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Volumn 39, Issue 11, 1983, Pages 1893-1907

On the role of singlet oxygen in the self-sensitized photo-oxygenation of bilirubin and its pyrromethenone models

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000148591     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)88703-2     Document Type: Article
Times cited : (47)

References (120)
  • 1
    • 33750246914 scopus 로고
    • K.P.M. Heirwegh, S.B. Brown, CRC Press, Boca Raton, Florida, Chap. 1.
    • (1982) Bilirubin , vol.1
    • Lightner1
  • 25
    • 84918391029 scopus 로고    scopus 로고
    • A.F. McDonagh, Hepatology, in press;
  • 38
    • 84918391025 scopus 로고    scopus 로고
    • W.P. Linnane, C.E. Ahlfors and D.A. Lightner, unpublished observations.
  • 56
    • 84918391024 scopus 로고    scopus 로고
    • E.J. Land, personal communication.
  • 62
    • 84918391022 scopus 로고    scopus 로고
    • A.A Lamola, S.E Braslavsky, K. Schaffner and D.A. Lightner, Photochem. Photobiol., in press.
  • 63
    • 84918391021 scopus 로고    scopus 로고
    • The isomerization of BR dimethyl ester has been followed by HPLC, ref. 2j, isomerization of BR has been followed by reverse phase HPLC in a system that cleanly separates all four isomers ref. 3b, c.
  • 74
    • 84918391020 scopus 로고    scopus 로고
    • 1H-NMR spectra have confirmed the structures of bilirubin E isomers (ref 2a) prepared as previously described (refs. 2j, k, l).
  • 75
    • 84918391019 scopus 로고    scopus 로고
    • Some studies of bilirubm E isomer hepatic excretion involved injection of photobilirubin preparations into jaundiced (Gunn) rats (refs. 2r,3a,g,h,i,n,o). Recent evidence indicates that some of these preparations (2o, p, r, 3g) do not have the structures ascribed to them and, in fact, contain relatively little of the BR E isomers (ref. 27).
  • 81
    • 0017807912 scopus 로고
    • 1Δl) dioxygen-all four reactions being spin-allowed although of different statistical probabilities. If reversible, it could mediate enhanced intersystem crossing for both species. Even if not significantly reversible, its intermediacy is not necessarily incompatible with either Type I or Type II photo-oxidation and indeed it might prevent any clear I/II distinction being drawn (if, for example, its decomposition to products were the rate-determining step)
    • (1978) Expenentia , vol.34 , pp. 555
    • Lightner1    Park2
  • 101
    • 84987341724 scopus 로고
    • Bilatriene-abcTetrapyrrole Synthesis by Acid-Catalyzed Oxidative Coupling of Dipyrroles
    • (1976) Synthesis , pp. 335
    • Lightner1    Quistad2    Pak3
  • 112


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.