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PLN-1474
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。
PLN-1474图片
CAS NO:2408065-32-5
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
200mg电议

产品介绍
PLN-1474 (compound 1) 是具有口服活性的,选择性的avss1 整合素抑制剂,IC50值 <50 nM。PLN-1474 在肝纤维化小鼠模型中显著降低肝脏 pSMAD3/SMAD3 水平、肝脏胶原蛋白基因表达和肝脏 OHP 浓度。PLN-1474 可用于预防、延缓或治疗纤维化或肝硬化疾病或紊乱的研究。
生物活性

PLN-1474 (compound 1) is an orally active and selectiveavss1integrininhibitor with anIC50value of <50 nM. PLN-1474 reduces levels of pSMAD3/SMAD3 in liver, hepatic collagen gene expression and hepatic OHP concentration in liver fibrosis mouse model. PLN-1474 can be used for the research of preventing, delaying or treating a fibrotic or cirrhotic disease or disorder[1].

IC50& Target

IC50: <50 nM (ανβ1), <50 nM (ανβ6)[1]

体外研究
(In Vitro)

PLN-1474 inhibits ανβ1 and ανβ6 with IC50s of <50 nM by solid phase assay[1].

体内研究
(In Vivo)

PLN-1474 (10 μM) decreases the expression level of profibrotic genes, including COL1A1 and TIMP1 in liver[1].
PLN-1474 significantly reduces levels of pSMAD3/SMAD3 in liver, hepatic collagen gene expression and hepatic OHP concentration in a mouse model of liver fibrosis[1].
PLN-1474 (6-12 weeks) prophylactically or therapeutically blocks SMAD3 phosphorylation and significantly decreases OHP levels, collagen gene expression, and collagen deposition examined histologically in the CDAHFD NASH mouse model[1].

分子量

431.57

性状

Solid

Formula

C24H37N3O4

CAS 号

2408065-32-5

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
溶解性数据
In Vitro: 

DMSO : ≥ 83.33 mg/mL(193.09 mM)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM2.3171 mL11.5856 mL23.1712 mL
5 mM0.4634 mL2.3171 mL4.6342 mL
10 mM0.2317 mL1.1586 mL2.3171 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℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。