Статті в журналах з теми "Pteridine ligands"
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Ознайомтеся з топ-27 статей у журналах для дослідження на тему "Pteridine ligands".
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Kaim, Wolfgang, Brigitte Schwederski, Oliver Heilmann, and Fridmann M. Hornung. "Coordination compounds of pteridine, alloxazine and flavin ligands: structures and properties." Coordination Chemistry Reviews 182, no. 1 (February 1999): 323–42. http://dx.doi.org/10.1016/s0010-8545(98)00193-3.
Повний текст джерелаKaim, Wolfgang, Brigitte Schwederski, Oliver Heilmann, and Fridmann M. Hornung. "ChemInform Abstract: Coordination Compounds of Pteridine, Alloxazine and Flavin Ligands: Structures and Properties." ChemInform 30, no. 18 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199918312.
Повний текст джерелаMullice, Lucy A., Huw J. Mottram, Andrew J. Hallett, and Simon J. A. Pope. "Gold(I) Complexes Incorporating Emissive Mercapto-Pteridine Ligands: Syntheses, X-ray Structure, Luminescence and Preliminary Cytotoxic Evaluation." European Journal of Inorganic Chemistry 2012, no. 18 (May 3, 2012): 3054–60. http://dx.doi.org/10.1002/ejic.201200147.
Повний текст джерелаSokolova, K. V., V. V. Stavytskyi, O. Yu Voskoboinik, O. A. Podpletnya, and S. I. Kovalenko. "In silico and in vivo screening of triamterene synthetic analogues as promising diuretics." Medicni perspektivi 27, no. 3 (September 30, 2022): 4–15. http://dx.doi.org/10.26641/2307-0404.2022.3.265739.
Повний текст джерелаShamshad, Hina, Abdul Hafiz, Ismail I. Althagafi, Maria Saeed, and Agha Zeeshan Mirza. "Characterization of the Trypanosoma brucei Pteridine Reductase Active- Site using Computational Docking and Virtual Screening Techniques." Current Computer-Aided Drug Design 16, no. 5 (November 9, 2020): 583–98. http://dx.doi.org/10.2174/1573409915666190827163327.
Повний текст джерелаKimuda, Magambo Phillip, Dustin Laming, Heinrich C. Hoppe, and Özlem Tastan Bishop. "Identification of Novel Potential Inhibitors of Pteridine Reductase 1 in Trypanosoma brucei via Computational Structure-Based Approaches and in Vitro Inhibition Assays." Molecules 24, no. 1 (January 1, 2019): 142. http://dx.doi.org/10.3390/molecules24010142.
Повний текст джерелаCummins, Peter L., and Jill E. Gready. "Prediction of Relative Binding Constants of Cofactors and Designed Ligands to Dihydrofolate Reductase by Computer Simulation." Pteridines 3, no. 1-2 (February 1991): 137–39. http://dx.doi.org/10.1515/pteridines.1991.3.12.137.
Повний текст джерелаFischer, B., A. Schafer, K. Hegetschweiler, and M. Viscontini. "Iron and Terahydropterin Complex with 1,3,5-Triamino-2,4,6-trihydroxycydohexane as Ligand." Pteridines 6, no. 3 (August 1995): 87–89. http://dx.doi.org/10.1515/pteridines.1995.6.3.87.
Повний текст джерелаIshii, Masakazu, Shunichi Shimizu, Kazuhiro Shiota, Yuji Kiuchi, and Toshinori Yamamoto. "Troglitazone Stimulates the Insulin-induced Tetrahydrobiopterin Synthesis In Vascular Endothelial Cells." Pteridines 11, no. 4 (November 2000): 137–41. http://dx.doi.org/10.1515/pteridines.2000.11.4.137.
Повний текст джерелаWirleitner, Barbara, Elisabeth Kowald, Bernhard Widner, Ulrike Ortner, Gabriele Baier-Bitterlich, Norbert Sepp, and Dietmar Fuchs. "Soluble Fas ligand and neopterin in patients with systemic and cutaneous discoid lupus erythematosus." Pteridines 11, no. 3 (August 2000): 85–89. http://dx.doi.org/10.1515/pteridines.2000.11.3.85.
Повний текст джерелаGhosh, Suparna, and Seung Joo Cho. "Binding Studies and Lead Generation of Pteridin-7(8H)-one Derivatives Targeting FLT3." International Journal of Molecular Sciences 23, no. 14 (July 12, 2022): 7696. http://dx.doi.org/10.3390/ijms23147696.
Повний текст джерелаHunter, W. N., M. S. Alphey, C. S. Bond, and A. W. Schüttelkopf. "Targeting metabolic pathways in microbial pathogens: oxidative stress and anti-folate drug resistance in trypanosomatids." Biochemical Society Transactions 31, no. 3 (June 1, 2003): 607–10. http://dx.doi.org/10.1042/bst0310607.
Повний текст джерелаHerrera-Acevedo, Chonny, Areli Flores-Gaspar, Luciana Scotti, Francisco Jaime Bezerra Mendonça-Junior, Marcus Tullius Scotti, and Ericsson Coy-Barrera. "Identification of Kaurane-Type Diterpenes as Inhibitors of Leishmania Pteridine Reductase I." Molecules 26, no. 11 (May 21, 2021): 3076. http://dx.doi.org/10.3390/molecules26113076.
Повний текст джерелаBaisya, Siddhartha S., та Parag S. Roy. "Crystal structure of (2-amino-7-methyl-4-oxidopteridine-6-carboxylato-κ3O4,N5,O6)aqua(1,10-phenanthroline-κ2N,N′)copper(II) trihydrate". Acta Crystallographica Section E Structure Reports Online 70, № 11 (18 жовтня 2014): 348–51. http://dx.doi.org/10.1107/s1600536814022302.
