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ICA
CAS No. 3374-88-7
ICA ( N-[4-(2-Pyridinyl)-2-thiazolyl]-2-pyridinamine )
产品货号. M26713 CAS No. 3374-88-7
ICA 是一种 SK 通道抑制剂,具有抗利什曼活性 (IC50:2.1 μM)。
纯度: >98% (HPLC)
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规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥3621 | 有现货 |
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10MG | ¥5338 | 有现货 |
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25MG | ¥7995 | 有现货 |
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50MG | ¥11259 | 有现货 |
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100MG | ¥15228 | 有现货 |
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500MG | ¥30618 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称ICA
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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ICA 是一种 SK 通道抑制剂,具有抗利什曼活性 (IC50:2.1 μM)。
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产品描述ICA is a SK channel inhibitor and exhibits antileishmanial activity (IC50: 2.1 μM).(In Vitro):ICA exhibited antiarrhythmic effects. ICA prevented electrically induced runs of atrial fibrillation in the isolated right atrium and induced atrial postrepolarization refractoriness and depolarized RMP. ICA (1-10 μM) was found to slow CV; however, because of a marked prolongation of effective refractory period, the calculated wavelength was increased. Furthermore, at increased pacing frequencies, SK channel inhibition by ICA (10-30 μM) demonstrated prominent depression of other sodium channel-dependent parameters. ICA did not inhibit IK,ACh, but at concentrations above 10 μM, ICA use dependently inhibited INa.
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体外实验The SK channel inhibitor ICA exhibits antiarrhythmic effects. ICA prevents electrically induced runs of atrial fibrillation in the isolated right atrium and induces atrial postrepolarization refractoriness and depolarizes resting membrane potential. ICA at 1 to 10 μM slows conduction velocity. At increased pacing frequencies, SK channel inhibition by ICA (10-30 μM) demonstrates prominent depression of other sodium channel-dependent parameters.
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体内实验——
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同义词N-[4-(2-Pyridinyl)-2-thiazolyl]-2-pyridinamine
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通路Cell Cycle/DNA Damage
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靶点Potassium Channel
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受体Alkyl/ether
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研究领域——
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适应症——
化学信息
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CAS Number3374-88-7
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分子量254.31
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分子式C13H10N4S
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : ≥ 49.5 mg/mL (194.64 m)
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SMILESN(c1nc(cs1)-c1ccccn1)c1ccccn1
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化学全称——
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
1.Zhang F, et al. Discovery of a new class of PROTAC BRD4 degraders based on a dihydroquinazolinone derivative and lenalidomide/pomalidomide.Bioorg Med Chem. 2020 Jan 1;28(1):115228.