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Journal articles on the topic 'Thiobarbiturate'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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1

Sams, R. A., W. W. Muir, R. L. Detra, and E. P. Robinson. "Comparative pharmacokinetics and anesthetic effects of methohexital, pentobarbital, thiamylal, and thiopental in Greyhound dogs and non-Greyhound, mixed-breed dogs." American Journal of Veterinary Research 46, no. 8 (1985): 1677–83. https://doi.org/10.2460/ajvr.1985.46.08.1677.

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SUMMARY Pharmacokinetics and duration of anesthesia of methohexital, pentobarbital, thiamylal, and thiopental in Greyhound and non-Greyhound, mixed-breed dogs were compared. In all dogs evaluated, pentobarbital induced the longest duration of anesthesia and methohexital induced the shortest duration. Pharmacokinetics of pentobarbital and methohexital were similar in both groups of dogs. Thiobarbiturates induced longer anesthetic effects in Greyhound dogs than in mixed-breed dogs. Plasma thiobarbiturate concentrations remained above normal longer in Greyhound dogs than in mixed-breed dogs. Disp

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2

Li, Chenming, Philipp Hilgeroth, Nazmul Hasan, Dieter Ströhl, Jörg Kressler, and Wolfgang H. Binder. "Comparing C2=O and C2=S Barbiturates: Different Hydrogen-Bonding Patterns of Thiobarbiturates in Solution and the Solid State." International Journal of Molecular Sciences 22, no. 23 (2021): 12679. http://dx.doi.org/10.3390/ijms222312679.

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Carbonyl-centered hydrogen bonds with various strength and geometries are often exploited in materials to embed dynamic and adaptive properties, with the use of thiocarbonyl groups as hydrogen-bonding acceptors remaining only scarcely investigated. We herein report a comparative study of C2=O and C2=S barbiturates in view of their differing hydrogen bonds, using the 5,5-disubstituted barbiturate B and the thiobarbiturate TB as model compounds. Owing to the different hydrogen-bonding strength and geometries of C2=O vs. C2=S, we postulate the formation of different hydrogen-bonding patterns in C

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3

Li, Chenming, Philipp Hilgeroth, Nazmul Hasan, Dieter Ströhl, Jörg Kressler, and Wolfgang H. Binder. "Comparing C2=O and C2=S Barbiturates: Different Hydrogen-Bonding Patterns of Thiobarbiturates in Solution and the Solid State." international Journal of Molecular Sciences 22, no. 23 (2021): 12679. https://doi.org/10.3390/ijms222312679.

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Abstract Carbonyl-centered hydrogen bonds with various strength and geometries are often exploited in materials to embed dynamic and adaptive properties, with the use of thiocarbonyl groups as hydrogen-bonding acceptors remaining only scarcely investigated. We herein report a comparative study of C2=O and C2=S barbiturates in view of their differing hydrogen bonds, using the 5,5-disubstituted barbiturate <strong>B</strong> and the thiobarbiturate <strong>TB</strong> as model compounds. Owing to the different hydrogen-bonding strength and geometries of C2=O vs. C2=S, we post

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4

Serrano, João L., Diana Lopes, Melani J. A. Reis, Renato E. F. Boto, Samuel Silvestre, and Paulo Almeida. "Bis-thiobarbiturates as Promising Xanthine Oxidase Inhibitors: Synthesis and Biological Evaluation." Biomedicines 9, no. 10 (2021): 1443. http://dx.doi.org/10.3390/biomedicines9101443.

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Xanthine oxidase (XO) is the enzyme responsible for the conversion of endogenous purines into uric acid. Therefore, this enzyme has been associated with pathological conditions caused by hyperuricemia, such as the disease commonly known as gout. Barbiturates and their congeners thiobarbiturates represent a class of heterocyclic drugs capable of influencing neurotransmission. However, in recent years a very large group of potential pharmaceutical and medicinal applications have been related to their structure. This great diversity of biological activities is directly linked to the enormous oppo

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5

Indutny, A. V., D. E. Bykov, and V. E. Vysokogorsky. "The level of free radical oxidation products in heart and blood plasma by diabetes mellitus with chronic alcohol intoxication." Biomeditsinskaya Khimiya 56, no. 2 (2010): 257–65. http://dx.doi.org/10.18097/pbmc20105602257.

