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首页 > 产品详情 > 应用 > 药物靶标 > 激酶 > TK:酪氨酸激酶
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包装 20mg | 50mg | 250mg | 1g
纯度 ≥98%
发货地 现货 品牌 阿拉丁
最小起订 1MG
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产品详情

中文名称 别名
CasNo 133550-30-8 产品类别 应用,药物靶标,激酶,TK:酪氨酸激酶

产品名称

英文名称:AG-490 (Tyrphostin B42)

同义词

133550-30-8、AG-490、Tyrphostin B42、AG 490、Tyrphostin AG 490、(E)-N-benzyl-2-cyano-3-(3,4-dihydroxyphenyl)acrylamide、AG490、Tyrphostin AG490、N-Benzyl-2-cyano-3-(3,4-dihydroxyphenyl)acrylamide、134036-52-5、(E)-N-benzyl-2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enam、酪氨酸激酶抑制剂AG 490

产品性质

CAS编号:133550-30-8

分子式:C17H14N2O3

分子量:294.3

MDL号:MFCD00236452

PubChem编号:5328779

别名:酪氨酸激酶抑制剂AG 490

英文别名:133550-30-8|AG-490|Tyrphostin B42|AG 490|Tyrphostin AG 490|(E)-N-benzyl-2-cyano-3-(3,4-dihydroxyphenyl)acrylamide|AG490|Tyrphostin AG490|N-Benzyl-2-cyano-3-(3,4-dihydroxyphenyl)acrylamide|134036-52-5|(E)-N-benzyl-2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enam

规格或纯度:≥98%

英文名称:AG-490 (Tyrphostin B42)

生化机理:AG-490 is a selective inhibitor of EGF receptor tyrosine kinase (IC50 values are 2 and 13.5 μM for EGFR and ErbB2 respectively). Inhibitor of JAK2, JAK3/STAT, JAK3/AP-1 and JAK3/MAPK pathways and potently inhibits cytokine-independent cell growth in vitro and tumor cell invasion in vivo.JAK2/3 inhibitor (IC 50 values are ~10 and 25 μM, respectively). Inhibits downstream activation of STAT5a/b. Effects synaptic plasticity and cytokine-independent cell growth in vitro and spatial learning, memory and tumor cell invasion in vivo .

应用:Tyrphostin AG has been used to block IL-6 cytokine signaling to study its effects on glial cell reactivity. AG 490 has also been used as a JAK2 inhibitor in human umbilical vein endothelial cells

储存温度:-20°C储存

运输条件:超低温冰袋运输

备注:如果有可能,您尽量在使用的当天配置溶液,并在当天使用完它。但是,如果您需要预先配制储备溶液,我们建议您将溶液等份保存在-20°C的密封小瓶中。通常,它们最多可以使用一个月。在使用前和打开样品瓶之前,我们建议您让您的产品在室温下平衡至少1小时。有毒,请参阅SDS以获取更多信息。需要更多关于溶解度,用法和处理的建议吗?请访问我们的常见问题(FAQ)页面以获取更多详细信息。

产品介绍:AG-490 (Tyrphostin AG 490)是EGFR抑制剂,IC50为100nM,比对ErbB2的抑制性高135倍,对Lck,Lyn,Btk,Syk和Src无活性。Tyrphostin AG has been used to block IL-6 cytokine signaling to study its effects on glial cell reactivity. AG 490 has also been used as a JAK2 inhibitor in human umbilical vein endothelial cellsAG-490 (Tyrphostin AG 490) is an inhibitor of EGFR with IC50 of 0.1 μM, 135-fold more selective for EGFR versus ErbB2, also inhibits JAK2 with no activity to Lck, Lyn, Btk, Syk and Src.Tyrphostin AG has been used to block IL-6 cytokine signaling to study its effects on glial cell reactivity. AG 490 has also been used as a JAK2 inhibitor in human umbilical vein endothelial cells

PubChem SID:488195367

PubChem SID url:https//pubchem.ncbi.nlm.nih.gov/substance/488195367

IUPAC Name:(E)-N-benzyl-2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enamide

INCHI:InChI=1S/C17H14N2O3/c18-10-14(8-13-6-7-15(20)16(21)9-13)17(22)19-11-12-4-2-1-3-5-12/h1-9,20-21H,11H2,(H,19,22)/b14-8+

InChi Key:TUCIOBMMDDOEMM-RIYZIHGNSA-N

Canonical SMILES:C1=CC=C(C=C1)CNC(=O)C(=CC2=CC(=C(C=C2)O)O)C#N

Isomeric SMILES:C1=CC=C(C=C1)CNC(=O)/C(=C/C2=CC(=C(C=C2)O)O)/C#N

WGK Germany:3

PubChem CID:5328779

CAS Registry No.:133550-30-8

ChEMBL Ligand:CHEMBL56543

溶解性:DMSO ≥57mg/mL Water <1.2mg/mL Ethanol ≥8mg/mL

敏感性:对光敏感、对空气敏感、对热敏感

熔点:215°C

象形图:

信号词:Danger

危险声明:H301 Toxic if swallowedH400 Very toxic to aquatic life

预防措施声明:P273,P321,P405,P501,P264,P270,P391,P330,P301+P316

产品包装

纯度包装库存所在地
≥98%20mg现货
≥98%50mg现货
≥98%250mg现货
≥98%1g现货
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