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CAS: 2049868-46-2
分子式: C14H18N2O
分子量: 230.31
中文名称: 
gsk′963
gsk′963a
gsk′ 963a
英文名称: 
gsk-963
gsk 963
gsk963
gsk963a
1-[(5S)-4,5-dihydro-5-phenyl-1h-pyrazol-1-yl]-2,2-dimethyl-1-propanone; 2,2-dimethyl-1-(5(S)-phenyl-4,5-dihydro-pyrazol-1-yl)-propan-1-one
gsk-963a
用途: GSK'963是RIP1 kinase的手性小分子抑制剂,在FP结合实验中IC50值为29 nM。它对RIP1的选择性是对其他339种激酶的10,000倍以上。
推荐供应商
货号品牌产品名称规格包装、参考价格详情
G795034MACKLINGSK'96310mM in DMSO598元/1ml;   展开
储存:-20°C
G873074MACKLINGSK'96399%809元/5mg;   2490元/25mg;   2988元/100mg;   展开
储存:-20℃
状态:粉末
SML2376Sigma-AldrichGSK′963≥98% (HPLC)1023.54元/5 MG;   4128.87元/25 MG;   展开

产品说明

生化/生理作用

GSK′963 (GSK′963A) is a brain-penetrant, highly potent and selective ATP site-targeting receptor-interacting protein 1 kinase (RIP1; RIPK1) inhibitor (IC50 = 0.8-8 nM with 50 μM ATP; IC50 >10 μM against RIPK2/3/5 and 335 other kinases) that protects against TNFα/zVAD-induced necroptosis (EC50 = 1/4 nM in mouse L929/human U937 cultures) and blocks Y. pestis-induced death of murine fetal liver macrophages (1 μM). GSK′963 prevents lethal hypothermia by acute sterile shock (2 mg/kg i.p. 15 min prior to TNFα/zVAD i.v.) and protects against acute neuronal death upon autologous blood intracerebral hemorrhage induction in mice in vivo (25 mg/kg/3 hr i.p.).

基本信息

经验(实验)分子式C14H18N2O
分子量230.31

产品性质

测定≥98% (HPLC)
形式powder
颜色 white to beige
溶解性DMSO: 2 mg/mL, clear
储存温度2-8℃
SMILES stringO=C(C(C)(C)C)N1[C@H](C2=CC=CC=C2)CC=N1

安全信息

储存分类代码13 - Non Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
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