CTx0294885
CAS No. 1439934-41-4
CTx0294885 ( CTX0294885 | CTX 0294885 | CTX-0294885 )
产品货号. M11865 CAS No. 1439934-41-4
CTX-0294885是一种新型双苯氨基嘧啶;在体外对多种激酶表现出抑制活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥504 | 有现货 |
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| 5MG | ¥781 | 有现货 |
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| 10MG | ¥1169 | 有现货 |
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| 25MG | ¥1972 | 有现货 |
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| 50MG | ¥2939 | 有现货 |
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| 100MG | ¥4167 | 有现货 |
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| 200MG | ¥5931 | 有现货 |
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| 500MG | ¥8901 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥752 | 有现货 |
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生物学信息
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产品名称CTx0294885
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述CTX-0294885是一种新型双苯氨基嘧啶;在体外对多种激酶表现出抑制活性。
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产品描述CTX-0294885 is a a novel bisanilino pyrimidine; exhibits inhibitory activity against a broad range of kinases in vitro, and further developed it into a Sepharose-supported kinase capture reagent.(In Vitro):CTX-0294885 is a kinase capture tool in large-scale kinome profiling experiments, with 185 kinases identified as total protein, and 179 identified from TiO2 enrichment for phosphopeptides in MDA-MB-231 cells (by quantitative MS).CTX-0294885 captures all members of the AKT family that is not identified from previous studies using other kinase capture reagents.
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体外实验CTX-0294885 is a kinase capture tool in large-scale kinome profiling experiments, with 185 kinases identified as total protein, and 179 identified from TiO2 enrichment for phosphopeptides in MDA-MB-231 cells (by quantitative MS).CTX-0294885 captures all members of the AKT family that is not identified from previous studies using other kinase capture reagents.
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体内实验——
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同义词CTX0294885 | CTX 0294885 | CTX-0294885
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通路Others
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靶点Other Targets
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受体Kinase capture reagent
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研究领域Other Indications
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适应症——
化学信息
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CAS Number1439934-41-4
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分子量437.93
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分子式C22H24ClN7O
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纯度>98% (HPLC)
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溶解度DMSO: 10 mM
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SMILESO=C(NC)C1=CC=CC=C1NC2=NC(NC3=CC=C(N4CCNCC4)C=C3)=NC=C2Cl
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化学全称2-((5-chloro-2-((4-(piperazin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)-N-methylbenzamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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BI-9321 trihydrochlo...
BI-9321 trihydrochloride 是一种有效的,选择性的,具有细胞活性的 NSD3-PWWP1 拮抗剂,Kd 值为 166 nM。BI-9321 对 NSD2-PWWP1 和 NSD3-PWWP2 无效。BI-9321 trihydrochloride 在 U2OS 细胞中特异性破坏 NSD3-PWWP1 与组蛋白相互作用,IC50 为 1.2 μM。
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VT103
VT103 是 VT101 的类似物,是一种具有口服活性和选择性的 TEAD1 蛋白棕榈酰化抑制剂。 VT103 抑制 YAP/TAZ-TEAD 促进的基因转录,阻断 TEAD auto-palmitoylation,阻断 YAP/TAZ和TEAD 之间的相互作用。VT103 可用于癌症研究。
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OD1
Potent rat Nav1.7, human Nav1.4 and rat Nav1.6 channel activator (EC50 values are 7, 10 and 47 nM, respectively). Exhibits minimal activation at mammalian Nav1.2, Nav1.3 and Nav1.5 (EC50 values >3 μM). Inhibits fast inactivation on all channels. Increases peak currents at all voltages and stimulates a persistent Na+ current at hNav1.7 channel. Increases hyperpolarization at Nav1.4 and Nav1.6 channels. Induces spontaneous pain in vivo.
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