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HJC0152 free base {[allProObj[0].p_purity_real_show]}

货号:A635939

HJC0152 free base是一种有效的STAT3抑制剂,具有口服活性,能够抑制细胞周期进程,诱导细胞凋亡,并显著抑制小鼠体内MDA-MB-231异种移植瘤的生长,显示出抗肿瘤活性,适用于STAT3相关癌症的研究。

HJC0152 free base 化学结构 CAS号:1420290-88-5
HJC0152 free base 化学结构
CAS号:1420290-88-5
HJC0152 free base 3D分子结构
CAS号:1420290-88-5
HJC0152 free base 化学结构 CAS号:1420290-88-5
HJC0152 free base 3D分子结构 CAS号:1420290-88-5
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HJC0152 free base 纯度/质量文件 产品仅供科研

货号:A635939 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 STAT1 STAT3 STAT5 其他靶点 纯度
Nifuroxazide 98%
Fludarabine 98%
Artesunate 98%
BP-1-102 +++

STAT3, Kd: 504 nM

99%+
Niclosamide ++

STAT3, IC50: 0.7 μM

98%
Napabucasin 98%
Cryptotanshinone ++

STAT3, IC50: 4.6 μM

98%
Stattic +

STAT3, IC50: 5.1 μM

98%
NSC 74859 +

STAT3, IC50: 86 μM

99%+
Ochromycinone 98%
HO-3867 97%
C188-9 ++++

STAT3, Kd: 4.7 nM

99%+
HJC0152 99%
SH5-07 95%
SH-4-54 ++++

STAT3, Kd: 300 nM

+++

STAT5, Kd: 464 nM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

HJC0152 free base 细胞实验

Cell Line
Concentration Treated Time Description References
H1299 1.25, 2.5, 5, 10, 20 μmol/L 24, 48, 72 hours HJC0152 significantly inhibited NSCLC cell proliferation with an IC50 value of 13.21 μmol/L (H1299). Cell Prolif. 2020 Mar;53(3):e12777
H460 1.25, 2.5, 5, 10, 20 μmol/L 24, 48, 72 hours HJC0152 significantly inhibited NSCLC cell proliferation with an IC50 value of 5.01 μmol/L (H460). Cell Prolif. 2020 Mar;53(3):e12777
A549 1.25, 2.5, 5, 10, 20 μmol/L 24, 48, 72 hours HJC0152 significantly inhibited NSCLC cell proliferation with an IC50 value of 5.11 μmol/L (A549). Cell Prolif. 2020 Mar;53(3):e12777
CAL27 cells 1 μM 24 hours Inhibited cell proliferation, migration and invasion, induced apoptosis Mol Cancer Ther. 2017 Apr;16(4):578-590
SCC25 cells 2 μM 24 hours Inhibited cell proliferation, migration and invasion, induced apoptosis Mol Cancer Ther. 2017 Apr;16(4):578-590
266-6 cells 10 µM 48 hours Inhibits STAT3 activity, rescues p-STAT1 nuclear translocation and enhances ISG expression Int J Mol Sci. 2024 Aug 19;25(16):9007
Human pulmonary artery endothelial cells (hPAECs) 1 μM 48 hours To investigate the effect of SERCA2a overexpression and STAT3 inhibitor HJC0152 on BMPR2 expression in hPAECs, results showed that STAT3i potentiated SERCA2a-induced BMPR2 expression. Int J Mol Sci. 2021 Aug 24;22(17):9105
Human pulmonary artery smooth muscle cells (hPASMCs) 1 μM 48 hours To evaluate the effect of STAT3 inhibitor HJC0152 on BMPR2 expression in hPASMCs, results showed that SERCA2a overexpression upregulated BMPR2 expression by inhibiting STAT3 activity. Int J Mol Sci. 2021 Aug 24;22(17):9105
HGC-27 cells 0, 5, 10, 20 µM 0, 24, 48, 72 hours To evaluate the effect of HJC0152 on cell growth, results showed that HJC0152 only inhibited the growth of HGC-27 cells at relatively high concentrations Cancer Manag Res. 2018 Dec 12;10:6857-6867
MKN45 cells 0, 5, 10, 20 µM 0, 24, 48, 72 hours To evaluate the effect of HJC0152 on cell growth, results showed that HJC0152 significantly inhibited the growth of MKN45 cells Cancer Manag Res. 2018 Dec 12;10:6857-6867
AGS cells 0, 5, 10, 20 µM 0, 24, 48, 72 hours To evaluate the effect of HJC0152 on cell growth, results showed that HJC0152 significantly inhibited the growth of AGS cells Cancer Manag Res. 2018 Dec 12;10:6857-6867

HJC0152 free base 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
BALB/c nude mice A549 NSCLC xenograft model Oral 7.5 mg/kg Once daily for 30 days HJC0152 significantly inhibited the growth of A549 xenograft tumours, extending the tumour volume doubling time from 2.03 days to 4.62 days. Cell Prolif. 2020 Mar;53(3):e12777
BALB/c-nu mice SCC25-derived orthotopic tongue tumor model Intraperitoneal injection 7.5 mg/kg Daily administration for 28 days Significantly inhibited tumor growth and invasion Mol Cancer Ther. 2017 Apr;16(4):578-590
C57BL/6 mice CVB3-induced acute pancreatitis and myocarditis model Intraperitoneal injection 12.5 mg/kg Once 24 hours before and once 24 hours after infection Alleviates viral-induced pancreatitis and myocarditis pathology by increasing IFNβ and ISG expression to reduce viral load Int J Mol Sci. 2024 Aug 19;25(16):9007
Rats Severe PAH model induced by unilateral left pneumonectomy combined with monocrotaline (PNT/MCT) Intraperitoneal injection 7.5 mg/kg Single injection, lasting 4 weeks To evaluate the therapeutic effect of STAT3 inhibitor HJC0152 combined with AAV1.hSERCA2a in the PAH model, results showed that combination therapy significantly reduced pulmonary artery pressure and vascular remodeling, and improved right ventricular function. Int J Mol Sci. 2021 Aug 24;22(17):9105
Nude mice MDA-MB-231 xenograft model Intraperitoneal injection and oral 7.5 mg/kg (ip), 25 mg/kg (po) Evaluate the inhibitory effect of HJC0152 on the growth of MDA-MB-231 xenograft tumors Am J Cancer Res. 2019 Apr 1;9(4):699-713
Nude mice MDA-MB-231 xenograft model Intraperitoneal injection and oral 7.5 mg/kg (ip), 25 mg/kg (po) Evaluate the inhibitory effect of HJC0152 on the growth of MDA-MB-231 xenograft tumors ACS Med Chem Lett. 2013 Feb 14;4(2):180-185
BALB/c nude mice MKN45 subcutaneous xenograft model Intraperitoneal injection 7.5 mg/kg Twice weekly for 21 days To evaluate the anti-tumor effect of HJC0152 in vivo, results showed that HJC0152 significantly inhibited tumor growth Cancer Manag Res. 2018 Dec 12;10:6857-6867

HJC0152 free base 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.70mL

0.54mL

0.27mL

13.51mL

2.70mL

1.35mL

27.01mL

5.40mL

2.70mL

HJC0152 free base 技术信息

CAS号1420290-88-5
分子式C15H13Cl2N3O4
分子量 370.19
SMILES Code O=C(NC1=CC=C([N+]([O-])=O)C=C1Cl)C2=CC(Cl)=CC=C2OCCN
MDL No. MFCD31704937
别名
运输蓝冰
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Keep in dark place, inert atmosphere, 2-8°C

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