Relevant bibliographies by topics / Pentetic Acid

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Pentetic Acid'

Author: Grafiati
Published: 4 June 2021
Last updated: 28 July 2025

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Journal articles on the topic "Pentetic Acid"

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&NA;. "Tc 99m pentetic acid." Reactions Weekly &NA;, no. 1411 (2012): 41. http://dx.doi.org/10.2165/00128415-201214110-00151.

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Mathew, Nimmi Mary, Sonu Ravindran, Sabir Muliyar, Alen Pious, and Suraj U. Menon. "Comparative Evaluation Of The Effect Of Different Chelating Agents On The Push-Out Bond Strength Of A Bioceramic Sealer: An In-Vitro Study." IOSR Journal of Dental and Medical Sciences 23, no. 11 (2024): 01–05. http://dx.doi.org/10.9790/0853-2311020105.

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Aim: This study aimed to assess how the push out bond strength of a bioceramic sealer (Meta CeraSeal) is affected by three different chelating agents: 17% EDTA, 7% Maleic acid, and 5% Pentetic acid. Methodology: 60 mandibular premolars were shaped using Pro Taper Gold rotary file upto size F2. The canals were irrigated with 2ml of 5.25% sodium hypochlorite (NaOCl) between instrumentation and then the NaOCl was removed by rinsing with five milliliters of distilled water.. The 60 specimens were divided into 4 groups of 15 each, in a random manner, depending on the final irrigating solution: Grou
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Coleman, R. Edward, Neil MacIntyre, Gary Snyder, Edward Pattishall, and David Zaccardelli. "Aerosol Characteristics of 99mTc-Pentetic Acid (DTPA) and Synthetic Surfactant (Exosurf)." Chest 105, no. 6 (1994): 1765–69. http://dx.doi.org/10.1378/chest.105.6.1765.

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Wallin, Martin, Peter Turner, Andrew Katsifis, Mingshi Yang та Hak-Kim Chan. "Crystal structure of aqua(2-{[2-({2-[bis(carboxylato-κO-methyl)amino-κN]ethyl}(carboxylato-κO-methyl)amino-κN)ethyl](carboxymethyl)azaniumyl}acetato)gallium(III) trihydrate". Acta Crystallographica Section E Crystallographic Communications 74, № 8 (2018): 1054–57. http://dx.doi.org/10.1107/s2056989018009428.

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In the title GaIIIcomplex compound with pentetic acid, [Ga(C14H20N3O10)(H2O)]·3H2O, the GaIIIcentre is bound in a slightly distorted octahedral coordination sphere by two amine N atoms, three carboxylate O atoms and one water O atom. The complex molecule exists as a zwitterion. In the crystal, the complexes are linked to each otherviaO—H...O and C—H...O hydrogen bonds, forming layers parallel to (001). Three uncoordinating water molecules link the complex layersviaO—H...O, N—H...O and C—H...O hydrogen bonds, forming a three-dimensional network.
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Capra, R., N. Marciano, L. A. Vignolo, A. Chiesa, and R. Gasparotti. "Gadolinium--Pentetic Acid Magnetic Resonance Imaging in Patients With Relapsing Remitting Multiple Sclerosis." Archives of Neurology 49, no. 7 (1992): 687–89. http://dx.doi.org/10.1001/archneur.1992.00530310029008.

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Bonatto, Fernando, Maria Luisa Puga, Annelise Kopp Alves, Jacqueline Arguello da Silva, Vladimir Lavayen Jimenez, and Carlos Pérez Bergmann. "Direct synthesis of singular silver dendrites over TiO2 nanotubes using pentetic acid as capping agent." Materials Letters 264 (April 2020): 127163. http://dx.doi.org/10.1016/j.matlet.2019.127163.

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Hussain, Afzal, Mohamed Fahad Alajmi, and S. Ganguly. "Pentetic acid derived dual purpose fluorescent carbon dots for pH responsive drug delivery and antioxidant proficiency." Diamond and Related Materials 145 (May 2024): 111101. http://dx.doi.org/10.1016/j.diamond.2024.111101.

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Hou, Lei, Alejandro López Valdivieso, Peng Chen, et al. "Pentetic acid/ammonia cooperatively stabilizes Cu(II) as an efficient oxidant for green thiosulfate leaching of gold." Minerals Engineering 218 (November 2024): 109043. http://dx.doi.org/10.1016/j.mineng.2024.109043.

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Gi, Mia, Junhui Jeong, Keehoon Lee, et al. "A Drug-Repositioning Screening Identifies Pentetic Acid as a Potential Therapeutic Agent for Suppressing the Elastase-Mediated Virulence of Pseudomonas aeruginosa." Antimicrobial Agents and Chemotherapy 58, no. 12 (2014): 7205–14. http://dx.doi.org/10.1128/aac.03063-14.

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ABSTRACTPseudomonas aeruginosa, a Gram-negative bacterium of clinical significance, produces elastase as a predominant exoprotease. Here, we screened a library of chemical compounds currently used for human medication and identified diethylene triamine penta-acetic acid (DTPA, pentetic acid) as an agent that suppresses the production of elastase. Elastase activity found in the prototypeP. aeruginosastrain PAO1 was significantly decreased when grown with a concentration as low as 20 μM DTPA. Supplementation with Zn2+or Mn2+ions restored the suppressive effect of DTPA, suggesting that the DTPA-m
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Patil, GayatriNitin, DipaliYogesh Shah, AshwiniManish Dadpe, SnehaRajendra Dole, BudhabhushanAshruba Sonvane, and NeerajEknath Kolge. "Impact of 5% pentetic acid on the pushout bond strength of AH Plus sealer to dentin: An in vitro study." Saudi Endodontic Journal 11, no. 2 (2021): 195. http://dx.doi.org/10.4103/sej.sej_71_20.

