17 beta hsd type 5 inhibitor

2009
OA: closed
⚙ AI-generated summary by qwen3.7-flash, 2026-09-26 ⓘ

An N-sulfonylindole derivative selectively inhibits 17beta HSD type 5, offering a potential treatment for endometriosis and other conditions associated with this enzyme without causing testosterone-related side effects.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

Abstract

It is intended to provide a novel and excellent method of treating and/or preventing prostate cancer, prostate enlargement, acne, seborrhea, hypertrichosis, calvities, alopecia, sexual precocity, adrenal hypertrophy, multilocular ovary syndrome, breast cancer, lung cancer, endometriosis, leiomyoma and so on based on an effect of selectively inhibiting 17beta HSD type 5. It is found out that an N-sulfonylindole derivative, in which a carbon atom in the indole group is substituted by a carboxy group, a carboxy-substituted lower alkyl group or a carboxy-substituted lower alkenyl group, has a potent activity of selectively inhibiting 17beta HSD type 5 and is usable as a remedy and/or a preventive for diseases, in which 17beta HSD type 5 participates, such as prostate enlargement and prostate cancer without showing any side effect caused by a decrease in testosterone.

My notes (saved in your browser only)

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.

Source provenance

europepmc
last seen: 2026-08-13T06:15:24.848197+00:00