المؤلفون: Palafox, M. A., Belskaya, N. P., Kostova, I. P.

المصدر: Pharmaceutics

مصطلحات موضوعية: 1,2,3-TRIAZOLES, ANTI-CANCER DRUGS, IR, SCALING, VIBRATIONAL ANALYSIS, 2 (4 CHLOROPHENYL) 5 (PYRROLIDIN 1 YL) 2H 1,2,3 TRIAZOLE 4 CARBOXYLIC ACID, DIMER, GELATINASE A, LEUCINE, MONOMER, TRIAZOLE, TRIAZOLE DERIVATIVE, UNCLASSIFIED DRUG, ACCURACY, ARTICLE, CALCULATION, CARBON NUCLEAR MAGNETIC RESONANCE, CHEMICAL STRUCTURE, DENSITY FUNCTIONAL THEORY, ENTROPY, EXPERIMENTAL DESIGN, GEOMETRY, INFRARED SPECTROSCOPY, MOLECULAR ARCHITECTURE, MOLECULAR DOCKING, POLYNOMIC SCALING EQUATION PROCEDURE, PROTON NUCLEAR MAGNETIC RESONANCE, QUANTUM CHEMISTRY, RAMAN SPECTROMETRY, SCALE UP

وصف الملف: application/pdf

العلاقة: Palafox, M, Belskaya, N & Kostova, I 2023, 'Study of the Molecular Architectures of 2-(4-Chlorophenyl)-5-(pyrrolidin-1-yl)-2H-1,2,3-triazole-4-carboxylic Acid Using Their Vibrational Spectra, Quantum Chemical Calculations and Molecular Docking with MMP-2 Receptor', Pharmaceutics, Том. 15, № 12, 2686. https://doi.org/10.3390/pharmaceutics15122686Test; Palafox, M., Belskaya, N., & Kostova, I. (2023). Study of the Molecular Architectures of 2-(4-Chlorophenyl)-5-(pyrrolidin-1-yl)-2H-1,2,3-triazole-4-carboxylic Acid Using Their Vibrational Spectra, Quantum Chemical Calculations and Molecular Docking with MMP-2 Receptor. Pharmaceutics, 15(12), [2686]. https://doi.org/10.3390/pharmaceutics15122686Test; Final; All Open Access, Gold, Green; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85180694443&doi=10.3390%2fpharmaceutics15122686&partnerID=40&md5=973d018ad4ba3a5621715acd67e4e08aTest; https://www.mdpi.com/1999-4923/15/12/2686/pdf?version=1701087791Test; http://elar.urfu.ru/handle/10995/131083Test; 85180694443; 001132704600001

الإتاحة: https://doi.org/10.3390/pharmaceutics15122686Test
http://elar.urfu.ru/handle/10995/131083Test
https://www.mdpi.com/1999-4923/15/12/2686/pdf?version=1701087791Test

المؤلفون: Alcolea, Palafox, M., Belskaya, N. P., Todorov, L. T., Kostova, I. P.

المصدر: Antioxidants

مصطلحات موضوعية: 1,2,3-TRIAZOLES, ANTIOXIDANT, LANTHANUM, SCALING, VIBRATIONAL ANALYSIS

وصف الملف: application/pdf

العلاقة: Alcolea Palafox, M, Belskaya, N, Todorov, L & Kostova, I 2023, 'Structural Study of a La(III) Complex of a 1,2,3-Triazole Ligand with Antioxidant Activity', Antioxidants, Том. 12, № 10, 1872. https://doi.org/10.3390/antiox12101872Test; Alcolea Palafox, M., Belskaya, N., Todorov, L., & Kostova, I. (2023). Structural Study of a La(III) Complex of a 1,2,3-Triazole Ligand with Antioxidant Activity. Antioxidants, 12(10), [1872]. https://doi.org/10.3390/antiox12101872Test; Final; All Open Access, Gold, Green; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85175324083&doi=10.3390%2fantiox12101872&partnerID=40&md5=90283e058bf85bca1df15a56beffe6afTest; https://www.mdpi.com/2076-3921/12/10/1872/pdf?version=1697530768Test; http://elar.urfu.ru/handle/10995/130905Test; 85175324083; 001119483800001

الإتاحة: https://doi.org/10.3390/antiox12101872Test
http://elar.urfu.ru/handle/10995/130905Test
https://www.mdpi.com/2076-3921/12/10/1872/pdf?version=1697530768Test

المؤلفون: Alcolea, Palafox, M., Belskaya, N. P., Kostova, I. P.

