Synthesis and biological evaluation of 3-tetrazolo steroidal analogs: Novel class of 5α-reductase inhibitors-Reference-Cited by-同舟云学术

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Synthesis and biological evaluation of 3-tetrazolo steroidal analogs: Novel class of 5α-reductase inhibitors

Published:2016-02 Issue:4 Volume:24 Page:779-788
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Aggarwal Saurabh,Mahapatra Manoj Kumar,Kumar Rajnish,Bhardwaj Tilak R.,Hartmann Rolf W.,Haupenthal Jörg,Kumar Manoj

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference32 articles.

1. Steroid 5 α-reductase inhibitors targeting BPH and prostate cancer

2. The Development of Human Benign Prostatic Hyperplasia with Age

3. Molecular Features of Hormone-Refractory Prostate Cancer Cells by Genome-Wide Gene Expression Profiles

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Tetrazoles: A multi-potent motif in drug design;European Journal of Medicinal Chemistry;2024-09

2. Synthesis and Pharmacological Properties of Modified A- and D-Ring in Dehydroepiandrosterone (DHEA): A Review;ACS Omega;2024-07-16

3. A chemoenzymatic process for preparation of highly purified dehydroepiandrosterone in high space-time yield;Bioorganic Chemistry;2023-04

4. Synthesis, Characterization and Evaluation of 5α, 6β-Dihalo Androsterone Derivatives as 5α-Reductase Inhibitors;Current Enzyme Inhibition;2022-10

5. 3D-QSAR, Molecular Docking and Pharmacokinetic Studies: In-Silico Approach to Search Novel Inhibitors of 5-Alpha Reductase for Treatment of Benign Prostatic Hyperplasia;Current Enzyme Inhibition;2022-10

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