Demonstration of the interaction of cysteamine with DNA using 23Na nmr technique
β Scribed by D. Vasilescu; G. Mallet
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1985
- Tongue
- English
- Weight
- 247 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0006-3525
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Calmidazolium 1R24571, 1-[ bis(4-chlorophenyl)methyl]-3-[2-(2,4dichloro-pheny1)-2- [ (2,4dichlorophenyl) methoxyl ethyl]-1H-imidazolium chloride} is a potent calmodulin inhibitor. This paper describes the synthesis and properties of the enantiomers of calmidazolium from the enantiomers of miconazole
Hedamycin, a member of the pluramycin class of antitumour antibiotics, consists of a planar anthrapyrantrione chromophore to which is attached two aminosugar rings at one end and a bisepoxidecontaining sidechain at the other end. Binding to double-stranded DNA is known to involve both reversible and