Supramolecular iron porphyrin/cyclodextrin dimer complex that mimics the functions of hemoglobin and methemoglobin.
暂无分享,去创建一个
[1] H. Kitagishi,et al. Supramolecular dioxygen receptors composed of an anionic water-soluble porphinatoiron(II) and cyclodextrin dimers. , 2012, Dalton transactions.
[2] Kenji Watanabe,et al. Supramolecular ferric porphyrins as cyanide receptors in aqueous solution. , 2011, ACS medicinal chemistry letters.
[3] A. Kiriyama,et al. A diatomic molecule receptor that removes CO in a living organism. , 2010, Angewandte Chemie.
[4] A. Hall,et al. Which cyanide antidote? , 2009, Critical reviews in toxicology.
[5] S. Hirota,et al. A supramolecular receptor of diatomic molecules (O2, CO, NO) in aqueous solution. , 2008, Journal of the American Chemical Society.
[6] S. Hirota,et al. A myoglobin functional model composed of a ferrous porphyrin and a cyclodextrin dimer with an imidazole linker. , 2006, Chemistry, an Asian journal.
[7] A. Crespo,et al. Heme protein oxygen affinity regulation exerted by proximal effects. , 2006, Journal of the American Chemical Society.
[8] S. Hirota,et al. Iron porphyrin-cyclodextrin supramolecular complex as a functional model of myoglobin in aqueous solution. , 2006, Inorganic chemistry.
[9] S. Hirota,et al. Dioxygen binding to a simple myoglobin model in aqueous solution. , 2005, Angewandte Chemie.
[10] S. Kundu,et al. The leghemoglobin proximal heme pocket directs oxygen dissociation and stabilizes bound heme , 2002, Proteins.
[11] H. Marques,et al. Kinetics and activation parameters of the reaction of cyanide with free aquocobalamin and aquocobalamin bound to a haptocorrin from chicken serum. , 1988, The Journal of biological chemistry.