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首页-小分子抑制剂&激动剂-Apoptosis-DAPK-HS-38
HS-38

Chemical Structure : HS-38

CAS No.: 1030203-81-6

HS-38 (HS38)

货号: PC-62870Not For Human Use, Lab Use Only.

HS-38 is a potent and selective DAPK1 and DAPK3 (ZIPK) inhibitor with IC50 of 200 nM for DAPK1 and Kd of 280 nM for ZIPK.

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25 mg ¥1880 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

HS-38 is a potent and selective DAPK1 and DAPK3 (ZIPK) inhibitor with IC50 of 200 nM for DAPK1 and Kd of 280 nM for ZIPK.
HS-38 also inhibits Pim3 (IC50=200 nM), and displays no activity against Src or Abl, little activity against EGFR.
HS-38 decreases RLC20 phosphorylation in cells, and decreases contractile force generated in mouse aorta, rabbit ileum, and calyculin A stimulated arterial muscle by decreasing RLC20 and MYPT1 phosphorylation.
HS-38 also promotes relaxation in Ca(2+)-sensitized vessels.

物理化学性质&存储条件

分子量 349.793
分子式 C14H12ClN5O2S
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

2-[[1-(3-Chlorophenyl)-4,5-dihydro-4-oxo-1H-pyrazolo[3,4-d]pyrimidin-6-yl]thio]propanamide

参考文献

1. Carlson DA, et al. ACS Chem Biol. 2013 Dec 20;8(12):2715-23.

2. MacDonald JA, et al. Mol Pharmacol. 2016 Jan;89(1):105-17.

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