Статті в журналах з теми "Lactam Based Molecules"
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Bai, Yuchen, Leina Dou, Weilin Wu, Zhimin Lu, Jiaqian Kou, Jianzhong Shen, Kai Wen та Zhanhui Wang. "Anti-Metatype Antibody Screening, Sandwich Immunoassay Development, and Structural Insights for β-Lactams Based on Penicillin Binding Protein". Molecules 26, № 18 (13 вересня 2021): 5569. http://dx.doi.org/10.3390/molecules26185569.
Повний текст джерелаBecker, D., M. Botoshansky, N. Gasper, F. H. Herbstein, and M. Karni. "2-Phenyl-4-hydroxyphthalazin-1-one: A Benzoannelated Derivative of Maleic Hydrazide." Acta Crystallographica Section B Structural Science 54, no. 5 (October 1, 1998): 671–76. http://dx.doi.org/10.1107/s0108768197015760.
Повний текст джерелаCox, Robin A. "Lactams in sulfuric acid. The mechanism of amide hydrolysis in weak to moderately strong aqueous mineral acid media." Canadian Journal of Chemistry 76, no. 6 (June 1, 1998): 649–56. http://dx.doi.org/10.1139/v98-012.
Повний текст джерелаPestana-Nobles, Roberto, Yani Aranguren-Díaz, Elwi Machado-Sierra, Juvenal Yosa, Nataly J. Galan-Freyle, Laura X. Sepulveda-Montaño, Daniel G. Kuroda, and Leonardo C. Pacheco-Londoño. "Docking and Molecular Dynamic of Microalgae Compounds as Potential Inhibitors of Beta-Lactamase." International Journal of Molecular Sciences 23, no. 3 (January 31, 2022): 1630. http://dx.doi.org/10.3390/ijms23031630.
Повний текст джерелаTwamley, Brendan, Niamh M. O'Boyle, and Mary J. Meegan. "Azetidin-2-ones: structures of antimitotic compounds based on the 1-(3,4,5-trimethoxyphenyl)azetidin-2-one core." Acta Crystallographica Section E Crystallographic Communications 76, no. 8 (July 3, 2020): 1187–94. http://dx.doi.org/10.1107/s2056989020008555.
Повний текст джерелаShiri, Pezhman. "Novel Hybrid Molecules Based on triazole-β-lactam as Potential Biological Agents". Mini-Reviews in Medicinal Chemistry 21, № 5 (2021): 536–53. http://dx.doi.org/10.2174/18755607mtewaotyn5.
Повний текст джерелаMolteni, Elena, Giovanni Onida, Matteo Ceccarelli, and Giancarlo Cappellini. "Ab Initio Spectroscopic Investigation of Pharmacologically Relevant Chiral Molecules: The Cases of Avibactam, Cephems, and Idelalisib as Benchmarks for Antibiotics and Anticancer Drugs." Symmetry 13, no. 4 (April 3, 2021): 601. http://dx.doi.org/10.3390/sym13040601.
Повний текст джерелаKurmaz, Svetlana V., Natalia V. Fadeeva, Vladislav M. Ignat’ev, Vladimir A. Kurmaz, Sergei A. Kurochkin, and Nina S. Emel’yanova. "Structure and State of Water in Branched N-Vinylpyrrolidone Copolymers as Carriers of a Hydrophilic Biologically Active Compound." Molecules 25, no. 24 (December 18, 2020): 6015. http://dx.doi.org/10.3390/molecules25246015.
Повний текст джерелаShlaes, D. M., та C. Currie-McCumber. "Mutations altering substrate specificity in OHIO-1, and SHV-1 family β-lactamase". Biochemical Journal 284, № 2 (1 червня 1992): 411–15. http://dx.doi.org/10.1042/bj2840411.
Повний текст джерелаMaity, Arindam, Sarmi Sardar, Shilpa Chatterjee, Nripendra Nath Bala, Sudhan Debnath та Debanjan Sen. "De-Novo Design of Hits Against New Delhi Metallo-β-Lactamase Enzyme". International Journal of Quantitative Structure-Property Relationships 7, № 2 (квітень 2022): 1–13. http://dx.doi.org/10.4018/ijqspr.290010.
