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1

Tadić, Živorad D., Bratislav Ž. Jovanovic, and Dušan G. Antonović. "The thermal dealkylation of 2-chloro-4,6-bis(bornyl- and norbornylamino)-s-triazines." Collection of Czechoslovak Chemical Communications 55, no. 1 (1990): 256–60. http://dx.doi.org/10.1135/cccc19900256.

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The thermal dealkylation of 2-chloro-4,6-bis(isobornylamino)-s-triazine (I), 2-chloro-4,6-bis(bornylamino)-s-triazine (II), 2-chloro-4,6-bis(exo-norbornylamino)-s-triazine (III) and 2-chloro-4,6-bis(endo-norbornylamino)-s-triazine (IV) was performed at 250 °C. The high degree of dealkylation in the case of isobornyl derivative I was ascribed to a reaction via a seven-membered cyclic transition state, as well as to steric interaction of the dimethylmethylene group and the triazine ring. The presence of tricyclenes in the dealkylation products of this derivative also indicates that the reaction
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2

Liang, Xiao Qin, Yan Zheng, Bi Qin Wang, and Xue Mei Pu. "Theoretical Studies on Structures and Properties of Pentazine,1,2,4,5-Tetrazine and s-Triazine Derivatives with Nitrogen - Containing Substitutents." Applied Mechanics and Materials 395-396 (September 2013): 104–15. http://dx.doi.org/10.4028/www.scientific.net/amm.395-396.104.

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B3LYP /aug-cc-pvdz level of theory, combined with NBO and G3 methods, is applied to study substituent effects on the geometries, bond dissociation energies and high energetic density material properties of 27 kinds of derivatives designed by substituted hydrogen atoms of pentazine, 1,2,4,5-tetrazine and s-triazine, of which the hydrogen atoms are substituted by CN, -NO2, -NH2, -N3, -N2H, -NHNH2, -N4H and-N4H3groups. The relatively small heats of formation are observed for the derivatives substituted by-NH2, -H, -NO2and-NHNH2. The order of heats of formation for the derivatives containing the s
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3

Mackay, Simon P., and Patrick J. O' Malley. "Molecular Modelling of the Interactions between Optically Active Triazine Herbicides and Photosystem II." Zeitschrift für Naturforschung C 48, no. 5-6 (1993): 474–81. http://dx.doi.org/10.1515/znc-1993-5-612.

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Abstract The QB binding site of photosystem II in green plants displays stereoselectivity for the (S′) stereoisomer of the α-methylbenzyl derivative of atrazine but not for derivatives with smaller substituents such as sec-butyl. We have shown that interactive models reflect the experimental data by determining the intermolecular energies between the D1 protein binding region (resi­dues Leu 210 to Val 280) and the triazine analogs. The intermolecular energy was calculated by van der Waals and electrostatic interactions after energy minimization of the combined structures to reduce inter and in
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4

Vora, J. J., S. B. Vasava, Asha D. Patel, K. C. Parmar, S. K. Chauhan, and S. S. Sharma. "Synthesis, Characterization and Antibacterial Activity of a New Series of s-Triazines Derived with Quinolines." E-Journal of Chemistry 6, no. 1 (2009): 201–6. http://dx.doi.org/10.1155/2009/812341.

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8-Hydroxy quinoline was synthesized using Skraup reaction. This was condensed with trichloro-s-triazine. The product of the above reaction was allowed to react with triazole derivative. Finally, urea derivatives were allowed to react and the products were characterized by conventional and instrumental methods. Their structures were determined and important biochemical properties were studied
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5

Ceyhan, Tanju, Mustafa Korkmaz, Mehmet K. Erbil, and Özer Bekaroğlu. "Synthesis, characterization and ESR spectroscopy of novel s-triazine bearing three oxygen-linked lutetium bisphthalocyanine sandwich complexes." Journal of Porphyrins and Phthalocyanines 09, no. 06 (2005): 423–29. http://dx.doi.org/10.1142/s1088424605000526.

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The conversion of compound 1 [2,4,6-tris(2-oxaphthalonitrile)-s-triazine] into its isoindoline derivative of 2,4,6-tris[2-oxa(1,3-hexaimino isoindoline)]-s-triazine 2 was accomplished by bubbling ammonia gas through a solution in methanol in the presence of sodium methoxide. The cyclization of two different isoindoline derivatives namely, compound 2 and 4,5-bis(hexylthio)-1,2-diimino-isoindoline 3 with lutetium(III) acetate, [ Lu ( OAc )3] in refluxed DMF by the method of statistically mixed condensation gave trimeric trilutetium phthalocyanine [( LuOAc )3( Pc )3]4. [ Lu 3( Pc )6]5 has been sy
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6

He, Zhan Rong, Zi Ran Chen, and You Hui Xu. "Second-Order Non-Linear Optical Properties of Y-Type S-Triazine Based Derivatives." Advanced Materials Research 683 (April 2013): 110–15. http://dx.doi.org/10.4028/www.scientific.net/amr.683.110.

