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DOI:
https://doi.org/10.34804/supra.20220628439 Cc Cc by 4.0

Title:
Eukaryotic Cell Toxicity and HSA Binding of [Ru(Me4phen)(bb7)]2+ and the Effect of Encapsulation in Cucurbit[10]uril

https://www.frontiersin.org/files/MyHome%20Article%20Library/423658/423658_Thumb_400.jpg

Description:
The toxicity (IC50) of a series of mononuclear ruthenium complexes containing bis[4(4′-methyl-2,2′-bipyridyl)]-1,n-alkane (bbn) as a tetradentate ligand against three eukaryotic cell lines—BHK (baby hamster kidney), Caco-2 (heterogeneous human epithelial colorectal adenocarcinoma) and Hep-G2 (liver carcinoma)—have been determined. The results demonstrate that cis-α-[Ru(Me4phen)(bb7)]2+ (designated as α-Me4phen-bb7, where Me4phen = 3,4,7,8-tetramethyl-1,10-phenanthroline) showed little toxicity toward the three cell lines, and was considerably less toxic than cis-α-[Ru(phen)(bb12)]2+ (α-phen-bb12) and the dinuclear complex [{Ru(phen)2}2{μ-bb12}]4+. Fluorescence spectroscopy was used to study the binding of the ruthenium complexes with human serum albumin (HSA). The binding of α-Me4phen-bb7 to the macrocyclic host molecule cucurbit[10]uril (Q[10]) was examined by NMR spectroscopy. Large upfield 1H NMR chemical shift changes observed for the methylene protons in the bb7 ligand upon addition of Q[10], coupled with the observation of several intermolecular ROEs in ROESY spectra, indicated that α-Me4phen-bb7 bound Q[10] with the bb7 methylene carbons within the cavity and the metal center positioned outside one of the portals. Simple molecular modeling confirmed the feasibility of the binding model. An α-Me4phen-bb7-Q[10] binding constant of 9.9 ± 0.2 × 106 M−1 was determined by luminescence spectroscopy. Q[10]-encapsulation decreased the toxicity of α-Me4phen-bb7 against the th...

Citation:

A. I. Day, B. Sun, I. F. Musgrave, K. Heimann, F. R. Keene, J. G. Collins, SupraBank 2024, Eukaryotic Cell Toxicity and HSA Binding of [Ru(Me4phen)(bb7)]2+ and the Effect of Encapsulation in Cucurbit[10]uril (dataset). https://doi.org/10.34804/supra.20220628439

Link: https://doi.org/10.34804/supra.20220628439
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Citation:

B. Sun, I. F. Musgrave, A. I. Day, K. Heimann, F. R. Keene, J. G. Collins, Front. Chem. 2018, 6, DOI 10.3389/fchem.2018.00595.

Link: https://doi.org/10.3389/fchem.2018.00595
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Creators:
Orcidid | Ror | Biyun Sun
Orcidid | Ror | Ian F. Musgrave
Orcidid | Ror | Anthony I. Day
Orcidid | Ror | Kirsten Heimann
Orcidid | Ror | F. Richard Keene
Orcidid | Ror | J. Grant Collins

Contributers:
Orcidid | Ror | Nilima Manoj Kumar | DataManager

Subjects:
general chemistry

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