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Recent Advances in Drug Design and Drug Discovery for Androgen-Dependent Diseases

This article summarizes the importance of different targets such as 5α-reductase, 17β-HSD, CYP17A, androgen receptor and protein kinase A for the treatment of prostate cancer and benign prostatic hyperplasia. It is a well known fact that dihydrotestosterone (DHT) is associated with the development o...

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Autores principales: Cabeza, Marisa, Sánchez-Márquez, Araceli, Garrido, Mariana, Silva, Aylín, Bratoeff, Eugene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412001/
https://www.ncbi.nlm.nih.gov/pubmed/26861003
http://dx.doi.org/10.2174/0929867323666160210125642
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author Cabeza, Marisa
Sánchez-Márquez, Araceli
Garrido, Mariana
Silva, Aylín
Bratoeff, Eugene
author_facet Cabeza, Marisa
Sánchez-Márquez, Araceli
Garrido, Mariana
Silva, Aylín
Bratoeff, Eugene
author_sort Cabeza, Marisa
collection PubMed
description This article summarizes the importance of different targets such as 5α-reductase, 17β-HSD, CYP17A, androgen receptor and protein kinase A for the treatment of prostate cancer and benign prostatic hyperplasia. It is a well known fact that dihydrotestosterone (DHT) is associated with the development of androgen-dependent afflictions. At the present time, several research groups are attempting to develop new steroidal and non-steroidal molecules with the purpose of inhibiting the synthesis and biological response of DHT. This review also discusses the most recent studies reported in the literature that describe the therapeutic potential of novel compounds, as well as the new drugs, principally inhibitors of 5α-reductase.
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spelling pubmed-54120012017-05-12 Recent Advances in Drug Design and Drug Discovery for Androgen-Dependent Diseases Cabeza, Marisa Sánchez-Márquez, Araceli Garrido, Mariana Silva, Aylín Bratoeff, Eugene Curr Med Chem Article This article summarizes the importance of different targets such as 5α-reductase, 17β-HSD, CYP17A, androgen receptor and protein kinase A for the treatment of prostate cancer and benign prostatic hyperplasia. It is a well known fact that dihydrotestosterone (DHT) is associated with the development of androgen-dependent afflictions. At the present time, several research groups are attempting to develop new steroidal and non-steroidal molecules with the purpose of inhibiting the synthesis and biological response of DHT. This review also discusses the most recent studies reported in the literature that describe the therapeutic potential of novel compounds, as well as the new drugs, principally inhibitors of 5α-reductase. Bentham Science Publishers 2016-03 2016-03 /pmc/articles/PMC5412001/ /pubmed/26861003 http://dx.doi.org/10.2174/0929867323666160210125642 Text en © 2016 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Cabeza, Marisa
Sánchez-Márquez, Araceli
Garrido, Mariana
Silva, Aylín
Bratoeff, Eugene
Recent Advances in Drug Design and Drug Discovery for Androgen-Dependent Diseases
title Recent Advances in Drug Design and Drug Discovery for Androgen-Dependent Diseases
title_full Recent Advances in Drug Design and Drug Discovery for Androgen-Dependent Diseases
title_fullStr Recent Advances in Drug Design and Drug Discovery for Androgen-Dependent Diseases
title_full_unstemmed Recent Advances in Drug Design and Drug Discovery for Androgen-Dependent Diseases
title_short Recent Advances in Drug Design and Drug Discovery for Androgen-Dependent Diseases
title_sort recent advances in drug design and drug discovery for androgen-dependent diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412001/
https://www.ncbi.nlm.nih.gov/pubmed/26861003
http://dx.doi.org/10.2174/0929867323666160210125642
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