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ChemicalBook--->CAS DataBase List--->667880-38-8

667880-38-8

667880-38-8 Structure

667880-38-8 Structure
IdentificationBack Directory
[Name]

5-({1-[2-(2,4-dimethylphenoxy)ethyl]-2-methyl-1H-indol-3-yl}methylene)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione
[CAS]

667880-38-8
[Synonyms]

IAC-8
5-({1-[2-(2,4-dimethylphenoxy)ethyl]-2-methyl-1H-indol-3-yl}methylene)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione
[Molecular Formula]

C24H23N3O3S
[MDL Number]

MFCD03699567
[MOL File]

667880-38-8.mol
[Molecular Weight]

433.523
Chemical PropertiesBack Directory
[density ]

1.30±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

62.5 mg/mL in DMSO
[form ]

Solid
[pka]

5.34±0.20(Predicted)
[color ]

Yellow to orange
Hazard InformationBack Directory
[Uses]

ZLDI-8 is a Notch activating/cleaving enzyme ADAM-17 inhibitor and inhibits the cleavage of Notch protein. ZLDI-8 decreases the expression of pro-survival/anti-apoptosis and epithelial-mesenchymal transition (EMT) related proteins. ZLDI-8 is also a competitive and irreversible tyrosine phosphatase (Lyp) inhibitor with an IC50 of 31.6 μM and a Ki of 26.22 μM. ZLDI-8 inhibits the growth of MHCC97-H cells with an IC50 of 5.32 μM[1][2].
[in vivo]

ZLDI-8 (0.2-2 mg/kg; intraperitoneal injection; every two days; for 20 days; nude mice) treatment enhances the effect of Sorafenib on inhibiting tumor growth in nude HCC-bearing mice model[1].

Animal Model:Nude mice with MHCC-97H cells[1]
Dosage:2?mg/kg, 1?mg/kg, 500?μg/kg, or 200?μg/kg
Administration:Intraperitoneal injection; every two days; for 20 days
Result: Inhibited tumor growth in nude HCC-bearing mice model.
[storage]

Store at -20°C
[References]

[1] Zhang Y, et al. Novel ADAM-17 inhibitor ZLDI-8 enhances the in vitro and in vivo chemotherapeutic effects of Sorafenib on hepatocellular carcinoma cells. Cell Death Dis. 2018 Jul 3;9(7):743. DOI:10.1038/s41419-018-0804-6
[2] Hou X, et al. Fast identification of novel lymphoid tyrosine phosphatase inhibitors using target-ligand interaction-based virtual screening. J Med Chem. 2014 Nov 26;57(22):9309-22. DOI:10.1021/jm500692u
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