Comprehensive Coordination Chemistry II 2003
DOI: 10.1016/b0-08-043748-6/03032-2
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Cited by 27 publications
(24 citation statements)
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“…[1] However, 2 is known to be metabolized by hepatic enzymes with the release of more reactive Cr III species. [28] Rapid hydrolysis of CrCl 3 in neutral aqueous media with the formation of insoluble products [16] is a likely reason for its relatively inefficient oxidation to Cr VI (Table 1), as well as for the controversies regarding its biological activity. [1] In conclusion, the ease of oxidation of 1 to carcinogenic Cr VI under biologically relevant conditions (Table 1) warrants further research into the safety of using 1 (or any other Cr III compound) as a nutritional supplement or therapeutic agent.…”
Section: Methodsmentioning
confidence: 99%
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“…[1] However, 2 is known to be metabolized by hepatic enzymes with the release of more reactive Cr III species. [28] Rapid hydrolysis of CrCl 3 in neutral aqueous media with the formation of insoluble products [16] is a likely reason for its relatively inefficient oxidation to Cr VI (Table 1), as well as for the controversies regarding its biological activity. [1] In conclusion, the ease of oxidation of 1 to carcinogenic Cr VI under biologically relevant conditions (Table 1) warrants further research into the safety of using 1 (or any other Cr III compound) as a nutritional supplement or therapeutic agent.…”
Section: Methodsmentioning
confidence: 99%
“…[4,7] Complex 1 can also serve as a representative example of numerous polynuclear species formed on hydrolysis of Cr III complexes in neutral aqueous solutions. [16] It is relatively stable at pH 7.4 and 37 8C, although partial hydrolysis (leading to di-and mononuclear species) occurs on the timescale of hours, as revealed by electrospray mass spectrometry (see the Supporting Information).…”
mentioning
confidence: 98%
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“…The specific interactions of Cr(III) ions with cellular insulin receptors[ 7 ] are caused by intra-or extracellular oxidations of Cr(III) to Cr(V) and/or Cr(VI) compounds, which act as protein tyrosine phosphatase (PTP) inhibitors. The oxidation of some Cr(III) complexes by H 2 O 2 in neutral or weakly basic aqueous media (pH 7.0–9.0), lead to polynuclear species formed on hydrolysis of Cr(III) complexes in neutral aqueous solutions [ 8 ]. The relative reactivities of various Cr(III) complexes towards H 2 O 2 may correlate with their reported activities as insulin activators [ 9 ].…”
Section: Introductionmentioning
confidence: 99%
“…In contrast to the V V , soluble Cr VI ions that enter cells are quickly reduced (Standeven and Wetterhan, 1989). As the Cr V and Cr IV species formed are unstable intracellularly (Lay and Lavina, 2004; Nag and Bose, 1985), the ion ultimately present is Cr III . Nevertheless, though unidirectionally-reduced, Cr VI ions are strong oxidants and can undergo redox/ligand displacement reactions with GSH, NAD(P)H, or other HS-bearing entities.…”
Section: Discussionmentioning
confidence: 99%