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The research results of level glycemia, contents of free radical oxidation products (thiobarbiturate-reactive substances, oxidized-modified proteins) in blood plasma and heart of diabetes mellitus rats with chronic alcohol intoxication are presented. It is shown, that at presence of a diabetes mellitus the chronic alcohol consumption does not change blood plasma levels of the oxidized-modified proteins, thiobarbiturate-reactive substances and glucose. However the contents of thiobarbiturate-reactive substances and oxidizing modification of proteins products in animals heart is more considerabl

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6

Gomathi, Sundaramoorthy, Jeyaraman Selvaraj Nirmalram, and Packianathan Thomas Muthiah. "Hydrogen bonding patterns in salts of derivatives of aminopyrimidine and thiobarbituric acid." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 71, no. 2 (2015): 144–52. http://dx.doi.org/10.1107/s2052520615001729.

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Three salts, namely 2-amino-4,6-dimethylpyrimidin-1-ium thiobarbiturate trihydrate (I), 2-amino-4,6-dimethoxypyrimidin-1-ium thiobarbiturate dihydrate (II) and 2,4-diamino-5-(3′,4′,5′-trimethoxybenzyl)pyrimidin-1-ium thiobarbiturate (III), were synthesized and characterized by IR and X-ray diffraction techniques. The primary interaction between the acid and base happensviaN—H...O hydrogen bonds in (II) and (III), andviawater-mediated N—H...OWand OW—HW...S in (I). The water molecules present in compound (I) form a (H2O)12water clusterviawater–water interactions. In all three compounds (I)–(III)

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7

Moskalenko, Ivan V., Vladimir V. Shilovskikh, Pavel V. Nesterov, et al. "Supramolecular Assemblies of Melamine-2-Thiobarbiturate and Melamine-Barbiturate-2-Thiobarbiturate: Experimental and Theoretical Studies." Crystals 13, no. 9 (2023): 1302. http://dx.doi.org/10.3390/cryst13091302.

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In this work, we considered the formation of supramolecular assemblies of melamine-thiobarbiturate and melamine-barbiturate-thiobarbiturate. It is known that thiobarbituric acid can form many tautomers, as well as different motifs due to the change of C2=O to C2=S hydrogen bonds. We formed the crystal. The resulting crystals were studied with scanning electron microscopy (SEM), optical fluorescence microscopy, single crystal and powder (PXRD) X-ray diffraction analyses, and solid state nuclear magnetic resonance (ss NMR). These systems were theoretically studied using density functional theory

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8

Mandal, Piyali, Diptendu Patra, and Raja Shunmugam. "Hierarchical self-assembled nanostructures of lactone-derived thiobarbiturate homopolymers for stimuli-responsive delivery applications." Polymer Chemistry 11, no. 19 (2020): 3340–48. http://dx.doi.org/10.1039/d0py00367k.

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9

Robinson, E. P., R. A. Sams, and W. W. Muir. "Barbiturate anesthesia in Greyhound and mixed-breed dogs: Comparative cardiopulmonary effects, anesthetic effects, and recovery rates." American Journal of Veterinary Research 47, no. 10 (1986): 2105–12. https://doi.org/10.2460/ajvr.1986.47.10.2105.

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SUMMARY The cardiovascular effects, anesthetic effects, and recovery rates were evaluated in racing Greyhounds under barbiturate anesthesia. Greyhounds and mixed-breed dogs of similar body weights were given (by iv route) thiopental (15 mg/kg), thiamylal (15 mg/kg), methohexital (10 mg/kg), and pentobarbital (20 mg/kg). The anesthesia lasted longer in Greyhound than in non-Greyhound mixed-breed dogs given thiopental, thiamylal, and methohexital. The mean times from recumbency to standing were 3 to 4 times longer for Greyhounds anesthetized with thiobarbiturates than for non-Greyhound mixed-bre

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10

Kessel, David, and Alan Morgan. "PHOTOSENSITIZATION WITH A CHLORIN-THIOBARBITURATE CONJUGATE." Photochemistry and Photobiology 59, no. 5 (1994): 547–49. http://dx.doi.org/10.1111/j.1751-1097.1994.tb02981.x.

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11

Golovnev, N. N., M. S. Molokeev, and M. Yu Belash. "Crystal structure of potassium 2-thiobarbiturate." Journal of Structural Chemistry 54, no. 3 (2013): 566–70. http://dx.doi.org/10.1134/s0022476613030141.

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12

Heine, Jörn, Dirk Scheinichen, Karsten Jaeger, Andreas Emmendoerffer, and Martin Leuwer. "Inhibition of neutrophil respiratory burst and chemotaxis in vitro by thiopentone but not methohexitone." Neurosurgical Focus 2, no. 6 (1997): E3. http://dx.doi.org/10.3171/foc.1997.2.6.4.

