找到约 23 条 “Androgen Receptor” 相关结果 (用时 0.112 秒)
目录号 | 产品名称 | 中文名称 | 靶点 |
---|---|---|---|
M25417 | Masofaniten | 马索法尼坦 | Androgen Receptor |
Androgen receptor-IN-2; EPI-7386 | |||
Masofaniten (Androgen receptor-IN-2,马索法尼坦) 是一种有效的,具有口服活性的雄激素受体(AR) 抑制剂。Masofaniten能抑制雄性激素与雄性激素受体的结合,在雄性激素诱导的PSA-荧光素酶试验中,IC50为535 nM。 | |||
M43584 | Androgen receptor antagonist 8 | Androgen receptor antagonist 8 | Androgen Receptor |
Androgen receptor antagonist 8 是雄激素受体 (androgen receptor) 拮抗剂。 | |||
M43586 | Androgen receptor degrader-1 | Androgen receptor degrader-1 | Androgen Receptor |
Androgen receptor degrader-1 是一种有效的雄激素受体降解剂。 | |||
M43587 | Androgen receptor degrader-2 | Androgen receptor degrader-2 | Androgen Receptor |
Androgen Receptor degrader-2 是一种有效的雄激素受体降解剂。 | |||
M43589 | Androgen receptor degrader-3 | Androgen receptor degrader-3 | Androgen Receptor |
Androgen receptor degrader-3 是一种选择性的雄激素受体降解剂。 | |||
M2344 | RU 58841 | RU 58841 | Androgen Receptor |
RU 58841是一种特殊的雄激素受体(androgen receptor)拮抗剂。 | |||
M4703 | Lupeol | 羽扇豆醇;羽扇醇;羽扇豆醇酯;蛇麻醇酯 | Androgen Receptor |
Clerodol; Monogynol B; Fagarasterol | |||
Lupeol (Clerodol, Monogynol B,Fagarasterol,羽扇豆醇,羽扇醇,羽扇豆醇酯,蛇麻醇酯) 是一个活跃的五环三萜,具有抗氧化,抗肿瘤和抗炎活性。Lupeol 是一种有效的雄激素受体 (androgen receptor) 抑制剂,可用于癌症研究,特别是雄激素依赖表型 (ADPC) 和去势抵抗表型 (CRPC) 的前列腺癌。 | |||
M6106 | 17α-Methyltestosterone | 17α-Methyltestosterone | Androgen Receptor |
Methyltestosterone; 17-Methyltestosterone | |||
17α-Methyltestosterone是一种雄激素受体(Androgen Receptor)抑制剂。 | |||
M7406 | TFM-4AS-1 | TFM-4AS-1 | Others |
TFM-4AS-1 is a selective androgen receptor modulator (SARM). | |||
M8053 | PF-998425 | PF-998425 | Others |
PF-998425 is a novel, nonsteroidal androgen receptor antagonist. | |||
M8301 | MJC13 | MJC13 | Others |
MJC13 inhibits the positive regulation of androgen receptor (AR) signaling by the cochaperone protein FKBP52. | |||
M8571 | VPC-14228 | VPC-14228 | Others |
VPC-14228 is a potent and specific inhibitor of human androgen receptor (AR) that binds to AR DNA-binding domain (AR DBD). | |||
M8718 | VPC-13566 | VPC-13566 | Others |
VPC-13566 is Binding Function 3 (BF3)-specific inhibitor of the androgen receptor. | |||
M14617 | GLPG0492 | GLPG0492 | Androgen Receptor |
GLPG0492 是一种非甾体选择性雄激素受体 (androgen receptor) 调节剂 (有效 12 nM)。GLPG0492 在肌肉骨骼疾病如肌萎缩和恶病质的研究方面具有潜在的潜力。 | |||
M14619 | MK-0773 | MK-0773 | Androgen Receptor |
PF-05314882 | |||
MK-0773 是一种选择性雄激素受体调节剂 (selective androgen receptor modulators),与 AR 结合,IC50 值为 6.6 nM。 | |||
M16523 | Ailanthone | 臭椿酮 | Androgen Receptor |
Δ13-Dehydrochaparrinone | |||
Ailanthone 是一种有效的雄激素受体 (androgen receptor,AR) 抑制剂,抑制完整雄激素受体,和持续活跃剪切变体的 IC50 值分别为 69 nM 和 309 nM。 | |||
M20488 | 4,4'-DDE | 4,4'-DDE | Estrogen Receptor |
p,p'-DDE; Dichlorodiphenyldichloroethylene; p,p'-dichlorodiphenyldichloroethylene | |||
DDE, a breakdown product of DDT, is an organochlorine pesticide and may behave as a potent androgen receptor antagonist. | |||
M20930 | 4-Methylcatechol | 4-Methylcatechol | Others |
2-Hydroxy-4-methylphenol; 4-Methyl-1,2-benzenediol (4-methylpyrocatechol); 4-Methyl-1,2-dihydroxybenzene; 4-methyl-2-benzenediol; 4-methyl-benzene-1,2-diol; 4-methyl-pyrocatecho | |||
an antagonist of the androgen receptor (AR) signaling pathway | |||
M20966 | Ligandrol (LGD-4033, VK-5211) | Ligandrol (LGD-4033, VK-5211) | Androgen Receptor |
Ligandrol (LGD-4033, VK-5211) is a novel nonsteroidal, oral selective androgen receptor modulator with high affinity (Ki of ∼1 nM) and selectivity. | |||
M21109 | Inobrodib | Inobrodib | Epigenetic Reader Domain |
CCS1477; CBP-IN-1; CBP/p300-IN-4 | |||
Inobrodib (CCS1477,CBP-IN-1) 是一种口服活性的、有效的选择性 p300/CBP 抑制剂。Inobrodib 与 p300 和 CBP 结合,Kd 值为 1.3 和 1.7 nM,与 Kd 为 222 nM 的 BRD4 相比,具有 170/130 倍的选择性。Inobrodib (CCS1477) 通过抑制 androgen receptor (AR) 的表达和功能以及抑制 c-Myc 起作用。 | |||
M21192 | ARD-2585 | ARD-2585 | PROTAC |
ARD-2585 是有效的、具有口服活性的雄激素受体 (androgen receptor) 的PROTAC 降解剂。 | |||
M29293 | EPI-7170 | EPI-7170 | Androgen Receptor |
EPI-7170,ralaniten 类似物,是一种有效的雄激素受体 N 端结构域 (androgen receptor N-terminal structural domain) 拮抗剂,可以阻断全长 AR (FL-AR) 和 AR 剪接变体 (AR-Vs) 的转录活性。EPI-7170 对 enzalutamide 耐药的去势抵抗性前列腺癌 (CRPC) 具有抗肿瘤作用。 | |||
M29958 | AR antagonist 3 | AR antagonist 3 | Androgen Receptor |
AR antagonist 3 是一种有效的选择性 androgen receptor (AR) 拮抗剂,IC50 为 0.47 µM。AR antagonist 3 呈剂量依赖性降低 FRET 信号 (IC50= 18.05 μM)。当瘤内给药时,AR antagonist 3 可有效抑制肿瘤生长。 |
产品仅供科学研究或药证申报的用途使用,不为任何个人或者非科研性质的其他用途提供服务。
Copyright © 2010-2022 AbMole版权所有 沪ICP备16047849号 沪公网安备 31011502012228号