The nuclear receptor known as the androgen receptor (AR) is activated when either the androgenic hormones testosterone or dihydrotestosterone bind to it in the cytoplasm before moving into the nucleus. The receptor separates from supporting proteins after binding the hormone ligand, moves into the nucleus, dimerizes, and then activates transcription of androgen-responsive genes. The progesterone receptor is most similar to the androgen receptor, and progestins can block the androgen receptor when used in higher doses. The androgen receptor's primary role is that of a DNA-binding transcription factor that controls gene expression. The development and maintenance of the male sexual phenotype depend heavily on genes that are regulated by androgen. Complete androgen insensitivity (CAIS) is a condition that is also correlated with mutations in this gene.
Structure | Cat No. | Product Name | CAS No. | Product Description |
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V98841 | (+)-JJ-74-138 | 2135545-34-3 | (+)-JJ-74-138 is a novel noncompetitive androgen receptor (AR) antagonist that inhibits enzalutamide-resistant castration-resistant prostate cancer (CRPC). |
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V89087 | (-)-Erteberel | 533884-08-1 | (-)-Erteberel is a selective estrogen receptor β (ERβ) agonist. |
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V89074 | (3β,4β,17β)-17-(2-Pyridinylmethyl)androst-5-ene-3,4,17-triol | 1393651-00-7 | (3β,4β,17β)-17-(2-Pyridinylmethyl)androst-5-ene-3,4,17-triol is an androstane derivative with anticancer activity. |
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V89081 | (R,R)-THC | 221368-54-3 | (R,R)-THC is an ERα agonist and ERβ antagonist, with Ki values of 9.0 nM and 3.6 nM for ERα and ERβ, respectively. |
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V89083 | 17-Epiestriol | 1228-72-4 | 17-Epiestriol is an estrogen metabolite and a selective estrogen receptor (ER) β agonist. |
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V8411 | AC-262536 | 870888-46-3 | AC-262536 (AC262536) is anovel selective androgen receptor modulator (SARM) with beneficial anabolic effects. |
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V10225 | ACP-105 | 899821-23-9 | ACP-105 (ACP105; ACP 105) is a novel, nonsteroidal and orally bioactive SARM (selective androgen receptor modulator) that has been investigated for the treatment of age-related cognitive decline. |
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V1761 | Andarine (GTx-007) | 401900-40-1 | Andarine (formerly known as GTx-007;S-4;GTx007;S4) is an orally bioactive and selective non-steroidal androgen receptor (AR) agonist,specifically a selective androgen receptor modulator (SARM),that has potential usefulness in muscle wasting and osteoporosis. |
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V88175 | Androgen receptor antagonist 10 | 876759-87-4 | Androgen receptor antagonist 10 (compound 6h) is an androgen receptor antagonist. |
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V93122 | Androgen receptor antagonist 12 | 6605-17-0 | Androgen receptor antagonist 12 (Compound EF2) is an orally active androgen receptor (AR) antagonist (IC50: 0.30 μM). |
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V85279 | Androgen receptor degrader-4 | 2505495-83-8 | |
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V98995 | Androgen receptor degrader-5 | 2902679-11-0 | Androgen receptor degrader-5 (compound 14k) exhibits favorable properties, including excellent androgen receptor (AR) degradation activity and antiproliferative activity. |
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V89078 | Androgen receptor-IN-3 | 926228-58-2 | Androgen Receptor-IN-3 (Compound 22) is an androgen receptor inhibitor. |
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V88176 | Androgen receptor-IN-4 | 2759137-87-4 | Androgen Receptor-IN-4 (Compound 206) is an androgen receptor inhibitor that can be used in the study of Kennedy's disease. |
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V85093 | AR antagonist 5 | 2902679-53-0 | |
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V88172 | AR antagonist 6 | 876760-08-6 | AR antagonist 6 (compound 6i) is a diphenyl ether androgen receptor (AR) antagonist that binds to AR at a concentration of 120 nM. |
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V89070 | AR antagonist 7 | 876759-97-6 | AR antagonist 7 (86) is an androgen receptor (AR) antagonist that can be used in the study of hair loss. |
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V89068 | AR antagonist 8 | AR antagonist 8 (compound 16) is ethinylestradiol, a potent Lupeol-inspired androgen receptor (AR) antagonist with IC50 of 0.76 μM. | |
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V88174 | AR Degrader-1 | AR Degrader-1 is a monovalent androgen receptor (AR) degrader. | |
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V89066 | AR Degrader-2 | 3023359-76-1 | AR Degrader-2 (Compound 2) is a degrader of androgen receptor (AR) with a DC50 of 0.3-0.5 μM in VCaP cells. |