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Administration of high-dose barbiturates may be used as an appropriate adjunctive treatment for control of intracranial pressure. The thiobarbiturate, thiopentone, has been reported to increase the rate of nosocomial pulmonary infection. This may be a substance-related effect of thiobarbiturates and it may be clinically important in barbiturate-sedated patients with severe head injury. Thus, the effects of the dose-response relationship of two commonly used barbiturates (thiopentone and methohexitone) on two vital aspects of neutrophil function were tested. We studied the production of superox

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13

Golovnev, N. N., and M. S. Molokeev. "Crystal structure of thallium(I) 2-thiobarbiturate." Russian Journal of Inorganic Chemistry 61, no. 4 (2016): 442–46. http://dx.doi.org/10.1134/s0036023616040100.

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14

Lenox, W. C., W. Mitzner, and C. A. Hirshman. "THIOBARBITURATE-INDUCED CONSTRICTION IN GUINEA PIG TRACHEAE." Anesthesiology 71, Supplement (1989): A1074. http://dx.doi.org/10.1097/00000542-198909001-01074.

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15

Pizov, Reuven, Robert H. Brown, Yuval S. Weiss, et al. "Wheezing during Induction of General Anesthesia in Patients with and without Asthma." Anesthesiology 82, no. 5 (1995): 1111–16. http://dx.doi.org/10.1097/00000542-199505000-00004.

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Background Patients with asthma who require general anesthesia and tracheal intubation are at increased risk for the development of bronchospasm during induction. The incidence of wheezing during induction with different intravenously administered agents is unknown. A randomized, double-blinded prospective study was undertaken to evaluate the incidence of wheezing in asymptomatic asthmatic and nonasthmatic patients receiving three commonly used intravenous anesthetic agents for induction of anesthesia. Methods Fifty-nine asymptomatic asthmatic and 96 nonasthmatic patients of ASA physical statu

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16

Jiménez, A., H. Jiménez, and J. Borrás. "2-Thiobarbiturate Copper Complexes: Preparation and Spectral Studies." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 17, no. 2 (1987): 159–71. http://dx.doi.org/10.1080/00945718708059421.

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17

Golovnev, N. N., and M. S. Molokeev. "Crystal structures of two barium 2-thiobarbiturate complexes." Journal of Structural Chemistry 55, no. 5 (2014): 871–78. http://dx.doi.org/10.1134/s0022476614050114.

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18

Hützler, Wilhelm Maximilian, Ernst Egert, and Michael Bolte. "One barbiturate and two solvated thiobarbiturates containing the triply hydrogen-bondedADA/DADsynthon, plus one ansolvate and three solvates of their coformer 2,4-diaminopyrimidine." Acta Crystallographica Section C Structural Chemistry 72, no. 9 (2016): 705–15. http://dx.doi.org/10.1107/s205322961601336x.

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A path to new synthons for application in crystal engineering is the replacement of a strong hydrogen-bond acceptor, like a C=O group, with a weaker acceptor, like a C=S group, in doubly or triply hydrogen-bonded synthons. For instance, if the C=O group at the 2-position of barbituric acid is changed into a C=S group, 2-thiobarbituric acid is obtained. Each of the compounds comprises twoADAhydrogen-bonding sites (D= donor andA= acceptor). We report the results of cocrystallization experiments of barbituric acid and 2-thiobarbituric acid, respectively, with 2,4-diaminopyrimidine, which contains

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19

Golovnev, Nikolay, and Maxim Molokeev. "Bridging behaviour of the 2-thiobarbiturate anion in its complexes with LiIand NaI." Acta Crystallographica Section C Crystal Structure Communications 69, no. 7 (2013): 704–8. http://dx.doi.org/10.1107/s0108270113014078.

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The structures of the LiIand NaIsalts of 2-thiobarbituric acid (2-sulfanylidene-1-3-diazinane-4,6-dione, H2TBA) have been studied. μ-Aqua-octaaquabis(μ-2-thiobarbiturato-κ2O:O′)bis(2-thiobarbiturato-κO)tetralithium(I) dihydrate, [Li4(C4H3N2O2S)4(H2O)9]·2H2O, (I), crystallizes with four symmetry-independent four-coordinated LiIcations and four independent HTBA−anions. The structure contains two structurally non-equivalent LiIcations and two non-equivalent HTBA−anions (bridging and terminal). Eight of the coordinated water ligands are terminal and the ninth acts as a bridge between LiIcations. D

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20

Vasylchenko, V., L. Korol, O. Kuchmenko, and N. Stepanova. "The oxidative status in patients with chronic kidney disease." Ukrainian Biochemical Journal 92, no. 5 (2020): 70–77. https://doi.org/10.15407/ubj92.05.070.