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Six modules (Y1~Y6) containing Y-type s-triazine based derivatives were optimized using density functional theory at B3LYP/6-31+G* level. On the basis of the optimized structure, electronic absorption spectrum was calculated with TD-DFT(TDB3LYP/6-31+G*) and the second-order nonlinear optical properties (NLO) were calculated with finite field (FF) method and coded programs. The results indicated that these molecules had good nonlinear optical properties with 106 order of magnitude a.u. (10-27 esu) of 0 value. Introducing different electron groups to the end of the tri-branched chain of this de
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7

Zhao, Ming-Zhe, Cai Tie, Yi-Wei Zhang, et al. "Deuterated hydrazino-s-triazine as highly-efficient labelling reagent for glycan relative quantification analysis using electrospray ionization mass spectrometry." RSC Advances 5, no. 97 (2015): 79317–22. http://dx.doi.org/10.1039/c5ra12005e.

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An innovative stable-isotope relative quantification strategy for N-glycans was achieved using self-designed non-reductive hydrazino-s-triazine deuterated derivative as labelling reagent combined with mass spectrometry.
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8

Atta, Ayman M., Mona A. Ahmed, Hamad A. Al-Lohedan, and Ayman El-Faham. "Multi-Functional Cardanol Triazine Schiff Base Polyimine Additives for Self-Healing and Super-Hydrophobic Epoxy of Steel Coating." Coatings 10, no. 4 (2020): 327. http://dx.doi.org/10.3390/coatings10040327.

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The designing of multifunctional materials in system-level efficiency is one of the main targets and a hot topic for the application of novel green or bio-based materials and structures. In this work, the chemical structure of bio-based cardanol that was derived from cashew oil was modified through a reaction with a bishydrazino-s-triazine derivative followed by condensation polymerization or reaction with terephthaldehyde to obtain a Schiff base polymer. The chemical structures of the modified cardanol-bishydrazino-s-triazine-based monomer and the Schiff base polymer were confirmed from FTIR
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9

Dona, Rahma, Rahmi Asrina Rizki, Jasril, Neni Frimayanti, and Rudi Hendra. "Molecular docking studies of novel s-triazine derivatives incorporating amino methoxy chalcone for EGFR inhibitor in breast cancer." Pharmacy Education 24, no. 2 (2024): 172–78. http://dx.doi.org/10.46542/pe.2024.242.172178.

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Background: The Epidermal growth factor receptor (EGFR) receptor is involved in both apoptosis and angiogenesis. An upregulation of EGFR activity can potentially expedite the proliferation of malignant cells. Anticancer activity is among the many pharmacological activities of s-triazine derivative compounds. The potential of amino chalcone derivatives as anticancer agents has been documented. The anticipated outcome is that the derivatives of these two compounds will enhance their efficacy as antiproliferative agents. Objective: Through molecular docking, this study aimed to assess the potenti
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10

Diao, Li Xiao, Yue Zhi Cui, Xiang Jian Meng, and Xing Wu Liu. "The Two-Photon Excited Fluorescence of Pyrazine Derivatives." Advanced Materials Research 535-537 (June 2012): 1266–69. http://dx.doi.org/10.4028/www.scientific.net/amr.535-537.1266.

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A series of multi-branched pyrazine derivatives have been synthesized, of which, the two-branched one with para-branching pattern shows much enhanced two-photon absorption cross section (σ) than that with meta-branching pattern (1.8 times). The three-branched pyrazine derivative, in which the branches are at ortho- or para-position, show strong two-photon absorption properties (σ=753GM), while its s-triazine analogue TSTA, with all the branches in meta-position, exhibit too weak two-photon excited fluorescence to be detected. These results indicate great effects of branching pattern on two-pho
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11

Cesarini, Silvia, Ilaria Vicenti, Federica Poggialini, et al. "Privileged Scaffold Decoration for the Identification of the First Trisubstituted Triazine with Anti-SARS-CoV-2 Activity." Molecules 27, no. 24 (2022): 8829. http://dx.doi.org/10.3390/molecules27248829.

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Current therapy against severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) are based on the use of Remdesivir 1, Molnupiravir 2, and the recently identified Nirmatrelvir 3. Unfortunately, these three drugs showed some limitations regarding potency and possible drug–drug interactions. A series of derivatives coming from a decoration approach of the privileged scaffold s-triazines were synthesized and evaluated against SAR-CoV-2. One derivative emerged as the hit of the series for its micromolar antiviral activity and low cytotoxicity. Mode of action and pharmacokinetic in vitro p
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12

Karthik, R., P. Muthukrishnan, A. Elangovan, M. M. Srividhya, B. Jeyaprabha, and P. Prakash. "Adsorption and corrosion inhibiting behavior of a new S-triazine derivative." Protection of Metals and Physical Chemistry of Surfaces 51, no. 4 (2015): 667–79. http://dx.doi.org/10.1134/s2070205115040152.

