Description:
Background: Benign Prostatic Hyperplasia (BPH), and Prostate Cancer (PCa) are androgendependent diseases. PPCa is associated with excessive signalling of the androgen receptor (AR)
due to the binding of 5?-dihydrotestosterone (5?-DHT) and testosterone (T). BPH is related
to high levels of 5?-DHT, biosynthesized from T by 5?-reductase (5RD5A). The inhibition
of 5RD5A and the blockage of AR are targets for their treatment. In this study, the synthesis
and determination of biological activity of the new N-cyclohexyl-3?-hydroxyandrosta-5,16-
diene-17-carboxamide (6), N-cyclohexyl-3-oxoandrosta-4,6,16-triene-17-carboxamide (7),
and N-cyclohexyl-3-oxoandrosta-4,16-diene-17-carboxamide (8) were carried out to find new
drugs to improve these afflictions.
Methods: The synthesis of 6 to 8 was confirmed by spectroscopic and spectrometric analyses.
Competitive binding assays determined the affinity of 6 to 8 to the AR. The inhibitory activity of
5RD5A isoform 2 (5RD5A2) (IC50) was established by the conversion of [3
H]-T to [3
H]-5?-DHT
and it was compared with finasteride (FIN). The pharmacological effect of 6 to 8 was determined
on the weight of the prostate and seminal vesicles glands of castrated hamsters treated with T,
and on the diameter size of their flank organs.
Results: Compounds 7 and 8 bound lightly (ca. 15 %) to AR. Comparing to FIN (IC50 = 8.5
nM), 6 to 8 (IC50 = 0.169, 0.105 and 0.155 nM, respectively) showed higher potency as inhibitors
of 5RD5A2. Compound 6 decreased the prostate and seminal vesicles weight, as well as the
hamsters’ diameter flank organs. However, 7 only decreased the diameter of flank organs.
Surprisingly, 8 increased these pharmacological parameters.
Conclusion: Androstane-17-caboxamide 6 is a 5RD5A2 inhibitor that reduces the weight of
androgen-dependent glands such as the prostate, suggesting it could be a lead for new drugs to
treat BPH and PCa.
URL:
http://103.158.96.210:88/web_repository/uploads/ps-28-433.pdf
Type:
Journal
Document:
Diploma III Farmasi
Date:
23-06-2024
Author:
Juan C. Lopez-Lezama