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An excess of free radicals accompanies the development of renal pathologies and causes numerous concomitant complications and syndromes. The most common of these are cardiometabolic syndromes in patients with chronic kidney disease. Therefore, the purpose of the study was to determine the activity of paraoxonase-1 and myeloperoxidase, which are associated with indicators of high-density lipoproteins content and oxidative stress in the blood of patients with the chronic stage of kidney disease. The activity of the enzymes, thiobarbiturate-active products concentration and  transferrin, cer

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21

Sweidan, Kamal, Mustafa M. El-Abadelah, Salim F. Haddad, and Wolfgang Voelter. "Synthesis and characterization of some new fluoroquinolone-barbiturate hybrid systems." Zeitschrift für Naturforschung B 70, no. 7 (2015): 513–17. http://dx.doi.org/10.1515/znb-2015-0037.

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AbstractNew hybrid molecules containing fluoroquinolone-barbiturate moieties were synthesized via simple routes, followed by characterization using various spectroscopic approaches. The THF solvent molecule was incorporated into compounds 2 and 3 through its oxygen atom based on its nucleophilicity. Facile displacement of the chloride ion in 4-oxoquinoline-3-carbonyl chloride by the nucleophilic methylene carbon of 1,3-dialkylbarbiturate/thiobarbiturate afforded the respective hybrids 5 and 6.

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22

Schade, Alexander, Ivan Tchernook, Mirko Bauer, et al. "Kinetics of Electrophilic Alkylations of Barbiturate and Thiobarbiturate Anions." Journal of Organic Chemistry 82, no. 16 (2017): 8476–88. http://dx.doi.org/10.1021/acs.joc.7b01223.

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23

Warrell, Raymond P., Josephia Muindi, Yee-Wan Stevens, Marian Isaacs, and Charles W. Young. "Induction of profound hypouricemia by a non-sedating thiobarbiturate." Metabolism 38, no. 6 (1989): 550–54. http://dx.doi.org/10.1016/0026-0495(89)90215-1.

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24

Hirshman, Carol A., Robert A. Edelstein, J. Mark Ebertz, and Jon M. Hanifin. "Thiobarbiturate-induced Histamine Release in Human Skin Mast Cells." Anesthesiology 63, no. 4 (1985): 353–56. http://dx.doi.org/10.1097/00000542-198510000-00002.

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25

Golovnev, N. N., M. S. Molokeev, and M. K. Lesnikov. "Crystal Structure and Properties of Levofloxacinium 2-Thiobarbiturate Trihydrate." Journal of Structural Chemistry 59, no. 3 (2018): 646–51. http://dx.doi.org/10.1134/s0022476618030204.

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26

Zhou, Xiaokun, Ling-Yan Chen, and Zhihua Sun. "A Versatile Approach for the Synthesis of Thiobarbiturate Analogues." Journal of Heterocyclic Chemistry 53, no. 1 (2015): 303–6. http://dx.doi.org/10.1002/jhet.2413.

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27

Golovnev, N. N., M. S. Molokeev, and I. I. Golovneva. "The crystal structure of lead(II) 1,3-diethyl-2-thiobarbiturate." Russian Journal of Coordination Chemistry 41, no. 5 (2015): 300–304. http://dx.doi.org/10.1134/s1070328415050012.

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28

Golovnev, N. N., M. S. Molokeev, I. V. Sterkhova, and I. I. Golovneva. "Structure of ionic cocrystals piperidinium 2-thiobarbiturate–2-thiobarbituric acid." Journal of Structural Chemistry 57, no. 6 (2016): 1266–69. http://dx.doi.org/10.1134/s0022476616060287.

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29

Hamidian, Hooshang, Najmeh Zahedian, Dadkhoda Ghazanfari, and Samieh Fozooni. "Synthesis and Evaluation of Changes Induced by Solvent and Substituent in Electronic Absorption Spectra of New Azo Disperse Dyes Containig Barbiturate Ring." Journal of Spectroscopy 2013 (2013): 1–6. http://dx.doi.org/10.1155/2013/276413.