Повний текст джерелаKhalesi, Maryam, Azim Ziyaei Halimehjani, and Jürgen Martens. "Synthesis of a novel category of pseudo-peptides using an Ugi three-component reaction of levulinic acid as bifunctional substrate, amines, and amino acid-based isocyanides." Beilstein Journal of Organic Chemistry 15 (April 4, 2019): 852–57. http://dx.doi.org/10.3762/bjoc.15.82.
Повний текст джерелаAbdullah, Shahla M., та Shwan Rachid. "On Column Binding a Real-Time Biosensor for β-lactam Antibiotics Quantification". Molecules 25, № 5 (10 березня 2020): 1248. http://dx.doi.org/10.3390/molecules25051248.
Повний текст джерелаMinhas, Gurdeep S., and Simon Newstead. "Structural basis for prodrug recognition by the SLC15 family of proton-coupled peptide transporters." Proceedings of the National Academy of Sciences 116, no. 3 (January 2, 2019): 804–9. http://dx.doi.org/10.1073/pnas.1813715116.
Повний текст джерелаLánská, B., L. Matisová-Rychlá, J. Broz̆ek, and J. Rychlý. "Chemiluminescence of polyamides II. Luminescence accompanying thermooxidation of lactam-based polyamides related to the content of end-groups of molecules." Polymer Degradation and Stability 66, no. 3 (December 1999): 433–44. http://dx.doi.org/10.1016/s0141-3910(99)00096-8.
Повний текст джерелаChepak, Aleksandr, Denis Balatskiy, Mikhail Tutov, Aleksandr Mironenko, and Svetlana Bratskaya. "Light Harvesting Nanoprobe for Trace Detection of Hg2+ in Water." Molecules 28, no. 4 (February 8, 2023): 1633. http://dx.doi.org/10.3390/molecules28041633.
Повний текст джерелаZarganes-Tzitzikas, Tryfon, Gonçalo Clemente, Philip Elsinga, and Alexander Dömling. "MCR Scaffolds Get Hotter with 18F-Labeling." Molecules 24, no. 7 (April 4, 2019): 1327. http://dx.doi.org/10.3390/molecules24071327.
Повний текст джерелаPresnova, Galina V., Denis E. Presnov, Anna A. Filippova, Ilia I. Tsiniaikin, Mariya M. Ulyashova та Maya Yu Rubtsova. "Multiplex Digital Quantification of β-Lactamase Genes in Antibiotic-Resistant Bacteria by Counting Gold Nanoparticle Labels on Silicon Microchips". Biosensors 12, № 4 (9 квітня 2022): 226. http://dx.doi.org/10.3390/bios12040226.
Повний текст джерелаMaham Khan, Shahid Wahab, Haroon Muhammad Ali, Sadia Khan, Reema Iqbal, and Tariq Khan. "Biogenic Nanomaterials: A Way Forward in Preventing Bacterial Infections." Proceedings of the Pakistan Academy of Sciences: B. Life and Environmental Sciences 60, S (January 22, 2023): 3–23. http://dx.doi.org/10.53560/ppasb(60-sp1)814.
Повний текст джерелаAslanli, Aysel, Ilya Lyagin, and Elena Efremenko. "Novel approach to quorum quenching: rational design of antibacterials in combination with hexahistidine-tagged organophosphorus hydrolase." Biological Chemistry 399, no. 8 (July 26, 2018): 869–79. http://dx.doi.org/10.1515/hsz-2018-0162.
Повний текст джерелаGaudêncio, Susana P., and Florbela Pereira. "Predicting Antifouling Activity and Acetylcholinesterase Inhibition of Marine-Derived Compounds Using a Computer-Aided Drug Design Approach." Marine Drugs 20, no. 2 (February 8, 2022): 129. http://dx.doi.org/10.3390/md20020129.
Повний текст джерелаKamat, Shweta, Pankaj Gupta та Akshata Mane. "2288. Role of Β Lactam-Β Lactamase Inhibitors in Indian Tertiary Care Hospitals: Results from a Nationwide Survey". Open Forum Infectious Diseases 6, Supplement_2 (жовтень 2019): S784. http://dx.doi.org/10.1093/ofid/ofz360.1966.
