Artículos de revistas sobre el tema "Lactam Based Molecules"
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Bai, Yuchen, Leina Dou, Weilin Wu, Zhimin Lu, Jiaqian Kou, Jianzhong Shen, Kai Wen y Zhanhui Wang. "Anti-Metatype Antibody Screening, Sandwich Immunoassay Development, and Structural Insights for β-Lactams Based on Penicillin Binding Protein". Molecules 26, n.º 18 (13 de septiembre de 2021): 5569. http://dx.doi.org/10.3390/molecules26185569.
Texto completoBecker, D., M. Botoshansky, N. Gasper, F. H. Herbstein y M. Karni. "2-Phenyl-4-hydroxyphthalazin-1-one: A Benzoannelated Derivative of Maleic Hydrazide". Acta Crystallographica Section B Structural Science 54, n.º 5 (1 de octubre de 1998): 671–76. http://dx.doi.org/10.1107/s0108768197015760.
Texto completoCox, 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, n.º 6 (1 de junio de 1998): 649–56. http://dx.doi.org/10.1139/v98-012.
Texto completoPestana-Nobles, Roberto, Yani Aranguren-Díaz, Elwi Machado-Sierra, Juvenal Yosa, Nataly J. Galan-Freyle, Laura X. Sepulveda-Montaño, Daniel G. Kuroda y Leonardo C. Pacheco-Londoño. "Docking and Molecular Dynamic of Microalgae Compounds as Potential Inhibitors of Beta-Lactamase". International Journal of Molecular Sciences 23, n.º 3 (31 de enero de 2022): 1630. http://dx.doi.org/10.3390/ijms23031630.
Texto completoTwamley, Brendan, Niamh M. O'Boyle y 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, n.º 8 (3 de julio de 2020): 1187–94. http://dx.doi.org/10.1107/s2056989020008555.
Texto completoShiri, Pezhman. "Novel Hybrid Molecules Based on triazole-β-lactam as Potential Biological Agents". Mini-Reviews in Medicinal Chemistry 21, n.º 5 (2021): 536–53. http://dx.doi.org/10.2174/18755607mtewaotyn5.
Texto completoMolteni, Elena, Giovanni Onida, Matteo Ceccarelli y 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, n.º 4 (3 de abril de 2021): 601. http://dx.doi.org/10.3390/sym13040601.
Texto completoKurmaz, Svetlana V., Natalia V. Fadeeva, Vladislav M. Ignat’ev, Vladimir A. Kurmaz, Sergei A. Kurochkin y Nina S. Emel’yanova. "Structure and State of Water in Branched N-Vinylpyrrolidone Copolymers as Carriers of a Hydrophilic Biologically Active Compound". Molecules 25, n.º 24 (18 de diciembre de 2020): 6015. http://dx.doi.org/10.3390/molecules25246015.
Texto completoShlaes, D. M. y C. Currie-McCumber. "Mutations altering substrate specificity in OHIO-1, and SHV-1 family β-lactamase". Biochemical Journal 284, n.º 2 (1 de junio de 1992): 411–15. http://dx.doi.org/10.1042/bj2840411.
Texto completoMaity, Arindam, Sarmi Sardar, Shilpa Chatterjee, Nripendra Nath Bala, Sudhan Debnath y Debanjan Sen. "De-Novo Design of Hits Against New Delhi Metallo-β-Lactamase Enzyme". International Journal of Quantitative Structure-Property Relationships 7, n.º 2 (abril de 2022): 1–13. http://dx.doi.org/10.4018/ijqspr.290010.
Texto completoKhalesi, Maryam, Azim Ziyaei Halimehjani y 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 (4 de abril de 2019): 852–57. http://dx.doi.org/10.3762/bjoc.15.82.
Texto completoAbdullah, Shahla M. y Shwan Rachid. "On Column Binding a Real-Time Biosensor for β-lactam Antibiotics Quantification". Molecules 25, n.º 5 (10 de marzo de 2020): 1248. http://dx.doi.org/10.3390/molecules25051248.
