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. |
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 (GTx-024) | 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. |
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 (LGD-4033, VK-5211) | Ligandrol (LGD-4033, VK-5211) is a novel nonsteroidal, oral selective androgen receptor modulator with high affinity (Ki of ∼1 nM) and selectivity. |
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. |
M14613 | 3,3'-Diindolylmethane | 3,3'-Diindolylmethane is a strong, pure androgen receptor (AR) antagonist. |
M11020 | Proxalutamide | Proxalutamide (GT0918) is an antagonist of the androgen receptor (AR) with oral activity. Proxalutamide (GT0918) can be used in prostate cancer and COVID-19 research. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2023 AbMole BioScience. All Rights Reserved.