LDC4297 hydrochloride
目录号: PL02852 纯度: ≥98%
CAS No. :2319747-14-1
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中文名称
LDC4297 hydrochloride
英文名称
LDC4297 hydrochloride
英文别名
Pyrazolo[1,5-a]-1,3,5-triazin-4-amine, 8-(1-methylethyl)-2-(3-piperidinyloxy)-N-[[2-(1H-pyrazol-1-yl)phenyl]methyl]-, hydrochloride (1:1);LDC4297 hydrochloride
Cas No.
2319747-14-1
分子式
C23H29ClN8O
分子量
468.98
包装储存
4°C, sealed storage, away from moisture and light In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
产品详情
LDC4297 hydrochloride 是 CDK7 的选择性抑制剂,IC50 值为 0.13 nM。LDC4297 hydrochloride 抑制人巨细胞病毒 (HCMV) 复制,EC50 值为 24.5 nM。LDC4297 hydrochloride 具有广谱的抗病毒活性,对疱疹病毒,腺病毒,痘病毒,逆转录病毒和正粘病毒的 EC50 值为 0.02-1.21 μM。LDC4297 hydrochloride 可用于感染的研究。
生物活性
LDC4297 hydrochloride is a selective inhibitor of CDK7 with an IC 50 value of 0.13 nM. LDC4297 hydrochloride inhibits human cytomegalovirus (HCMV) replication with an EC 50 value of 24.5 nM. LDC4297 hydrochloride shows broad antiviral activities to Herpesviridae, Adenoviridae, Poxviridae, Retroviridae and Orthomyxoviridae with EC 50 values of 0.02-1.21 μM. LDC4297 hydrochloride can be used for the research of infection.
性状
Solid
IC50 & Target[1][2]
CDK7 0.13 nM (IC50) 166v VP22-GFP 0.02 μM
体外研究(In Vitro)
LDC4297 hydrochloride (0-10 μM; 6 d) dose-dependently inhibits HCMV replication with an EC50 value of 24.5 nM.
LDC4297 hydrochloride (0-10 μM; 4 d) shows anti-proliferative activity to primary cultures of fibroblasts derived from human (HFF) with a GI50 value of 4.5 μM.
LDC4297 hydrochloride (20 μM; 12-96 h) shows anti-HCMV activity through a multifaceted mode of action that involves an interference with virus-induced Rb phosphorylation.
LDC4297 hydrochloride (0-10 μM; 7 d) shows broad antiviral activities to HCMV, GPCMV, MCMV, HVV-6A, HSV-1, HSV-2, VZV, EBV, HAdV-2, Vaccinia virus, HIV-1 (nl4-3), HIV-1 (4LIG7) and Influenza A virus with EC50 values of 0.02, 0.05, 0.07, 0.04, 0.02, 0.27, 0.06, 1.21, 0.25, 0.77, 1.04, 1.13 and 0.99 μM, respectively. has not independently confi
体内研究(In Vivo)
LDC4297 hydrochloride (100 mg/kg; p.o. once) shows promising pharmacokinetic analyses. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: CD1 mice
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moisture and light In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
参考文献
[1]. Hutterer C, et al. A novel CDK7 inhibitor of the Pyrazolotriazine class exerts broad-spectrum antiviral activity at nanomolar concentrations. Antimicrob Agents Chemother. 2015 Apr;59(4):2062-71.
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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