Статті в журналах з теми "Enzyme Inhibition Potency"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Enzyme Inhibition Potency".
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Yamali, Cem, Halise Inci Gul, Tahir Cakir, Yeliz Demir, and Ilhami Gulcin. "Aminoalkylated Phenolic Chalcones: Investigation of Biological Effects on Acetylcholinesterase and Carbonic Anhydrase I and II as Potential Lead Enzyme Inhibitors." Letters in Drug Design & Discovery 17, no. 10 (October 12, 2020): 1283–92. http://dx.doi.org/10.2174/1570180817999200520123510.
Повний текст джерелаGiresha, Aladahalli S., Deepadarshan Urs, Sophiya Pundalik, Rajkumar S. Meti, Siddanakoppalu N. Pramod, Ballenahalli H. Supreetha, Madhusudana Somegowda, et al. "Sinapicacid Inhibits Group IIA Secretory Phospholipase A2 and Its Inflammatory Response in Mice." Antioxidants 11, no. 7 (June 25, 2022): 1251. http://dx.doi.org/10.3390/antiox11071251.
Повний текст джерелаMartyn, Derek C., Michael J. B. Moore, and Andrew D. Abell. "Succinimide and Saccharin-based Enzyme-activated Inhibitors of Serine Proteases." Current Pharmaceutical Design 5, no. 6 (June 1999): 405–15. http://dx.doi.org/10.2174/138161280505230110110545.
Повний текст джерелаLiu, Liqin, Violeta Yu, Jeanne Pistillo, Josie Lee, Laurie B. Schenkel, Stephanie Geuns-Meyer, Ivonne Archibeque, Angus Sinclair, Renee Emkey, and Graham Molineux. "New Insights on Assessing Intra-Family Selectivity for Jak2 Inhibitors." Blood 118, no. 21 (November 18, 2011): 5150. http://dx.doi.org/10.1182/blood.v118.21.5150.5150.
Повний текст джерелаPratasik, Veronika, Revolson Mege, and Mokosuli Semuel Yermia. "In Vitro Antidiabetic Activity Of Apis dorsata Binghami Nest Extract." JURNAL PEMBELAJARAN DAN BIOLOGI NUKLEUS 8, no. 3 (November 25, 2022): 733–43. http://dx.doi.org/10.36987/jpbn.v8i3.3196.
Повний текст джерелаKern, Gunther, Tiffany Palmer, David E. Ehmann, Adam B. Shapiro, Beth Andrews, Gregory S. Basarab, Peter Doig, et al. "Inhibition of Neisseria gonorrhoeae Type II Topoisomerases by the Novel Spiropyrimidinetrione AZD0914." Journal of Biological Chemistry 290, no. 34 (July 6, 2015): 20984–94. http://dx.doi.org/10.1074/jbc.m115.663534.
Повний текст джерелаBetari, Nibal, Kristoffer Sahlholm, Yuta Ishizuka, Knut Teigen, and Jan Haavik. "Discovery and biological characterization of a novel scaffold for potent inhibitors of peripheral serotonin synthesis." Future Medicinal Chemistry 12, no. 16 (August 2020): 1461–74. http://dx.doi.org/10.4155/fmc-2020-0127.
Повний текст джерелаOUELLET, Marc, Jean-Pierre FALGUEYRET, and M. David PERCIVAL. "Detergents profoundly affect inhibitor potencies against both cyclo-oxygenase isoforms." Biochemical Journal 377, no. 3 (February 1, 2004): 675–84. http://dx.doi.org/10.1042/bj20030969.
Повний текст джерелаDavies, Gareth, Hannah Semple, Megan McCandless, Jonathan Cairns, and Geoffrey A. Holdgate. "High-Throughput Mechanism of Inhibition." SLAS DISCOVERY: Advancing the Science of Drug Discovery 26, no. 2 (January 22, 2021): 248–56. http://dx.doi.org/10.1177/2472555220983809.
Повний текст джерелаHaehner, Thomas, Ulrich Massing, Torsten Diesinger, and Dieter Müller-Enoch. "Inhibition of Cytochrome P450 Mediated Enzyme Activity by Alkylphosphocholines." Zeitschrift für Naturforschung C 59, no. 7-8 (August 1, 2004): 599–605. http://dx.doi.org/10.1515/znc-2004-7-826.
