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Journal articles on the topic 'Dimercapto'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Pazalja, Mirha. "Electrochemical Oxidation of 2,5-Dimercapto-1,3,4-thiadiazole on Carbon Electrodes Modified with Ru(III) Schiff Base Complex." Kemija u industriji 70, no. 7-8 (2021): 401–10. http://dx.doi.org/10.15255/kui.2020.068.

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The thiol compound 2,5-dimercapto-1,3,4-thiadiazole is a potential cathode material. The redox reactions of the mentioned thiol compound are slow at room temperature but can be enhanced using electron transfer mediators. The electrochemical oxidation of 2,5-dimercapto-1,3,4-thiadiazole on the surface of carbon electrodes modified with Ruthenium(III) Schiff base complex was studied by voltammetric methods and amperometric flow injection analysis. The electrocatalytic properties of Ruthenium(III) Schiff base complex on glassy carbon and screen printed carbon electrodes are enhanced by the addition of multi-walled carbon nanotubes and Nafion. Voltammetric studies showed that anodic oxidation of DMcT on a modified glassy carbon electrode occurs at a potential of +0.28 V vs. Ag/AgCl in Britton-Robinson buffer (pH 6.50). Flow injection amperometric measurements were performed at +0.20 V vs. Ag/AgCl in Britton-Robinson buffer solutions pH 6.50 at a 0.40 cm3 min–1 flow rate. The results of amperometric measurements for modified screen printed and glassy carbon electrodes showed that the screen printed electrode had a lower value of detection limit (0.38 mg dm–3) and quantification (1.28 mg dm–3), and a linear dynamic range from 1 to 500 mg dm–3 of 2,5-dimercapto-1,3,4-thiadiazole. Modified glassy carbon electrode provided a linear dynamic range up to 750 mg dm–3 of 2,5-dimercapto-1,3,4-thiadiazole with a detection limit of 3.90 mg dm–3 and quantification of 13.20 mg dm–3.

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2

Inns, R. H., P. Rice, J. E. Bright, and T. C. Marrs. "Evaluation of the Efficacy of Dimercapto Chelating Agents for the Treatment of Systemic Organic Arsenic Poisoning in Rabbits." Human & Experimental Toxicology 9, no. 4 (July 1990): 215–20. http://dx.doi.org/10.1177/096032719000900403.

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1 The standard drug for the treatment of arsenic poisoning is BAL (dimercaprol). BAL possesses marked side-effects and a low safety ratio, drawbacks which new BAL analogues, DMPS and DMSA, do not possess. 2 The efficacy of three chelating agents, BAL, DMPS and DMSA, has been evaluated as a treatment for systemic organic arsenic poisoning, induced by intravenous dichloro(2-chlorovinyl)arsine (lewisite) administration to rabbits. Equimolar dosing schedules were used based upon realistic doses for the most toxic agent, BAL. 3 It was concluded that all three dimercapto chelating agents provided signficant protection against the lethal systemic effects of lewisite, and, under the test conditions reported here, there was no significant difference between them in therapeutic efficacy. 4 The cause of mortality following intravenous lewisite in treated and untreated rabbits was pulmonary damage. 5 It is considered that DMPS and DMSA are worthy of further study as replacements for BAL in the treatment of systemic poisoning by lewisite.

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3

Kuliev, K. A., and N. A. Verdizadeh. "SPECTROPHOTOMETRIC DETERMINATION OF HEAVY METALS IN SOILS." Industrial laboratory. Diagnostics of materials 85, no. 5 (June 5, 2019): 18–27. http://dx.doi.org/10.26896/1028-6861-2019-85-5-18-27.

