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Home > Inhibitors & Agonists > Nuclear Receptor/Transcription Factor > Androgen Receptor (AR)

RU58841

  Cat. No.:  DC4163   Featured
Chemical Structure
154992-24-2
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More than 5000 active chemicals with high quality for research!
Field of application
RU58841 is a nonsteroidal anti-androgen with potency (IC50 = 100 nM, Ka = 1.1 nM) comparable to hydroxyflutamide.
Chemicals PropertiesBiological activity COA & MSDSRelated productsDatasheet
Cas No.: 154992-24-2
Chemical Name: RU58841,RU 58841,RU-58841
Synonyms: RU58841,RU 58841,RU-58841
SMILES: O=C(N1CCCCO)N(C(C1(C)C)=O)C2=CC=C(C#N)C(C(F)(F)F)=C2
Formula: C17H18F3N3O3
M.Wt: 369.34
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: RU 58841 (PSK-3841) is a specific androgen receptor antagonist or anti-androgen. RU 58841 (PSK-3841) has a dramatic effect on hair regrowth.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
DC10811 S23 S23 is a novel Selective Androgen Receptor Modulator(SARM)
DC4163 RU58841 RU58841 is a nonsteroidal anti-androgen with potency (IC50 = 100 nM, Ka = 1.1 nM) comparable to hydroxyflutamide.
DC9657 RAD140 RAD140 is a potent, orally bioavailable, nonsteroidal selective androgen receptor modulator (SARM).
DC8248 Ostarine(MK-2286) Ostarine (MK-2866) is a selective androgen receptor modulator (SARMs) that regulates cardiomyocyte function, improves bone healing, regulates uterine function, and influences muscle tissue metabolism.
DC8700 ODM-201(Darolutamide) ODM-201 is a potent and full antagonists for human AR (hAR) with IC50 values of 26 nM by transactivation assays in AR-HEK293 cells.
DC5069 Enzalutamide (MDV3100) MDV3100 is an androgen-receptor (AR) antagonist with IC50 of 36 nM.
DC7633 Ligandrol (VK5211, LGD-4033) Ligandrol (LGD-4033) is a novel nonsteroidal, oral SARM that binds to androgen receptor with high affinity (Ki of 1 nM) and selectivity.
DC9738 GSK2881078 GSK-2881078 is an orally active and nonsteroidal selective androgen receptor modulator (SARM) which act as partial AR agonists in androgenic tissues while mainly as complete AR agonists in synthetic metabolic tissues,induces AR-mediated transcriptional activation in PC3(AR)2 cells (EC50 = 3.99 nM) and the effect can be inhibited by the non-steroidal AR antagonist Bicalutamide. GSK-2881078 can be used in research of muscle weakness and cachexia associated with both chronic and acute illness.
DC8856 EPI-001 EPI-001 is an androgen receptor N-terminal domain antagonist with IC50 of ∼6 μM and a selective PPAR-gamma modulator
DC4160 CB-03-01 CB-03-01 is a steroidal ester, androgen antagonist derived from 11-deoxycortisone, which tightly mimics the profile of an ideal anti-androgen for topical use.
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