Повний текст джерелаJiménez-Pulido, Sonia B., Fátima M. Linares-Ordóñez, and Miguel N. Moreno-Carretero. "Novel coordination behavior of a pteridine-benzoylhydrazone ligand (BZLMH): Theoretical calculations, XRD structures and luminescence studies." Polyhedron 28, no. 13 (September 2009): 2641–48. http://dx.doi.org/10.1016/j.poly.2009.05.061.
Повний текст джерелаSantucci, Matteo, Rosaria Luciani, Eleonora Gianquinto, Cecilia Pozzi, Flavio di Pisa, Lucia dello Iacono, Giacomo Landi, et al. "Repurposing the Trypanosomatidic GSK Kinetobox for the Inhibition of Parasitic Pteridine and Dihydrofolate Reductases." Pharmaceuticals 14, no. 12 (November 30, 2021): 1246. http://dx.doi.org/10.3390/ph14121246.
Повний текст джерелаJiménez-Pulido, Sonia B., Fátima M. Linares-Ordóñez, Miguel N. Moreno-Carretero, and Miguel Quirós-Olozábal. "Versatile Coordinative Abilities of a New Hybrid Pteridine−Thiosemicarbazone Ligand: Crystal Structure, Spectroscopic Characterization, and Luminescent Properties." Inorganic Chemistry 47, no. 3 (February 2008): 1096–106. http://dx.doi.org/10.1021/ic701994s.
Повний текст джерелаJedwabny, Wiktoria, Joanna Panecka-Hofman, Edyta Dyguda-Kazimierowicz, Rebecca C. Wade, and W. Andrzej Sokalski. "Application of a simple quantum chemical approach to ligand fragment scoring for Trypanosoma brucei pteridine reductase 1 inhibition." Journal of Computer-Aided Molecular Design 31, no. 8 (July 7, 2017): 715–28. http://dx.doi.org/10.1007/s10822-017-0035-4.
Повний текст джерелаEr-rajy, Mohammed, Mohamed El fadili, Hamada Imtara, Aamir Saeed, Abid Ur Rehman, Sara Zarougui, Shaef A. Abdullah, Ahmad Alahdab, Mohammad Khalid Parvez, and Menana Elhallaoui. "3D-QSAR Studies, Molecular Docking, Molecular Dynamic Simulation, and ADMET Proprieties of Novel Pteridinone Derivatives as PLK1 Inhibitors for the Treatment of Prostate Cancer." Life 13, no. 1 (January 2, 2023): 127. http://dx.doi.org/10.3390/life13010127.
Повний текст джерелаSchüttelkopf, Alexander W., Larry W. Hardy, Stephen M. Beverley, and William N. Hunter. "Structures of Leishmania major Pteridine Reductase Complexes Reveal the Active Site Features Important for Ligand Binding and to Guide Inhibitor Design." Journal of Molecular Biology 352, no. 1 (September 2005): 105–16. http://dx.doi.org/10.1016/j.jmb.2005.06.076.
Повний текст джерелаSahi, Shakti, Parul Tewatia, and Sabari Ghosal. "Leishmania donovani pteridine reductase 1: comparative protein modeling and protein–ligand interaction studies of the leishmanicidal constituents isolated from the fruits of Piper longum." Journal of Molecular Modeling 18, no. 12 (July 3, 2012): 5065–73. http://dx.doi.org/10.1007/s00894-012-1508-y.
Повний текст джерелаHueso-Ureña, Francisco, Sonia B. Jiménez-Pulido, Maria P. Fernández-Liencres, Manuel Fernández-Gómez, and Miguel N. Moreno-Carretero. "A new five-coordinated CuIP2NO2 system: XRD structure of 6-acetyl-1,3,7-trimethyl-pteridine-2,4(1H,3H)-dione and its Cu(i) (N5,O61,O4)-tridentate complex with triphenylphosphine. An AIM study of the nature of metal–ligand bonds." Dalton Transactions, no. 45 (2008): 6461. http://dx.doi.org/10.1039/b807634k.
Повний текст джерелаPhadke, Shraddha, Devender Pathak, and Rakesh Somani. "Design and In silico Studies of 2,5-Disubstituted 1,2,4-Triazole and 1,3,4-Thiadiazole Derivatives as Pteridine Reductase 1 Inhibitors." Journal of Pharmaceutical Research International, May 21, 2021, 166–78. http://dx.doi.org/10.9734/jpri/2021/v33i29a31575.
Повний текст джерела"Automated site-directed drug design : the formation of molecular templates in primary structure generation." Proceedings of the Royal Society of London. B. Biological Sciences 236, no. 1283 (March 22, 1989): 141–62. http://dx.doi.org/10.1098/rspb.1989.0018.
Повний текст джерелаNeda Adibpour. "In silico designing selective inhibitor of drugs, medicinal plants compounds and experimental ligands for pteridine reductase targeting visceral leishmaniasis." African Journal of Microbiology Research 6, no. 5 (February 9, 2012). http://dx.doi.org/10.5897/ajmr-11-738.
Повний текст джерелаChinedu, Shalom N., Mercy Bella-Omunagbe, Esther Okafor, Rufus Afolabi, and Ezekiel Adebiyi. "Computational Studies on 6-Pyruvoyl Tetrahydropterin Synthase (6-PTPS) of Plasmodium falciparum." Bioinformatics and Biology Insights 18 (January 2024). http://dx.doi.org/10.1177/11779322241230214.
Повний текст джерелаPanecka-Hofman, Joanna, and Ina Poehner. "Structure and dynamics of pteridine reductase 1: the key phenomena relevant to enzyme function and drug design." European Biophysics Journal, August 22, 2023. http://dx.doi.org/10.1007/s00249-023-01677-6.
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