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IZCZ-3

Catalog No. T11698   CAS 2223019-53-0

IZCZ-3,antitumor activity. is a potent c-MYC transcription inhibitor.

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IZCZ-3 Chemical Structure
IZCZ-3, CAS 2223019-53-0
Pack Size Availability Price/USD Quantity
25 mg 6-8 weeks $ 1,230.00
50 mg 6-8 weeks $ 1,610.00
100 mg 6-8 weeks $ 2,390.00
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This compound is a customized synthesis product. We have a strong synthesis team with excellent synthesis technology and capabilities. However, due to various objective factors, there is a low probability that the synthesis will not be successful. If you need to learn more, please feel free to consult us, we will serve you wholeheartedly.
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Biological Description
Chemical Properties
Storage & Solubility Information
Description IZCZ-3,antitumor activity. is a potent c-MYC transcription inhibitor.
In vitro IZCZ-3 induces only weak growth inhibition in the BJ fibroblasts (IC50=15.9 μM) and mouse mesangial cells (IC50=15.6 μM), suggesting that IZCZ-3 is more effective against cancer cells than against c-MYC-independent normal cells. IZCZ-3 (0-5 μM; 12 hours) induces an apparent accumulation of cells in the G0/G1 phase in SiHa cells in a dose-dependent manner.IZCZ-3 (2.1 μM-15.9 μM; 24 hours) significantly inhibits SiHa, HeLa, Huh7, and A375 cancer cell proliferation (IC50s of 3.3, 2.1,4.1, and 4.2 μM, respectively).
In vivo IZCZ-3 inhibits tumor growth in BALB/c nude mice with SiHa human cervical squamous cancer xenograft.
Molecular Weight 715.93
Formula C46H49N7O
CAS No. 2223019-53-0

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 5 mg/mL (6.98 mM), Sonication and heating to 80℃ are recommended.

TargetMolReferences and Literature

1. Hu MH, et al. Discovery of a New Four-Leaf Clover-Like Ligand as a Potent c-MYC Transcription Inhibitor Specifically Targeting the Promoter G-Quadruplex. J Med Chem. 2018 Mar 22;61(6):2447-2459.

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Keywords

IZCZ-3 2223019-53-0 Others IZCZ3 IZCZ 3 inhibitor inhibit

 

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