Title of article :
Inhibition of 3(17)α-hydroxysteroid dehydrogenase (AKR1C21) by aldose reductase inhibitors Original Research Article
Author/Authors :
Urmi Dhagat، نويسنده , , Satoshi Endo، نويسنده , , Akira Hara and Yukio Mitsui، نويسنده , , Ossama El-Kabbani، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Abstract :
Mouse 3(17)α-hydroxysteroid dehydrogenase (AKR1C21) is a member of the aldo-keto reductase superfamily that catalyses the oxido-reduction of steroid hormones such as estrogens, androgens and neurosteroids. Inhibitors of aldose reductase (AR), a member of the same superfamily, were evaluated against AKR1C21. Models of the enzyme–inhibitor complexes suggest that Tyr118 and Phe311 are important residues for inhibitor recognition and orientation in the active site of AKR1C21.
Keywords :
drug design , Hydroxysteroid dehydrogenases , Aldose reductase , Enzyme inhibition , Molecular modeling , Aldo-keto reductases
Journal title :
Bioorganic and Medicinal Chemistry
Journal title :
Bioorganic and Medicinal Chemistry