 2008): 999–1006. http://dx.doi.org/10.1177/1087057108326536.
Повний текст джерелаNayak, Riddhi A., and Anvita D. Mangte. "Synthesis and Antimicrobial Studies of Novel N-Glycosyl Hydrazino Carbothioamide." Asian Journal of Chemistry 33, no. 1 (2020): 127–31. http://dx.doi.org/10.14233/ajchem.2021.22967.
Повний текст джерелаKim, Dong, Yae Choi, Jaewon Shim, Yun-Sang Choi, Yun Kim, Mina Kim, and Min Kim. "Suppressive Effect of Arctium Lappa L. Leaves on Retinal Damage Against A2E-Induced ARPE-19 Cells and Mice." Molecules 25, no. 7 (April 9, 2020): 1737. http://dx.doi.org/10.3390/molecules25071737.
Повний текст джерелаDamdindorj, Mungunnaran, Gereltu Borjihan, Odontuya Gendaram, and Bayarmaa Bold. "Synthesis and antihyperlipidaemic activity of a new piperine derivative." Mongolian Journal of Chemistry 22, no. 48 (December 29, 2021): 13–18. http://dx.doi.org/10.5564/mjc.v22i48.1782.
Повний текст джерелаAmrati, Fatima Ez-Zahra, Mohammed Bourhia, Hamza Saghrouchni, Meryem Slighoua, Andriy Grafov, Riaz Ullah, Essam Ezzeldin, et al. "Caralluma europaea (Guss.) N.E.Br.: Anti-Inflammatory, Antifungal, and Antibacterial Activities against Nosocomial Antibiotic-Resistant Microbes of Chemically Characterized Fractions." Molecules 26, no. 3 (January 26, 2021): 636. http://dx.doi.org/10.3390/molecules26030636.
Повний текст джерелаGülten, Şirin, Ufuk Gezer, and Elmas Aksanli Gündoğan. "Fast and Efficient One-Pot Three-Component Synthesis of Some 1,2,3,4- Tetrahydro-6-methyl-N-phenyl-5-pyrimidinecarboxamide Derivatives via Biginelli Condensation Reaction." Letters in Organic Chemistry 17, no. 5 (April 28, 2020): 366–71. http://dx.doi.org/10.2174/1570178616666190819142221.
Повний текст джерелаYu, Da Qing, Xiao Jing Han, Ting Yu Shan, Rui Xu, Jin Hu, Wang Xing Cheng, Liang Ping Zha, and Hua Sheng Peng. "Microscopic Characteristic and Chemical Composition Analysis of Three Medicinal Plants and Surface Frosts." Molecules 24, no. 24 (December 12, 2019): 4548. http://dx.doi.org/10.3390/molecules24244548.
Повний текст джерелаBai, Xiuyun, Hengye Chen, Wanjun Long, Wei Lan, Siyu Wang, Guanghua Lei, Yuting Guan, Jian Yang, and Haiyan Fu. "Accurate Traceability of Stable C, H, O, N Isotope Ratios and Multi-Element Analysis Combined with Chemometrics for Chrysanthemi Flos ‘Hangbaiju’ from Different Origins." Chemosensors 10, no. 12 (December 12, 2022): 529. http://dx.doi.org/10.3390/chemosensors10120529.
Повний текст джерелаJung, In-Geun, Jae-Young Jeong, Seung-Hoon Yum, and You-Jin Hwang. "Inhibitory Effects of Selected Medicinal Plants on Bacterial Growth of Methicillin-Resistant Staphylococcus aureus." Molecules 27, no. 22 (November 11, 2022): 7780. http://dx.doi.org/10.3390/molecules27227780.
Повний текст джерелаInnes, Dylan, Michael V. Perkins, Andris J. Liepa, and Craig L. Francis. "N,N-Dialkyl-N′-Chlorosulfonyl Chloroformamidines in Heterocyclic Synthesis. Part XIV. Synthesis and Reactivity of the New Benzo[4,5]imidazo[1,2-b][1,2,6]thiadiazine Ring System." Australian Journal of Chemistry 71, no. 1 (2018): 58. http://dx.doi.org/10.1071/ch17255.
Повний текст джерелаSemenyuk, Pavel I., Lidia P. Kurochkina, Lauri Mäkinen, Vladimir I. Muronetz, and Sami Hietala. "Thermocontrolled Reversible Enzyme Complexation-Inactivation-Protection by Poly(N-acryloyl glycinamide)." Polymers 13, no. 20 (October 19, 2021): 3601. http://dx.doi.org/10.3390/polym13203601.
