Androgen Receptor
Androgen Receptor(雄激素受体)
AR (androgen receptor) is a member of steroid hormone receptor and ligand-activated transcription factor. It plays a crucial role in prostate cellular proliferation and male sexual differentiation.
Androgen Receptor 相关产品(148)
- GC11070Dehydroepiandrosterone (DHEA)CAS: 53-43-0纯度: >99.00%
脱氢表雄酮 (DHEA) 及其硫酸酯 DHEAS 共同代表了人体内最丰富的类固醇激素。
- GC12271BicalutamideCAS: 90357-06-5纯度: >98.00%
Bicalutamide是一种非甾体抗雄激素药物,可通过选择性和竞争性地阻断雄激素与雄激素受体(AR)的结合,在外周组织中发挥抗雄激素作用。
- GC12385MDV3100 (Enzalutamide)CAS: 915087-33-1纯度: >99.50%
MDV3100(enzalutamide) 是第二代 AR 拮抗剂,在 LNCaP 前列腺细胞中的 IC50 为 36nM。
- GC127913,3'-DiindolylmethaneCAS: 1968-05-4纯度: >98.00%
A phytochemical with antiradiation and chemopreventative effects
- GC12974Medroxyprogesterone acetateCAS: 71-58-9纯度: >99.50%
Medroxyprogesterone acetate(MPA)是一种人工合成的孕激素。
- GC16649TAK-700 (Orteronel)CAS: 426219-18-3
A non-steroidal inhibitor of the 17,20-lyase activity of CYP17A1
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC13362 | TOK-001 | 851983-85-2 | >99.50% | |
A CYP17 inhibitor | ||||
| GC13971 | Cyproterone Acetate | 427-51-0 | >99.50% / >98.00% | |
An androgen receptor antagonist | ||||
| GC10372 | AZD3514 | 1240299-33-5 | >99.00% | |
A SARD | ||||
| GC10547 | ASC-J9 | 52328-98-0 | >98.00% | |
A selective enhancer of AR degradation | ||||
| GC10567 | TCPOBOP | 76150-91-9 | >98.00% | |
TCPOBOP是一种构成性雄酮受体(CAR)激动剂(EC 50 =0.05μM),能够小鼠诱导肝细胞增殖和肝肿大,但不会造成肝损伤。 | ||||
| GC10618 | Fluoxymesterone | 76-43-7 | - | |
An Analytical Reference Standard | ||||
| GC10785 | Danazol | 17230-88-5 | >99.50% / >98.00% | |
An androgen receptor agonist | ||||
| GC11070 | Dehydroepiandrosterone (DHEA) | 53-43-0 | >99.00% | |
脱氢表雄酮 (DHEA) 及其硫酸酯 DHEAS 共同代表了人体内最丰富的类固醇激素。 | ||||
| GC11386 | ODM-201 | 1297538-32-9 | >99.00% | |
ODM-201是一种强效的雄激素受体拮抗剂,K i 值为11nM,IC 50 值为26nM。 | ||||
| GC11837 | MI-136 | 1628316-74-4 | >98.50% | |
A menin-MLL inhibitor | ||||
| GC11957 | RD162 | 915087-27-3 | - | |
A second-generation androgen receptor antagonist | ||||
| GC12271 | Bicalutamide | 90357-06-5 | >98.00% | |
Bicalutamide是一种非甾体抗雄激素药物,可通过选择性和竞争性地阻断雄激素与雄激素受体(AR)的结合,在外周组织中发挥抗雄激素作用。 | ||||
| GC12385 | MDV3100 (Enzalutamide) | 915087-33-1 | >99.50% | |
MDV3100(enzalutamide) 是第二代 AR 拮抗剂,在 LNCaP 前列腺细胞中的 IC50 为 36nM。 | ||||
| GC12445 | TFM-4AS-1 | 188589-61-9 | - | |
androgen receptor modulator | ||||
| GC12791 | 3,3'-Diindolylmethane | 1968-05-4 | >98.00% | |
A phytochemical with antiradiation and chemopreventative effects | ||||
| GC12933 | RU 58841 | 154992-24-2 | >99.50% | |
A non-steroidal antiandrogen | ||||
| GC12938 | PF 998425 | 1076225-27-8 | >98.00% | |
A non-steroidal androgen receptor antagonist | ||||
| GC12974 | Medroxyprogesterone acetate | 71-58-9 | >99.50% | |
Medroxyprogesterone acetate(MPA)是一种人工合成的孕激素。 | ||||
| GC13685 | Andarine | 401900-40-1 | >99.50% | |
A selective androgen receptor modulator | ||||
| GC14221 | HE-3235 | 183387-50-0 | - | |
Androgen receptor antagonist | ||||
| GC14560 | Cl-4AS-1 | 188589-66-4 | - | |
Cl-4AS-1 是一种有效的甾体雄激素受体 (AR) 激动剂 (IC50 = 12 nM),也是 5α-还原酶 I 型和 II 型的抑制剂(IC50 分别为 6 和 10 nM)。 | ||||
| GC15774 | 5α-dihydro-11-keto Testosterone | 32694-37-4 | >98.00% | |
An Analytical Reference Standard | ||||
| GC16631 | EPI-001 | 227947-06-0 | >98.00% | |
An androgen receptor antagonist | ||||
| GC16649 | TAK-700 (Orteronel) | 426219-18-3 | - | |
A non-steroidal inhibitor of the 17,20-lyase activity of CYP17A1 | ||||
