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1030203-81-6

中文名称 2-[[1-(3-Chlorophenyl)-4-oxo-5H-pyrazolo[5,4-d]pyrimidin-6-yl]sulfanyl]propanamide
CAS 1030203-81-6
分子式 C14H12ClN5O2S
分子量 349.8
MOL 文件 1030203-81-6.mol
更新日期 2024/08/27 10:38:56
1030203-81-6 结构式 1030203-81-6 结构式

基本信息

英文别名
HS38
HS-38 (HS38)
HS38 >=95% (HPLC)
NASYEGAVCTZSDO-UHFFFAOYSA-N
2-[[1-(3-Chlorophenyl)-4-oxo-5H-pyrazolo[5,4-d]pyrimidin-6-yl]sulfanyl]propanamide
2-[[1-(3-Chlorophenyl)-4,5-dihydro-4-oxo-1H-pyrazolo[3,4-d]pyrimidin-6-yl]thio]-propanamide
Propanamide, 2-[[1-(3-chlorophenyl)-4,5-dihydro-4-oxo-1H-pyrazolo[3,4-d]pyrimidin-6-yl]thio]-

物理化学性质

储存条件2-8°C
溶解度DMSO:可溶5mg/mL,澄清(加热)
形态粉末
颜色白色至米色

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H315-H319-H335
危险品标志Xi
危险类别码36/37/38
安全说明26
WGK Germany3

常见问题列表

生物活性
HS38 是一种高效、选择性的,ATP 竞争性的 DAPK1 和 ZIPK (DAPK3) 抑制剂,Kd 值分别为 300 nM 和 280 nM。HS38 也是 PIM3 的抑制剂,其 IC50 值为 200 nM。HS38 可用于平滑肌相关疾病的研究。
靶点

Kd: 300 nM (DAPK1), 79 nM (DAPK2), 280 nM (ZIPK), IC50: 200 nM (DAPK1), 200 nM (PIM3)

体外研究

HS38 displays high affinity toward DAPK2, with a K d of 79 nM. DAPK2 is not implicated in smooth muscle contractility.
HS38 significantly reduces relative RLC20 phosphorylation in both the basal and sphingosine 1-phosphate (S1P) activated states in human aortic SM cells.
HS38 reduces contractile forces generated by intact mouse aorta in aortic tissue.
HS38 reduces the contractile force, RLC20 phosphorylation, and MYPT1 phosphorylation in Ca 2+ -sensitized rabbit ileum.

Western Blot Analysis

Cell Line: CA-VSMCs
Concentration: 10 µM
Incubation Time: 40 minutes
Result: Reduced relative RLC20 phosphorylation in both the basal and S1P activated states.
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