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Androgen Receptor Androgen Receptor

Cat.No.  Name Information
M1973 Ostarine Ostarine (GTx-024 and MK-2866) is an investigational selective androgen receptor modulator (SARM) with Ki of 3.8 nM.
M6033 Dihydrotestosterone Dihydrotestosterone is an androgen (male hormone). Specifically it's the strongest of the androgens. It can be used to construct animal models of polycystic ovary syndrome (PCOS).
M5565 Dexmedetomidine HCl Dexmedetomidine Hydrochloride is an agonist of adrenergic alpha-2 receptor, which is used in veterinary medicine for its analgesic and sedative properties.
M5805 Nandrolone Nandrolone is a synthetic, anabolic steroid analog of testosterone.
M1839 MDV3100 MDV3100 is an orally bioavailable, organic, non-steroidal small molecule targeting the androgen receptor (AR) with potential antineoplastic activity.
M5764 Medroxyprogesterone acetate Medroxyprogesterone acetate (MPA) is a synthetic progestin and act as a potent progesterone receptor agonist, used to treat abnormal menstruation or irregular vaginal bleeding.
M2270 Apalutamide (ARN-509) Apalutamide (ARN-509) is a novel androgen receptor (AR) antagonist for the treatment of castration-resistant prostate cancer (CRPC).
M10306 Bavdegalutamide (ARV-110) Bavdegalutamide (ARV-110) is an oral, specific androgen receptor (AR) PROTAC degrader.
M6269 Indacaterol Indacaterol is an orally active ultra-long-acting β2 adrenergic receptor (ADRB2) agonist. Indacaterol inhibits NF-κB activity in a β-arrestin2-dependent manner.
M6123 Nandrolone phenylpropionate Nandrolone phenylpropionate (NPP) is an anabolic-androgenic steroid. The low androgenicity and enhanced anabolic activity of NPP has shown to positively influence calcium metabolism and to increase bone mass in osteoporosis.
M6122 ChlordehydroMethyl Testosterone A male hormone.
M6115 Drostanolone Propionate Drostanolone propionate can reduce the uptake of oestradiol-17B by tumour cells
M6114 Metandienone Metandienone is a synthetic anabolic steroid that is prohibited in sports by the World Anti-Doping Agency (WADA).
M6099 Boldenone Undecylenate Boldenone undecylenate(Equipoise) is a synthetic steroid which has a similar effect as the natural steroid testosterone.
M5778 Methenolone acetate Metenolone (Methenolone) is a long-acting anabolic steroid with weak androgenic properties.
M5586 DL-Epinephrine DL-Epinephrine(DL-Adrenaline) is a hormone and a neurotransmitter.
M5544 Cyproterone Acetate Cyproterone acetate is an androgen receptor (AR) antagonist with IC50 of 7.1 nM.
M5454 Betaxolol hydrochloride Betaxolol hydrochloride is a β1 adrenergic receptor blocker with IC50 of 6 μM.
M5396 Alfuzosin HCl Alfuzosin HCl is an alpha1 receptor antagonist used to treat benign prostatic hyperplasia (BPH).
M5395 Alfuzosin Alfuzosin is an α1 adrenergic receptor antagonist used to treat benign prostatic hyperplasia (BPH).
M5035 Clascoterone Clascoterone (Cortexolone 17α-propionate, CB-03-01) is a new selective androgen receptor (AR) antagonist.
M4703 Lupeol Lupeol (Clerodol; Monogynol B; Fagarasterol (Fagarasterol) is an active pentacyclic triterpenoid with antioxidant, anti-tumor and anti-inflammatory activities. Lupeol is a potent androgen receptor inhibitor that can be used in cancer research, especially in prostate cancer with androgen-dependent phenotypes (ADPC) and castration-resistant phenotypes (CRPC).
M4199 Triptophenolide Triptophenolide is a colorless crystal isolated from the ethyl acetate extract of Triptophenolide.
M3933 Danazol Danazol is a derivative of the synthetic steroid ethisterone that suppresses the production of gonadotrophins and has some weak androgenic effects.
M3750 TAK-700 TAK-700 (Orteronel) is an investigational, oral, nonsteroidal, selective, reversible inhibitor of 17,20-lyase, a key enzyme in the production of androgenic hormones.
M3748 Mestanolone Mestanolone is the 17α-methylated version of dihydrotestosterone (DHT).
M3685 Mesterolone The Mesterolone is an orally applicable androgen, and DHT derivative.
M3234 (R)-Bicalutamide (R)-Bicalutamide is an active competitive non-steroidal androgen receptor antagonist with an IC50 of 0.17 μM for MDA 453 cells.




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