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13

Othman, Muhammad Bisyrul Hafi, Zulkifli Ahmad, Hasnah Osman, Mohd Firdaus Omar, and Hazizan Md Akil. "Thermal degradation behavior of a flame retardant melamine derivative hyperbranched polyimide with different terminal groups." RSC Advances 5, no. 112 (2015): 92664–76. http://dx.doi.org/10.1039/c5ra12923k.

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The non-isothermal kinetic degradation behaviour of hyperbranched polyimide series containing s-triazine rings has been contributed by an effects of different terminal groups. The solid state mechanism proposed is one-dimensional diffusions.
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14

Mikulová, Mária Bodnár, Dáša Kružlicová, Daniel Pecher, Claudiu T. Supuran, and Peter Mikuš. "Synthetic Strategies and Computational Inhibition Activity Study for Triazinyl-Substituted Benzenesulfonamide Conjugates with Polar and Hydrophobic Amino Acids as Inhibitors of Carbonic Anhydrases." International Journal of Molecular Sciences 21, no. 10 (2020): 3661. http://dx.doi.org/10.3390/ijms21103661.

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Various sulfonamide derivatives are intensively studied as anticancer agents owing to their inhibitory activity against human tumor-associated carbonic anhydrase isoforms. In this work, different synthetic procedures for the series of 1,3,5-triazinyl-aminobenzenesulfonamide conjugates with amino acids, possessing polar uncharged, negatively charged, and hydrophobic side chain, were studied and optimized with respect to the yield/purity of the synthesis/product as well as the time of synthetic reaction. These procedures were compared to each other via characteristic HPLC-ESI-DAD/QTOF/MS analyti
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15

Takahashi, M., T. Kayo, T. Karakida, et al. "Potent and selective aromatase inhibitor:in vitroandin vivostudies with s-triazine derivative sef19." Endocrine Research 23, no. 1-2 (1997): 1–13. http://dx.doi.org/10.1080/07435809709031838.

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16

Xiong, Li Ping, Zhong Yi He, Jun Xiao Wang, Liang Qian, and Sheng Han. "Tribological Property of a Triazine Derivative in Rapeseed Oil." Advanced Materials Research 284-286 (July 2011): 293–96. http://dx.doi.org/10.4028/www.scientific.net/amr.284-286.293.

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2-propylamino-4,6-(O,O’-dibuthyldithiophosphate)-s-1,3,5-triazine(DPOB)was synthesized and it’s tribological behavior as lubricant in rapeseed oil (RSO) were evaluated using a four-ball tester. The lubrication mechanism was investigated by X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The results indicate that the compound possess excellent load-carrying capacity and antiwear ability, and has some friction-reducing property only under the low load condition. Based on the results of XPS and SEM analysis, it can be seen that tribochemical reaction occurred betwee
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17

Rybakova, A., D. Kim, and N. Stolpovskaya. "Synthesis and structure of new 4-amino-1,3,5-triazine-2-thione S-derivatives and their study by 1H, 13C NMR and chromatography-mass spectrometry." Bulletin of the South Ural State University series "Chemistry" 16, no. 1 (2024): 93–107. http://dx.doi.org/10.14529/chem240107.

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4-Amino-1,3,5-triazine-2-thione 1 interacts with allyl bromide, 2-methyl-3-chloro-1-propene, 2,3-dibromopropene-1, prenyl bromide in DMFA/K2CO3 and with cinnamyl chloride, butenyl bromide in DMFA/NaOH to form 4-allylsulfanyl- 2, 4-(2-methylpropene-2-yl)sulfanyl- 3, 4-(2-bromopropene-2-yl)sulfanyl- 4, 4-(2-methylbutene-2-yl)sulfanyl- 5, 4-cinnamylsulfanyl- 6 and 4-(butene-1-yl)sulfanyl-1,3,5-triazine-2-amines 7, respectively. The structure of compounds 2–7 was studied by 1H NMR, as well as of compounds 5 and 7, in their case including 13C NMR; allyl sulfide 2, prenyl sulfide 5 and butenyl sulfi
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18

Yao, Tianfu, Peixuan Sun, and Wenjin Zhao. "Triazine Herbicides Risk Management Strategies on Environmental and Human Health Aspects Using In-Silico Methods." International Journal of Molecular Sciences 24, no. 6 (2023): 5691. http://dx.doi.org/10.3390/ijms24065691.

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As an effective herbicide, 1, 3, 5-Triazine herbicides (S-THs) are used widely in the pesticide market. However, due to their chemical properties, S-THs severely threaten the environment and human health (e.g., human lung cytotoxicity). In this study, molecular docking, Analytic Hierarchy Process—Technique for Order Preference by Similarity to the Ideal Solution (AHP-TOPSIS), and a three-dimensional quantitative structure-active relationship (3D-QSAR) model were used to design S-TH substitutes with high herbicidal functionality, high microbial degradability, and low human lung cytotoxicity. We
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19

Cui, Yue-zhi, Qi Fang, Zhen-li Huang, Gang Xue, Wen-tao Yu та Hong Lei. "Synthesis, structure, and intense second harmonic generation of Λ-shaped s-triazine derivative". Optical Materials 27, № 10 (2005): 1571–75. http://dx.doi.org/10.1016/j.optmat.2004.12.009.