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Dissertations / Theses on the topic "Pentetic Acid"

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Lee, Ronald Duane. "The synthesis of 2-((E)-1'-propenyl)-(E)-2-pentenoic acid and its metabolism and pharmacokinetics in rats." Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26437.

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The anticonvulsant drug valproic acid (VPA) is extensively metabolized with 16 metabolites identified in man. Of interest are the unsaturated metabolites which appear to be responsible for the observed secondary antiepileptic activity and/or idiosyncratic hepatotoxicity. A study by Abbott et al . (1986) has shown 2-((E)-1'-propenyl)-(E)-2-pentenoic acid ((E,E)-2,3'-diene VPA) to be a major unsaturated metabolite of VPA. Acheampong (1985) demonstrated that an isomeric mixture of 2,3'-diene VPA prevented pentylenetetrazole-induced seizures in mice and had 60% the potency of VPA. Research on (E,
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Books on the topic "Pentetic Acid"

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Robert C., M.D. Brasch. Mri Contrast Enhancement in the Central Nervous System: A Case Study Approach. Raven Pr, 1993.

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Book chapters on the topic "Pentetic Acid"

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Bährle-Rapp, Marina. "Pentetic Acid." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_7790.

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Kapil, Shikha, and Ziad N. Kazzi. "Pentetic Acid." In Critical Care Toxicology. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-20790-2_180-1.

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Kapil, Shikha, and Ziad N. Kazzi. "Pentetic Acid." In Critical Care Toxicology. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-17900-1_180.

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Holze, Rudolf. "Ionic conductance of Δαn-pentenoic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_481.

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Holze, Rudolf. "Ionic conductance of Δβn-pentenoic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_482.

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Holze, Rudolf. "Ionic conductance of Δγn-pentenoic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_483.

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Holze, Rudolf. "Ionic conductance of γ-methyl–Δα-pentenoic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_506.

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Holze, Rudolf. "Ionic conductance of γ-methyl –Δβ-pentenoic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_507.

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Holze, Rudolf. "Ionic conductance of cis-β-methyl-Δα-pentenoic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_504.

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Holze, Rudolf. "Ionic conductance of trans-β-methyl-Δα-pentenoic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_505.

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Conference papers on the topic "Pentetic Acid"

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Quintela, J., M. Fernández, V. Ojea, M. Ruiz, S. Conde, and A. Díaz. "Stereoselective Synthesis of 2-Amino-4-phosphono-4-pentenoic Acid Derivatives (AP4 Analogues)." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02021.

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Saeki, T., K. HARADA, T. Youshimura, et al. "MODE OF ACTION OF A NOVEL ANTI-PLATELET AGENT (E-5510)." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643427.

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A novel anti-platelet agent, 4-cyano-5,5-bis(4-methoxy-phenyl)-4-pentenoic acid(E-5510), has been shown to inhibit platelet aggregation and secretion induced by thrombin as well as by other inducers such as ADP, collagen and PAF. Although E-5510 can act as a cyclooxygenase inhibitor,inhibition of cyclooxygenase may not be the primary mode of action since this compound effectively inhibits thrombin-induced platelet activation. In this paper, effects^of E-5510 on arachidonic acid (AA) metabolism, intracellular Ca++ and cAMP in human platelets are examined.(1) Effect on AA metabolism. Platelets p
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Fujimori, T., T. Saeki, K. Harada, M. Sato, and N. Ohshima. "ANTI-THROMBOTIC EFFECTS OF E-5510 IN EXPERIMENTAL THROMBOSIS MODELS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643429.

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A new agent developed in our laboratory, 4-cyano-5,5-bis(4-methoxyphenyl)-4-pentenoic acid (E-5510), suppressed various human platelet functions in vitro. The compound also showed quite potent ex vivo anti-platelet effects in many experimentalanimals. It is well known that anti-platelet effects are not always parallel to anti-thrombotic effects. Thus, in order to predict the efficacy of E-5510 in thrombotic disorders, the anti-thrombotic effects were examined in 3 different animal models of thrombosis.(1) Anti-thrombotic effect in an extracorporeal shunt model Two hrs after oral administration
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Harada, K., T. Fujimori, M. Kogushi, M. Kogushi, I. Yamatsu, and Y. Ikeda. "THE NEWLY SYNTHESIZED COMPOUND E-5510 IS A HIGHLY POTENT ANTIPLATELET AGENT." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643428.

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Our newly synthesized compound, 4-cyano-5,5-bis(methoxy-phenyl)-4-pentenoic acid (E-5510) has highly potent antiplatelet activity. In this paper, the effects of E-5510 on platelet functions in vitro and ex vivo in human and in various experimental animals are examined.E-5510 inhibited human platelet aggregation induced by collagen, arachidonate, ADP, PAF and epinephrine (IC50: 1.5, 0.7, 2.0, 1.6 and 1.1 uM, respectively). Thrombin-induced platelet aggregation, which was not inhibited by aspirin and U-53059 (lC50s: 100 uM), was also inhibited by this compound (IC50: 21uM). The IC50 of E-5510 in
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