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Fidarestat

    级别和纯度:
  • 10mM in DMSO
  • CAS编号: 136087-85-9
  • 分子式: C12H10FN3O4
  • 分子量: 279.22
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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
F656826-1ml
1ml 期货 Stock Image

基本描述

别名 非达司他
规格或纯度 10mM in DMSO
英文名称 Fidarestat
生化机理 Fidarestat (SNK 860) 是一种醛糖还原酶抑制剂,对醛糖还原酶、AKR1B10 和 V301L AKR1B10 的 IC 50 s 分别为 26 nM、33 μM 和 1.8 μM;Fidarestat (SNK 860) 具有治疗糖尿病的潜力。
储存温度 -80℃储存
运输条件 超低温冰袋运输
产品介绍


Fidarestat (SNK 860) is an inhibitor of aldose reductase , with IC 50 s of 26 nM, 33 μM, and 1.8 μM for aldose reductase , AKR1B10 and V301L AKR1B10, respectively; Fidarestat (SNK 860) has the potential to treat diabetic disease.

In Vitro

Fidarestat is an inhibitor of aldose reductase, with IC 50 s of 26 nM, 33 μM, and 1.8 μM for aldose reductase, AKR1B10 and V301L AKR1B10, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Fidarestat (SNK-860; 1 or 4 mg/kg. p.o., daily for 4 weeks) reduces the concentrations of sorbitol and fructose in diabetic rats. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

IC50& Target:IC50: 26 nM (Aldose reductase), 33 μM (AKR1B10), 1.8 μM (V301L AKR1B10)

关联靶点(人)

AKR1B1 Tclin 醛糖还原酶(Aldose reductase) (7 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)

名称和识别符

分子类型 小分子
Isomeric SMILES C1[C@H](OC2=C([C@]13C(=O)NC(=O)N3)C=C(C=C2)F)C(=O)N
关联CAS 136087-85-9
PubChem CID 160024
MeSH Entry Terms (2S,4S)-6-fluoro-2',5'-dioxospiro(chroman-4,4'-imidazolidine)-2-carboxamide;fidarestat;SNK 860;SNK-860
分子量 279.22

安全和危险性(GHS)

质检证书(CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):
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