货号:A1164834
                
                同义名:
                    
                        
                            
                                diABZI STING Agonist-1 (hydrochloride); STING Agonist diABZI
                            
                        
                    
                
                
                
                    
                     
                
            
diABZI STING agonist-1 is a selective STING receptor agonist with EC50 value of 130nM.
 
                                 
                                
                            

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| 描述 | diABZI STING agonist-1 3HCl is a selective STING agonist with EC50 values of 130 and 186 nM in humans and mice, respectively. diABZI STING agonist-1 3HCl is highly selective for more than 350 kinases at a concentration of 1 μM[1]. | 
| Administration | Dosage | Frequency | Description | References | ||
| Female BALB/cJ mice | Skin inflammation model | Subcutaneous injection | 2.5 mg/kg | Single injection, monitored for up to 6 weeks | To investigate the role of STING activation in skin inflammation, results showed that diABZI injection induced severe skin inflammation including erythema, scaling, and induration, which resolved within 6 weeks. | Int J Mol Sci. 2023 Feb 18;24(4):4128 | 
| Animal study | Administered intravenously at a dose of 3 mg/kg, diABZI STING agonist-1 3HCl demonstrated a systemic exposure half-life of 1.4 hours and achieved systemic concentrations higher than the EC50 for mouse STING (200 ng/ml). Administered subcutaneously at a dose of 2.5 mg/kg, diABZI STING agonist-1 3HCl induced STING-dependent activation of type I interferons and pro-inflammatory cytokines in in vivo experiments. In the BALB/c mouse colorectal tumour homozygous mouse model (CT-26), diABZI STING agonist-1 3HCl, administered intravenously at a dose of 1.5 mg/kg, significantly inhibited tumour growth and significantly increased animal survival. At the end of the study on day 43, 8 out of 10 mice remained tumour free[1]. | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 1.04mL 0.21mL 0.10mL | 5.21mL 1.04mL 0.52mL | 10.42mL 2.08mL 1.04mL | |
| CAS号 | 2138299-34-8 | 
| 分子式 | C42H54Cl3N13O7 | 
| 分子量 | 959.32 | 
| SMILES Code | O=C(C1=CC(OC)=C2C(N=C(NC(C3=CC(C)=NN3CC)=O)N2C/C=C/CN4C(NC(C5=CC(C)=NN5CC)=O)=NC6=CC(C(N)=O)=CC(OCCCN7CCOCC7)=C46)=C1)N.[H]Cl.[H]Cl.[H]Cl | 
| MDL No. | MFCD31746912 | 
| 别名 | diABZI STING Agonist-1 (hydrochloride); STING Agonist diABZI; STING Agonist (Compound 3); Diamidobenzimidazole STING Agonist-1; diABZI STING agonist-1 trihydrochloride | 
| 运输 | 蓝冰 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, 2-8°C | 
| 溶解方案 | DMSO: 95 mg/mL(99.03 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 25 mg/mL(26.06 mM),配合低频超声助溶 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶 
 
 
 
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