Повний текст джерелаBorgianni, Luisa, Julie Vandenameele, André Matagne, Luca Bini, Robert A. Bonomo, Jean-Marie Frère, Gian Maria Rossolini та Jean-Denis Docquier. "Mutational Analysis of VIM-2 Reveals an Essential Determinant for Metallo-β-Lactamase Stability and Folding". Antimicrobial Agents and Chemotherapy 54, № 8 (24 травня 2010): 3197–204. http://dx.doi.org/10.1128/aac.01336-09.
Повний текст джерелаDiarra, M. S., M. C. Lavoie, M. Jacques, I. Darwish, E. K. Dolence, J. A. Dolence, A. Ghosh, M. Ghosh, M. J. Miller, and F. Malouin. "Species selectivity of new siderophore-drug conjugates that use specific iron uptake for entry into bacteria." Antimicrobial Agents and Chemotherapy 40, no. 11 (November 1996): 2610–17. http://dx.doi.org/10.1128/aac.40.11.2610.
Повний текст джерелаBhagwanth, Swapna, Ram K. Mishra, and Rodney L. Johnson. "Development of peptidomimetic ligands of Pro-Leu-Gly-NH2 as allosteric modulators of the dopamine D2 receptor." Beilstein Journal of Organic Chemistry 9 (January 30, 2013): 204–14. http://dx.doi.org/10.3762/bjoc.9.24.
Повний текст джерелаBiswal, Sarmistha, Karina Caetano, Diamond Jain, Anusha Sarrila, Tulika Munshi, Rachael Dickman, Alethea B. Tabor, Surya Narayan Rath, Sanjib Bhakta та Anindya S. Ghosh. "Antimicrobial Peptides Designed against the Ω-Loop of Class A β-Lactamases to Potentiate the Efficacy of β-Lactam Antibiotics". Antibiotics 12, № 3 (10 березня 2023): 553. http://dx.doi.org/10.3390/antibiotics12030553.
Повний текст джерелаSharan, Deepti, та Erin E. Carlson. "Expanded profiling of β-lactam selectivity for penicillin-binding proteins in Streptococcus pneumoniae D39". Biological Chemistry 403, № 4 (28 лютого 2022): 433–43. http://dx.doi.org/10.1515/hsz-2021-0386.
Повний текст джерелаAnant, Prem Singh, and Pratima Gupta. "Application of machine learning in understanding bioactivity of beta-lactamase AmpC." Journal of Physics: Conference Series 2273, no. 1 (May 1, 2022): 012005. http://dx.doi.org/10.1088/1742-6596/2273/1/012005.
Повний текст джерелаAslanli, Aysel, and Elena Efremenko. "Simultaneous molecular docking of different ligands to His6-tagged organophosphorus hydrolase as an effective tool for assessing their effect on the enzyme." PeerJ 7 (September 12, 2019): e7684. http://dx.doi.org/10.7717/peerj.7684.
Повний текст джерелаYamada, Masanori, and Itaru Honma. "An Anhydrous Proton Conductor Based on Lactam–Lactim Tautomerism of Uracil." ChemPhysChem 5, no. 5 (May 17, 2004): 724–28. http://dx.doi.org/10.1002/cphc.200301015.
Повний текст джерелаFlores, Anthony R., Linda M. Parsons та Martin S. Pavelka. "Characterization of Novel Mycobacterium tuberculosis and Mycobacterium smegmatis Mutants Hypersusceptible to β-Lactam Antibiotics". Journal of Bacteriology 187, № 6 (15 березня 2005): 1892–900. http://dx.doi.org/10.1128/jb.187.6.1892-1900.2005.
Повний текст джерелаBobba, Sudheer, V. K. Chaithanya Ponnaluri, Mridul Mukherji, and William G. Gutheil. "Microtiter Plate-Based Assay for Inhibitors of Penicillin-Binding Protein 2a from Methicillin-Resistant Staphylococcus aureus." Antimicrobial Agents and Chemotherapy 55, no. 6 (March 14, 2011): 2783–87. http://dx.doi.org/10.1128/aac.01327-10.
