Characterization of Isomers Which Are Produced by Reactions of (1R,3S-Cyclohexanediamine)platinum(II) with Nucleotide d(GpG)
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/66/6/66_6_1822/_pdf
Reference14 articles.
1. Specific Binding of Chromosomal Protein HMG1 to DNA Damaged by the Anticancer Drug Cisplatin
2. Antibodies against (1R,2R)-cyclohexanediamineplatinum(II)-DNA adduct recognize the conformational differences of isomeric analogues of cyclohexanediamine
3. Reaction of symmetrically and asymmetrically substituted derivatives of cisplatin with r(ApG). Influence of the nonleaving groups on structures and kinetics
4. Characterization of (1,2-cyclohexanediamine)platinum(II) isomers and their d(GpG) adducts by means of proton NMR spectroscopy. A minor structural change induced by the isomers
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1. Interactions with DNA Models of the Oxaliplatin Analog (cis-1,3-DACH)PtCl2;International Journal of Molecular Sciences;2024-07-05
2. Isomer formation in the binding of [PtCl2(cis-cyclohexane-1,3-diamine)] to oligonucleotides and the X-ray crystal structure of [PtCl2(cis-cyclohexane-1,3-diamine)]·dimethylformamide†;Journal of the Chemical Society, Dalton Transactions;2001
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