Texto completoMinhas, Gurdeep S. y Simon Newstead. "Structural basis for prodrug recognition by the SLC15 family of proton-coupled peptide transporters". Proceedings of the National Academy of Sciences 116, n.º 3 (2 de enero de 2019): 804–9. http://dx.doi.org/10.1073/pnas.1813715116.
Texto completoLánská, B., L. Matisová-Rychlá, J. Broz̆ek y 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, n.º 3 (diciembre de 1999): 433–44. http://dx.doi.org/10.1016/s0141-3910(99)00096-8.
Texto completoChepak, Aleksandr, Denis Balatskiy, Mikhail Tutov, Aleksandr Mironenko y Svetlana Bratskaya. "Light Harvesting Nanoprobe for Trace Detection of Hg2+ in Water". Molecules 28, n.º 4 (8 de febrero de 2023): 1633. http://dx.doi.org/10.3390/molecules28041633.
Texto completoZarganes-Tzitzikas, Tryfon, Gonçalo Clemente, Philip Elsinga y Alexander Dömling. "MCR Scaffolds Get Hotter with 18F-Labeling". Molecules 24, n.º 7 (4 de abril de 2019): 1327. http://dx.doi.org/10.3390/molecules24071327.
Texto completoPresnova, Galina V., Denis E. Presnov, Anna A. Filippova, Ilia I. Tsiniaikin, Mariya M. Ulyashova y Maya Yu Rubtsova. "Multiplex Digital Quantification of β-Lactamase Genes in Antibiotic-Resistant Bacteria by Counting Gold Nanoparticle Labels on Silicon Microchips". Biosensors 12, n.º 4 (9 de abril de 2022): 226. http://dx.doi.org/10.3390/bios12040226.
Texto completoMaham Khan, Shahid Wahab, Haroon Muhammad Ali, Sadia Khan, Reema Iqbal y 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 (22 de enero de 2023): 3–23. http://dx.doi.org/10.53560/ppasb(60-sp1)814.
Texto completoAslanli, Aysel, Ilya Lyagin y Elena Efremenko. "Novel approach to quorum quenching: rational design of antibacterials in combination with hexahistidine-tagged organophosphorus hydrolase". Biological Chemistry 399, n.º 8 (26 de julio de 2018): 869–79. http://dx.doi.org/10.1515/hsz-2018-0162.
Texto completoGaudêncio, Susana P. y Florbela Pereira. "Predicting Antifouling Activity and Acetylcholinesterase Inhibition of Marine-Derived Compounds Using a Computer-Aided Drug Design Approach". Marine Drugs 20, n.º 2 (8 de febrero de 2022): 129. http://dx.doi.org/10.3390/md20020129.
Texto completoKamat, Shweta, Pankaj Gupta y 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 (octubre de 2019): S784. http://dx.doi.org/10.1093/ofid/ofz360.1966.
Texto completoBorgianni, Luisa, Julie Vandenameele, André Matagne, Luca Bini, Robert A. Bonomo, Jean-Marie Frère, Gian Maria Rossolini y Jean-Denis Docquier. "Mutational Analysis of VIM-2 Reveals an Essential Determinant for Metallo-β-Lactamase Stability and Folding". Antimicrobial Agents and Chemotherapy 54, n.º 8 (24 de mayo de 2010): 3197–204. http://dx.doi.org/10.1128/aac.01336-09.
Texto completoDiarra, M. S., M. C. Lavoie, M. Jacques, I. Darwish, E. K. Dolence, J. A. Dolence, A. Ghosh, M. Ghosh, M. J. Miller y F. Malouin. "Species selectivity of new siderophore-drug conjugates that use specific iron uptake for entry into bacteria." Antimicrobial Agents and Chemotherapy 40, n.º 11 (noviembre de 1996): 2610–17. http://dx.doi.org/10.1128/aac.40.11.2610.
Texto completoBhagwanth, Swapna, Ram K. Mishra y 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 (30 de enero de 2013): 204–14. http://dx.doi.org/10.3762/bjoc.9.24.