Повний текст джерелаHulcová, Daniela, Kateřina Breiterová, Lucie Zemanová, Tomáš Siatka, Marcela Šafratová, Nina Vaněčková, Anna Hošťálková, Vladimír Wsól, and Lucie Cahlíková. "AKR1C3 Inhibitory Potency of Naturally-occurring Amaryllidaceae Alkaloids of Different Structural Types." Natural Product Communications 12, no. 2 (February 2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200226.
Повний текст джерелаSari, Desi Ratna, Aurelia Afra, Erni Yupita Sari Br Sembiring, and Cico Jhon Karunia Simamora. "Fat-Rich Food Review on Obesity Control through Induction Enzyme Inhibitors." BIOEDUSCIENCE 5, no. 3 (December 31, 2021): 211–17. http://dx.doi.org/10.22236/j.bes/536903.
Повний текст джерелаPrasa, D., L. Svendsen, and J. Stürzebecher. "Inhibition of Thrombin Generation in Plasma by Inhibitors of Factor Xa." Thrombosis and Haemostasis 78, no. 04 (1997): 1215–20. http://dx.doi.org/10.1055/s-0038-1657717.
Повний текст джерелаAragaw, Wassihun Wedajo, Brendon M. Lee, Xuan Yang, Matthew D. Zimmerman, Martin Gengenbacher, Véronique Dartois, Wai-Keung Chui, Colin J. Jackson, and Thomas Dick. "Potency boost of a Mycobacterium tuberculosis dihydrofolate reductase inhibitor by multienzyme F420H2-dependent reduction." Proceedings of the National Academy of Sciences 118, no. 25 (June 14, 2021): e2025172118. http://dx.doi.org/10.1073/pnas.2025172118.
Повний текст джерелаHasinoff, B. B., and J. P. Davey. "The inhibition of a membrane-bound enzyme as a model for anaesthetic action and drug toxicity." Biochemical Journal 258, no. 1 (February 15, 1989): 101–7. http://dx.doi.org/10.1042/bj2580101.
Повний текст джерелаOjo, Kayode K., J. Robert Gillespie, Aaron J. Riechers, Alberto J. Napuli, Christophe L. M. J. Verlinde, Frederick S. Buckner, Michael H. Gelb, et al. "Glycogen Synthase Kinase 3 Is a Potential Drug Target for African Trypanosomiasis Therapy." Antimicrobial Agents and Chemotherapy 52, no. 10 (July 21, 2008): 3710–17. http://dx.doi.org/10.1128/aac.00364-08.
Повний текст джерелаHara, A., M. Shinoda, T. Kanazu, T. Nakayama, Y. Deyashiki, and H. Sawada. "Inhibition of dimeric dihydrodiol dehydrogenases of rabbit and pig lens by ascorbic acid." Biochemical Journal 275, no. 1 (April 1, 1991): 121–26. http://dx.doi.org/10.1042/bj2750121.
Повний текст джерелаRožman, Kaja, Evan M. Alexander, Eva Ogorevc, Krištof Bozovičar, Izidor Sosič, Courtney C. Aldrich, and Stanislav Gobec. "Psoralen Derivatives as Inhibitors of Mycobacterium tuberculosis Proteasome." Molecules 25, no. 6 (March 12, 2020): 1305. http://dx.doi.org/10.3390/molecules25061305.
Повний текст джерелаBaruah, Prayasee, Mostofa Ataur Rohman, Semen O. Yesylevskyy, and Sivaprasad Mitra. "Therapeutic potency of substituted chromones as Alzheimer’s drug: Elucidation of acetylcholinesterase inhibitory activity through spectroscopic and molecular modelling investigation." BioImpacts 9, no. 2 (March 8, 2019): 79–88. http://dx.doi.org/10.15171/bi.2019.11.
Повний текст джерелаConnor, M. J., and M. H. Smit. "Terminal-group oxidation of retinol by mouse epidermis. Inhibition in vitro and in vivo." Biochemical Journal 244, no. 2 (June 1, 1987): 489–92. http://dx.doi.org/10.1042/bj2440489.
