化合物 Turosteride T71703
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
100 mg | 137099-09-3 | ¥9,870.00 | 询底价 |
5 mg | 137099-09-3 | ¥2,230.00 | 询底价 |
1 mg | 137099-09-3 | ¥910.00 | 询底价 |
25 mg | 137099-09-3 | ¥5,460.00 | 询底价 |
10 mg | 137099-09-3 | ¥3,350.00 | 询底价 |
50 mg | 137099-09-3 | ¥7,670.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Turosteride
描述: Turosteride是一种小分子类固醇5α还原酶(5α-reductase)抑制剂。Turosteride具有抗肿瘤活性,可用于治疗肿瘤疾病和泌尿生殖系统疾病,可用于研究前列腺癌。
体内活性: Turosteride caused inhibition of rat and human prostatic enzymes, with IC50 values of 55 and 53 nM, respectively. In addition, turosteride did not show any relevant binding affinity to the rat prostate androgen receptor (IC50 84 μM; relative binding affinity 0.004% of DHT). The endocrine effects of turosteride were evaluated in adult male rats, treated orally at daily doses of 3, 10 and 30 mg/kg for 20 days. At these doses, the compound reduced the ventral prostate weight by 10, 33 and 42% and the intraprostatic total DHT content by 61, 74 and 78%, respectively, whereas no change in the intraprostatic content of T was observed. Turosteride caused a 40% reduction of serum DHT levels which, however, did not reach statistical significance, whereas serum T levels were similar to control animals. No effect on serum luteinizing hormone or prolactin was observed. These results indicate that the antiprostatic effect of turosteride in the adult rat is related to inhibition of the conversion of T to DHT.[1]
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 45 mg/mL (97.9 mM)
相关产品: Quercetin 3-gentiobioside | Ponalrestat | Sorbinil | Ginsenoside Ro | DL-Glyceraldehyde | Risarestat | Dutasteride | Fidarestat | AT-007 | Torilin
相关库: Anti-Cancer Compound Library | Bioactive Compounds Library Max | Inhibitor Library | Anti-Cancer Active Compound Library | Bioactive Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途