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Simple, selective and highly sensitive extraction-photometric methods for determination of Cu, Hg, У Mn, Fe, Co, and Ni are developed using dimercaptophenols (DF) and hydrophobic amines (Am) (2,6-dimercaptophenol(DMP), 2,6-dimercapto-4-methylphenol(DMMP), 2,6-dimercapto-4-ethylphenol(DMEP), 2,6-dimercapto-4-propylphenol(DMPP), and 2,6-dimercapto-4-tertbutylphenol(DMBP)) as complexing reagents. Optimal conditions for formation and extraction of heteroligand compounds (HLC) are specified and the ratios of the components in the complexes are determined. The optimum pH value providing maximum and constant optical density ranges within 3.0-8.1, chloroform (extraction ratio: 98.4-99.6%) being used as an extractant. Optimal concentrations of DP and Am are (0.6 - 0.8) x 10-3and (0.8 - 1.2) x 10-3mol/liter, respectively. HLC are stable and do not decompose for three days in aqueous and organic solvents, and after extraction for more than a month. The maximum analytical signal for M(II) complexing with DP and Am is observed at 464 - 630 nm (εk= 1.82 - 4.40 x 104). The structure of the HLC was studied using thermogravimetry and IR-spectroscopy Comparison of the analytical capabilities of the studied reagents showed that the contrast and sensitivity of the reaction decreases in the series DMBP — DMPP — DMEP — DMMP — DME The interfering impact of ions can be eliminated through changing pH of the medium, masking substances and extraction. The limits of photometric detection and quantitative determination of M (II) in the form of HLC were calculated using calibration graphs. The developed procedures have been successfully used in determination of the trace amounts of Cu, Hg, У Mn, Fe, Co, Ni in different soils: sod-podzolic sandy and sandy-loamy sod-podzolic loamy and clayey, gray forest, black soils, chestnut and river (soil of river floodplains) soils. The determination limits range within 27 - 43 ng/cm3.

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4

Lv, Li-Ping, Shuai Jiang, Alper Inan, Katharina Landfester, and Daniel Crespy. "Redox-responsive release of active payloads from depolymerized nanoparticles." RSC Advances 7, no. 14 (2017): 8272–79. http://dx.doi.org/10.1039/c6ra24796b.

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5

Al-Madani, W. A., N. J. Siddiqi, and A. S. Alhomida. "Renal Toxicity of Mercuric Chloride at Different Time Intervals in Rats." Biochemistry Insights 2 (January 2009): BCI.S2928. http://dx.doi.org/10.4137/bci.s2928.

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This study was undertaken to study the renal toxicity of mercuric chloride in rats at different periods of time. The following groups of rats were studied: i) control, ii) placebo, iii) rats injected with a single ip dose of 100 mg/kg body weight of 2, 3 dimercapto-1-propanesulfonic acid, iv) rats injected with a single ip dose of 100 mg/kg body weight of 2, 3 dimercapto-1-propanesulfonic acid (DMPS) followed by a single dose ip of 2.0 mg HgCl2/kg body weight one hour after DMPS injection v) rats injected with a single ip dose of 2.0 mg HgCl2/kg body weight. Results indicate that mercuric chloride was more toxic after 48 hours of its administration when compared to 24 hours. Mercuric chloride administration caused an impairment of renal function which was evident from a significant decrease in urine volume, urinary excretion of urea, creatinine and glomerular filteration rate (P < 0.001) when compared to other treated groups. There was an increased excretion of protein, albumin and γ–-glutamyltransferase in the urine of mercuric chloride treated rats. Administration of 2, 3 dimercapto-1-propanesulfonic acid before mercuric chloride treatment caused the altered indices to return to near normal levels.

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6

Kuodis, Z., A. Rutavichyus, and S. Valiulene. "Salts of 2,5-dimercapto-1,3,4-thiadiazole." Chemistry of Heterocyclic Compounds 36, no. 5 (May 2000): 598–602. http://dx.doi.org/10.1007/bf02290852.

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7

Klyuchko, S. V., B. M. Khutova, and L. P. Prikazchikova. "Amidoalkylation of mono- and dimercapto-pyrimidines." Chemistry of Heterocyclic Compounds 30, no. 9 (September 1994): 1069–73. http://dx.doi.org/10.1007/bf01171167.

