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GSK3326595(EPZ-015938)
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。
GSK3326595(EPZ-015938)图片
CAS NO:1616392-22-3
规格:≥98%
包装与价格:
包装价格(元)
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理化性质和储存条件
Molecular Weight (MW) 452.55
Formula C24H32N6O3
CAS No. 1616392-22-3
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 90 mg/mL (198.8 mM)
Water:<1 mg/mL
Ethanol: 90 mg/mL (198.8 mM)
Solubility (In vivo) 2.2 mg/mL in 10% DMSO : 40% PEG300 : 5% Tween-80 : 45% saline
Synonyms

EPZ-015938; EPZ 015938; EPZ015938; Pemrametostat; GSK3326595; GSK 3326595; GSK-3326595;

Chemical Name: (S)-6-((1-acetylpiperidin-4-yl)amino)-N-(3-(3,4-dihydroisoquinolin-2(1H)-yl)-2-hydroxypropyl)pyrimidine-4-carboxamide

SMILES CodeO=C(C)N1CCC(NC2=NC=NC(C(NC[C@H](O)CN3CCC(C=CC=C4)=C4C3)=O)=C2)CC1
实验参考方法
In Vitro

In vitro activity: GSK3326595 (formerly known as EPZ015938) is an orally bioactive, potent and selective inhibitor of protein arginine methyltransferase 5 (PRMT5). It potently inhibits tumor growth in vitro and in vivo in animal models. GSK3326595 is able to halt cell proliferation and induce apoptosis in numerous solid and hematologic tumor cell lines. It has demonstrated potent in vivo anti-tumor activity in animal models. The protein arginine methyltransferases (PRMT) are a family of 11 enzymes that catalyze mono- or dimethylation of arginine residues on histones. so far PRMT inhibitors (PRMTi) are still limited to preclinical studies.


Kinase Assay: GSK3326595 (formerly known as EPZ015938) is an orally bioactive, potent and selective inhibitor of protein arginine methyltransferase 5 (PRMT5).


Cell Assay: GSK3326595 is able to halt cell proliferation and induce apoptosis in numerous solid and hematologic tumor cell lines. I

In VivoGSK3326595 has demonstrated potent in vivo anti-tumor activity in animal models. The protein arginine methyltransferases (PRMT) are a family of 11 enzymes that catalyze mono- or dimethylation of arginine residues on histones. so far PRMT inhibitors (PRMTi) are still limited to preclinical studies.
Animal model
Formulation & Dosage
References Biomolecules. 2017 Mar; 7(1): 3; WO 2016022605 A1
 
 
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