Inhibition of porphobilinogen synthase by heme and an enol-ether amino acid
Author:
Publisher
Elsevier BV
Subject
General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine
Reference16 articles.
1. Inhibition of δ-aminolevulinic acid synthetase and δ-aminolevulinic acid dehydrase by L-2-amino-4-methoxy--3-butenoic acid in the rat
2. Mechanisms of action of naturally occurring irreversible enzyme inhibitors
3. The Genetic and Developmental Regulation of Hepatic δ-Aminolevulinate Dehydratase in Mice
4. Liver and red-cell porphobilinogen synthase in the adult and fetal guinea pig
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1. α-Vinylic amino acids: occurrence, asymmetric synthesis, and biochemical mechanisms;Tetrahedron: Asymmetry;2006-03
2. A Convenient Synthesis of (E)-4-Alkoxy-2-amino-3-butenoic Acid Derivatives;Bulletin of the Chemical Society of Japan;1999-10
3. A New Synthesis of (E)-4-Alkoxy-2-formylamino-3-butenoic Acid Derivatives Utilizing 3-Alkoxy-1-isocyano-1-lithiopropenes;Chemistry Letters;1997-06
4. New non-proteogenic aminoacids bearing an enol aryl-ether moiety.;Tetrahedron;1992-03
5. Improved synthetic access to the β,γ-enol ether amino acids, L-2-amino-4-methoxy-trans-but-3-enoic acid and l-2-amino-4-methoxy--but-3-enoic acid;Tetrahedron Letters;1990-01
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