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. 1982 Jan 1;201(1):179–188. doi: 10.1042/bj2010179

Concerning the structure of photobilirubin II.

M S Stoll, N Vicker, C H Gray, R Bonnett
PMCID: PMC1163624  PMID: 7082282

Abstract

Evidence is presented which supports the postulate that the photobilirubins IIA and IIB are diastereoisomers in which the C-3 vinyl group has cyclized intramolecularly. The evidence comes principally from proton n.m.r. spectroscopy at 400 MHz and from chemical considerations. The cyclic structures require the E-configuration at the C-4 double bond in the precursor; this is the first structural evidence for the Z leads to E isomerization in bilirubin and supports the view that the precursor (photobilirubin IA or IB) is (4E, 15Z)-bilirubin. Brief irradiation of photobilirubin II gives bilirubin, a new compound (photobilirubin III) and unchanged starting material. The various photoisomers are discussed in terms of their inter-relationships and biological fates.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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