2000
DOI: 10.1016/s0020-1693(00)00139-0
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Acetylenehexacarbonyldicobalt complexes, a novel class of antitumor drugs

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Cited by 92 publications
(90 citation statements)
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“…Interestingly, the effects were most marked in human breast cancer cells [24,34,35]. This was also the fact in experiments on human tumour xenografts using a clonogenic assay which has been found to have a high predictive value for further in vivo evaluation [36].…”
Section: Cobalt Compoundsmentioning
confidence: 92%
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“…Interestingly, the effects were most marked in human breast cancer cells [24,34,35]. This was also the fact in experiments on human tumour xenografts using a clonogenic assay which has been found to have a high predictive value for further in vivo evaluation [36].…”
Section: Cobalt Compoundsmentioning
confidence: 92%
“…Interestingly, the properties of the alkyne bond are changed towards that of an alkene upon coordination to the hexacarbonyldicobalt cluster. Thus, the angle between the triple bond and the substituents on both sides of the alkyne (X -C=C -X dihedral angle) was found to be significantly lower than 180 degrees, the C - C distance of the triple bond was increased and high signal shifts could be noted in 1 H-and 13 C-NMR spectra [23,24].…”
Section: Cobalt Compoundsmentioning
confidence: 95%
“…[4] Ferrocifen, a ferrocene derivative of the drug tamoxifen shows activity even on hormone-independent cell lines for which tamoxifen is inactive. [5,6] Further examples include {Ru(arene)} complexes, [7] several {Co(CO) 2 (alkyne)} derivatives [8][9][10][11] in addition to the well-studied titanocene dichloride which has been in clinical trials. [12][13][14][15] DNA interaction has been suggested as the mode of action, at least for some of the organometallic antitumor agents.…”
mentioning
confidence: 99%
“…[4] Ein Ferrocenderivat des bekannten Wirkstoffs Tamoxifen, Ferrocifen, zeigt eine gute cytostatische Aktivität, selbst bei hormonunabhängigen Zelllinien, die auf Tamoxifen naturgemäß nicht ansprechen. [5,6] Weitere Beispiele sind {Ru(aren)}-Komplexe, [7] verschiedene {Co(CO) 2 -(alkin)}-Derivate [8][9][10][11] und Titanocendichlorid, das bereits in klinischen Studien getestet wurde. [12][13][14][15] Für die meisten dieser Verbindungen ist eine Wechselwirkung mit der DNA als Wirkmechanismus vorgeschlagen worden.…”
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