Повний текст джерелаListro, Roberta, Giacomo Rossino, Serena Della Volpe, Rita Stabile, Massimo Boiocchi, Lorenzo Malavasi, Daniela Rossi та Simona Collina. "Enantiomeric Resolution and Absolute Configuration of a Chiral δ-Lactam, Useful Intermediate for the Synthesis of Bioactive Compounds". Molecules 25, № 24 (19 грудня 2020): 6023. http://dx.doi.org/10.3390/molecules25246023.
Повний текст джерелаdel Corte, Xabier, Adrián López-Francés, Ilia Villate-Beitia, Myriam Sainz-Ramos, Edorta Martínez de Marigorta, Francisco Palacios, Concepción Alonso, Jesús M. de los Santos, José Luis Pedraz та Javier Vicario. "Multicomponent Synthesis of Unsaturated γ-Lactam Derivatives. Applications as Antiproliferative Agents through the Bioisosterism Approach: Carbonyl vs. Phosphoryl Group". Pharmaceuticals 15, № 5 (22 квітня 2022): 511. http://dx.doi.org/10.3390/ph15050511.
Повний текст джерелаPathompong, Paomephan, Sebastian Pfütze, Frank Surup, Thitiya Boonpratuang, Rattaket Choeyklin, Josphat C. Matasyoh, Cony Decock, Marc Stadler, and Chuenchit Boonchird. "Drimane-Type Sesquiterpenoids Derived from the Tropical Basidiomycetes Perenniporia centrali-africana and Cerrena sp. nov." Molecules 27, no. 18 (September 14, 2022): 5968. http://dx.doi.org/10.3390/molecules27185968.
Повний текст джерелаCollia, Deanna, Thomas D. Bannister, Hao Tan, Shouguang Jin, Taimour Langaee, Justin Shumate, Louis Scampavia та Timothy P. Spicer. "A Rapid Phenotypic Whole-Cell Screening Approach for the Identification of Small-Molecule Inhibitors That Counter β-Lactamase Resistance in Pseudomonas aeruginosa". SLAS DISCOVERY: Advancing the Science of Drug Discovery 23, № 1 (29 серпня 2017): 55–64. http://dx.doi.org/10.1177/2472555217728489.
Повний текст джерелаLiu, Xinyu, Shengjie Dong, Yuru Ma, Hu Xu, Hongxia Zhao та Qingzhi Gao. "N-(Sulfamoylbenzoyl)-L-proline Derivatives as Potential Non-β-lactam ESBL Inhibitors: Structure-Based Lead Identification, Medicinal Chemistry and Synergistic Antibacterial Activities". Medicinal Chemistry 15, № 2 (12 лютого 2019): 196–206. http://dx.doi.org/10.2174/1573406414666180816123232.
Повний текст джерелаAhmadvand, Parvaneh, Johannetsy J. Avillan, Jacob A. Lewis, Douglas R. Call, and ChulHee Kang. "Characterization of Interactions between CTX-M-15 and Clavulanic Acid, Desfuroylceftiofur, Ceftiofur, Ampicillin, and Nitrocefin." International Journal of Molecular Sciences 23, no. 9 (May 7, 2022): 5229. http://dx.doi.org/10.3390/ijms23095229.
Повний текст джерелаAbordo, Alecks Megxel S., Mark B. Carascal, Roland Remenyi, Doralyn S. Dalisay та Jonel P. Saludes. "Clinically Isolated β-Lactam-Resistant Gram-Negative Bacilli in a Philippine Tertiary Care Hospital Harbor Multi-Class β-Lactamase Genes". Pathogens 12, № 8 (8 серпня 2023): 1019. http://dx.doi.org/10.3390/pathogens12081019.
Повний текст джерелаT. Mohd Ali, M., and . "Synthesis of -Hydroxy -Proline: Potential for Organocataly-sis Reactions." International Journal of Engineering & Technology 7, no. 4.14 (December 24, 2019): 237. http://dx.doi.org/10.14419/ijet.v7i4.14.27571.
