Acivicin(Synonyms: 阿西维辛; AT-125; U-42126)

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Acivicin (Synonyms: 阿西维辛; AT-125; U-42126) 纯度: 98.26%

Acivicin (AT-125) 是一种由猪链霉菌产生的天然产物,是 γ-谷氨酰转肽酶 (GGT) 抑制剂。Acivicin 可以透过血脑屏障,并具有抗癌,抗寄生虫的特性。

Acivicin(Synonyms: 阿西维辛; AT-125;  U-42126)

Acivicin Chemical Structure

CAS No. : 42228-92-2

规格 价格 是否有货 数量
10 mM * 1 mL in Water ¥2950 In-stock
1 mg ¥2850 In-stock
5 mg   询价  
10 mg   询价  

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Acivicin 相关产品

相关化合物库:

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  • CNS-Penetrant Compound Library
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  • Microbial Metabolite Library

生物活性

Acivicin (AT-125), a natural product produced by Streptomyces sviceus is a γ-glutamyl transpeptidase (GGT) inhibitor. Acivicin can across the blood-brain barrier and has anti-cancer, anti-parasitic properties[1][2].

IC50 & Target

γ-glutamyl transpeptidase[1]

体外研究
(In Vitro)

Acivicin (AT-125; 0.1-50 μM; 5 days) has an IC50 of 0.7 μM in human HepG2 cells[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Acivicin (AT-125; 5 mg/kg; IP; twice weekly) reduces urinary γ-GT by 70-78%[3].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male pigmented Long-Evans rats weighed between 250 g and 300 g exposed to Toluene[3]
Dosage: 5 mg/kg
Administration: IP; twice weekly (monday and wednesday)
Result: Reduced urinary γ-GT by 70-78%.

分子量

178.57

Formula

C5H7ClN2O3

CAS 号

42228-92-2

中文名称

阿西维辛;异恶唑醋酸

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, stored under nitrogen

*In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

溶解性数据
In Vitro: 

H2O : 6.67 mg/mL (37.35 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 5.6000 mL 28.0002 mL 56.0004 mL
5 mM 1.1200 mL 5.6000 mL 11.2001 mL
10 mM 0.5600 mL 2.8000 mL 5.6000 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 (stored under nitrogen)。-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。

参考文献
  • [1]. Kreuzer J, et al. Target discovery of acivicin in cancer cells elucidates its mechanism of growth inhibition. Chem Sci. 2014 Dec 1;6(1):237-245. Epub 2014 Sep 26.

    [2]. Chikhale EG, et al. Carrier-mediated transport of the antitumor agent acivicin across the blood-brain barrier. Biochem Pharmacol. 1995 Mar 30;49(7):941-5.

    [3]. Delphine Waniusiow, et al. Toluene-induced hearing loss in acivicin-treated rats. Neurotoxicol Teratol. May-Jun 2008;30(3):154-60.

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