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ChemInform Abstract: PORPHOBILINOGEN‐SYNTH.

Chemischer Informationsdienst, 1973
Abstractβ‐Oxo‐adipinsäure‐diäthylester (I) wird mit Pentylnitrit und anschließend mit Acetylaceton in Essigsäure in Gegenwart von Zink und Ammoniumacetat in 50%iger Ausbeute zu dem Acetylpyrrol (II) umgesetzt, das mit Thallium(III)‐ nitrat in‐Methanol das Methoxycarbonylmethyl‐pyrrol (III) ergibt.
G. W. KENNER   +2 more
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[19] Preparation of porphobilinogen

1970
Publisher Summary This chapter illustrates the preparation of porphobilinogen (PBG). PBG is a normal intermediate in the biosynthesis of heme. An enzymatic method has been considered for the preparation of porphobilinogen with good yield using both δ-aminolevulinic acid and the enzyme aminolevulinic acid dehydratase.
H.A. Sancovich   +3 more
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The porphobilinogen synthase catalyzed reaction mechanism

Bioorganic Chemistry, 2004
Porphobilinogen synthase (PBGS) catalyzes the first common reaction in the biosynthesis of the tetrapyrroles, the asymmetric condensation of two molecules of delta-aminolevulinic acid to form porphobilinogen. There is a variable requirement for an essential active site zinc that necessitates consideration of PBGS as an enzyme that may exhibit ...
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Porphobilinogen synthesis

Journal of the Chemical Society, Chemical Communications, 1973
G. W. Kenner   +2 more
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Porphobilinogen

2017
T. Arndt, T. Stauch
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PORPHOBILINOGEN

The Lancet, 1952
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Porphobilinogen

Fresenius' Zeitschrift f�r Analytische Chemie, 1957
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Porphobilinogen synthase

1990
Dietmar Schomburg, Margit Salzmann
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