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词条 Bisthiosemicarbazone
释义

  1. See also

  2. References

In organic chemistry, a bisthiosemicarbazone is a derivative from an elimination reaction between a thiosemicarbazide and a diketone. Their structure is H2NHC(=S)NN=C(R1)-R2-C(R3)=NNHC(=S)NH2. A 'thiosemicarbazone' contains a sulfur atom in lieu of the ketonic oxygen in semicarbazone. Bisthiosemicarbazones are known to have anti-viral, anti-malarial and anti-cancer activity,[1] usually mediated through binding to copper or iron in cells. They have also been identified as potential ligands for radioisotope delivery, with selectivity towards hypoxic tissues, particularly in the heart and brain.[2][3][4] When chelated to zinc atoms some bisthiosemicarbazones may have uses as fluorescing agents in optical microscopy.

See also

  • Salen ligand
  • Ambazone - structurally related

References

1. ^{{cite journal|last1=Palanimuthu|first1=Duraippandi|last2=Shinde|first2=Sridevi Vijay|last3=Somasundaram|first3=Kumaravel|last4=Samuelson|first4=Ashoka G.|title=In Vitro and in Vivo Anticancer Activity of Copper Bis(thiosemicarbazone) Complexes|journal=Journal of Medicinal Chemistry|date=14 February 2013|volume=56|issue=3|pages=722–734|doi=10.1021/jm300938r|pmid=23320568}}
2. ^{{cite journal|last1=Dearling|first1=Jason L.|last2=Lewis|first2=Jason S.|last3=Mullen|first3=Gregory E.|last4=Welch|first4=Michael J.|last5=Blower|first5=Philip J.|title=Copper bis(thiosemicarbazone) complexes as hypoxia imaging agents: structure-activity relationships|journal=JBIC Journal of Biological Inorganic Chemistry|date=20 April 2014|volume=7|issue=3|pages=249–259|doi=10.1007/s007750100291}}
3. ^{{cite journal|last1=Maurer|first1=Richard I.|last2=Blower|first2=Philip J.|last3=Dilworth|first3=Jonathan R.|last4=Reynolds|first4=Christopher A.|last5=Zheng|first5=Yifan|last6=Mullen|first6=Gregory E. D.|title=Studies on the Mechanism of Hypoxic Selectivity in Copper Bis(Thiosemicarbazone) Radiopharmaceuticals|journal=Journal of Medicinal Chemistry|date=March 2002|volume=45|issue=7|pages=1420–1431|doi=10.1021/jm0104217}}
4. ^{{cite journal|last1=Cowley|first1=Andrew R.|last2=Dilworth|first2=Jonathan R.|last3=Donnelly|first3=Paul S.|last4=Labisbal|first4=Elena|last5=Sousa|first5=Antonio|title=An Unusual Dimeric Structure of a Cu(I) Bis(thiosemicarbazone) Complex: Implications for the Mechanism of Hypoxic Selectivity of the Cu(II) Derivatives|journal=Journal of the American Chemical Society|date=May 2002|volume=124|issue=19|pages=5270–5271|doi=10.1021/ja012668z}}
{{Organic-chemistry-stub}}

3 : Functional groups|Thiocarbonyl compounds|Thiosemicarbazone

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