Повний текст джерелаBisz, Elwira, Pamela Podchorodecka, Hengzhao Li, Wioletta Ochędzan-Siodłak, Jie An, and Michal Szostak. "Sequential Iron-Catalyzed C(sp2)–C(sp3) Cross-Coupling of Chlorobenzamides/Chemoselective Amide Reduction and Reductive Deuteration to Benzylic Alcohols." Molecules 28, no. 1 (December 27, 2022): 223. http://dx.doi.org/10.3390/molecules28010223.
Повний текст джерелаGao, Meng, Wenting Zhao, Hongyi Zhao, Ziyun Lin, Dongfeng Zhang, and Haihong Huang. "An efficient and facile access to highly functionalized pyrrole derivatives." Beilstein Journal of Organic Chemistry 14 (April 20, 2018): 884–90. http://dx.doi.org/10.3762/bjoc.14.75.
Повний текст джерелаShafiq, Nusrat, Farah Yasmin, Sadia Noreen, Alina Shahzad, Zill-I.-huma Nazli, Shagufta Parveen, Basharat Ali, Zaheer Ahmad, Maryam Rashid, and Muhammad Bilal. "Phytochemical Profiling of Medicinal Plants Extracts and Their Antioxidant and Anticancer Potentialities Against Human Liver Cancer (Hep G2) Cell Lines." Revista de Chimie 72, no. 1 (February 3, 2021): 100–110. http://dx.doi.org/10.37358/rc.21.1.8407.
Повний текст джерелаZhang, Lin, Wei Xie, Xiaojun Teng, Kui Wang, Wei Xie, and Caiyan Wang. "Improving the Extraction of Active Ingredients from Medicinal Plants by XynA Modification." Journal of Chemistry 2022 (February 3, 2022): 1–8. http://dx.doi.org/10.1155/2022/2483797.
Повний текст джерелаAsilbekova, Daniya Tolimbekovna, та Khairulla Mamadievich Bobakulov. "STUDY OF LIPIDS, FATTY ACIDS AND LIPOPHILIC SUBSTANCES OF СONSOLIDA AMBIGUA (L.) P.W. BALL & HEYWOOD AND NIGELLA SATIVA L. SEEDS". chemistry of plant raw material, № 1 (16 березня 2021): 105–12. http://dx.doi.org/10.14258/jcprm.2021018384.
Повний текст джерелаCilia, Giovanni, Giacomo Luchetti, and Antonio Nanetti. "Polymorphism of 16s rRNA Gene: Any Effect on the Biomolecular Quantitation of the Honey Bee (Apis mellifera L., 1758) Pathogen Nosema ceranae?" Applied Sciences 12, no. 1 (January 2, 2022): 422. http://dx.doi.org/10.3390/app12010422.
Повний текст джерелаRasool, Rabia, Inam Ullah, Samiah Shahid, Bismillah Mubeen, Syed Sarim Imam, Sultan Alshehri, Mohammed M. Ghoneim, et al. "In Vivo Assessment of the Ameliorative Impact of Some Medicinal Plant Extracts on Lipopolysaccharide-Induced Multiple Sclerosis in Wistar Rats." Molecules 27, no. 5 (February 28, 2022): 1608. http://dx.doi.org/10.3390/molecules27051608.
Повний текст джерелаKatugampala, Supun, Inoka C. Perera, Chandrika Nanayakkara, and Theshini Perera. "Synthesis, Characterization, and Antimicrobial Activity of Novel Sulfonated Copper-Triazine Complexes." Bioinorganic Chemistry and Applications 2018 (August 29, 2018): 1–7. http://dx.doi.org/10.1155/2018/2530851.
Повний текст джерелаChuang, Lu-Te, Ya-Hsin Shih, Wen-Cheng Huang, Lie-Chwen Lin, Chin Hsu, Jong-Ho Chyuan, Tsung-Hsien Tsai, and Po-Jung Tsai. "In Vitro and In Vivo Screening of Wild Bitter Melon Leaf for Anti-Inflammatory Activity against Cutibacterium acnes." Molecules 25, no. 18 (September 18, 2020): 4277. http://dx.doi.org/10.3390/molecules25184277.
