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- W1998117518 abstract "Haem a with denatured proteins in strongly alkaline solutions forms haemochromes whose α -absorption bands lie 15 to 20 m μ more towards shorter wavelengths than those of haemochromes with other nitrogenous ligands. It is found that this is due to the formation of Schiff’s bases, the formyl side chain of haem a being condensed with amino groups of the protein. The same reaction is given by other haems and porphyrins with formyl side chains. The Schiff’s bases are stable only at high pH and are dissociated at pH 7 to 8. Schiff’s bases with methylamine are also obtained with high concentration of methylamine at high pH. These compounds are compared with alkaline indicator yellow (retinal-opsin) and retinylidene methylamine." @default.
- W1998117518 created "2016-06-24" @default.
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- W1998117518 date "1962-01-09" @default.
- W1998117518 modified "2023-09-27" @default.
- W1998117518 title "Haem a compounds as models for cytochromes of group a III. Schiff’s bases of haem a and other formylhaems and formyl-porphyrins" @default.
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- W1998117518 doi "https://doi.org/10.1098/rspb.1962.0005" @default.
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