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RO8191 {[allProObj[0].p_purity_real_show]}

货号:A888527 同义名: CDM-3008

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。

RO8191 化学结构 CAS号:691868-88-9
RO8191 化学结构
CAS号:691868-88-9
RO8191 3D分子结构
CAS号:691868-88-9
RO8191 化学结构 CAS号:691868-88-9
RO8191 3D分子结构 CAS号:691868-88-9
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RO8191 纯度/质量文件 产品仅供科研

货号:A888527 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。

RO8191 细胞实验

Cell Line
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

RO8191 动物实验

Species
Animal Model
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

RO8191 实验方案

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

RO8191 技术信息

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

请根据您的动物给药指南选择适当的溶解方案。
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
方案 一
方案 二
方案 三
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