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Six azo disperse dyes were prepared by diazotizing 4-amino hippuric acid and coupled with barbituric acid and 2-thiobarbituric acid. Then, the products were reacted with aromatic aldehyde, sodium acetate, and acetic anhydride, and oxazolone derivatives were formed. Characterization of the dyes was carried out by using UV-Vis, FT-IR,1H NMR and13C NMR, and mass spectroscopic techniques. The solvatochromic behavior of azo disperse dyes was evaluated in various solvents. The effects of substituents of aromatic aldehyde, barbiturate, and thiobarbiturate ring on the color of dyes were investigated.

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30

Mandal, Piyali, Madhumita Mukherjee, Diptendu Patra, and Raja Shunmugam. "Unique vesicular nano‐architecture of thiobarbiturate derived chitosan with excellent hydrophilicity." Journal of Polymer Science 60, no. 1 (2021): 122–30. http://dx.doi.org/10.1002/pol.20210700.

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31

Semrad, S. D., C. M. Trim, and G. E. Hardee. "Hypertension in bulls and steers anesthetized with guaifenesin-thiobarbiturate-halothane combination." American Journal of Veterinary Research 47, no. 7 (1986): 1577–82. https://doi.org/10.2460/ajvr.1986.47.07.1577.

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SUMMARY Eight bulls and steers (research animals) and 18 bulls (surgical patients) were anesthetized with guaifenesin and thiopental or thiamylal and for 90 minutes with halothane. Arterial blood pressure and heart rate were recorded in all animals. Cardiac output, plasma glucose and lactate concentrations, pcv, plasma proteins and plasma thromboxane B2 values were determined before (control) and every 15 minutes during anesthesia in the research animals. Plasma catecholamine concentrations were measured in 3 of the research animals and 3 of the surgical patients. Arterial pressure, heart rate

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32

Carof, Martine, Souad Lebbar, and Ladislas Szabó. "Detection of 3-deoxy-2-octulosonic acid in thiobarbiturate-negative endotoxins." Carbohydrate Research 161, no. 1 (1987): C4—C7. http://dx.doi.org/10.1016/0008-6215(87)84019-3.

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33

Golovnev, N. N., M. S. Molokeev, I. V. Sterkhova, M. K. Lesnikov, and A. S. Samoilo. "Structure of bis(2-Thiobarbiturate)Tris (2,2-Bipyridyl)Nickel(II) Hexahydrate." Journal of Structural Chemistry 60, no. 1 (2019): 111–16. http://dx.doi.org/10.1134/s0022476619010153.

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34

Vanhaeverbeek, M., D. Brohee, A. Lefevre, P. Piro, B. Kennes, and P. Neve. "Thiobarbiturate and fructosamine assays: significance and interest of the borohydride blank." Acta Diabetologica 31, no. 1 (1994): 43–46. http://dx.doi.org/10.1007/bf00580760.

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35

Hagege, Daniel, André Nouvelot, Jean Boucaud, and Thomas Gaspar. "Malondialdehyde titration with thiobarbiturate in plant extracts: Avoidance of pigment interference." Phytochemical Analysis 1, no. 2 (1990): 86–89. http://dx.doi.org/10.1002/pca.2800010208.

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36

Raja, S., and R. Dhamodharan. "Synthesis and characterization of water-soluble barbiturate- and thiobarbiturate-functionalized polystyrene." Journal of Polymer Science Part A: Polymer Chemistry 40, no. 6 (2002): 731–37. http://dx.doi.org/10.1002/pola.10154.

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37

Rakhimov, A. I., S. A. Avdeev, and Thi Doan Le Chang. "Specific features of the reaction of m-phenoxybenzyl chloride with sodium thiobarbiturate." Russian Journal of General Chemistry 79, no. 2 (2009): 338–39. http://dx.doi.org/10.1134/s1070363209020339.

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38

Mane, Shivshankar R., Vijayakameswara Rao N., and Raja Shunmugam. "Reversible pH- and Lipid-Sensitive Vesicles from Amphiphilic Norbornene-Derived Thiobarbiturate Homopolymers." ACS Macro Letters 1, no. 4 (2012): 482–88. http://dx.doi.org/10.1021/mz2002092.

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39

Takechi, Haruko, Kanji Kubo, Hajime Takahashi, and Taisuke Matsumoto. "Crystal Structures of Thiobarbiturate with N-Phenylalkyl Group and Its Photocyclization Product." Journal of Oleo Science 60, no. 8 (2011): 439–43. http://dx.doi.org/10.5650/jos.60.439.