المصدر: International Journal of Molecular Sciences

مصطلحات موضوعية: 1,2,3-TRIAZOLES, ANTICANCER DRUGS DESIGN, DIMER CALCULATION, SCALING, VIBRATIONAL ANALYSIS, ANTINEOPLASTIC AGENT, DIMER, MONOMER, TRIAZOLE, TRIAZOLE DERIVATIVE, CARBOXYLIC ACID, POLYMER, SODIUM CHLORIDE, ANTINEOPLASTIC ACTIVITY, ARTICLE, BIOLOGICAL ACTIVITY, CALCULATION, CHEMICAL STRUCTURE, CONFORMATION, CONTROLLED STUDY, DENSITY FUNCTIONAL THEORY, GEOMETRY, HYDROGEN BOND, MECHANICAL TORSION, MICROENVIRONMENT, NUCLEAR MAGNETIC RESONANCE, SOLID STATE, SUBSTITUTION REACTION, X RAY ANALYSIS, CARBOXYLIC ACIDS

وصف الملف: application/pdf

العلاقة: Palafox, MA, Belskaya, N & Kostova, I 2023, 'Peculiarities of the Spatial and Electronic Structure of 2-Aryl-1,2,3-Triazol-5-Carboxylic Acids and Their Salts on the Basis of Spectral Studies and DFT Calculations', International Journal of Molecular Sciences, Том. 24, № 18, 14001. https://doi.org/10.3390/ijms241814001Test; Palafox, M. A., Belskaya, N., & Kostova, I. (2023). Peculiarities of the Spatial and Electronic Structure of 2-Aryl-1,2,3-Triazol-5-Carboxylic Acids and Their Salts on the Basis of Spectral Studies and DFT Calculations. International Journal of Molecular Sciences, 24(18), [14001]. https://doi.org/10.3390/ijms241814001Test; Final; All Open Access, Gold; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85172022877&doi=10.3390%2fijms241814001&partnerID=40&md5=4f44ef16922cce5d0fe566c45b2ab4cfTest; https://www.mdpi.com/1422-0067/24/18/14001/pdf?version=1694517851Test; http://elar.urfu.ru/handle/10995/130795Test; 85172022877; 001119235600001

الإتاحة: https://doi.org/10.3390/ijms241814001Test
http://elar.urfu.ru/handle/10995/130795Test
https://www.mdpi.com/1422-0067/24/18/14001/pdf?version=1694517851Test

المؤلفون: Safronov, N. E., Kostova, I. P., Palafox, M. A., Belskaya, N. P.

المصدر: International Journal of Molecular Sciences

مصطلحات موضوعية: 1,2,3-TRIAZOLES, CARBOXYLIC ACID, DIMER, FLUORESCENCE, PKA, TDDFT, 1,2,3 TRIAZOLE 4 CARBOXYLIC ACID, ANION, CARBOXYLIC ACID DERIVATIVE, DIMETHYL SULFOXIDE, DIOXANE, METHANOL, SODIUM, UNCLASSIFIED DRUG, WATER, SODIUM CHLORIDE, SOLVENT, TRIAZOLE DERIVATIVE, ARTICLE, CARBON NUCLEAR MAGNETIC RESONANCE, CHEMICAL STRUCTURE, CONTROLLED STUDY, DENSITY FUNCTIONAL THEORY, IONIZATION, MOLECULAR INTERACTION, NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, PROTON NUCLEAR MAGNETIC RESONANCE, QUANTUM CHEMISTRY, SPECTROFLUOROMETRY, ULTRAVIOLET VISIBLE SPECTROSCOPY

وصف الملف: application/pdf

العلاقة: Safronov, NE, Kostova, IP, Palafox, MA & Belskaya, NP 2023, 'Combined NMR Spectroscopy and Quantum-Chemical Calculations in Fluorescent 1,2,3-Triazole-4-carboxylic Acids Fine Structures Analysis', International Journal of Molecular Sciences, Том. 24, № 10, 8947. https://doi.org/10.3390/ijms24108947Test; Safronov, N. E., Kostova, I. P., Palafox, M. A., & Belskaya, N. P. (2023). Combined NMR Spectroscopy and Quantum-Chemical Calculations in Fluorescent 1,2,3-Triazole-4-carboxylic Acids Fine Structures Analysis. International Journal of Molecular Sciences, 24(10), [8947]. https://doi.org/10.3390/ijms24108947Test; Final; All Open Access, Gold, Green; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85160376599&doi=10.3390%2fijms24108947&partnerID=40&md5=c71224dcfc837a512239ec8a77fdb623Test; https://www.mdpi.com/1422-0067/24/10/8947/pdf?version=1684400993Test; http://elar.urfu.ru/handle/10995/130516Test; 85160376599; 000998011100001

الإتاحة: https://doi.org/10.3390/ijms24108947Test
http://elar.urfu.ru/handle/10995/130516Test
https://www.mdpi.com/1422-0067/24/10/8947/pdf?version=1684400993Test

المؤلفون: Sadchikova, E. V., Safronov, N. E., Beliaev, N. A., Nenajdenko, V. G., Belskaya, N. P.