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8

Ngatijo, Ngatijo, Diah Riski Gusti, Abdurrazaq Habib Fadhilah, and Resilta Khairunnisah. "Adsorben Magnetit Terlapis Dimerkaptosilika untuk Adsorpsi Anion Logam [AuCl4]- dan [Cr2O7]-." Jurnal Riset Kimia 11, no. 2 (August 27, 2020): 113–20. http://dx.doi.org/10.25077/jrk.v11i2.353.

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Adsorbent magnetite-dimercapto-silica (Fe3O4 - DMS) is a synthesis of magnetite with 2,3-dimercapto-1-propanol which has been applied to adsorb anions [AuCl4] - and [Cr2O7]-2. The adsorption process of metal anion [AuCl4]- at pH 5 with a contact time of 100 minutes was found optimum results at an adsorption capacity of 77.58 mg/g and an adsorption efficiency value of 96.975%. While the optimum conditions of metal anion [Cr2O7]-2 after the adsorption process at pH 4 with a contact time of 90 minutes was found an adsorption capacity of 85.0426 mg/g and an adsorption efficiency value of 85.0426%. The adsorption efficiency of metal anions [AuCl4]- is higher than the adsorption efficiency of metal anions [Cr2O7] -2

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9

Flora, Swaran J. S. "Influence of Simultaneous Supplementation of Zinc and Copper During Chelation of Lead in Rats." Human & Experimental Toxicology 10, no. 5 (September 1991): 331–36. http://dx.doi.org/10.1177/096032719101000506.

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The influence of zinc and copper supplementation during chelation therapy to reduce zinc and copper imbalance and promote lead elimination from the body, was investigated in rats poisoned with lead. The simultaneous supplementation of zinc and copper increased urinary lead excretion by calcium disodium ethylenediamine tetraacetic acid (CaNa2EDTA) compared to treatment with CaNa2EDTA alone. Combination therapy was effective in potentiating the depletion of blood and renal lead by CaNa2EDTA and meso 2,3-dimercapto succinic acid (DMSA). Combination therapy was also more effective in reducing hepatic lead by CaNa2EDTA and blood lead by 2,3-dimercapto propane sulphonate (DMPS). Zinc and copper supplementation produced a more effective reversal of inhibited blood δ-aminolevulinic acid dehydratase (ALAD) activity, urinary δ-aminolevulinic acid excretion and depleted body zinc and copper status.

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10

Vasimalai, N., K. Rajalakshmi, and S. Abraham John. "Economically viable sensitive and selective luminescent sensor for the determination of Au(iii) in environmental samples." RSC Adv. 4, no. 73 (2014): 38812–19. http://dx.doi.org/10.1039/c4ra05217j.

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11

Valyulene, S., and A. Rutavichyus. "Some derivatives of 2,5-dimercapto-1,3,4-thiadiazole." Chemistry of Heterocyclic Compounds 34, no. 12 (December 1998): 1431–35. http://dx.doi.org/10.1007/bf02317816.

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12

Steimecke, Günter, Reinhard Kirmse, and Eberhard Hoyer. "Dimercapto-isotrithion - ein neuer, ungesättigter 1,2-Dithiolatligand." Zeitschrift für Chemie 15, no. 1 (September 1, 2010): 28–29. http://dx.doi.org/10.1002/zfch.19750150117.

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13

Dart, RC, KV Iserson, and HV Aposhian. "Treatment of polonium poisoning with dimercapto chelating agents." Annals of Emergency Medicine 14, no. 5 (May 1985): 508. http://dx.doi.org/10.1016/s0196-0644(85)80392-9.

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14

O'Driscoll, John, Michael Beck, and Stuart Taylor. "Occupational contact allergy to 2,5-dimercapto-1,3,4-thiadiazole." Contact Dermatitis 23, no. 4 (October 1990): 268. http://dx.doi.org/10.1111/j.1600-0536.1990.tb05085.x.

