Investigations of the reactivity, stability and biological activity of halido (NHC)gold(i) complexes. Issue 4 (6th January 2022)
- Record Type:
- Journal Article
- Title:
- Investigations of the reactivity, stability and biological activity of halido (NHC)gold(i) complexes. Issue 4 (6th January 2022)
- Main Title:
- Investigations of the reactivity, stability and biological activity of halido (NHC)gold(i) complexes
- Authors:
- Goetzfried, Sina Katharina
Kapitza, Paul
Gallati, Caroline Marie
Nindl, Anna
Cziferszky, Monika
Hermann, Martin
Wurst, Klaus
Kircher, Brigitte
Gust, Ronald - Abstract:
- Abstract : The significance of the halido ligand (Cl −, Br −, I − ) in (NHC)gold(i ) complexes in ligand exchange reactions, including the ligand scrambling to the bis(NHC)gold(i ) complex 5, was evaluated by HPLC and discussed in relation to the biological activity in A2780 cell lines. Abstract : The significance of the halido ligand (Cl −, Br −, I − ) in halido[3-ethyl-4-phenyl-5-(2-methoxypyridin-5-yl)-1-propyl-1, 3-dihydro-2 H -imidazol-2-ylidene]gold(i ) complexes (2 –4 ) in terms of ligand exchange reactions, including the ligand scrambling to the bis[3-ethyl-4-phenyl-5-(2-methoxypyridin-5-yl)-1-propyl-1, 3-dihydro-2 H -imidazol-2-ylidene]gold(i ) complex (5 ), was evaluated by HPLC in acetonitrile/water = 50:50 (v/v) mixtures. In the presence of 0.9% NaCl, the bromido (NHC)gold(i ) complex 3 was immediately transformed into the chlorido (NHC)gold(i ) complex 2 . The iodido (NHC)gold(i ) complex 4 converted under the same conditions during 0.5 h of incubation by 52.83% to 2 and by 8.77% to 5 . This proportion remained nearly constant for 72 h. The halido (NHC)gold(i ) complexes also reacted very rapidly with 1 eq. of model nucleophiles, e.g., iodide or selenocysteine (Sec). For instance, Sec transformed 3 in the proportion 73.03% to the (NHC)Au(i )Sec complex during 5 min of incubation. This high reactivity against this amino acid, present in the active site of the thioredoxin reductase (TrxR), correlates with the complete inhibition of the isolated TrxR enzyme at 1Abstract : The significance of the halido ligand (Cl −, Br −, I − ) in (NHC)gold(i ) complexes in ligand exchange reactions, including the ligand scrambling to the bis(NHC)gold(i ) complex 5, was evaluated by HPLC and discussed in relation to the biological activity in A2780 cell lines. Abstract : The significance of the halido ligand (Cl −, Br −, I − ) in halido[3-ethyl-4-phenyl-5-(2-methoxypyridin-5-yl)-1-propyl-1, 3-dihydro-2 H -imidazol-2-ylidene]gold(i ) complexes (2 –4 ) in terms of ligand exchange reactions, including the ligand scrambling to the bis[3-ethyl-4-phenyl-5-(2-methoxypyridin-5-yl)-1-propyl-1, 3-dihydro-2 H -imidazol-2-ylidene]gold(i ) complex (5 ), was evaluated by HPLC in acetonitrile/water = 50:50 (v/v) mixtures. In the presence of 0.9% NaCl, the bromido (NHC)gold(i ) complex 3 was immediately transformed into the chlorido (NHC)gold(i ) complex 2 . The iodido (NHC)gold(i ) complex 4 converted under the same conditions during 0.5 h of incubation by 52.83% to 2 and by 8.77% to 5 . This proportion remained nearly constant for 72 h. The halido (NHC)gold(i ) complexes also reacted very rapidly with 1 eq. of model nucleophiles, e.g., iodide or selenocysteine (Sec). For instance, Sec transformed 3 in the proportion 73.03% to the (NHC)Au(i )Sec complex during 5 min of incubation. This high reactivity against this amino acid, present in the active site of the thioredoxin reductase (TrxR), correlates with the complete inhibition of the isolated TrxR enzyme at 1 μM. Interestingly, in cellular systems (A2780cis cells), even at a 5-fold higher concentration, no increased ROS levels were detected. The concentration required for ROS generation was about 20 μM. Superficially considered, the antiproliferative and antimetabolic activities of the halido (NHC)Au(i ) complexes correlate with the reactivity of the Au(i )–X bond (2 < 3 < 4 ). However, it is very likely that degradation products formed during the incubation in cell culture medium participated in the biological activity. In particular, the high-cytotoxic [(NHC)2 Au(i )] + complex (5 ) distorts the results. … (more)
- Is Part Of:
- Dalton transactions. Volume 51:Issue 4(2022)
- Journal:
- Dalton transactions
- Issue:
- Volume 51:Issue 4(2022)
- Issue Display:
- Volume 51, Issue 4 (2022)
- Year:
- 2022
- Volume:
- 51
- Issue:
- 4
- Issue Sort Value:
- 2022-0051-0004-0000
- Page Start:
- 1395
- Page End:
- 1406
- Publication Date:
- 2022-01-06
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1dt03528b ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 20754.xml