(C^Npz^C)AuIII complexes of acyclic carbene ligands: synthesis and anticancer properties. Issue 39 (25th September 2017)
- Record Type:
- Journal Article
- Title:
- (C^Npz^C)AuIII complexes of acyclic carbene ligands: synthesis and anticancer properties. Issue 39 (25th September 2017)
- Main Title:
- (C^Npz^C)AuIII complexes of acyclic carbene ligands: synthesis and anticancer properties
- Authors:
- Williams, Morwen
Green, Adam I.
Fernandez-Cestau, Julio
Hughes, David L.
O'Connell, Maria A.
Searcey, Mark
Bertrand, Benoît
Bochmann, Manfred - Abstract:
- Abstract : Synthesis of amino ester conjugated (C^N pz ^C)Au acyclic carbene complexes with low micromolar cytotoxicity on human cancer cells. Abstract : A series of cyclometallated gold(iii ) complexes supported by pyrazine-based (C^N pz ^C)-type pincer ligands were synthesized via two different pathways. Nucleophilic attack on the isocyanide complex [(C^N pz ^C)Au(CNC6 H3 Me2 -2, 6)]SbF6 (2 ) gave [(C^N pz ^C)Au(ACC)]SbF6 complexes with aniline (4 ·SbF 6 ), adamantylamine (5 ), glycine ethyl ester (6 ), alanine methyl ester (7 ), valine methyl ester (8 ), phenylglycine methyl ester (9 ) and methionine methyl ester (10 ) substituents (ACC = acyclic carbene). The pathway via isocyanide insertion into gold–amide bonds was also investigated; e.g. the reaction of xylyl isocyanide with (C^N pz ^C)AuNHPh followed by protonation with HBF4 ·OEt2 gave the acyclic carbene complex4 ·BF 4 . To the best of our knowledge compounds6–10 represent the first examples of gold(iii ) acyclic carbene complexes bearing amino acid functions. The compounds provide a versatile platform for the study of the anti-proliferative properties of gold(iii ) complexes. Tests against human adenoma-type lung cancer cells identified5, 6, 7 and10 as particularly promising and demonstrate the synthetic flexibility of acyclic carbene complexes and the potential of that class of compounds for anticancer applications. Compared to cisplatin, amino ester-containing ACC complexes showed improved selectivity for MCF-7Abstract : Synthesis of amino ester conjugated (C^N pz ^C)Au acyclic carbene complexes with low micromolar cytotoxicity on human cancer cells. Abstract : A series of cyclometallated gold(iii ) complexes supported by pyrazine-based (C^N pz ^C)-type pincer ligands were synthesized via two different pathways. Nucleophilic attack on the isocyanide complex [(C^N pz ^C)Au(CNC6 H3 Me2 -2, 6)]SbF6 (2 ) gave [(C^N pz ^C)Au(ACC)]SbF6 complexes with aniline (4 ·SbF 6 ), adamantylamine (5 ), glycine ethyl ester (6 ), alanine methyl ester (7 ), valine methyl ester (8 ), phenylglycine methyl ester (9 ) and methionine methyl ester (10 ) substituents (ACC = acyclic carbene). The pathway via isocyanide insertion into gold–amide bonds was also investigated; e.g. the reaction of xylyl isocyanide with (C^N pz ^C)AuNHPh followed by protonation with HBF4 ·OEt2 gave the acyclic carbene complex4 ·BF 4 . To the best of our knowledge compounds6–10 represent the first examples of gold(iii ) acyclic carbene complexes bearing amino acid functions. The compounds provide a versatile platform for the study of the anti-proliferative properties of gold(iii ) complexes. Tests against human adenoma-type lung cancer cells identified5, 6, 7 and10 as particularly promising and demonstrate the synthetic flexibility of acyclic carbene complexes and the potential of that class of compounds for anticancer applications. Compared to cisplatin, amino ester-containing ACC complexes showed improved selectivity for MCF-7 breast cancer cells over that for healthy fibroblasts. … (more)
- Is Part Of:
- Dalton transactions. Volume 46:Issue 39(2017)
- Journal:
- Dalton transactions
- Issue:
- Volume 46:Issue 39(2017)
- Issue Display:
- Volume 46, Issue 39 (2017)
- Year:
- 2017
- Volume:
- 46
- Issue:
- 39
- Issue Sort Value:
- 2017-0046-0039-0000
- Page Start:
- 13397
- Page End:
- 13408
- Publication Date:
- 2017-09-25
- 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/c7dt02804k ↗
- 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:
- 4813.xml