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KIRA-7
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
KIRA-7图片
CAS NO:1937235-76-1

KIRA-7 是一种咪唑并吡嗪化合物,可与IRE1α激酶结合 (IC50为 110 nM) 以变构方式抑制其 RNase 活性。KIRA-7 具有抗纤维化作用。
生物活性

KIRA-7, an imidazopyrazine compound, binds theIRE1α kinase(IC50of 110 nM) to allosterically inhibit its RNase activity. KIRA-7 has an anti-fibrotic effect[1].

IC50& Target

IC50: 110 nM (IRE1α kinase)[1]

体外研究
(In Vitro)

KIRA-7 can inhibit XBP1 splicing in the alveolar epithelial cell line MLE12[1].

体内研究
(In Vivo)

KIRA-7 (5 mg/kg; intraperitoneal injection; daily for 14 days; C57BL6 mice) treatment results in decreased spliced XBP1 and ATF4, compared to bleomycin exposed mice treated with vehicle. Likewise, mRNA levels of BiP and CHOP are significantly elevated after Bleomycin exposure, and treatment of Bleomycin-exposed mice with KIRA-7 decreased these levels. mRNA levels of collagen 1A1 and fibronectin are both significantly decreased by KIRA-7 treatment[1].

Animal Model:C57BL6 mice (12 weeks of age) with Bleomycin (1.5 units/kg)[1]
Dosage:5 mg/kg
Administration:Intraperitoneal injection; daily; for 14 days
Result:Resulted in decreased spliced XBP1 and ATF4. Likewise, mRNA levels of BiP and CHOP were significantly decreased.
分子量

466.51

性状

Solid

Formula

C27H23FN6O

CAS 号

1937235-76-1

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
 
 
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