In silico structural prediction of human steroid 5α-reductase type II-Reference-Cited by-同舟云学术

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In silico structural prediction of human steroid 5α-reductase type II

Published:2016-03-09 Issue:6 Volume:25 Page:1049-1056
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Karnsomwan Wiranpat,Rungrotmongkol Thanyada,De-Eknamkul Wanchai,Chamni Supakarn^ORCID

Funder

New Researcher Grants of National Science and Technology Development Agency sponsored by Ministry of Science & Technology, Thailand

Chulalongkorn University and ICS-UNIDO collaborative research project

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/s00044-016-1541-y.pdf

Reference31 articles.

1. Aggarwal S, Thareja S, Verma A, Bhardwaj TR, Kumar M (2010) An overview on 5α-reductase inhibitors. Steroids 75:109–153

2. Arnold K, Bordoli L, Kopp J, Schwede T (2006) The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling. Bioinformatics 22:195–201

3. Azzouni F, Godoy A, Li Y, Mohler J (2012) The 5α-reductase isozyme family: a review of basic biology and their role in human diseases. Adv Urol 12:1–18

4. Berséus O, Björkhem I (1967) Enzymatic conversion of a Δ4-3-ketosteroid into a 3α-hydroxy-5β-steroid: mechanism and stereochemistry of hydrogen transfer from NADPH. Eur J Biochem 2:503–507

5. Björkhem I (1969) Mechanism and stereochemistry of the enzymatic conversion of a Δ4-3-oxosteroid into a 3-oxo-5α-steroid. Eur J Biochem 8:345–351

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4. Erratum to: In silico structural prediction of human steroid 5α-reductase type II;Medicinal Chemistry Research;2017-03-18

5. Synthesis, Biological Evaluation and Molecular Docking of Avicequinone C Analogues as Potential Steroid 5α-Reductase Inhibitors;Chemical and Pharmaceutical Bulletin;2017

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