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IMP-1088 {[allProObj[0].p_purity_real_show]}

货号:A1365252

IMP-1088是一种有效的人 N-肉豆蔻酰基转移酶 NMT1 和 NMT2 双重抑制剂,对 HsNMT1 和 HsNMT2 的 IC50 小于 1 nM。IMP-1088 对 HsNMT1 的 Kd 小于 210 pM。IMP-1088 通过阻断鼻病毒的 N-肉豆蔻酰化蛋白 (VP0) 有效阻断鼻病毒的复制,并保护宿主细胞免受病毒感染的细胞毒作用。

IMP-1088 化学结构 CAS号:2059148-82-0
IMP-1088 化学结构
CAS号:2059148-82-0
IMP-1088 3D分子结构
CAS号:2059148-82-0
IMP-1088 化学结构 CAS号:2059148-82-0
IMP-1088 3D分子结构 CAS号:2059148-82-0
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IMP-1088 纯度/质量文件 产品仅供科研

货号:A1365252 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 DNA synthesis helicase RdRp ribonucleotide reductase tRNA synthetase YB-1 其他靶点 纯度
Fexinidazole 98%
Daptomycin 98%
Blasticidin S·HCl 98%
Metronidazole 98%
Daunorubicin HCl +++

DNA synthesis, Ki: 20 nM

98%
Triglycidyl isocyanurate p53 98+%
Nedaplatin 99%+
Oxolinic acid 98+%
Bendamustine 98+%
Trifluridine 98%
Robinetin 99%+
Carboplatin 99%
Cidofovir 99%
Cisplatin 99%
Cytarabine ++++

DNA synthesis, IC50: 16 nM

98%
Acelarin ++++

DNA synthesis, EC50: 0.2 nM

99%+
Oxaliplatin 98%
YK-4-279 99%+
ML216 +

BLM636-1298, IC50: 0.97 μM

BLMfull-length, IC50: 2.98 μM

99%+
RK-33 98%
Brr2-IN-3 99%+
Phen-DC3 Trifluoromethanesulfonate 95%
Favipiravir 99%
Suramin sodium salt ++

RdRp, IC50: 0.26 μM

99%+
Clofarabine ++

Ribonucleotide reductase, IC50: 65 nM

97%
Didox 98%
(E)-3-AP 99%
Halofuginone +++

prolyl-tRNA synthetase, Ki: 18.3nM

99%+
BC-LI-0186 +++

Leucyl-tRNA synthetase, Kd: 42.1 nM

Leucyl-tRNA synthetase, IC50: 46.11 nM

98%
SU056 +

YB-1, IC50: 1.73 μM

98%
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。

IMP-1088 生物活性

描述 IMP-1088 is a potent dual inhibitor of HsNMT1/2 with IC50 values of less than 1 nM, and the Kd value of IMP-1088 against HsNMT1 is less than 210 pM. IMP-1088 effectively blocks rhinovirus replication by blocking the N-myristoylation of rhinovirus-encoded protein (VP0). IMP-1088 protects host cells from cytotoxicity caused by viral infection. At concentrations less than 1000 nM, IMP-1088 prevented virus-induced cytopathic effects in a dose-dependent manner, with IC50 values of 17 nM, respectively, and at a concentration of 125 nM, IMP-1088 completely inhibited newly infected viruses, with an IC50 value of 5.8 nM. IMP-1088 blocks infectious virus production and inhibits single-cycle replication 7 hours after infection of primary human bronchial epithelial cells (hBEC) with rhinovirus RV-A1 (MOI 5). IMP-1088 significantly inhibits the production of infectious virus even within 3 hours of infection[1].

IMP-1088 细胞实验

Cell Line
Concentration Treated Time Description References
HeLa cells 125 nM 6 hours Complete suppression of infectious virus production Nat Chem. 2018 Jun;10(6):599-606
HeLa cells 50 nM 6 hours Inhibition of RV-A16 VP0 myristoylation post-infection Nat Chem. 2018 Jun;10(6):599-606
human fibroblasts 100 nM To study the inhibitory effect of IMP-1088 on N-myristoylation Brain. 2024 Apr 4;147(4):1436-1456
HeLa 1 nM, 10 nM, 100 nM 24 hours To evaluate the inhibitory effect of IMP-1088 on NMT activity, results showed that IMP-1088 significantly inhibited NMT activity. Mol Cell Proteomics. 2019 Jan;18(1):115-126
Panc-1 1 nM, 10 nM, 100 nM 24 hours To evaluate the inhibitory effect of IMP-1088 on NMT activity, results showed that IMP-1088 significantly inhibited NMT activity. Mol Cell Proteomics. 2019 Jan;18(1):115-126
MDA-MB-231 1 nM, 10 nM, 100 nM 24 hours To evaluate the inhibitory effect of IMP-1088 on NMT activity, results showed that IMP-1088 significantly inhibited NMT activity. Mol Cell Proteomics. 2019 Jan;18(1):115-126
HeLa cells 500 nM 6 hours Blockade of viral assembly, preventing infectious virion formation Nat Chem. 2018 Jun;10(6):599-606
ST cells 50 nM and 100 nM 24 hours To evaluate the effect of IMP-1088 on SVA replication, results showed that IMP-1088 significantly inhibited SVA replication. Pathogens. 2024 Jul 21;13(7):601
BHK-21 cells 100 nM 24 hours To evaluate the effect of IMP-1088 on SVA replication, results showed that IMP-1088 significantly inhibited SVA replication. Pathogens. 2024 Jul 21;13(7):601

IMP-1088 参考文献

[1]Aurélie Mousnier, et al. Fragment-derived Inhibitors of Human N-myristoyltransferase Block Capsid Assembly and Replication of the Common Cold Virus. Nat Chem. 2018 Jun;10(6):599-606.

IMP-1088 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.20mL

0.44mL

0.22mL

11.02mL

2.20mL

1.10mL

22.05mL

4.41mL

2.20mL

IMP-1088 技术信息

CAS号2059148-82-0
分子式C25H29F2N5O
分子量 453.53
SMILES Code FC=1C=CC(C2=CC=C3C(=C2)C(=NN3C)CN(C)C)=C(OCCC=4C(=NN(C4C)C)C)C1F
MDL No. MFCD32708500
别名
运输蓝冰
InChI Key SOXNKJCQBRQUMS-UHFFFAOYSA-N
Pubchem ID 132274735
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry, store in freezer, under -20°C

溶解方案

DMSO: 105 mg/mL(231.52 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

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
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