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20

Dennis, Matthew L., Lygie Esquirol, Tom Nebl, Janet Newman, Colin Scott, and Thomas S. Peat. "The evolving story of AtzT, a periplasmic binding protein." Acta Crystallographica Section D Structural Biology 75, no. 11 (2019): 995–1002. http://dx.doi.org/10.1107/s2059798319013883.

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Atrazine is an s-triazine-based herbicide that is used in many countries around the world in many millions of tons per year. A small number of organisms, such as Pseudomonas sp. strain ADP, have evolved to use this modified s-triazine as a food source, and the various genes required to metabolize atrazine can be found on a single plasmid. The atomic structures of seven of the eight proteins involved in the breakdown of atrazine by Pseudomonas sp. strain ADP have been determined by X-ray crystallography, but the structures of the proteins required by the cell to import atrazine for use as an en
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21

Barakat, Assem, Saied M. Soliman, Ayman El-Faham, et al. "Three Multi-Components Reaction: Synthesis and X-Ray Single-Crystal of Hydroacridinone-Based Hydrazino-S-Triazine Derivative as a New Class of Urease Inhibitor." Crystals 10, no. 1 (2019): 14. http://dx.doi.org/10.3390/cryst10010014.

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The one-pot fashion of three multi-component reaction provides the desired hydroacridinone-based hydrazino-s-triazine scaffold 4. Compound 4 was crystallized in an orthorhombic crystal system and Pbca space group with a = 11.6271(2) Å, b = 18.2018(4) Å, c = 32.4721(6) Å, and α = β = γ = 90° with one formula unit per asymmetric unit and eight molecules per unit cell. Additionally, structural features, Hirshfeld surfaces, and DFT studies were also investigated. Its packing in the crystal is controlled by H…H (63.4%), O…H (12.7%), Cl…H (7.2%), N…H (4.7%), and C…H (10.2%) contacts, where the O…H a
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22

Wang, Lei, Shijing Yan, Lei Zhang, Yuliang Mai, Weihao Li, and Hao Pang. "An Acid-/Base-Degradable Epoxy Resin Cured by 1,3,5-Triacroylamino-hexahydro-s-triazine Derivative." Macromolecular Research 29, no. 7 (2021): 462–69. http://dx.doi.org/10.1007/s13233-021-9060-1.

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23

Motaleb, Mohamed A., Ismail T. Ibrahim, Mona O. Sarhan, and Wafaa A. Zaghary. "Radioiodination and biological distribution of a new s -triazine derivative for tumor uptake evaluation." Journal of Labelled Compounds and Radiopharmaceuticals 61, no. 14 (2018): 1058–68. http://dx.doi.org/10.1002/jlcr.3682.

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24

Ibrahim, Ahmad, Bandar El Fouhaili, Aurélie Chan Yong, Christian Ley, Xavier Allonas, and Christiane Carré. "Optimization of a Safranine O three-component photoinitiating system for use in holographic recording." Canadian Journal of Chemistry 93, no. 12 (2015): 1345–53. http://dx.doi.org/10.1139/cjc-2014-0606.

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The coupling between a holographic resin, combining multiple monomers and additives, with photoinitiating systems (PIS) is not straightforward. In this paper, a classic PIS based on Safranine O (SFH+) as dye, an amine (ethyl-4-(dimethylamino)benzoate) as electron donor, and a triazine derivative (2-(4-methoxyphenyl)-4,6-bis(trichloromethyl)-1,3,5-triazine) as electron acceptor for holographic recording was studied using time-resolved spectroscopic experiments. By taking into account the viscosity of the matrix, a method to evaluate the overall quantum yield of radicals released is proposed and
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25

Al-Khodir, Fatima A. I., Hana M. A. Abumelha, Tarfah Al-Warhi, and S. A. Al-Issa. "New Platinum(IV) and Palladium(II) Transition Metal Complexes of s-Triazine Derivative: Synthesis, Spectral, and Anticancer Agents Studies." BioMed Research International 2019 (February 17, 2019): 1–14. http://dx.doi.org/10.1155/2019/9835745.

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New Pd(II) and Pt(IV) triazine complexes [Pt3(L1)2(Cl)9(H2O)3].3Cl.3H2O (1), [Pt3(L2)2(Cl)9(H2O)3].3Cl (2), [Pt3(L3)2(Cl)9(H2O)3].3Cl (3), [Pt2(L4)2(Cl)6(H2O)2] .2Cl.4H2O (4), [Pd3(L1)2(H2O)6] .3Cl2(5), [Pd3(L2)2(H2O)6].3Cl2(6), [Pd3(L3)2(H2O)6].3Cl2(7), and [Pd2(L4)2(H2O)4].2Cl2(8) were synthesized and well characterized using elemental analyses, molar conductance, IR, UV-Vis, magnetic susceptibility,1H,13C-NMR spectra, and thermal analyses. These analyses deduced that theL1,L2,andL3ligands act as tridentate forming octahedral geometry with Pt(IV) metal ions and square planar geometry in case
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26

Yamada, Yoichi, Heinosuke Yasuda, and Kazue Yoshizawa. "A Simple Synthesis of 1-Substituted 5-Aminopyrazoles and Pyrazolo[1,5-a]-s-triazine Derivative." HETEROCYCLES 48, no. 10 (1998): 2095. http://dx.doi.org/10.3987/com-98-8262.

