“Tutalthromycin second gen”的搜索结果
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Androgen receptor 拮抗剂
Flutamide是一种抗雄激素药物,其活性代谢洛丽塔与Ki值为55nM的雄激素受体结合,可作用于前列腺癌。
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androgen receptor modulator
GSK-2881078是一种选择性雄激素受体调节剂(SARM),正在针对肌肉萎缩以改善其身体功能的受试者的肌肉生长和力量进行评估。
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Androgen Receptor 拮抗剂
EPI-001是雄激素受体(AR)的拮抗剂,它通过与AR的N末端结构域(NTD)共价结合并阻断AR及其剪接变体(转录因子IC50)的转录活性所需的蛋白质相互作用抑制AR NTD反式激活6μM)
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Androgen receptor 拮抗剂
ODM-201是一种有效且完全的人类AR(hAR)拮抗剂,IC50值为26 nM。
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Androgen receptor modulator
MK-0773是一种选择性雄激素受体调节剂(SARMs),是一种4-氮杂-类固醇,在人体中表现出组织选择性(IC50 = 6.6 nM)。
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androgen-receptor (AR) 拮抗剂
N-desMethyl EnzalutaMide用于治疗涉及雄激素,雌激素和孕激素受体的疾病。
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Androgen receptor (AR) modulator
BMS-564929是一种新型,高效,口服活性,非甾体组织选择性雄激素受体(AR)调节剂,结合到雄激素受体,Ki 为 2.11±0.16 nM。该化合物已被推进临床试验,以治疗与年龄相关的功能衰退。
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Androgen 拮抗剂
17 alpha-propionate是一种新型的局部和外周选择性雄激素拮抗剂。
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Androgen Receptor 拮抗剂
Cyproterone acetate是17-羟孕酮的合成衍生物,可作为雄激素受体拮抗剂以及具有弱孕激素和糖皮质激素活性的弱孕激素受体激动剂。
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Androgen Receptor 激动剂
Andarine (GTX-007)是研究性的选择性雄激素受体调节剂(SARM)。
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Androgen Receptor 拮抗剂
Bicalutamide (Casodex)是一种口服非甾体抗雄激素,用于治疗前列腺癌和多毛症。
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- Mi Chen, .et al. TRIM33 drives prostate tumor growth by stabilizing androgen receptor from Skp2-mediated degradation, EMBO Rep, 2022, Aug 3;23(8):e53468 PMID: 35785414
- Takashi Azuma, .et al. Removal of pharmaceuticals in water by introduction of ozonated microbubbles, SEP PURIF TECHNOL, 2019, Apr; 212: 483-489
- Anowara Khatun, .et al. Transcriptional Repression and Protein Degradation of the Ca2+-Activated K+ Channel KCa1.1 by Androgen Receptor Inhibition in Human Breast Cancer Cells, Front Physiol, 2018, 9: 312 PMID: 29713287
- Azuma T, .et al. Distribution of six anticancer drugs and a variety of other pharmaceuticals, and their sorption onto sediments, in an urban Japanese river, Environ Sci Pollut Res Int, 2017, Aug;24(23):19021-19030 PMID: 28660504
- Azuma T, .et al. Detection of pharmaceuticals and phytochemicals together with their metabolites in hospital effluents in Japan, and their contribution to sewage treatment plant influents, Sci Total Environ, 2016, Apr 1;548-549:189-197 PMID: 26802347
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Androgen Receptor 拮抗剂
(R)-Bicalutamide是一种活性的竞争性非甾体雄激素受体拮抗剂,对MDA 453细胞的IC50为0.17μM。
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Androgen receptor 拮抗剂
MDV3100(Enzalutamide)是一种androgen-receptor (AR)拮抗剂。在AR研究中强烈推荐的抑制剂。
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- Shiv Verma, .et al. Increased cytokine gene expression and cognition risk associated with androgen deprivation therapy, Prostate, 2022, Oct;82(14):1389-1399 PMID: 35821621
- Mi Chen, .et al. TRIM33 drives prostate tumor growth by stabilizing androgen receptor from Skp2-mediated degradation, EMBO Rep, 2022, Aug 3;23(8):e53468 PMID: 35785414
- Prem P Kushwaha, .et al. Role of solute carrier transporters SLC25A17 and SLC27A6 in acquired resistance to enzalutamide in castration-resistant prostate cancer, Mol Carcinog, 2021, Dec 22 PMID: 34939235
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Androgen Receptor Modulators
Ostarine (MK-2866,GTX-024)是一种雄激素受体调节剂(SARM)。
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