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Androgen Receptor Androgen Receptor

Cat.No.  Name Information
M8128 R1881 R1881 (Metribolone) is an orally active, non-aromatisable androgen and anabolic steroid.
M6105 Testosterone Testosterone is an androgen, which binds the androgen receptor.
M5805 Nandrolone Nandrolone is a synthetic, anabolic steroid analog of testosterone.
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.
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.
M3502 Testosterone cypionate Testosterone cypionate is the oil-soluble 17 (beta)-cyclopentylpropionate ester of the androgenic hormone testosterone.
M1973 Ostarine (MK-2866) Ostarine (GTx-024 and MK-2866) is an investigational selective androgen receptor modulator (SARM) with Ki of 3.8 nM.
M1839 MDV3100 MDV3100 is an orally bioavailable, organic, non-steroidal small molecule targeting the androgen receptor (AR) with potential antineoplastic activity.
M54872 BMS-986365 BMS-986365 (CC-94676) is a selective heterobifunctional ligand-directed degrader (LDD) with a dual mechanism-of-action and best-in-class potential, targeting the androgen receptor (AR). In animal models of advanced prostate cancer, BMS-986365 demonstrates on-target activity, degrading AR, suppressing AR signaling, and inhibiting tumor growth.
M54608 Androstenone Androstenone is a steroid pheromone and also a metabolite of androgens.
M43897 APC-100 APC-100 is the antioxidant portion of vitamin E (α-tocopherol) and an androgen receptor (AR) inhibitor that may be used in studies related to prostate cancer.
M20966 Ligandrol Ligandrol (LGD-4033) is a novel nonsteroidal, oral selective androgen receptor modulator with high affinity (Ki of ∼1 nM) and selectivity. Ligandrol (LGD-4033) has demonstrated anabolic activity in the muscle, anti-resorptive and anabolic activity in bone, and robust selectivity for muscle versus prostate In animal models.
M16523 Ailanthone Ailanthone is a potent inhibitor of both full-length androgen receptor (AR) (IC50=69 nM) and constitutively active truncated AR splice variants (AR1-651 IC50=309 nM).
M14622 Stanolone benzoate Stanolone benzoate (Androstanolone benzoate) is a synthetic androgen and anabolic steroid.
M14620 Vosilasarm Vosilasarm (RAD140) is a potent, orally active, nonsteroidal selective androgen receptor modulator (SARM) with a Ki of 7 nM. Vosilasarm shows good selectivity over other steroid hormone nuclear receptors.
M14619 MK-0773 MK-0773 is a selective androgen receptor modulators (SARMs) that binds to AR with an IC50 of 6.6 nM.
M14618 LY2452473 LY2452473 is an orally bioavailable, selective androgen receptor modulator (SARM).
M14617 GLPG0492 GLPG0492 is a non-steroidal selective androgen receptor modulator (potency 12 nM). GLPG0492 has the potential for the research of musculo-skeletal diseases such as sarcopenia and cachexia.
M14615 BMS-564929 BMS-564929 is an androgen receptor (AR) agonist, binds to androgen receptor (AR) with a Ki of 2.11±0.16 nM.
M14614 ACP-105 ACP-105 is an orally available, selective amd potent androgen receptor modulator (SARM), with pEC50s of 9.0 and 9.3 for AR wild type and T877A mutant, respectively.




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