Повний текст джерелаBalasuriya, Nileeka, McShane McKenna, Xuguang Liu, Shawn Li, and Patrick O’Donoghue. "Phosphorylation-Dependent Inhibition of Akt1." Genes 9, no. 9 (September 7, 2018): 450. http://dx.doi.org/10.3390/genes9090450.
Повний текст джерелаPrinsloo, Denise, Sandra van Dyk, Anél Petzer, and Jacobus P. Petzer. "Monoamine Oxidase Inhibition by Kavalactones from Kava (Piper Methysticum)." Planta Medica 85, no. 14/15 (September 20, 2019): 1136–42. http://dx.doi.org/10.1055/a-1008-9491.
Повний текст джерелаMostafa, Amany S., Waleed A. Bayoumi, Mohamed El-Mesery, and Abdelaziz Elgaml. "Molecular Design and Synthesis of New 3,4-Dihydropyrimidin-2(1H)-Ones as Potential Anticancer Agents with VEGFR-2 Inhibiting Activity." Anti-Cancer Agents in Medicinal Chemistry 19, no. 3 (June 25, 2019): 310–22. http://dx.doi.org/10.2174/1871520618666180717125906.
Повний текст джерелаGalardy, R. E., and Z. P. Kortylewicz. "Inhibitors of angiotensin-converting enzyme containing a tetrahedral arsenic atom." Biochemical Journal 226, no. 2 (March 1, 1985): 447–54. http://dx.doi.org/10.1042/bj2260447.
Повний текст джерелаGüzel-Akdemir, Özlen, Simone Carradori, Rossella Grande, Kübra Demir-Yazıcı, Andrea Angeli, Claudiu T. Supuran, and Atilla Akdemir. "Development of Thiazolidinones as Fungal Carbonic Anhydrase Inhibitors." International Journal of Molecular Sciences 21, no. 8 (April 22, 2020): 2960. http://dx.doi.org/10.3390/ijms21082960.
Повний текст джерелаOWENS, Raymond J., Cath CATTERALL, Dawn BATTY, John JAPPY, Annette RUSSELL, Bryan SMITH, Jimi O'CONNELL, and Martin J. PERRY. "Human phosphodiesterase 4A: characterization of full-length and truncated enzymes expressed in COS cells." Biochemical Journal 326, no. 1 (August 15, 1997): 53–60. http://dx.doi.org/10.1042/bj3260053.
Повний текст джерелаSivaraman, Bhuvaneswari, Vijaykumar Raji, Bala Aakash Velmurugan, and Ramalakshmi Natarajan. "Acetylcholinesterase Enzyme Inhibitor Molecules with Therapeutic Potential for Alzheimer's Disease." CNS & Neurological Disorders - Drug Targets 21, no. 5 (June 2022): 427–49. http://dx.doi.org/10.2174/1871527320666210928160159.
Повний текст джерелаGholivand, Khodayar, Ahlam Madani Alizadehgan, Fresia Mojahed, Gholamreza Dehghan, Azadeh Mohammadirad, and Mohammad Abdollahi. "Some New Carbacylamidophosphates as Inhibitors of Acetylcholinesterase and Butyrylcholinesterase." Zeitschrift für Naturforschung C 63, no. 3-4 (April 1, 2008): 241–50. http://dx.doi.org/10.1515/znc-2008-3-414.
Повний текст джерелаGreen, Louis S., James M. Bullard, Wendy Ribble, Frank Dean, David F. Ayers, Urs A. Ochsner, Nebojsa Janjic, and Thale C. Jarvis. "Inhibition of Methionyl-tRNA Synthetase by REP8839 and Effects of Resistance Mutations on Enzyme Activity." Antimicrobial Agents and Chemotherapy 53, no. 1 (November 17, 2008): 86–94. http://dx.doi.org/10.1128/aac.00275-08.
Повний текст джерелаGoedken, Eric R., Andrew I. Gagnon, Gary T. Overmeyer, Junjian Liu, Richard A. Petrillo, Andrew F. Burchat, and Medha J. Tomlinson. "HTRF-Based Assay for Microsomal Prostaglandin E2 Synthase-1 Activity." Journal of Biomolecular Screening 13, no. 7 (July 1, 2008): 619–25. http://dx.doi.org/10.1177/1087057108321145.