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27

Liu, Tianye, Hongxia Yan, Zhengyan Chen, Peilun Xu, and Shikun Su. "A Derivative of s-Triazine Modified Reduced Graphene Oxide with the Function of UV-absorbing." Chinese Journal of Chemistry 34, no. 1 (2015): 123–28. http://dx.doi.org/10.1002/cjoc.201500506.

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28

Dai, Qiuzi, Qinsheng Sun, Xiaorong Ouyang, et al. "Antitumor Activity of s-Triazine Derivatives: A Systematic Review." Molecules 28, no. 11 (2023): 4278. http://dx.doi.org/10.3390/molecules28114278.

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1,3,5-triazine derivatives, also called s-triazines, are a series of containing-nitrogen heterocyclic compounds that play an important role in anticancer drug design and development. To date, three s-triazine derivatives, including altretamine, gedatolisib, and enasidenib, have already been approved for refractory ovarian cancer, metastatic breast cancer, and leukemia therapy, respectively, demonstrating that the s-triazine core is a useful scaffold for the discovery of novel anticancer drugs. In this review, we mainly focus on s-triazines targeting topoisomerases, tyrosine kinases, phosphoino
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29

Jain, Sonika, Pankaj Kumar Jain, Shalu Sain, Dharma Kishore, and Jaya Dwivedi. "Anticancer s-Triazine Derivatives: A Synthetic Attribute." Mini-Reviews in Organic Chemistry 17, no. 8 (2020): 904–21. http://dx.doi.org/10.2174/1570193x17666200131111851.

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1, 3, 5-Triazine (s-Triazine) is a versatile nucleus to design and develop potent bioactive molecules for drug discovery, particularly in cancer therapy. The aim of this review is to present the most recent trends in the field of synthetic strategies made for functionalized triazine derivatives active against cell proliferation. This review article covers the synthesis of aryl methylamino, morpholino, triamino substituted triazines, antimitotic agents coupled triazines and many more. Many 1,3,5- triazine derivatives, both hetero-fused and uncondensed, have shown remarkable antitumor activities
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30

Shanmugakala, R., P. Tharmaraj, C. D. Sheela, and N. Chidambaranathan. "Transition metal complexes of s-triazine derivative: new class of anticonvulsant, anti-inflammatory, and neuroprotective agents." Medicinal Chemistry Research 23, no. 1 (2013): 329–42. http://dx.doi.org/10.1007/s00044-013-0634-0.

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31

Darwish, Elham S. "Facile Synthesis and Antimicrobial Evaluation of Some New Heterocyclic Compounds Incorporating a Biologically Active Sulfamoyl Moiety." Scientific World Journal 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/165495.

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A facile and convenient synthesis of new heterocyclic compounds containing a sulfamoyl moiety suitable for use as antimicrobial agents was reported. The precursor 3-oxo-3-phenyl-N-(4-sulfamoylphenyl)propionamide was coupled smoothly with arenediazonium salt producing hydrazones which reacted with malononitrile or triethylorthoformate affording pyridazine and triazine derivatives, respectively. Also, the reactivity of the same precursor with DMF-DMA was followed by aminotriazole; aromatic aldehydes was followed by hydrazine hydrate, triethylorthoformate, or thiourea affording triazolo[1,5-a]pyr
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32

Schuster, David I., Joel Rosenthal, Shaun MacMahon, Peter D. Jarowski, Christopher A. Alabi, and Dirk M. Guldi. "Formation and photophysics of a stable concave–convex supramolecular complex of C60and a substituted s-triazine derivative." Chem. Commun., no. 21 (2002): 2538–39. http://dx.doi.org/10.1039/b207661f.

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33

YAMADA, Y., H. YASUDA, and K. YOSHIZAWA. "ChemInform Abstract: A Simple Synthesis of 1-Substituted 5-Aminopyrazoles and Pyrazolo[1,5-a]-s-triazine Derivative." ChemInform 30, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199907140.

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34

Akpe, Victor, Timothy J. Biddle, Christian Madu, Christopher L. Brown, Tak H. Kim, and Ian E. Cock. "A Computational Comparative Study for the Spectroscopic Evaluation of Triazine Derivative Dyes in Implicit Solvation Model Systems Using Semi-Empirical and Time-Dependent Density Functional Theory Approaches." Australian Journal of Chemistry 74, no. 12 (2021): 856. http://dx.doi.org/10.1071/ch21196.