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15

Hruby, K., and A. Donner. "2,3-Dimercapto-1-Propanesulphonate in Heavy Metal Poisoning." Medical Toxicology 2, no. 5 (October 1987): 317–23. http://dx.doi.org/10.1007/bf03259951.

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16

Domingo, JoséL, M. Angeles Bosque, Juan M. Llobet, and Jacinto Corbella. "Amelioration by BAL (2,3-dimercapto-1-propanol) and DMPS (Sodium 2,3-dimercapto-1-propanesulfonic acid) of arsenite developmental toxicity in mice." Ecotoxicology and Environmental Safety 23, no. 3 (June 1992): 274–81. http://dx.doi.org/10.1016/0147-6513(92)90077-g.

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17

Valiunene, S., and A. Rutavichius. "ChemInform Abstract: Some Derivatives of 2,5-Dimercapto-1,3,4-thiadiazole." ChemInform 30, no. 18 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199918110.

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18

Kutkevicius, S., A. Stanisauskaite, V. Getautis, A. Railaite, and S. Uss. "Synthesis of carbazole containing Organic Photosemiconductors using dimercapto compounds." Journal f�r Praktische Chemie/Chemiker-Zeitung 337, no. 1 (1995): 315–18. http://dx.doi.org/10.1002/prac.19953370165.

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19

Picart, Sébastien, and Eugène Geniès. "Electrochemical study of 2,5-dimercapto-1,3,4-thiadiazole in acetonitrile." Journal of Electroanalytical Chemistry 408, no. 1-2 (May 1996): 53–60. http://dx.doi.org/10.1016/0022-0728(95)04460-4.

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20

Ramírez, Augusto V. "El cuadro clínico de la intoxicación ocupacional por plomo." Anales de la Facultad de Medicina 66, no. 1 (March 6, 2013): 57. http://dx.doi.org/10.15381/anales.v66i1.1352.

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Al plomo, metal pesado grisáceo y ubicuo, se le ha encontrado en lugares tan inverosímiles como los hielos fósiles de Groenlandia. Egipcios y hebreos lo usaron. Los fenicios c. 2000 AC trabajaron menas de plomo en España. Al final del s XX, en países desarrollados, la intoxicación por plomo pasó de problema ocupacional a problema de salud pública. Entre nosotros aún es frecuente la intoxicación ocupacional. El diagnóstico pasa por reconocer la existencia de plomo en el ambiente laboral y en tomar una buena historia clínica y ocupacional. El diagnóstico diferencial considera cuadros dolorosos neurológicos y abdominales. Plomo-sanguíneo y zinc-protoporfirina son análisis cruciales y fidedignos. En expuestos, el plomo-sanguíneo suele llegar a 40 ug/100 mL, aunque en trabajadores de industrias insalubres puede alcanzar 80 ug/100 mL y la zinc-protoporfirina ser mayor de 4 ug/g de hemoglobina. El tratamiento se basa en quelar el plomo casi específicamente con edetato disódico monocálcico, sin olvidar la penicilamida ni los nuevos ácido dimercapto-succínico y ácido dimercapto-propanosulfónico, que han mejorado las opciones terapéuticas, son menos tóxicos y más fáciles de administrar. Se resalta la importancia del problema plomo como prioritario en salud pública y ocupacional, además de coadyuvar al grave problema ecológico actual.

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21

Ceconi, C., S. Curello, A. Cargnoni, G. M. Boffa, and R. Ferrari. "Antioxidant protection against ischaemia: Effect of 2,3-Dimercapto-1-propanol." Pharmacological Research Communications 20 (September 1988): 86. http://dx.doi.org/10.1016/s0031-6989(88)80216-9.

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22

Gordon, I. "Indications for 99m Technetium Dimercapto-Succinic Acid Scan in Children." Journal of Urology 137, no. 3 (March 1987): 464–67. http://dx.doi.org/10.1016/s0022-5347(17)44069-9.

