购物车
- 全部删除
- 您的购物车当前为空
Bazedoxifene hydrochloride (TSE 424 hydrochloride) 是一种能透过血脑屏障且具有口服活性、选择性和高效性的雌激素受体调节剂 (SERM),也是 IL-6/GP130 蛋白相互作用抑制剂,对 ERα 和 ERβ 具有很高的亲和力,可用于研究绝经后骨质疏松症和血管舒缩相关疾病。
Bazedoxifene hydrochloride (TSE 424 hydrochloride) 是一种能透过血脑屏障且具有口服活性、选择性和高效性的雌激素受体调节剂 (SERM),也是 IL-6/GP130 蛋白相互作用抑制剂,对 ERα 和 ERβ 具有很高的亲和力,可用于研究绝经后骨质疏松症和血管舒缩相关疾病。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 492 | 现货 | |
5 mg | ¥ 1,270 | 现货 | |
10 mg | ¥ 2,300 | 现货 | |
25 mg | ¥ 3,590 | 现货 | |
50 mg | ¥ 5,680 | 现货 | |
100 mg | ¥ 7,690 | 现货 | |
500 mg | ¥ 15,300 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 1,980 | 现货 |
产品描述 | Bazedoxifene hydrochloride (TSE 424 hydrochloride) is an orally active, selective, and potent estrogen receptor modulator (SERM) that crosses the blood-brain barrier and is an inhibitor of IL-6/GP130 protein interactions with high affinity for ERα and ERβ. It has a high affinity for ERα and ERβ and can be used to study postmenopausal osteoporosis and vasodilator-related diseases. |
靶点活性 | ERβ (rat):99 nM, ERα:26 nM, ERα:23 nM, ERβ:89 nM |
体外活性 | 在 AsPC-1 细胞中,Bazedoxifene hydrochloride(10 μM-20 μM;2 小时)能够抑制由 IL-6、IL-11 或 OSM(各50 ng/mL)诱导的 STAT3 磷酸化[2]。 |
体内活性 | 在 6 周龄的雌性无胸腺裸鼠中,Bazedoxifene hydrochloride(剂量为5 mg/kg;通过口服灌胃,每日一次,持续 18 天)被用于抑制胰腺癌异种移植瘤的生长,并在肿瘤细胞中诱导凋亡[2]。 |
激酶实验 | Ligand binding competition experiments: Test compounds are initially solubilized in DMSO and the final concentration of DMSO in the binding assay is ≤ 1%. Eight dilutions of each test compound are used as an unlabelled competitor for [3H]17β-estradiol. Typically, a set of compound dilutions would be tested simultaneously on human, rat and mouse ER-α and ER-β. The results are plotted as measured DPM vs. concentration of test compound. For dose-response curve fitting, a four parameter logistic model on the transformed, weighted data are fit and the IC50 is defined as the concentration of compound decreasing maximum [3H]estradiol binding by 50%. For active compounds, the IC50 is determined at least three times. It should be noted that IC50 values are not direct measures of a ligand's affinity for the receptor. Rather, they can only be compared as relative values, in this case to 17β-estradiol. |
细胞实验 | For the proliferation assay, cells are plated at 20,000 cells/well in a 24-well plate in DMEM/F12 (50:50) (phenol red-free) with 10% charcoal/dextran-treated FBS and 1 × GlutaMAX-1. After overnight incubation, the medium is aspirated and treatments in DMEM/F12 (50:50) (phenol red-free) with 2% charcoal/dextran-treated FBS and 1 × GlutaMAX-1 are added to the wells. Each plate has a vehicle (baseline proliferation) and treatments. Treatments included 10 pM 17β-estradiol determined to be the EC80 for 17β-estradiol and 17β-estradiol in combination with six concentrations of BZA. Treatments from d 1 are renewed on d 3 and d 6 by aspirating medium from wells and replacing with fresh medium and treatments. On d 7, cells are detached from the plate using trypsin-EDTA and counted using a Multisizer II.(Only for Reference) |
别名 | WAY 140424 hydrochloride, TSE-424 hydrochloride, TSE424 hydrochloride, TSE 424 hydrochloride |
分子量 | 507.06 |
分子式 | C30H35ClN2O3 |
CAS No. | 198480-56-7 |
Smiles | Cl.OC=1C=CC(=CC1)C2=C(C3=CC(O)=CC=C3N2CC4=CC=C(OCCN5CCCCCC5)C=C4)C |
密度 | no data available |
存储 | store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | H2O: <1 mg/mL Ethanol: <1 mg/mL DMSO: 93 mg/mL (183.4 mM) | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
|
版权所有©2015-2024 TargetMol Chemicals Inc.保留所有权利.
评论内容