Texto completoBiswal, Sarmistha, Karina Caetano, Diamond Jain, Anusha Sarrila, Tulika Munshi, Rachael Dickman, Alethea B. Tabor, Surya Narayan Rath, Sanjib Bhakta y 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, n.º 3 (10 de marzo de 2023): 553. http://dx.doi.org/10.3390/antibiotics12030553.
Texto completoSharan, Deepti y Erin E. Carlson. "Expanded profiling of β-lactam selectivity for penicillin-binding proteins in Streptococcus pneumoniae D39". Biological Chemistry 403, n.º 4 (28 de febrero de 2022): 433–43. http://dx.doi.org/10.1515/hsz-2021-0386.
Texto completoAnant, Prem Singh y Pratima Gupta. "Application of machine learning in understanding bioactivity of beta-lactamase AmpC". Journal of Physics: Conference Series 2273, n.º 1 (1 de mayo de 2022): 012005. http://dx.doi.org/10.1088/1742-6596/2273/1/012005.
Texto completoAslanli, Aysel y 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 (12 de septiembre de 2019): e7684. http://dx.doi.org/10.7717/peerj.7684.
Texto completoYamada, Masanori y Itaru Honma. "An Anhydrous Proton Conductor Based on Lactam–Lactim Tautomerism of Uracil". ChemPhysChem 5, n.º 5 (17 de mayo de 2004): 724–28. http://dx.doi.org/10.1002/cphc.200301015.
Texto completoFlores, Anthony R., Linda M. Parsons y Martin S. Pavelka. "Characterization of Novel Mycobacterium tuberculosis and Mycobacterium smegmatis Mutants Hypersusceptible to β-Lactam Antibiotics". Journal of Bacteriology 187, n.º 6 (15 de marzo de 2005): 1892–900. http://dx.doi.org/10.1128/jb.187.6.1892-1900.2005.
Texto completoBobba, Sudheer, V. K. Chaithanya Ponnaluri, Mridul Mukherji y William G. Gutheil. "Microtiter Plate-Based Assay for Inhibitors of Penicillin-Binding Protein 2a from Methicillin-Resistant Staphylococcus aureus". Antimicrobial Agents and Chemotherapy 55, n.º 6 (14 de marzo de 2011): 2783–87. http://dx.doi.org/10.1128/aac.01327-10.
Texto completoListro, Roberta, Giacomo Rossino, Serena Della Volpe, Rita Stabile, Massimo Boiocchi, Lorenzo Malavasi, Daniela Rossi y Simona Collina. "Enantiomeric Resolution and Absolute Configuration of a Chiral δ-Lactam, Useful Intermediate for the Synthesis of Bioactive Compounds". Molecules 25, n.º 24 (19 de diciembre de 2020): 6023. http://dx.doi.org/10.3390/molecules25246023.
Texto completodel 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 y Javier Vicario. "Multicomponent Synthesis of Unsaturated γ-Lactam Derivatives. Applications as Antiproliferative Agents through the Bioisosterism Approach: Carbonyl vs. Phosphoryl Group". Pharmaceuticals 15, n.º 5 (22 de abril de 2022): 511. http://dx.doi.org/10.3390/ph15050511.
Texto completoPathompong, Paomephan, Sebastian Pfütze, Frank Surup, Thitiya Boonpratuang, Rattaket Choeyklin, Josphat C. Matasyoh, Cony Decock, Marc Stadler y Chuenchit Boonchird. "Drimane-Type Sesquiterpenoids Derived from the Tropical Basidiomycetes Perenniporia centrali-africana and Cerrena sp. nov". Molecules 27, n.º 18 (14 de septiembre de 2022): 5968. http://dx.doi.org/10.3390/molecules27185968.
Texto completoCollia, Deanna, Thomas D. Bannister, Hao Tan, Shouguang Jin, Taimour Langaee, Justin Shumate, Louis Scampavia y 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, n.º 1 (29 de agosto de 2017): 55–64. http://dx.doi.org/10.1177/2472555217728489.
Texto completoLiu, Xinyu, Shengjie Dong, Yuru Ma, Hu Xu, Hongxia Zhao y 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, n.º 2 (12 de febrero de 2019): 196–206. http://dx.doi.org/10.2174/1573406414666180816123232.