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23

Pohl, Hans. "Renal Scars, Dimercapto-Succinic Acid Defects—What's in a Name?" Journal of Urology 180, no. 6 (December 2008): 2303–4. http://dx.doi.org/10.1016/j.juro.2008.09.068.

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24

Amiel, Pascale, Abdallah Mahamoud, Pierre Brouant, Jean Pierre Galy, Jacques Barbe, Janina Karolak-Wojciechowska, and Maciej Posel. "Tautomérie du 2,5-dimercapto-1,3,4-thiadiazole et synthèse de thiadiazoloacridiniques." Canadian Journal of Chemistry 73, no. 8 (August 1, 1995): 1258–66. http://dx.doi.org/10.1139/v95-154.

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Some 2(3H)-thione-5-alkylthio-1,3,4-thiadiazoles were prepared with a view to arylating these compounds with 9-chloroacridines. Using pyridine as solvent and base, this arylation led to the 2-thione-(N)3-acridinyl-5-alkylthio-1,3,4-thiadiazoles. Molecular structures of the latter were determined either by NMR spectroscopy or by referring to X-ray crystallography of the 5-(diethylaminoethylthio)-1,3,4-thiadiazole-2-thione. Thus, with respect to the tautomeric equilibrium of the compound investigated, the thione group was detected either in the solid state or in solution. In contrast, 2-acridinylthio-5-alkylthio-1,3,4-thiadiazoles were prepared by using the sodium salt of 2-mercapto-5-alkylthio-1,3,4-thiadiazoles as starting material. Keywords: acridines, thiadiazoles, tautomerism.

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25

Stewart, J. R., and G. L. Diamond. "Renal tubular secretion of the alkanesulfonate 2,3-dimercapto-1-propanesulfonate." American Journal of Physiology-Renal Physiology 252, no. 5 (May 1, 1987): F800—F810. http://dx.doi.org/10.1152/ajprenal.1987.252.5.f800.

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The in vivo tubular secretion and metabolism of 2,3-dimercapto-1-propanesulfonate (DMPS) was examined in the chicken by use of the Sperber technique. Infusion of DMPS into the renal portal circulation of the chicken at rates equal to or less than 7.5 mumol X min-1 X kg body wt-1, resulted in a tubular excretion ratio of 0.5 for DMPS with 90% of the infused DMPS excreted in the urine unchanged. Renal tubular secretion accounted for approximately 90% of the total DMPS excreted into the urine during the infusion of DMPS at a rate of 0.75 mumol X min-1 X kg-1. The secretion of DMPS was saturable and was inhibited by p-aminohippurate (PAH), probenecid, and heptanesulfonate. Taurine (2-aminoethanesulfonate), isethionate (2-hydroxyethanesulfonate), and 2-mercaptoethanesulfonate had no effect on the secretion of DMPS or PAH. Renal tubular secretion may explain several pharmacological characteristics previously reported for DMPS, including the selective removal of heavy metals from the kidney.

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26

Yu, Lei, Xianhong Wang, Ji Li, Xiabin Jing, and Fosong Wang. "Soluble 2,5‐Dimercapto‐1,3,4‐thiadiazole/Poly(o‐toluidine) Electroactive Composite." Journal of The Electrochemical Society 146, no. 5 (May 1, 1999): 1712–16. http://dx.doi.org/10.1149/1.1391831.

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27

Guzmán Barrón, Alberto. "Efecto del 2,3 dimercapto-propanol (BAL) en la policitemia por el cobalto." Anales de la Facultad de Medicina 32, no. 2 (October 18, 2014): 97. http://dx.doi.org/10.15381/anales.v32i2.9570.

