Design, synthesis, antiproliferative and antimicrobial evaluation of a new class of disulfides containing 1,3,4-thiadiazole units-Reference-Cited by-同舟云学术

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Design, synthesis, antiproliferative and antimicrobial evaluation of a new class of disulfides containing 1,3,4-thiadiazole units

Published:2022-07-28 Issue:9 Volume:31 Page:1571-1583
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Zhang Ruilian,Li Bo,Chi Chunlan,Liu Yang,Liu Xuguang,Li Junjie,Li Wei,Chen Baoquan^ORCID

Funder

Tianjin Municipal Natural Science Foundation

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

https://link.springer.com/content/pdf/10.1007/s00044-022-02937-4.pdf

Reference38 articles.

1. Branowska D, Ławecka J, Sobiczewski M, Karczmarzyk Z, Wysocki W, Wolińska E, et al. Synthesis of unsymmetrical disulfanes bearing 1,2,4-triazine scaffold and their in vitro screening towards anti-breast cancer activity. Monatsh Chem. 2018;149:1409–20. https://doi.org/10.1007/s00706-018-2206-y

2. Lee TH, Khan Z, Subedi L, Kim SY, Lee KR. New bis-thioglycosyl-1,1′-disulfides from Nasturtium officinale R. Br. And their anti-neuroinflammatory effect. Bioorg Chem. 2019;86:501–6. https://doi.org/10.1016/j.bioorg.2019.01.062

3. Sheppard JG, Frazier KR, Saralkar P, Hossain MF, Geldenhuys WJ, Long TE. Disulfiram-based disulfides as narrow-spectrum antibacterial agents. Bioorg Med Chem Lett. 2018;28:1298–302. https://doi.org/10.1016/j.bmcl.2018.03.023

4. Diraimondo TR, Plugis NM, Jin X, Khosla C. Selective inhibition of extracellular thioredoxin by asymmetric disulfides. J Med Chem. 2013;56:1301–10. https://doi.org/10.1021/jm301775s

5. Baker AF, Adab KN, Raghunand N, Chow HHS, Stratton SP, Squire SW, et al. A phase IB trial of 24-hour intravenous PX-12, a thioredoxin-1 inhibitor, inpatients with advanced gastrointestinal cancers. Invest N. Drugs. 2013;31:631–41. https://doi.org/10.1007/s10637-012-9846-2

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1. Synthesis, docking and characterization of some novel 5-(S-alkyl)-1.3.4-thiadiazole-2-carboxamide derivatives as anti-inflammatory and antibacterial agents;BMC Chemistry;2024-07-27

2. Visible light mediated eosin-Y catalysed direct synthesis of biologically potent [1,2,4]Triazolo [3,4-b] [1,3,4] Thiadiazols;Indian Journal of Chemistry;2024-07-19

3. Anti‐Biofilm and Anti‐Virulence Potential of 2‐Amino‐1,3,4‐Thiadiazole Derivatives;ChemistrySelect;2024-04-11

4. Molecular modeling, synthesis, and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory activities of novel benzimidazole-bearing thiadiazole derivatives;Journal of Molecular Structure;2024-01

5. 1,3,4-Thiadiazole: A Versatile Scaffold for Drug Discovery;Letters in Organic Chemistry;2023-12-22

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