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The spectroscopic data for a range of cyclopenta-[d][1,2,3]-triazine derivative dyes have been evaluated using various standard computational approaches. Absorption data of these dyes were obtained using the ZINDO/S semi-empirical model for vertical excitation energies of structures optimised with the AM1, PM3, and PM6 methods. These studies were conducted under vacuum and solution states using the polarisation continuum model (PCM) for implicit solvation in the linear response model. The accuracy, along with the modest computational costs of using the ZINDO/S prediction, combined with the PM3
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35

Allahverdiyeva, G. E., V. M. Ismailov, I. A. Mamedov, and N. N. Yusubov. "Reactions of triethyl phosphonoacetate, bromoacetaldehyde diethyl acetal, and (diethoxyphosphoryl)acetaldehyde with thiourea and (thio)semicarbazide." Журнал общей химии 93, no. 5 (2023): 711–16. http://dx.doi.org/10.31857/s0044460x23050062.

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Condensation of thiocarbamide with triethyl phosphonoacetate leads to S -phosphorylated 2-ethoxy-4-oxo3,4,5-trihydro-1,5,2-diazaphosphinine-2-oxide, an isostere of thiobarbiturate. Under similar conditions, triethyl phosphonoacetate reacts with semicarbazide with the intermediate formation of 2-(diethoxyphosphorylacetyl) hydrazine-1-carboxamide, which forms a triazine upon cleavage of the P-C bond and 1,2,3-phosphadiazole upon cleavage of the C-N bond. Under analogous conditions, the condensation of triethyl phosphonoacetate with thiosemicarbazide proceeds with cleavage of the Р-С bond and het
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36

Khattab, Sara M., Mezna Saleh Altowyan, Ayman El-Faham, et al. "A New Bromo-Mn(II) Complex with 1,3,5-Triazine Derivative: Synthesis, Crystal Structure, DFT and Biological Studies." Inorganics 12, no. 11 (2024): 284. http://dx.doi.org/10.3390/inorganics12110284.

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The crystal structure and topology analyses of a new bromo-Mn(II) complex with 2,4-bis(3,5dimethyl-1H-pyrazol-1-yl)-6-methoxy-1,3,5-triazine (MBPT) were reported. Its structure was confirmed using single-crystal X-ray diffraction to create the formula [Mn(MBPT)Br(H2O)2]ClO4. Its crystal system was monoclinic and its space group was p21. The Mn(II) was coordinated with MBPT as a NNN-pincer ligand, with one bromide ion in the equatorial plane. The two axial terminals were occupied by two trans water molecules. H…H, N…H, Br…H, C…H and O…H were the predominant intermolecular contacts, while Br…H,
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37

Dahlous, Kholood, Zainab Almarhoon, Ahmed-Yacine Badjah-Hadj-Ahmed, Zeid AL Othman, and Ayman El-Faham. "Microwave Irradiation Assists the Synthesis of a Novel Series of bis-Arm s-Triazine Oxy-Schiff Base and Oxybenzylidene Barbiturate Derivatives." Molecules 23, no. 11 (2018): 2976. http://dx.doi.org/10.3390/molecules23112976.

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A novel series of s-triazines incorporating 4-hydroxybenzaldehyde and 4-hydroxy-3-methoxybenzaldehyde was prepared and fully characterized. The reaction was carried out via stepwise nucleophilic aromatic substitution of chlorine atoms in cyanuric chloride. The first chlorine was substituted by different amines (morpholine, piperidine, or diethylamine) to afford 2,4-dichloro-6-substituted-1,3,5-triazine. The second and third chlorines were substituted by benzaldehyde derivatives in the presence of Na2CO3 as a HCl scavenger to afford the target products: s-triazine oxyaldehyde derivatives (dipod
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38

Meng, Qi, Gui Yong Wu, Ying Shao, and Xiao Qiang Sun. "Convenient Synthesis and Characterization of Star-Shaped Dendrimers: 2,4,6-Trisubstituted 1,3,5-Triazine Derivatives." Advanced Materials Research 396-398 (November 2011): 2476–84. http://dx.doi.org/10.4028/www.scientific.net/amr.396-398.2476.

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A serial of novel star-shaped 2,4,6-trisubstituted 1,3,5-triazine (s-triazine) dendrimers were synthesized via step-by-step nucleophilic substitution starting from 2,4,6-trichloro-1,3,5-triazine, and were characterized by1H,13C NMR, FT-IR and ESI-MS spectra. The crystal structures for 2b, 2d and 4c have been determined by X-ray diffraction analysis, which indicate that there are hydrogen bonding and short contact interactions existing in intermolecules result in forming three-dimensional network architecture. D NMR experiments demonstrate that symmetrical trialkylamino-s-triazine shows correla
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39

DESAI, K. R., and B. D. MISTRY. "ChemInform Abstract: Synthesis and Antimicrobial Activity of 2-(4′-(4′′-Acetamidophenyl) thiazol-2′-ylamino)-4-(4′-methoxyphenylamino)-6-(arylureido)-s- triazine and 2-(4′-(4′′-Acetamidophenyl)thiazol-2′-ylamino)-4,6-bis( arylureido)-s-triazine Derivative." ChemInform 26, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.199522207.