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Durante la última guerra mundial se han realizado interesantes investigaciones sobre la acción de 2,3 dimercapto-propanol en intoxicaciones por diversas sustancias, tanto en animales como en hombres, siendo de especial interés de aquellos de uso terapéutico. Como en trabajos llegados a nuestras manos no hemos encontrado estudios con relación al cobalto, que en dosis elevadas ejerce una acción tóxica y en dosis pequeñas es capaz de originar una policitemia en diversos animales, cuyo mecanismo hasta hoy aún permanece sin aclararse, nos decidimos estudiar el efecto que el Bal podría ejercer frente al cobalto. Los primeros resultados hallados son materia de esta comunicación.

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28

Fang, Q., X. Z. You, J. H. Cai, and M. Y. He. "Cobaltocenium bis[(4,5-dimercapto-S4,S5)-1,3-dithiole-2-thionato]nickelate." Acta Crystallographica Section C Crystal Structure Communications 49, no. 7 (July 15, 1993): 1347–50. http://dx.doi.org/10.1107/s0108270193000332.

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29

KUTKEVICIUS, S., A. STANISAUSKAITE, V. GETAUTIS, A. RAILAITE, and S. USS. "ChemInform Abstract: Synthesis of Carbazole Containing Organic Photosemiconductors Using Dimercapto Compounds." ChemInform 26, no. 37 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199537154.

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30

Aldhaheri, Sarah R., Roohi Jeelani, Hamid-Reza Kohan-Ghadr, Sana N. Khan, Sasha Mikhael, Christina Washington, Robert T. Morris, and Husam M. Abu-Soud. "Dimercapto-1-propanesulfonic acid (DMPS) induces metaphase II mouse oocyte deterioration." Free Radical Biology and Medicine 112 (November 2017): 445–51. http://dx.doi.org/10.1016/j.freeradbiomed.2017.08.015.

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31

Albulescu, Laura-Oana, Melissa S. Hale, Stuart Ainsworth, Jaffer Alsolaiss, Edouard Crittenden, Juan J. Calvete, Chloe Evans, et al. "Preclinical validation of a repurposed metal chelator as an early-intervention therapeutic for hemotoxic snakebite." Science Translational Medicine 12, no. 542 (May 6, 2020): eaay8314. http://dx.doi.org/10.1126/scitranslmed.aay8314.

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Snakebite envenoming causes 138,000 deaths annually, and ~400,000 victims are left with permanent disabilities. Envenoming by saw-scaled vipers (Viperidae: Echis) leads to systemic hemorrhage and coagulopathy and represents a major cause of snakebite mortality and morbidity in Africa and Asia. The only specific treatment for snakebite, antivenom, has poor specificity and low affordability and must be administered in clinical settings because of its intravenous delivery and high rates of adverse reactions. This requirement results in major treatment delays in resource-poor regions and substantially affects patient outcomes after envenoming. Here, we investigated the value of metal ion chelators as prehospital therapeutics for snakebite. Among the tested chelators, dimercaprol (British anti-Lewisite) and its derivative 2,3-dimercapto-1-propanesulfonic acid (DMPS) were found to potently antagonize the activity of Zn2+-dependent snake venom metalloproteinases in vitro. Moreover, DMPS prolonged or conferred complete survival in murine preclinical models of envenoming against a variety of saw-scaled viper venoms. DMPS also considerably extended survival in a “challenge and treat” model, where drug administration was delayed after venom injection and the oral administration of this chelator provided partial protection against envenoming. Last, the potential clinical scenario of early oral DMPS therapy combined with a delayed, intravenous dose of conventional antivenom provided prolonged protection against the lethal effects of envenoming in vivo. Our findings demonstrate that the safe and affordable repurposed metal chelator DMPS can effectively neutralize saw-scaled viper venoms in vitro and in vivo and highlight the promise of this drug as an early, prehospital, therapeutic intervention for hemotoxic snakebite envenoming.