Повний текст джерелаKlabe, Ronald M., Lee T. Bacheler, Paul J. Ala, Susan Erickson-Viitanen, and James L. Meek. "Resistance to HIV Protease Inhibitors: A Comparison of Enzyme Inhibition and Antiviral Potency." Biochemistry 37, no. 24 (June 1998): 8735–42. http://dx.doi.org/10.1021/bi972555l.
Повний текст джерелаLamba, Doriano, and Alessandro Pesaresi. "Kinetic Modeling of Time-Dependent Enzyme Inhibition by Pre-Steady-State Analysis of Progress Curves: The Case Study of the Anti-Alzheimer’s Drug Galantamine." International Journal of Molecular Sciences 23, no. 9 (May 3, 2022): 5072. http://dx.doi.org/10.3390/ijms23095072.
Повний текст джерелаHuppatz, John L., та John E. Casida. "Acetohydroxyacid Synthase Inhibitors: N-Phthalyl-ʟ-valine Anilide and Related Compounds". Zeitschrift für Naturforschung C 40, № 9-10 (1 серпня 1985): 652–56. http://dx.doi.org/10.1515/znc-1985-9-1010.
Повний текст джерелаShen, L. L., and D. T. W. Chu. "Type II DNA Topoisomerases as Antibacterial Targets." Current Pharmaceutical Design 2, no. 2 (April 1996): 195–208. http://dx.doi.org/10.2174/1381612802666220921174531.
Повний текст джерелаNga, Bui T. T., Yuki Takeshita, Misa Yamamoto, and Yoshimi Yamamoto. "Studies of Inhibitory Mechanisms of Propeptide-Like Cysteine Protease Inhibitors." Enzyme Research 2014 (June 19, 2014): 1–10. http://dx.doi.org/10.1155/2014/848937.
Повний текст джерелаRodríguez Núñez, Yeray A., Margarita Gutíerrez, Jans Alzate-Morales, Francisco Adasme-Carreño, Fausto M. Güiza, Cristian C. Bernal, and Arnold R. Romero Bohórquez. "Tetrahydroquinoline-Isoxazole/Isoxazoline Hybrid Compounds as Potential Cholinesterases Inhibitors: Synthesis, Enzyme Inhibition Assays, and Molecular Modeling Studies." International Journal of Molecular Sciences 21, no. 1 (December 18, 2019): 5. http://dx.doi.org/10.3390/ijms21010005.
Повний текст джерелаMalunga, Lovemore Nkhata, Marta Izydorczyk, and Trust Beta. "Antiglycemic Effect of Water Extractable Arabinoxylan from Wheat Aleurone and Bran." Journal of Nutrition and Metabolism 2017 (2017): 1–6. http://dx.doi.org/10.1155/2017/5784759.
Повний текст джерелаMatsuda, Y., S. Nakanishi, K. Nagasawa, K. Iwahashi, and H. Kase. "The effect of K-252a, a potent microbial inhibitor of protein kinase, on activated cyclic nucleotide phosphodiesterase." Biochemical Journal 256, no. 1 (November 15, 1988): 75–80. http://dx.doi.org/10.1042/bj2560075.
Повний текст джерелаKalalinia, Fatemeh, Mohammad Jouya, Alireza K. Komachali, Seyed M. Aboutourabzadeh, Gholamreza Karimi, Javad Behravan, Khalil Abnous, Leila Etemad, Hossein Kamali, and Farzin Hadizadeh. "Design, Synthesis, and Biological Evaluation of New Azole Derivatives as Potent Aromatase Inhibitors with Potential Effects against Breast Cancer." Anti-Cancer Agents in Medicinal Chemistry 18, no. 7 (November 30, 2018): 1016–24. http://dx.doi.org/10.2174/1871520618666180116105858.
Повний текст джерелаde Jonge, Boudewijn L. M., Grant K. Walkup, Sushmita D. Lahiri, Hoan Huynh, Georg Neckermann, Luke Utley, Tory J. Nash, et al. "Discovery of Inhibitors of 4′-Phosphopantetheine Adenylyltransferase (PPAT) To Validate PPAT as a Target for Antibacterial Therapy." Antimicrobial Agents and Chemotherapy 57, no. 12 (September 16, 2013): 6005–15. http://dx.doi.org/10.1128/aac.01661-13.
