Efficient isolation of carbonyl-reducing enzymes using affinity approach with anticancer drug oracin as a specific ligand-Reference-Cited by-同舟云学术

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Efficient isolation of carbonyl-reducing enzymes using affinity approach with anticancer drug oracin as a specific ligand

Published:2013-03-13 Issue:7 Volume:36 Page:1176-1184
ISSN:1615-9306
Container-title:Journal of Separation Science
language:en
Short-container-title:J. Sep. Science

Author:

Škarydová Lucie¹,Andrýs Rudolf¹,Holubová Lucie²,Štambergová Hana¹,Kňavová Jana²,Wsól Vladimír¹,Bílková Zuzana²

Affiliation:

1. Department of Biochemical Sciences; Faculty of Pharmacy in Hradec Králové; Charles University in Prague; Hradec Králové Czech Republic

2. Department of Biological and Biochemical Sciences; Faculty of Chemical Technology; University of Pardubice; Pardubice Czech Republic

Funder

Agency of Charles University

Agency of the Czech Republic

Charles University

Publisher

Wiley

Subject

Filtration and Separation,Analytical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jssc.201201141/fullpdf

Reference39 articles.

1. Human Carbonyl Reduction Pathways and a Strategy for Their Study In Vitro

2. Classification and nomenclature of the superfamily of short-chain dehydrogenases/reductases (SDRs)

3. The Aldo-Keto Reductase Superfamily and its Role in Drug Metabolism and Detoxification

4. Carbonyl Reductases and Pluripotent Hydroxysteroid Dehydrogenases of the Short-chain Dehydrogenase/reductase Superfamily

5. Classification of the short-chain dehydrogenase/reductase superfamily using hidden Markov models

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1. Towards cost-effective drug discovery: Reusable immobilized enzymes for neurological disease research;Talanta;2024-08

2. Imac-Immobilized Enzymes as a Cost-Effective and Sustainable Approach in an Early Phase of Drug Development for Neurological Diseases;2023

3. Carbonyl-reducing enzymes as targets of a drug-immobilised affinity carrier;Chemico-Biological Interactions;2015-06

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