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32

Samee, Weerasak. "Antifungal, cytotoxic activities and docking studies of 2,5-dimercapto-1,3,4-thiadiazole derivatives." African Journal of Pharmacy and Pharmacology 5, no. 4 (April 30, 2011): 477–85. http://dx.doi.org/10.5897/ajpp10.156.

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33

TERADA, Kikuo, Ken MATSUMOTO, and Yukiko NANAO. "Preconcentration of bismuth with 2,5-dimercapto-1,3,4-thiadiazole loaded on silica gel." Analytical Sciences 1, no. 2 (1985): 145–49. http://dx.doi.org/10.2116/analsci.1.145.

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34

Li, Jinxia, Hui Zhan, and Yunhong Zhou. "Synthesis and electrochemical properties of polypyrrole-coated poly(2,5-dimercapto-1,3,4-thiadiazole)." Electrochemistry Communications 5, no. 7 (July 2003): 555–60. http://dx.doi.org/10.1016/s1388-2481(03)00121-8.

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35

Swaminathan, K., P. J. Carroll, Kochurani, H. B. Singh, and H. D. Bhargava. "Structure of trimethyltelluronium bis(4,5-dimercapto-1,3-dithiole-2-thionato)aurate(III)." Acta Crystallographica Section C Crystal Structure Communications 49, no. 7 (July 15, 1993): 1243–46. http://dx.doi.org/10.1107/s0108270193002999.

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36

Rodríguez-Calero, Gabriel G., Michael A. Lowe, Stephen E. Burkhardt, and Héctor D. Abruña. "Electrocatalysis of 2,5-Dimercapto-1,3,5-thiadiazole by 3,4-Ethylenedioxy-Substituted Conducting Polymers." Langmuir 27, no. 22 (November 15, 2011): 13904–9. http://dx.doi.org/10.1021/la202706s.

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37

Kaminaga, Akiko, Tetsu Tatsuma, Tadashi Sotomura, and Noboru Oyama. "Reactivation and Reduction of Electrochemically Inactivated Polyaniline by 2,5‐Dimercapto‐1,3,4‐thiadiazole." Journal of The Electrochemical Society 142, no. 4 (April 1, 1995): L47—L49. http://dx.doi.org/10.1149/1.2044178.

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38

Ma, Chunlin, Junhong Zhang, Feng Li, and Rufen Zhang. "Syntheses and Crystal Structures of Diorganotin Derivatives of 2,5-Dimercapto-1,3,4-thiadiazole." European Journal of Inorganic Chemistry 2004, no. 13 (July 2004): 2775–83. http://dx.doi.org/10.1002/ejic.200300860.

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AMIEL, P., A. MAHAMOUD, P. BROUANT, J. P. GALY, J. BARBE, J. KAROLAK-WOJCIECHOWSKA, and M. POSEL. "ChemInform Abstract: Tautomerism of 2,5-Dimercapto-1,3,4-thiadiazole and Synthesis of Thiadiazoloacridines." ChemInform 27, no. 13 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199613156.

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Hoyer, Eberhard, Wolfgang Dietzsch, and Hans Müuller. "Dithiolen-Chelate; Neue Übergangsmetallchelate von cis-Äthylenbisthiol und 4,5-Dimercapto-o-xylol." Zeitschrift für Chemie 7, no. 9 (September 2, 2010): 354–55. http://dx.doi.org/10.1002/zfch.19670070921.

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Kuodis, Z., A. Rutavichyus, and S. Valiulene. "Kinetic investigation of the alkylation of salts of 2,5-dimercapto-1,3,4-thiadiazole." Chemistry of Heterocyclic Compounds 36, no. 7 (July 2000): 857–61. http://dx.doi.org/10.1007/bf02256923.

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Shagun, L. G., L. V. Klyba, I. A. Dorofeev, E. R. Zhanchipova, I. A. Mikhailova, and M. G. Voronkov. "Synthesis and characteristics of the mass spectra of 2,5-dimercapto-2,5-dimethyltetrahydrothiophene." Chemistry of Heterocyclic Compounds 43, no. 2 (February 2007): 166–68. http://dx.doi.org/10.1007/s10593-007-0027-8.

