2005
DOI: 10.1016/j.jinorgbio.2005.05.003
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Synthesis, characterization and antiproliferative behavior of tricarbonyl complexes of rhenium(I) with some 6-amino-5-nitrosouracil derivatives: Crystal structure of fac-[ReCl(CO)3(DANU-N5,O4)] (DANU=6-amino-1,3-dimethyl-5-nitrosouracil)

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Cited by 46 publications
(30 citation statements)
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“…This indicates a π-accepting character of the N,N′-chelates. Re-N distances in 6a-7d show no recognizable preference for a shorter imine or oxime bonding and are close to bond lengths recently reported for an ortho-quinoid diimine Re(I) complex [46] or a Re(I) nitroso complex [66]. Only few structurally characterized rhenium oximato complexes suitable for comparison are known.…”
Section: Synthesis and Characterization Of Re(i) Complexes 6a-7dsupporting
confidence: 82%
“…This indicates a π-accepting character of the N,N′-chelates. Re-N distances in 6a-7d show no recognizable preference for a shorter imine or oxime bonding and are close to bond lengths recently reported for an ortho-quinoid diimine Re(I) complex [46] or a Re(I) nitroso complex [66]. Only few structurally characterized rhenium oximato complexes suitable for comparison are known.…”
Section: Synthesis and Characterization Of Re(i) Complexes 6a-7dsupporting
confidence: 82%
“…2.34 Å) because of the different basicity degree. The geometrical features of the uracil rings are very similar to those found in other related uracil derivatives [24,25]. The C2@O carbonyl length (ca.…”
Section: Synthetic Proceduressupporting
confidence: 74%
“…The treatment of the different complexes in DMSO showed similar effect in the tumoral cell line used as it was previously reported [63]. The solvent dimethyl sulphoxide (DMSO) shows no effect in cell growth.…”
Section: Electron Spin Resonance (Esr)supporting
confidence: 72%
“…It seems that, changing the anion and the nature of the metal ion has effect on the biological behavior, due to alter binding ability of DNA binding, so testing of different complexes is very interesting from this point of view. Chemotherapeutic activity of the complexes may be attributed to the central metal atom which was explained by Tweedy's chelation theory [63,64]. Also, the positive charge of the metal increases the acidity of coordinated ligand that bears protons, leading to stronger hydrogen bonds he biological activity [65,66].…”
Section: Table 2bmentioning
confidence: 97%