EGPI-1
Cat. No.: DC70380
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Chemical Structure
2355263-33-9
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Field of application
EGPI-1 is a potent small molecule that inhibits the translation initiation factors eIF4E/eIF4G interaction.EGPI-1 has potent antiproliferative and proapoptotic activity in multiple myeloma cells, Jurkat cells, and A549 lung cancer cell lines, inhibts A549 proliferation with IC50 of 2.61 uM, which is better than that of 4EGI-1 (IC50=58.6 uM), inhibits cancer cell growth by inhibiting eIF4E phosphorylation and inhibiting PI3K/Akt/mTOR signal pathway.EGPI-1 induces autophagy, apoptosis, G0/G1 cell cycle arrest and ROS generation in A549 cells, disrupts the mitochondrial membrane potential (∆ψ m).EGPI-1 demonstrated in vivo anti-tumor activities in A549-xenografted athymic mice (25 mg/kg/day, 50 mg/kg/day, i.p.).
Cas No.: |
2355263-33-9 |
Chemical Name: |
EGPI-1 |
Synonyms: |
EGPI 1;Benzaldehyde, 3,4-difluoro-, 2-[4-[4-(trifluoromethyl)phenyl]-2-thiazolyl]hydrazone, [C(E)]- |
SMILES: |
C1=C(/C=N/NC2SC=C(N=2)C2C=CC(C(F)(F)F)=CC=2)C=CC(F)=C1F |
Formula: |
C17H10F5N3S |
M.Wt: |
383.34 |
Purity: |
>97% |
Sotrage: |
2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Publication: |
1. Lijun Wang, et al. Eur J Med Chem. 2019 Sep 1;177:153-170. 2. Qi X, et al. Chem Biol Interact. 2022 Jan 25;352:109773. |
Description: |
EGPI-1 is a potent small molecule that inhibits the translation initiation factors eIF4E/eIF4G interaction.EGPI-1 has potent antiproliferative and proapoptotic activity in multiple myeloma cells, Jurkat cells, and A549 lung cancer cell lines, inhibts A549 proliferation with IC50 of 2.61 uM, which is better than that of 4EGI-1 (IC50=58.6 uM), inhibits cancer cell growth by inhibiting eIF4E phosphorylation and inhibiting PI3K/Akt/mTOR signal pathway.EGPI-1 induces autophagy, apoptosis, G0/G1 cell cycle arrest and ROS generation in A549 cells, disrupts the mitochondrial membrane potential (∆ψ m).EGPI-1 demonstrated in vivo anti-tumor activities in A549-xenografted athymic mice (25 mg/kg/day, 50 mg/kg/day, i.p.). |
References: |
1. Lijun Wang, et al. Eur J Med Chem. 2019 Sep 1;177:153-170. 2. Qi X, et al. Chem Biol Interact. 2022 Jan 25;352:109773. |
MSDS
COA
LOT NO. |
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2018-0101 |
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