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Volumn 384, Issue 1, 2009, Pages 74-78

Reduction of porphyrins to porphyrinogens with palladium on carbon

Author keywords

Heme biosynthetic pathway; HPLC; Porphyria; Porphyrin; Porphyrinogen; Uroporphyrinogen decarboxylase

Indexed keywords

ALKALINITY; BIOSYNTHESIS; CARBON; ENZYMES; INERT GASES; IONIC STRENGTH; PALLADIUM; SODIUM BOROHYDRIDE;

EID: 56549109912     PISSN: 00032697     EISSN: 10960309     Source Type: Journal    
DOI: 10.1016/j.ab.2008.09.027     Document Type: Article
Times cited : (12)

References (12)
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    • (2003) EMBO J. , vol.22 , pp. 6225-6233
    • Phillips, J.D.1    Whitby, F.G.2    Kushner, J.P.3    Hill, C.P.4
  • 3
    • 0020407640 scopus 로고
    • Uroporphyrinogen decarboxylase: a method for measuring enzymatic activity
    • Straka J.G., Kushner J.P., and Pryor M.A. Uroporphyrinogen decarboxylase: a method for measuring enzymatic activity. Enzyme 28 (1982) 170-185
    • (1982) Enzyme , vol.28 , pp. 170-185
    • Straka, J.G.1    Kushner, J.P.2    Pryor, M.A.3
  • 4
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    • Studies in the chlorophyll series: II. Reduction and catalytic hydrogenation
    • Conant J.B., and Hyde J.F. Studies in the chlorophyll series: II. Reduction and catalytic hydrogenation. J. Am. Chem. Soc. 52 (1930) 1233-1239
    • (1930) J. Am. Chem. Soc. , vol.52 , pp. 1233-1239
    • Conant, J.B.1    Hyde, J.F.2
  • 5
    • 84926433255 scopus 로고
    • The natural porphyrins: VIII. Uroporphyrinogen heptamethyl ester and a new conversion of uro- into coproporphyrin
    • Fischer H., and Zerweck W. The natural porphyrins: VIII. Uroporphyrinogen heptamethyl ester and a new conversion of uro- into coproporphyrin. Z. Physiol. Chem. 137 (1924) 242-264
    • (1924) Z. Physiol. Chem. , vol.137 , pp. 242-264
    • Fischer, H.1    Zerweck, W.2
  • 6
    • 0038341842 scopus 로고    scopus 로고
    • Quantitative microscale hydrogenation of vegetable oils
    • Blanchard D.E. Quantitative microscale hydrogenation of vegetable oils. J. Chem. Educ. 80 (2003) 544-546
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    • Synthesis and crystal structure of a novel tripyrrane-containing porphyrinogen-like macrocycle
    • Sessler J.L., Johnson M.R., and Lynch V. Synthesis and crystal structure of a novel tripyrrane-containing porphyrinogen-like macrocycle. J. Org. Chem. 52 (1987) 4394-4397
    • (1987) J. Org. Chem. , vol.52 , pp. 4394-4397
    • Sessler, J.L.1    Johnson, M.R.2    Lynch, V.3
  • 11
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    • Measurement of uroporphyrinogen decarboxylase activity
    • Maines M.D., Costa L.G., Reed D.J., Sassa S., and Sipes I.G. (Eds), John Wiley, New York
    • Phillips J.D., and Kushner J.P. Measurement of uroporphyrinogen decarboxylase activity. In: Maines M.D., Costa L.G., Reed D.J., Sassa S., and Sipes I.G. (Eds). Current Protocols in Toxicology (1999), John Wiley, New York 841-8413
    • (1999) Current Protocols in Toxicology , pp. 841-8413
    • Phillips, J.D.1    Kushner, J.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.