A New and Efficient Synthesis of the HMG-CoA Reductase Inhibitor Pitavastatin-Reference-Cited by-同舟云学术

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A New and Efficient Synthesis of the HMG-CoA Reductase Inhibitor Pitavastatin

Published:2007-06 Issue:6 Volume:90 Page:1069-1081
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:en
Short-container-title:HCA

Author:

Acemoglu Murat,Brodbeck Andre,Garcia Angel,Grimler Dominique,Hassel Marc,Riss Bernhard,Schreiber Robert

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference30 articles.

1. Mode of interaction of .beta.-hydroxy-.beta.-methylglutaryl coenzyme A reductase with strong binding inhibitors: compactin and related compounds

2. ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogensis produced by Penicillium citrinum.

3. Competitive inhibition of 3-hydroxy-3-methylglutaryl coenzyme a reductase by ML-236A and ML-236B fungal metabolites, having hypocholesterolemic activity

4. Inhibition of Cholesterol Synthesis in vitro and in vivo by ML-236A and ML-236B, Competitive Inhibitors of 3-Hydroxy-3-methylglutaryl-Coenzyme A Reductase

5. Compactin (ML-236B) and related compounds as potential cholesterol-lowering agents that inhibit HMG-CoA reductase

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4. Chemoenzymatic Synthesis of δ-Keto β-Hydroxy Esters as Useful Intermediates for Preparing Statins;European Journal of Organic Chemistry;2016-05-20

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