Synthesis and characterization of targeted 17β-hydroxysteroid dehydrogenase type 7 inhibitors.
In: The Journal of steroid biochemistry and molecular biology, Jg. 242 (2024-09-01), S. 106544
academicJournal
Zugriff:
Sex steroid hormones such as estrogen estradiol (E2) and androgen dihydrotestosterone (DHT) are involved in the development of hormone-dependent cancers. Blockade of 17β-hydroxysteroid dehydrogenase type 7 (17β-HSD7), a member of the short chain dehydrogenase/reductase superfamily, is thought to decrease E2 levels while increasing those of DHT. Therefore, its unique double action makes this enzyme as an interesting drug target for treatment of breast cancer. The chemical synthesis, molecular characterization, and preliminary biological evaluation as 17β-HSD7 inhibitors of novel carbamate derivatives 3 and 4 are described. Like previous 17β-HSD7 inhibitors 1 and 2, compounds 3 and 4 bear a hydrophobic nonyl side chain at the C-17β position of a 4-aza-5α-androstane nucleus, but compound 3 has an oxygen atom replacing the CH 2 in the steroid A-ring C-2 position, while compound 4 has a C17-spiranic E-ring containing a carbamate function. They both inhibited the in vitro transformation of estrone (E1) into E2 by 17β-HSD7, but the introduction of a (17 R)-spirocarbamate is preferable to replacing C-2 methylene with an oxygen atom since compound 4 (IC 50 = 63 nM) is an inhibitor 14 times more powerful than compound 3 (IC 50 = 900 nM). Furthermore, when compared to the reference inhibitor 1 (IC 50 = 111 nM), the use of a C17-spiranic E-ring made it possible to introduce differently the hydrophobic nonyl side chain, without reducing the inhibitory activity.
Competing Interests: Declaration of Competing Interests MZ declares no competing interests, while JYS, RM, SXL, and DP are owners of a patent on 17β-HSD type 7 inhibitors.
(Copyright © 2024 Elsevier Ltd. All rights reserved.)
Titel: |
Synthesis and characterization of targeted 17β-hydroxysteroid dehydrogenase type 7 inhibitors.
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Autor/in / Beteiligte Person: | Sancéau, JY ; Maltais, R ; Zhou, M ; Lin, SX ; Poirier, D |
Zeitschrift: | The Journal of steroid biochemistry and molecular biology, Jg. 242 (2024-09-01), S. 106544 |
Veröffentlichung: | Oxford ; New York : Pergamon, c1990-, 2024 |
Medientyp: | academicJournal |
ISSN: | 1879-1220 (electronic) |
DOI: | 10.1016/j.jsbmb.2024.106544 |
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