S-23,99.95%

产品编号:Bellancom-112257| CAS NO:1010396-29-8| 分子式:C18H13ClF4N2O3| 分子量:416.75

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
Bellancom-112257
500.00 杭州 北京(现货)
Bellancom-112257
800.00 杭州 北京(现货)
Bellancom-112257
1600.00 杭州 北京(现货)
Bellancom-112257
2500.00 杭州 北京(现货)
Bellancom-112257
3900.00 杭州 北京(现货)

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S-23

产品介绍 S-23 是一种口服选择性雄激素受体调节剂 (SARM)Ki 为 1.7 nM。S-23 诱导 CV-1 细胞雄激素受体介导的转录激活。S-23 增加去势大鼠前列腺、精囊和肛提肌重量。
生物活性

S-23 is an orally active selective androgen receptor modulator (SARM) with a Ki of 1.7 nM. S-23 induces androgen receptor (AR)-mediated transcriptional activation in CV-1 cells. S-23 increases prostate, seminal vesicle, and levator ani muscle weights in castrated rats.

体外研究

S-23 induces AR-mediated transcriptional activation in CV-1 cells when used at a concentration of 10 nM.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

By administration of S-23 to castrated animals, androgen-dependent organ weights increased in a dose-dependent manner. The ED50 of S-23 in the prostate and levator ani muscle is 0.43 and 0.079 mg/d, respectively.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male Sprague Dawley rats (in castrated male rats)
Dosage: 0.01-3 mg
Administration: S.c.; daily for 14 d
Result: Androgen-dependent organ weights increased in a dose-dependent manner. At a dose rate as low as 0.1 mg/d, S-23 is able to selectively maintain the weight of the levator ani muscle at the intact control level, whereas its effects on the prostate and seminal vesicles are lower than 30% of those observed in intact controls.
体内研究

By administration of S-23 to castrated animals, androgen-dependent organ weights increased in a dose-dependent manner. The ED50 of S-23 in the prostate and levator ani muscle is 0.43 and 0.079 mg/d, respectively.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male Sprague Dawley rats (in castrated male rats)
Dosage: 0.01-3 mg
Administration: S.c.; daily for 14 d
Result: Androgen-dependent organ weights increased in a dose-dependent manner. At a dose rate as low as 0.1 mg/d, S-23 is able to selectively maintain the weight of the levator ani muscle at the intact control level, whereas its effects on the prostate and seminal vesicles are lower than 30% of those observed in intact controls.
性状Solid
溶解性数据
In Vitro: 

DMSO : 100 mg/mL (239.95 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.3995 mL 11.9976 mL 23.9952 mL
5 mM 0.4799 mL 2.3995 mL 4.7990 mL
10 mM 0.2400 mL 1.1998 mL 2.3995 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献

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