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RU58841 – Powder, 5 grams

RU58841 (PSK-3841) is a non-steroidal androgen receptor (AR) antagonist developed to selectively inhibit AR-mediated signaling pathways.

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RU58841 (PSK-3841) is a non-steroidal androgen receptor (AR) antagonist developed to selectively inhibit AR-mediated signaling pathways. Experimental investigations have demonstrated that RU58841 competes with androgenic ligands for binding to the androgen receptor, preventing receptor activation and downstream transcriptional activity.

Research has examined its interactions with AR-associated regulatory mechanisms, ligand-receptor dynamics, nuclear receptor signaling pathways, and transcriptional control processes governed by androgen receptor activation.

Its well-characterized antagonist profile makes RU58841 a valuable research tool for studies of androgen receptor pharmacology, AR-mediated signal transduction, receptor-ligand competition, nuclear receptor regulation, and comparative investigations of androgen receptor antagonists.

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3D Molecular Structure

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Chemical Formula C17H18F3N3O3
Synonyms PSK-3841, HMR-3841, 4-[3-(4-Hydroxybutyl)-4,4-dimethyl-2,5-dioxo-1-imidazolidinyl]-2-(trifluoromethyl)benzonitrile
Molar Mass 369.34 g/mol
CAS Number 154992-24-2
PubChem CID 132981
Total Compound Content 5 g powder
Shelf Life 36 months
RU58841 (PSK-3841) is a hydantoin-class non-steroidal androgen receptor (AR) antagonist that functions through competitive inhibition of androgen receptor signaling. Experimental investigations have demonstrated that RU58841 competes with androgenic ligands for binding to the AR ligand-binding domain, preventing receptor activation and subsequent transcriptional activity. Research has examined its interactions with AR-associated regulatory mechanisms, ligand-receptor dynamics, nuclear receptor signaling pathways, and androgen-responsive gene regulation. Its antagonist profile and well-characterized receptor interactions make RU58841 a valuable research tool for studies of androgen receptor pharmacology, AR-mediated signal transduction, receptor-ligand competition, nuclear receptor regulation, and comparative investigations of androgen receptor antagonists. Supplied as powder (5 g). Independently third-party HPLC-tested; COA available per batch.

Every batch is independently lab tested for identity, purity and potency. View our lab testing program →

Why was RU58841 developed as a locally acting androgen receptor antagonist?

RU58841 was developed as a non-steroidal androgen receptor antagonist for investigations of localized AR-mediated signaling pathways.

Its pharmacological profile has made it a useful research tool for examining androgen receptor activity within defined experimental systems while studying receptor-ligand interactions, androgen-responsive gene regulation, and AR-dependent signal transduction mechanisms. This distinguishes RU58841 from compounds primarily utilized for broader systemic androgen receptor pharmacology studies.

How does RU58841's androgen receptor affinity compare with other AR ligands?

RU58841 exhibits high affinity for the androgen receptor and functions as a competitive antagonist at the AR ligand-binding domain. Experimental studies have utilized RU58841 in receptor-binding assays, ligand competition experiments, and investigations of androgen receptor activation mechanisms.

Its well-characterized antagonist profile makes it a valuable reference compound for comparative studies of androgen receptor pharmacology and receptor-ligand dynamics.

What formulation characteristics make RU58841 powder useful for research applications?

RU58841 powder provides flexibility for preparation in a variety of experimental systems, including receptor-binding assays, cell-based signaling studies, gene expression analyses, and formulation development investigations. The powder format allows researchers to prepare defined concentrations in assay-specific solvents and vehicles, supporting studies of androgen receptor signaling, concentration-response relationships, receptor occupancy, and comparative pharmacological evaluation of AR antagonists.

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