المصدر: Molecules

مصطلحات موضوعية: AIE EFFECT, DIAZOIMIDAZOLE, DIAZOPYRAZOLE, DIHYDROAZOLO[5,1-C][1,2,4]TRIAZINES, ENAMINE, FLUORESCENCE, ISOXAZOLE, SOLVATOCHROMISM

وصف الملف: application/pdf

العلاقة: Sadchikova, EV, Safronov, NE, Beliaev, NA, Nenajdenko, VG & Belskaya, NP 2023, 'Isoxazolyl-Derived 1,4-Dihydroazolo[5,1-c][1,2,4]Triazines: Synthesis and Photochemical Properties', Molecules, Том. 28, № 7, 3192. https://doi.org/10.3390/molecules28073192Test; Sadchikova, E. V., Safronov, N. E., Beliaev, N. A., Nenajdenko, V. G., & Belskaya, N. P. (2023). Isoxazolyl-Derived 1,4-Dihydroazolo[5,1-c][1,2,4]Triazines: Synthesis and Photochemical Properties. Molecules, 28(7), [3192]. https://doi.org/10.3390/molecules28073192Test; Final; All Open Access, Gold, Green; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85152355537&doi=10.3390%2fmolecules28073192&partnerID=40&md5=2d904e295c41c9d908ab6399054bfb70Test; https://www.mdpi.com/1420-3049/28/7/3192/pdf?version=1680579793Test; http://elar.urfu.ru/handle/10995/130379Test; 85152355537

الإتاحة: https://doi.org/10.3390/molecules28073192Test
http://elar.urfu.ru/handle/10995/130379Test
https://www.mdpi.com/1420-3049/28/7/3192/pdf?version=1680579793Test

المؤلفون: Eltyshev, A. K., Belskaya, N. P.

مصطلحات موضوعية: DIHYDROTRIAZOLOPYRIMIDINES, ACIDS, BASES, FLUORESCENCE RESPONSE, CHEMOSENSOR

وصف الملف: application/pdf

العلاقة: Chimica Techno Acta. 2021. Vol. 8. № 3; Eltyshev A. K. Sensitivity of the Phenoxy Derivatives of 2,4-dihydro-5H-[1,2,3]triazolo[4,5-d]pyrimidin-5-ones to Acidic and Basic Stimuli / A. K. Eltyshev, N. P. Belskaya // Chimica Techno Acta. — 2021. — Vol. 8, No. 3. — № 20218303.; http://elar.urfu.ru/handle/10995/104751Test; https://elibrary.ru/item.asp?id=46654757Test

الإتاحة: https://doi.org/10.15826/chimtech.2021.8.3.03Test
http://elar.urfu.ru/handle/10995/104751Test
https://elibrary.ru/item.asp?id=46654757Test

المؤلفون: Belskaya, N. P., Lugovik, K. I., Ivina, A. D., Bakulev, V. A., Fan, Z. J.

المصدر: ChemInform ; volume 46, issue 9 ; ISSN 0931-7597 1522-2667

الإتاحة: https://doi.org/10.1002/chin.201509031Test

المؤلفون: Gavlik, К. D., Belskaya, N. P., Гавлик, К. Д., Бельская, Н. П.

وصف الملف: application/pdf

العلاقة: Химия в федеральных университетах. — Екатеринбург, 2013.; Гавлик К. Д. Синтез 2,3-дигидро-1,2,4-триазинов / К. Д. Гавлик, Н. П. Бельская // Химия в федеральных университетах : материалы докладов конф. — Екатеринбург, 2013. — С. 49-53.; http://elar.urfu.ru/handle/10995/20488Test

الإتاحة: http://elar.urfu.ru/handle/10995/20488Test

المؤلفون: Barykin, N. V., Belskaya, N. P., Барыкин, Н. В., Бельская, Н. П.

وصف الملف: application/pdf

العلاقة: Химия в федеральных университетах. — Екатеринбург, 2013.; Барыкин Н. В. Синтез и свойства бис(гидразонотиоамидов) / Н. В. Барыкин, Н. П. Бельская // Химия в федеральных университетах : материалы докладов конф. — Екатеринбург, 2013. — С. 25-28.; http://elar.urfu.ru/handle/10995/20476Test

الإتاحة: http://elar.urfu.ru/handle/10995/20476Test

المؤلفون: Lugovik, К. I., Belskaya, N. P., Луговик, К. И., Бельская, Н. П.

وصف الملف: application/pdf

العلاقة: Химия в федеральных университетах. — Екатеринбург, 2013.; Луговик К. И. Синтез и окислительная циклизация арилминопропентиоамидов / К. И. Луговик, Н. П. Бельская // Химия в федеральных университетах : материалы докладов конф. — Екатеринбург, 2013. — С. 101-103.; http://elar.urfu.ru/handle/10995/20456Test

الإتاحة: http://elar.urfu.ru/handle/10995/20456Test