The role of the heterocycle in bis(hydroxyphenyl)triazoles for inhibition of 17beta-Hydroxysteroid Dehydrogenase (17beta-HSD) type 1 and type 2
Yaseen A Al-Soud,
Al-Soud YA,
Bey E,
Emmanuel Bey,
Alexander Oster,
Oster A,
Marchais-Oberwinkler S,
Sandrine Marchais-Oberwinkler,
Werth R,
Ruth Werth,
Patricia Kruchten,
Kruchten P,
Martin Frotscher,
Frotscher M,
Hartmann RW,
Rolf W. Hartmann
Lab / animal
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AI-generated summary
by gemini-2.5-flash-lite, 2026-06-11
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This study investigated bis(hydroxyphenyl)triazoles as inhibitors of 17beta-HSD1 and 17beta-HSD2, finding 3-[4-(4-Hydroxyphenyl)-1H-1,2,3-triazol-1-yl]phenol to be the most potent inhibitor of 17beta-HSD1 with good selectivity.
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AI-generated deep summary
by claude@2026-06, 2026-06-11
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The content provided does not include the actual scientific paper text (it is blocked by a Proof-of-Work page), so the study’s objectives, methods, results, and stated limitations cannot be determined. No experimental or analytical findings about bis(hydroxyphenyl)triazoles or 17β-hydroxysteroid dehydrogenase are accessible from the message. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.
Abstract
17beta-Hydroxysteroid dehydrogenase type 1 (17beta-HSD1) is responsible for the catalytic reduction of the weak estrogen estrone (E1) into the highly potent 17beta-estradiol (E2). As 17beta-HSD1 is often overexpressed in mammary tumors and endometriosis, the selective inhibition of this enzyme is discussed as a promising approach for the treatment of estrogen-dependent diseases. Recently, we reported on bis(hydroxyphenyl)azoles as a new class of potent inhibitors of 17beta-HSD1. In this paper, we focused on bis(hydroxyphenyl)triazoles. The influence of nitrogens on the potency as well as the space available around the heterocycle was investigated. Substituents were introduced on the triazole core in order to establish additional interactions with the enzyme active site. The compounds were evaluated for activity towards 17beta-HSD1 and selectivity with regard to 17beta-HSD2, the enzyme which is responsible for the deactivation of E2 into E1. 3-[4-(4-Hydroxyphenyl)-1H-1,2,3-triazol-1-yl]phenol (3) was the most active compound discovered in this study with an IC(50) value of 840nM and a reasonable selectivity towards 17beta-HSD2.
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Condition tags
endometriosis
MeSH descriptors
Enzyme Inhibitors
Enzyme Inhibitors
Estradiol Dehydrogenases
Triazoles
Triazoles
Enzyme Inhibitors
Enzyme Inhibitors
Estradiol
Estradiol
Estradiol
Estradiol
Estradiol Dehydrogenases
Estradiol Dehydrogenases
Estrone
Estrone
Estrone
Estrone
Humans
Humans
Triazoles
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Source provenance
- europepmc
- last seen: 2026-10-25T09:32:14.900964+00:00
- pubmed
- last seen: 2026-10-08T21:05:50.299847+00:00
- unpaywall
- last seen: 2026-05-14T19:30:52.867331+00:00
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