Abstract
OF the three urobilinoid pigments excreted by man (i-urobilin, d-urobilin and stercobilin), only i-urobilin has a structure established by degradation and synthesis1. The structure of i-urobilin is as shown in (I), except that the end rings, in common with all so-called hydroxypyrroles, are probably lactam in nature2. The other two pigments are formally derived from i-urobilin by dehydrogenation and tetrahydrogenation respectively3.
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References
Siedel, W., and Meier, E., Hoppe-Seyl. Z., 242, 101 (1936).
Plieninger, H., and Decker, M., Liebigs Annalen, 598, 198 (1956).
Lowry, P. T., Ziegler, N. R., and Watson, C. J., Bull. Univ. Minn. Hosp. and Med. Found., 24, 166 (1952).
Linstead, R. P., J. Chem. Soc., 3728 (1954).
Fischer, H., and Halbach, H., Hoppe-Seyl. Z., 238, 59 (1936).
Pruckner, F., and Stern, A., Z. phys. Chem., 182A, 117 (1938).
Birch, A. J., Chem. and Indust., 652 (1955).
Siedel, W., and Grams, E., Hoppe-Seyl. Z., 267, 49 (1940).
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GRAY, C., NICHOLSON, D. Structure of Stercobilin. Nature 179, 264–265 (1957). https://doi.org/10.1038/179264a0
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DOI: https://doi.org/10.1038/179264a0
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