RO8191是一种口服活性干扰素 (IFN) 受体激动剂,能够与 IFNAR2 结合,激活干扰素刺激基因 (ISGs) 的表达。其表现出对 HCV 和 HBV 的显著抗病毒活性,适用于抗病毒治疗的研究。
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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。 |
Concentration | Treated Time | Description | References | |
HeLa cells | 0.01-100 µM | 1 day | CDM-3008 showed anti-SARS-CoV-2 activity in HeLa cells with an IC50 of 0.78 μM | Int J Mol Sci. 2021 Oct 28;22(21):11641 |
NCI-H1395 cells | 2 µM | 24 hours | RO8191 treatment slowed down the changes induced by Amuc_1100, inhibiting the recruitment and toxicity of CD8+ T cells. | Microb Biotechnol. 2024 Jul;17(7):e14522 |
A549 cells | 2 µM | 24 hours | RO8191 treatment slowed down the changes induced by Amuc_1100, inhibiting the recruitment and toxicity of CD8+ T cells. | Microb Biotechnol. 2024 Jul;17(7):e14522 |
Calu-3 cells | 0.001-10 µM | 3 days | CDM-3008 showed anti-SARS-CoV-2 activity in Calu-3 cells with an IC50 of 2.54 μM | Int J Mol Sci. 2021 Oct 28;22(21):11641 |
N2a-58 cells | 0.5, 5, 50, 250, 500 µM | 48 hours | RO8191 treatment did not alter PrPC levels in N2a-58 cells but dose-dependently increased OAS1a expression. | Brain. 2019 Apr 1;142(4):1035-1050 |
N2a-22L cells | 0.5, 5, 50, 250, 500 µM | 48 hours | RO8191 treatment significantly reduced PrPSc levels in N2a-22L cells in a dose-dependent manner. | Brain. 2019 Apr 1;142(4):1035-1050 |
REP-HepG2-NTCP cells | 1 and 10 µM | 9 days | Evaluated the anti-HBV effect of CDM-3008, showing significant reduction in HBV DNA levels | Cell Death Discov. 2021 Jun 2;7(1):130 |
Administration | Dosage | Frequency | Description | References | ||
Mice | Myocardial infarction model | Intragastric administration | 10 mg/kg | Single dose 30 min before MI surgery | To assess the effect of RO8191 on the anti-inflammatory and cardiac reparative effects of hEPs in MI treatment, showing that RO8191 attenuated these beneficial effects of hEPs. | Adv Sci (Weinh). 2023 Sep;10(27):e2300470 |
C57BL/6 mice | Subcutaneous allograft tumour model | Intraperitoneal injection | 2 mg/kg | Not specified | RO8191 attenuated the inhibitory effect of Amuc_1100 on tumour growth and reduced the number of tumour-infiltrating CD8+ T cells. | Microb Biotechnol. 2024 Jul;17(7):e14522 |
ICR mice | LPS-induced acute lung injury model | In vitro | 2 μM | Not used | Partially reversed the inhibitory effects of IRD on inflammation | J Inflamm Res. 2021 Feb 5;14:341-354. |
DdY mice | 22L prion infection model | Intraperitoneal injection | 2.0 mg/kg/day | Administered every other day starting from 2 days post-inoculation until sacrifice | RO8191 treatment significantly prolonged the survival of infected mice and reduced PrPSc levels and pathological changes in the brain and spleen. | Brain. 2019 Apr 1;142(4):1035-1050 |
Rats | Post-LT liver fibrosis model | Oral | 20 mg/kg | Daily for 10 days | To study the effect of RO8191 on liver fibrosis, results showed RO8191 increased the stage of liver fibrosis and the levels of COL1A1 and ACTA2. | Stem Cell Res Ther. 2025 May 1;16(1):217 |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.68mL 0.54mL 0.27mL |
13.40mL 2.68mL 1.34mL |
26.79mL 5.36mL 2.68mL |
CAS号 | 691868-88-9 |
分子式 | C14H5F6N5O |
分子量 | 373.21 |
SMILES Code | FC(C1=CC(C(F)(F)F)=NC2=C1C=CC3=NC(C4=NN=CO4)=CN32)(F)F |
MDL No. | MFCD03102493 |
别名 | CDM-3008 |
运输 | 蓝冰 |
InChI Key | GRHYZVJEXKTJOS-UHFFFAOYSA-N |
Pubchem ID | 2768133 |
存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
溶解方案 |
DMSO: 4 mg/mL(10.72 mM),配合低频超声,并水浴加热至45℃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 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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