Повний текст джерелаFranceschini, Nicola, Berardo Caravelli, Jean-Denis Docquier, Moreno Galleni, Jean-Marie Frère, Gianfranco Amicosante та Gian Maria Rossolini. "Purification and Biochemical Characterization of the VIM-1 Metallo-β-Lactamase". Antimicrobial Agents and Chemotherapy 44, № 11 (1 листопада 2000): 3003–7. http://dx.doi.org/10.1128/aac.44.11.3003-3007.2000.
Повний текст джерелаGórecki, Marcin, та Jadwiga Frelek. "A Holistic Approach to Determining Stereochemistry of Potential Pharmaceuticals by Circular Dichroism with β-Lactams as Test Cases". International Journal of Molecular Sciences 23, № 1 (27 грудня 2021): 273. http://dx.doi.org/10.3390/ijms23010273.
Повний текст джерелаKonaklieva, Monika. "Molecular Targets of β-Lactam-Based Antimicrobials: Beyond the Usual Suspects". Antibiotics 3, № 2 (3 квітня 2014): 128–42. http://dx.doi.org/10.3390/antibiotics3020128.
Повний текст джерелаPiotrowska, Marta, Lukasz Dziewit, Rafał Ostrowski, Cora Chmielowska, and Magdalena Popowska. "Molecular Characterization and Comparative Genomics of IncQ-3 Plasmids Conferring Resistance to Various Antibiotics Isolated from a Wastewater Treatment Plant in Warsaw (Poland)." Antibiotics 9, no. 9 (September 17, 2020): 613. http://dx.doi.org/10.3390/antibiotics9090613.
Повний текст джерелаVitus Silago. "Beta-lactam antibiotics and extended spectrum beta-lactamases." GSC Advanced Research and Reviews 9, no. 2 (November 30, 2021): 015–24. http://dx.doi.org/10.30574/gscarr.2021.9.2.0200.
Повний текст джерелаWolfe, Saul, та Tova Hoz. "A semiempirical molecular orbital study of the methanolysis of complex azetidinones. A combined MM and QM analysis of the interaction of Δ2- and Δ3-cephems with the penicillin receptor". Canadian Journal of Chemistry 72, № 4 (1 квітня 1994): 1044–50. http://dx.doi.org/10.1139/v94-132.
Повний текст джерелаLouis, Bruno, and Vijay K. Agrawal. "Quantitative structure-pharmacokinetic relationship (QSPkP) analysis of the volume of distribution values of anti-infective agents from j group of the ATC classification in humans." Acta Pharmaceutica 62, no. 3 (September 1, 2012): 305–23. http://dx.doi.org/10.2478/v10007-012-0024-z.
Повний текст джерелаElliott, Jason M., Emma J. Carlson, Gary G. Chicchi, Olivier Dirat, Maria Dominguez, Ute Gerhard, Richard Jelley, et al. "NK1 antagonists based on seven membered lactam scaffolds." Bioorganic & Medicinal Chemistry Letters 16, no. 11 (June 2006): 2929–32. http://dx.doi.org/10.1016/j.bmcl.2006.02.080.
Повний текст джерелаAli, Tanveer, Abdul Basit, Asad Mustafa Karim, Jung-Hun Lee, Jeong-Ho Jeon, Shafiq ur Rehman, and Sang-Hee Lee. "Mutation-Based Antibiotic Resistance Mechanism in Methicillin-Resistant Staphylococcus aureus Clinical Isolates." Pharmaceuticals 14, no. 5 (May 1, 2021): 420. http://dx.doi.org/10.3390/ph14050420.
Повний текст джерелаSanbongi, Yumiko, Takahisa Suzuki, Yumi Osaki, Nami Senju, Takashi Ida та Kimiko Ubukata. "Molecular Evolution of β-Lactam-Resistant Haemophilus influenzae: 9-Year Surveillance of Penicillin-Binding Protein 3 Mutations in Isolates from Japan". Antimicrobial Agents and Chemotherapy 50, № 7 (липень 2006): 2487–92. http://dx.doi.org/10.1128/aac.01316-05.
Повний текст джерелаBiondi, S., S. Long, M. Panunzio, and W. L. Qin. "Current Trends in β-Lactam Based β-Lactamases Inhibitors." Current Medicinal Chemistry 18, no. 27 (September 1, 2011): 4223–36. http://dx.doi.org/10.2174/092986711797189655.
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