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40

Yebga, A., S. Ménager, P. Vérité, C. Combet Farnoux, and O. Lafont. "Competition between two metabolic pathways: oxidation and desulfuration in the thiobarbiturate series." European Journal of Medicinal Chemistry 30, no. 10 (1995): 769–77. http://dx.doi.org/10.1016/0223-5234(96)88296-1.

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41

Khan, Abbas, Iltaf Khan, Momin Khan, and Hussain Gulab. "Physicochemical Investigation of Some Thiobarbiturate Derivatives and Their Binding Study with Deoxyribonucleic Acid." Russian Journal of Physical Chemistry B 12, no. 3 (2018): 485–94. http://dx.doi.org/10.1134/s1990793118030028.

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42

Zhou, Lily, and John R. J. Sorenson. "Formation of Cu or Fe thiobarbiturate complexes interfere with the determination of malondialdehyde." Journal of Inorganic Biochemistry 72, no. 3-4 (1998): 217–25. http://dx.doi.org/10.1016/s0162-0134(98)10083-1.

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43

Ofri, R., W. W. Dawson, K. Foli, and K. N. Gelatt. "Primary Open-angle Glaucoma Alters Retinal Recovery from a Thiobarbiturate: Spatial Frequency Dependence." Experimental Eye Research 56, no. 4 (1993): 481–88. http://dx.doi.org/10.1006/exer.1993.1061.

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44

Stošić, Biljana, Radmilo Janković, Marija Stošić, et al. "In silico development of anesthetics based on barbiturate and thiobarbiturate inhibition of GABAA." Computational Biology and Chemistry 88 (October 2020): 107318. http://dx.doi.org/10.1016/j.compbiolchem.2020.107318.

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45

Zharikov, A. Yu, S. O. Filinova, O. N. Mazko, I. P. Bobrov, O. G. Makarova, and A. S. Kalnitsky. "Effect of Carnosine on Oxidative Damage to the Kidneys in Experinental Diabetes Mellitus." Journal Biomed 20, no. 1 (2024): 52–61. http://dx.doi.org/10.33647/2074-5982-20-1-52-61.

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The article presents the results of a study into the effect of carnosine on oxidative damage to the kidneys in experimental diabetes mellitus. The experiment was carried out using two groups of Wistar rats: control (n=8) and experimental (n=11). In both groups, streptozotocin-induced diabetes mellitus was simulated for eight weeks. Experimental animals were intragastrically injected with carnosine (15 mg/kg) from weeks 4 to 8. The concentration of glucose, protein and creatinine excretion in urine were determined. At the end of eight weeks, the kidneys were removed from the rats to determine t

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46

Abbas Khan, Iltaf Khan, Muhammad Usman, Zahoor H. Farooqi, and Momin Khan. "Physicochemical Study of Some Thiobarbiturate Derivatives and Their Interaction with DNA in Aqueous Media." Russian Journal of Physical Chemistry A 92, no. 10 (2018): 1987–95. http://dx.doi.org/10.1134/s0036024418100023.

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47

Gong, Yun, Zhi Hao, JingHua Li, Tao Wu, and JianHua Lin. "Mg(ii)-induced second-harmonic generation based on bis-monodentate coordination mode of thiobarbiturate." Dalton Transactions 42, no. 18 (2013): 6489. http://dx.doi.org/10.1039/c3dt32380c.

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48

Golovnev, Nicolay N., Maxim S. Molokeev, Maxim K. Lesnikov, Irina V. Sterkhova, and Victor V. Atuchin. "Thiobarbiturate and barbiturate salts of pefloxacin drug: Growth, structure, thermal stability and IR-spectra." Journal of Molecular Structure 1149 (December 2017): 367–72. http://dx.doi.org/10.1016/j.molstruc.2017.08.011.

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García-Tasende, M. S., M. García Bugarín, and M. Filella. "Potentiometric investigation of the complexation of dimethylthallium(III) by 2-thiobarbiturate in aqueous solution." Polyhedron 10, no. 4-5 (1991): 517–21. http://dx.doi.org/10.1016/s0277-5387(00)80222-3.

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Golovnev, N. N., M. S. Molokeev, and S. N. Vereshchagin. "Crystal structure and some properties of europium(III) Catena-{tris(1,3-diethyl-2-thiobarbiturate)}." Journal of Structural Chemistry 57, no. 1 (2016): 167–74. http://dx.doi.org/10.1134/s0022476616010200.

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