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40

PREJMEREANU, I., N. CARP, M. VASILESCU, L. FLORU та I. SEBE. "ChemInform Abstract: Study of Some Triazin-Δ2-Pyrazolines by Derivative Absorption and Emission Spectrophotometry. Part 2. Effects of the Substituents of the s-Triazine Cycle upon UV Absorption." ChemInform 29, № 11 (2010): no. http://dx.doi.org/10.1002/chin.199811032.

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41

Yamashita, Katsumi, Akemi Yasukawa, and Hideo Sawada. "Fabrication of Cotton Fabric with Superoleophilic/Superhydrophobic Characteristic on the Modified Surface by Using Fluoroalkylated Oligomeric Silica/Triazine Derivative Nanocomposites." Coatings 10, no. 2 (2020): 174. http://dx.doi.org/10.3390/coatings10020174.

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Two fluoroalkylated vinyltrimethoxysilane oligomer (RF-(CH2CHSi(OMe)3)n-RF; n = 2, 3; RF = CF(CF3)OC3F7:RF-VMSi) in methanol reacted with aqueous sodium carbonate solution containing 2-hydroxy-4,6-dichloro-1,3,5-triazine sodium salt (TAZ) to provide two fluoroalkylated oligomeric silica/TAZ nanocomposites (RF-VMSiO2/TAZ). The original cotton fabric gives an oleophilic/hydrophilic property on its surface; however, modified cotton fabric surface with RF-VMSiO2/TAZ composites was demonstrated to provide highly oleophobic/superhydrophobic property on the surface. We can observe a remarkable time-d
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42

Bacchi, Cyrus J., Marcus Vargas, Donna Rattendi, Burt Goldberg, and Weicheng Zhou. "Antitrypanosomal Activity of a New Triazine Derivative, SIPI 1029, In Vitro and in Model Infections." Antimicrobial Agents and Chemotherapy 42, no. 10 (1998): 2718–21. http://dx.doi.org/10.1128/aac.42.10.2718.

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ABSTRACT A recently developed diaminotriazine derivative [O,O′-bis(1,2-dihydro-2,2-tetramethylene-4,6-diamino-S-triazin-1-yl)-1,6-hexanediol dihydrochloride; T-46; SIPI 1029] was examined for activity against African trypanosomes in in vitro and in vivo model systems. In vitro, SIPI 1029 was 50% inhibitory for growth of bloodstream trypomastigotes of four strains of Trypanosoma brucei brucei and Trypanosoma brucei rhodesiense at 0.15 to 2.15 nM (50% inhibitory concentrations). In in vivo mouse laboratory models of T. b. rhodesiense clinical isolate infections, SIPI 1029 was curative for 12 of
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43

Schwarzer, Anke, and Edwin Kroke. "5,8-Bis[bis(pyridin-2-yl)amino]-1,3,4,6,7,9,9b-heptaazaphenalen-2(1H)-one dimethyl sulfoxide monosolvate dihydrate." Acta Crystallographica Section E Structure Reports Online 70, no. 4 (2014): o456—o457. http://dx.doi.org/10.1107/s1600536814005698.

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In the asymmetric unit of the title compound, C26H17N13O·C2H6OS·2H2O, there is one independent heptazine-based main molecule, one dimethyl sulfoxide molecule and two water molecules as solvents. The tri-s-triazine unit is substituted with two dipyridyl amine moieties and a carbonylic O atom. As indicated by the bond lengths in this acid unit of the heptazine derivative [C=O = 1.213 (2) Å, while the adjacent C—N(H) bond = 1.405 (2) Å] it is best described by the keto form. The cyameluric nucleus is close to planar (r.m.s. deviation = 0.061 Å) and the pyridine rings are inclined to its mean plan
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44

L., M. Patel, H. Chikhalia K., and S. Desai P. "Synthesis of substituted s-triazine derivatives and studies of their antimicrobial activities." Journal of Indian Chemical Society Vol. 82, Jan 2005 (2005): 83–85. https://doi.org/10.5281/zenodo.5824391.

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Department of Chemistry, B. K. M. Science College, Valsad-396 001, India <em>Manuscript received 7 July 2003, revised /6 June 2004, accepted 3 August 2004</em> Some new s-triazine derivatives have been synthesised. These compounds act as anti-bacterial, fungal and tubercular agents.
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45

P., S. DESAl, and R. DESAl K. "Synthesis of Benzothiazolyl-s-triazine Derivatives and their Antimicrobial Activity." Journal of Indian Chemical Society Vol. 71, March 1994 (1994): 155–57. https://doi.org/10.5281/zenodo.5894044.

