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ChemicalBook--->CAS DataBase List--->1919828-81-1

1919828-81-1

1919828-81-1 Structure

1919828-81-1 Structure
IdentificationBack Directory
[Name]

Urea, N-[4-(4-butyl-1H-1,2,3-triazol-1-yl)phenyl]-N'-(2-methylphenyl)-
[CAS]

1919828-81-1
[Synonyms]

Urea, N-[4-(4-butyl-1H-1,2,3-triazol-1-yl)phenyl]-N'-(2-methylphenyl)-
[Molecular Formula]

C20H23N5O
[MOL File]

1919828-81-1.mol
[Molecular Weight]

349.43
Chemical PropertiesBack Directory
[density ]

1.18±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[form ]

Solid
[pka]

13.83±0.70(Predicted)
[color ]

Off-white to gray
Hazard InformationBack Directory
[Uses]

DDX3-IN-2 is an active DEADbox polypeptide 3 (DDX3) inhibitor with an IC50 value of 0.3 μM. DDX3-IN-2 shows a broad spectrum of antiviral activity. DDX3-IN-2 has the potential to overcome HIV resistance[1].
[Biological Activity]

DDX3-IN-2 is an active DEADbox polypeptide 3 (DDX3) inhibitor with an IC50 value of 0.3 μM. DDX3-IN-2 shows a broad spectrum of antiviral activity. DDX3-IN-2 has the potential to overcome HIV resistance[1]. DDX3-IN-2 behaves as a competitive inhibitor with respect to the RNA substrate, which can be seen by the decrease in its inhibition potency as a function of increasing RNA substrate concentrations. DDX3-IN-2 is found to be completely inactive against the ATPase of DDX3, DDX1 helicase, and DENV NS3 helicase[1]. DDX3-IN-2 (20 mg/kg; tail vein injection) possesses excellent biocompatibility, and Wistar rats shows a good tolerance to the dose of 20 mg/kg[1].DDX3-IN-2 (10 mg/kg; i.v. bolus injection; 0~25 hours) rapidly eliminates the half-life elimination and the plasmatic clearance values[1].
[in vivo]

DDX3-IN-2 (20 mg/kg; tail vein injection) possesses excellent biocompatibility, and Wistar rats shows a good tolerance to the dose of 20 mg/kg[1].
DDX3-IN-2 (10 mg/kg; i.v. bolus injection; 0~25 hours) rapidly eliminates the half-life elimination and the plasmatic clearance values[1].

Animal Model:Wistar rats[1]
Dosage:Tail vein injection
Administration:20 mg/kg
Result:Possessed excellent biocompatibility, and Wistar rats showed a good tolerance to the dose of 20 mg/kg.
Animal Model:Rats[1]
Dosage:I.v. bolus injection (Pharmacokinetic Analysis)
Administration:10 mg/kg; 0~25 hours
Result:Rapidly eliminated the half-life elimination and the plasmatic clearance values.
[IC 50]

HIV
[References]

[1]. Brai A, et al. Human DDX3 protein is a valuable target to develop broad spectrum antiviral agents. Proc Natl Acad Sci U S A. 2016;113(19):5388-5393.
1919828-81-1 suppliers list
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Website: https://www.targetmol.cn/
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