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Schulze, Klaus, Eva-Maria Dietrich, and Manfred Mühlstädt. "Umsetzungen mit 1,3-Dichlor-2-methylenpropan; Synthese von 1,3-Dimercapto-2-methylenpropan." Zeitschrift für Chemie 15, no. 8 (September 1, 2010): 302–3. http://dx.doi.org/10.1002/zfch.19750150805.

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Prasad, Michaella M., and Earl Y. Cheng. "Radiographic Evaluation of Children with Febrile Urinary Tract Infection: Bottom-Up, Top-Down, or None of the Above?" Advances in Urology 2012 (2012): 1–8. http://dx.doi.org/10.1155/2012/716739.

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Abstract:

The proper algorithm for the radiographic evaluation of children with febrile urinary tract infection (FUTI) is hotly debated. Three studies are commonly administered: renal-bladder ultrasound (RUS), voiding cystourethrogram (VCUG), and dimercapto-succinic acid (DMSA) scan. However, the order in which these tests are obtained depends on the methodology followed: bottom-up or top-down. Each strategy carries advantages and disadvantages, and some groups now advocate even less of a workup (none of the above) due to the current controversies about treatment when abnormalities are diagnosed. New technology is available and still under investigation, but it may help to clarify the interplay between vesicoureteral reflux, renal scarring, and dysfunctional elimination in the future.

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Rushton, H. Gil, Massoud Majd, Roma Chandra, and Dae Yim. "Evaluation of99Mtechnetium-Dimercapto-Succinic Acid Renal Scans in Experimental Acute Pyelonephritis in Piglets." Journal of Urology 140, no. 5 Part 2 (November 1988): 1169–74. http://dx.doi.org/10.1016/s0022-5347(17)41992-6.

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Chowdhury, A. Z. M. Shaifullah, Yasuyuki Shibata, Masatoshi Morita, and Kunimitsu Kaya. "Synthesis of Arsenical Adduct: Synthesis and Transformation of Dimercapto Compound to Arsenical Adduct." Phosphorus, Sulfur, and Silicon and the Related Elements 177, no. 2 (February 1, 2002): 497–509. http://dx.doi.org/10.1080/10426500210241.

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Donner, C., O. Valet, Y. Yang, and H. Baumgärtel. "The Chemisorption of 2,3-Dimercapto-n-Propane Sulfonate at the Au(111)-Electrode." Zeitschrift für Physikalische Chemie 217, no. 10-2003 (October 2003): 1319–30. http://dx.doi.org/10.1524/zpch.217.10.1319.20491.

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KUBOTA, SATOSHI, MOHAMED A. EL-FARRASH, MASATOSHI MAKI, SHINJI HARADA, and MASAKAZU HATANAKA. "2,3 Dimercapto-1-Propanol Inhibits HIV-1tatActivity, Viral Production, and Infectivity In Vitro." AIDS Research and Human Retroviruses 6, no. 7 (July 1990): 919–27. http://dx.doi.org/10.1089/aid.1990.6.919.

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Tatsuma, Tetsu, Yasuyuki Yokoyama, Daniel A. Buttry, and Noboru Oyama. "Electrochemical Polymerization and Depolymerization of 2,5-Dimercapto-1,3,4-thiadiazole. QCM and Spectroscopic Analysis." Journal of Physical Chemistry B 101, no. 38 (September 1997): 7556–62. http://dx.doi.org/10.1021/jp971502a.

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Tomura, Masaaki, and Yoshiro Yamashita. "Bis(tetra-n-butylammonium) bis(2-dicyanomethylene-4,5-dimercapto-1,3-dithiole)nickel(II)." Acta Crystallographica Section E Structure Reports Online 58, no. 4 (March 22, 2002): m133—m135. http://dx.doi.org/10.1107/s1600536802004816.

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