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Department of Chemistry, B. K. M. Science College, Valsad-396 007 Department of Chemistry, South Gujarat University, Surat-395 007 <em>Manuscript received 26 September 1991, revised 17 May 1993, accepted 15 June 1993</em> Synthesis of Benzothiazolyl-s-triazine Derivatives and their Antimicrobial Activity.
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46

Abd Alhameed, Rakia, Zainab Almarhoon, Essam N. Sholkamy, et al. "Novel 4,6-Disubstituted s-Triazin-2-yl Amino Acid Derivatives as Promising Antifungal Agents." Journal of Fungi 6, no. 4 (2020): 237. http://dx.doi.org/10.3390/jof6040237.

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A novel series of 4,6-disubstituted s-triazin-2-yl amino acid derivatives was prepared and characterized. Most of them showed antifungal activity against Candida albicans compared to clotrimazole (standard drug). Compounds bearing aniline derivatives, piperidine and glycine on the triazine core showed the highest inhibition zones at concentrations of 50, 100, 200, and 300 μg per disc. In addition, docking studies revealed that all the compounds accommodated well in the active site residues of N-myristoltransferase (NMT) and exhibited complementarity, which explains the observed antifungal acti
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47

Cai, Dong, Tai Li, Qian Xie, et al. "Synthesis, Characterization, and Biological Evaluation of Novel 7-Oxo-7H-thiazolo[3,2-b]-1,2,4-triazine-2-carboxylic Acid Derivatives." Molecules 25, no. 6 (2020): 1307. http://dx.doi.org/10.3390/molecules25061307.

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A series of novel 7-oxo-7H-thiazolo[3,2-b]-1,2,4-triazine-2-carboxylic acid derivatives was synthesized in good yields by a multi-step procedure that included the generation of the S-alkylated derivatives from 6-substituted arylmethyl-3-mercapto-1,2,4-triazin-5-ones with ethyl 2-chloroacetoacetate, intramolecular cyclization with microwave irradiation, hydrolysis and amidation. All of the target compounds were fully characterized through 1H-NMR, 13C-NMR and HRMS spectra. The intramolecular cyclization occurred regioselectively at the N2-position of 1,2,4-triazine ring, which was confirmed by c
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48

Al-Rasheed, Hessa H., Kholood A. Dahlous, Essam N. Sholkamy, Sameh M. Osman, Omar H. Abd-Elkader, and Ayman El-Faham. "Chitosan-S-triazinyl-bis(2-aminomethylpyridine) and Chitosan-S-triazinyl-bis(8-oxyquinoline) Derivatives: New Reagents for Silver Nanoparticle Preparation and Their Effect of Antimicrobial Evaluation." Journal of Chemistry 2020 (June 25, 2020): 1–8. http://dx.doi.org/10.1155/2020/9590120.

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Herein, we described the modification of chitosan with cyanuric chloride as a mediator for preparation of chitosan-s-triazinyl-bis(2-aminomethylpyridine) and chitosan-s-triazinyl-bis(8-oxyquinoline) derivatives to be used as reagents for preparation of silver nanoparticles under ecofriendly conditions. These two reagents are convenient and effective for reduction of silver ions to silver nanoparticles with particle size less than 10 nm that might be suitable for industrial and medicinal applications. The formation and particle size of AgNPs are characterized by transmission electron microscopy
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49

Patel, Rahul V., Premlata Kumari, and Kishor H. Chikhalia. "Fluorinated s-Triazinyl Piperazines as Antimicrobial Agents." Zeitschrift für Naturforschung C 66, no. 7-8 (2011): 345–52. http://dx.doi.org/10.1515/znc-2011-7-805.

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A series of 1,3,5-triazine derivatives that contain 4-amino-2-trifl uoromethyl-benzonitrile, 8-hydroxyquinoline, and different piperazines as substituents at the carbon atoms of the triazine ring have been synthesized by a simple and efficient synthetic protocol. The chemical structures of the compounds were elucidated with the aid of IR, 1H NMR and 13C NMR spectroscopy, and elemental analysis. The antimicrobial activity of the compounds was tested against seven bacteria (Staphylococcus aureus MTCC 96, Bacillus cereus MTCC 619, Escherichia coli MTCC 739, Pseudomonas aeruginosa MTCC 741, Klebsi
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50

Jevric, Lidija, Sanja Podunavac-Kuzmanovic, Strahinja Kovacevic, Natasa Kalajdzija, and Bratislav Jovanovic. "Estimation of the retention behaviour of s-triazine derivatives applying multiple regression analysis of selected molecular descriptors." Acta Periodica Technologica, no. 44 (2013): 229–37. http://dx.doi.org/10.2298/apt1344229j.

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The estimation of retention factors by correlation equations with physico-chemical properties can be of great helpl in chromatographic studies. The retention factors were experimentally measured by RP-HPTLC on impregnated silica gel with paraffin oil using two-component solvent systems. The relationships between solute retention and modifier concentration were described by Snyder?s linear equation. A quantitative structure-retention relationship was developed for a series of s-triazine compounds by the multiple linear regression (MLR) analysis. The MLR procedure was used to model the relations
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