Повний текст джерелаHasserodt, Jens, Arnaud Gautier, Romain Barbe, and Michael Waibel. "ChemInform Abstract: The N→C=O Interaction: A Weak Bond with Attractive Properties for the Deliberate Exploitation in Medicinal and Supramolecular Chemistry." ChemInform 42, no. 24 (May 19, 2011): no. http://dx.doi.org/10.1002/chin.201124215.
Повний текст джерелаTang, Xue Song, and Ming Li. "Synthesis of n-Hexadecylphosphonic Acid-Coated Monodisperse Fe3O4 Superparamagnetic Nanoparticles." Key Engineering Materials 512-515 (June 2012): 170–73. http://dx.doi.org/10.4028/www.scientific.net/kem.512-515.170.
Повний текст джерелаDoan, Chien, Thi Tran, Minh Nguyen, Van Nguyen, Anh Nguyen та San-Lang Wang. "Anti-α-Glucosidase Activity by a Protease from Bacillus licheniformis". Molecules 24, № 4 (15 лютого 2019): 691. http://dx.doi.org/10.3390/molecules24040691.
Повний текст джерелаLu, Cheng Wei, Tzu Yu Lin та Su Jane Wang. "11-Keto-β-Boswellic Acid Attenuates Glutamate Release and Kainic Acid-Induced Excitotoxicity in the Rat Hippocampus". Planta Medica 86, № 06 (25 лютого 2020): 434–41. http://dx.doi.org/10.1055/a-1107-9337.
Повний текст джерелаAl-Ostoot, Fares Hezam, Jigmat Stondus, Sumati Anthal, Geetha Doddenahally Venkatesh, Yasser Hussein Eissa Mohammed, Mandayam Anandalwar Sridhar, Shaukath Ara Khanum, and Rajni Kant. "Synthesis, spectroscopic and X-ray crystallographic analysis of N-(2-(2-(4-chlorophenoxy)acetamido)phenyl)-1H-indole-2-carboxamide." European Journal of Chemistry 10, no. 3 (September 30, 2019): 234–38. http://dx.doi.org/10.5155/eurjchem.10.3.234-238.1874.
Повний текст джерелаDhanalakshmi, G., Velu Saravanan, Arasambattu K. Mohanakrishnan, and S. Aravindhan. "Synthesis, Crystal Structure, Hirshfeld Surface, Energy Framework and Molecular Docking Analysis of Two Novel Carbazole Derivatives." Asian Journal of Chemistry 31, no. 12 (November 16, 2019): 3017–28. http://dx.doi.org/10.14233/ajchem.2019.22430.
Повний текст джерелаBACKES, Luana Taís Hartmann, Telma Elita BERTOLIN, Silvana Souza ROMAN, Janaine de Oliveira PAIVA, Vanusa MANFREDINI, Luciane Noal CALIL, Daliane Paula FATURI, and Adelina MEZZARI. "ASCORBIC ACID AND THE PROTECTIVE EFFECT IN SWISS MICE TREATED WITH GREEN TEA INFUSIONS." Periódico Tchê Química 12, no. 24 (August 20, 2015): 17–27. http://dx.doi.org/10.52571/ptq.v12.n24.2015.17_p_24_pgs_17_27.pdf.
Повний текст джерелаJeffs, Joshua W., Nilojan Jehanathan, Stephanie M. F. Thibert, Shadi Ferdosi, Linda Pham, Zachary T. Wilson, Christian Breburda, and Chad R. Borges. "Delta-S-Cys-Albumin: A Lab Test that Quantifies Cumulative Exposure of Archived Human Blood Plasma and Serum Samples to Thawed Conditions." Molecular & Cellular Proteomics 18, no. 10 (July 19, 2019): 2121–37. http://dx.doi.org/10.1074/mcp.tir119.001659.
Повний текст джерелаPiontek, Aleksandra, Elwira Bisz, Błażej Dziuk, Roman Szostak, and Michal Szostak. "Structures and energetic properties of 4-halobenzamides." Acta Crystallographica Section C Structural Chemistry 74, no. 11 (October 23, 2018): 1395–402. http://dx.doi.org/10.1107/s2053229618013463.
Повний текст джерелаTsai, Yueh-Ting, Shung-Te Kao, and Chin-Yi Cheng. "Medicinal Herbs and Their Derived Ingredients Protect against Cognitive Decline in In Vivo Models of Alzheimer’s Disease." International Journal of Molecular Sciences 23, no. 19 (September 25, 2022): 11311. http://dx.doi.org/10.3390/ijms231911311.
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