Synthesis and cytogenetic effects of aminoquinone derivatives with a di- and a tripeptide

 
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Synthesis and cytogenetic effects of aminoquinone derivatives with a di- and a tripeptide

Mourelatos, Dionysios
Pachatouridis, C.
Mioglou-Kalouptsi, Eleftheria
Liakopoulou-Kyriakidou, Maria
Papageorgiou, Vasileios
Kotsis, Alexandros
Pantazaki, Anastasia
Iakovidou-Kritsi, Zafeiroula

Quinones are of significant interest due to their important role in specific cellular functions. Quinoproteins are a big class of oxyreductative agents occurring in bacteria and other organisms. In this investigation derivatives of 2-amino-1,4-benzoquinone, 2-amino-1,4-naphthoquinone and 2-amino-5,8-dihydroxy-1,4-naphthoquinone with a di- and a tripeptide were prepared for first time. The effect of the synthesized compounds on sister chomatid exchange (SCE) rates and human lymphocyte proliferation kinetics on a molar basis was studied. Among these coupled products the most effective in inducing SCEs and depressing proliferation rate indices is the coupling product of 2-amino-1,4-naphthoquinone with the tripeptide GHK (10). Next in order of magnitude in inducing cytogenetic effects Is 2-amino-1,4-naphthoquinone (2) and its coupling products with glycine and serine (4 and 5), while the rest displayed marginal activity. [(C) 2002 Lippincott Williams Wilkins.].

Article / Άρθρο
info:eu-repo/semantics/article

Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (EL)
Aristotle University of Thessaloniki (EN)

2002
2009-07-17T11:21:39Z


Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης, Πολυτεχνική Σχολή, Τμήμα Χημικών Μηχανικών
Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης, Σχολή Επιστημών Υγείας, Τμήμα Ιατρικής

urn:ISSN:09594973
Anti-Cancer Drugs, vol.13 no.4 [2002] p.367-372 [Published Version]

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info:eu-repo/semantics/openAccess



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