Повний текст джерелаHafifani, Witya, Indun D. Puspita, and Masagus M. P. Putra. "The effect of hydrolysis duration on the antibacterial activity of swamp eel head protein hydrolysate produced by papain against histamine-producing bacteria." E3S Web of Conferences 322 (2021): 04005. http://dx.doi.org/10.1051/e3sconf/202132204005.
Повний текст джерелаRani, Nidhi, and Randhir Singh. "Molecular Modelling Studies of 1,4-Diaryl-2-Mercaptoimidazole Derivatives for Antimicrobial Potency." Current Computer-Aided Drug Design 15, no. 5 (September 23, 2019): 409–20. http://dx.doi.org/10.2174/1573409915666181219124956.
Повний текст джерелаGiovanny, Lisa, Faliha Arinda Lestari, Nurul Marfira, Laksmi Ambarsari, and Siti Warnasih. "Potency of Ethanol Extracts Palm Seeds (Phoenix dactylifera L.) as Antidiabetic with Inhibition Kinetics Parameter." Current Biochemistry 6, no. 2 (February 3, 2020): 1–10. http://dx.doi.org/10.29244/cb.6.2.1.
Повний текст джерелаHumnabadkar, Vaishali, Prashanti Madhavapeddi, Halesha Basavarajappa, Md Gulebahar Sheikh, Rajendra Rane, Reetobrata Basu, Prateek Verma, Aishwarya Sundaram, Kakoli Mukherjee, and Sunita M. de Sousa. "Assays, Surrogates, and Alternative Technologies for a TB Lead Identification Program Targeting DNA Gyrase ATPase." Journal of Biomolecular Screening 20, no. 2 (October 9, 2014): 265–74. http://dx.doi.org/10.1177/1087057114554170.
Повний текст джерелаFINNEY, Sarah, Lisa SEALE, Roy T. SAWYER, and Robert B. WALLIS. "Tridegin, a new peptidic inhibitor of factor XIIIa, from the blood-sucking leech Haementeria ghilianii." Biochemical Journal 324, no. 3 (June 15, 1997): 797–805. http://dx.doi.org/10.1042/bj3240797.
Повний текст джерелаAsan, Tandiah, I. Nyoman Ehrich Lister, Edy Fachrial, Annisa Amalia, Wahyu Widowati, Buter Samin, and Liena Liena. "Potency of Black Soybean (Glycine max (L.) Merr) Extract and Daidzein as Antioxidant and Antihyaluronidase." Majalah Obat Tradisional 24, no. 1 (April 30, 2019): 52. http://dx.doi.org/10.22146/mot.43615.
Повний текст джерелаBeattie, R. E., D. T. Elmore, C. H. Williams, and D. J. S. Guthrie. "The behaviour of leucine aminopeptidase towards thionopeptides." Biochemical Journal 245, no. 1 (July 1, 1987): 285–88. http://dx.doi.org/10.1042/bj2450285.
Повний текст джерелаSamira, Nia, Benarous Khedidja, Abdelalim Fatima Zahra, Chellali Khadidja Nour Elyakine, and Yousfi Mohamed. "In silico and in vitro Study of the Inhibitory Effect of Antiinflammatory Drug Betamethasone on Two Lipases." Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry 19, no. 4 (October 15, 2020): 387–92. http://dx.doi.org/10.2174/1871523018666190906165944.
Повний текст джерелаHermanto, Sandra, Aldi Octavio, Azrifitria Azrifitria, and Susi Kusumaningrum. "The HMG-CoA Reductase Inhibitor Activities of Soy Protein Hydrolysates from Papain Hydrolysis." Molekul 16, no. 2 (July 20, 2021): 145. http://dx.doi.org/10.20884/1.jm.2021.16.2.724.
Повний текст джерелаBaldwin, Jeffrey, Carolyn H. Michnoff, Nicholas A. Malmquist, John White, Michael G. Roth, Pradipsinh K. Rathod, and Margaret A. Phillips. "High-throughput Screening for Potent and Selective Inhibitors of Plasmodium falciparum Dihydroorotate Dehydrogenase." Journal of Biological Chemistry 280, no. 23 (March 28, 2005): 21847–53. http://dx.doi.org/10.1074/jbc.m501100200.
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