Texto completoAhmadvand, Parvaneh, Johannetsy J. Avillan, Jacob A. Lewis, Douglas R. Call y ChulHee Kang. "Characterization of Interactions between CTX-M-15 and Clavulanic Acid, Desfuroylceftiofur, Ceftiofur, Ampicillin, and Nitrocefin". International Journal of Molecular Sciences 23, n.º 9 (7 de mayo de 2022): 5229. http://dx.doi.org/10.3390/ijms23095229.
Texto completoAbordo, Alecks Megxel S., Mark B. Carascal, Roland Remenyi, Doralyn S. Dalisay y 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, n.º 8 (8 de agosto de 2023): 1019. http://dx.doi.org/10.3390/pathogens12081019.
Texto completoT. Mohd Ali, M. y . "Synthesis of -Hydroxy -Proline: Potential for Organocataly-sis Reactions". International Journal of Engineering & Technology 7, n.º 4.14 (24 de diciembre de 2019): 237. http://dx.doi.org/10.14419/ijet.v7i4.14.27571.
Texto completoFranceschini, Nicola, Berardo Caravelli, Jean-Denis Docquier, Moreno Galleni, Jean-Marie Frère, Gianfranco Amicosante y Gian Maria Rossolini. "Purification and Biochemical Characterization of the VIM-1 Metallo-β-Lactamase". Antimicrobial Agents and Chemotherapy 44, n.º 11 (1 de noviembre de 2000): 3003–7. http://dx.doi.org/10.1128/aac.44.11.3003-3007.2000.
Texto completoGórecki, Marcin y 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, n.º 1 (27 de diciembre de 2021): 273. http://dx.doi.org/10.3390/ijms23010273.
Texto completoKonaklieva, Monika. "Molecular Targets of β-Lactam-Based Antimicrobials: Beyond the Usual Suspects". Antibiotics 3, n.º 2 (3 de abril de 2014): 128–42. http://dx.doi.org/10.3390/antibiotics3020128.
Texto completoPiotrowska, Marta, Lukasz Dziewit, Rafał Ostrowski, Cora Chmielowska y 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, n.º 9 (17 de septiembre de 2020): 613. http://dx.doi.org/10.3390/antibiotics9090613.
Texto completoVitus Silago. "Beta-lactam antibiotics and extended spectrum beta-lactamases". GSC Advanced Research and Reviews 9, n.º 2 (30 de noviembre de 2021): 015–24. http://dx.doi.org/10.30574/gscarr.2021.9.2.0200.
Texto completoWolfe, Saul y 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, n.º 4 (1 de abril de 1994): 1044–50. http://dx.doi.org/10.1139/v94-132.
Texto completoLouis, Bruno y 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, n.º 3 (1 de septiembre de 2012): 305–23. http://dx.doi.org/10.2478/v10007-012-0024-z.
Texto completoElliott, 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, n.º 11 (junio de 2006): 2929–32. http://dx.doi.org/10.1016/j.bmcl.2006.02.080.
Texto completoAli, Tanveer, Abdul Basit, Asad Mustafa Karim, Jung-Hun Lee, Jeong-Ho Jeon, Shafiq ur Rehman y Sang-Hee Lee. "Mutation-Based Antibiotic Resistance Mechanism in Methicillin-Resistant Staphylococcus aureus Clinical Isolates". Pharmaceuticals 14, n.º 5 (1 de mayo de 2021): 420. http://dx.doi.org/10.3390/ph14050420.
Texto completoSanbongi, Yumiko, Takahisa Suzuki, Yumi Osaki, Nami Senju, Takashi Ida y 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, n.º 7 (julio de 2006): 2487–92. http://dx.doi.org/10.1128/aac.01316-05.
Texto completoBiondi, S., S. Long, M. Panunzio y W. L. Qin. "Current Trends in β-Lactam Based β-Lactamases Inhibitors". Current Medicinal Chemistry 18, n.º 27 (1 de septiembre de 2011): 4223–36. http://dx.doi.org/10.2174/092986711797189655.
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