Kevetrin HCl

This product is for research use only, not for human use. We do not sell to patients.

Kevetrin HCl
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Size Price Stock
1g$250Check With Us
2g$400Check With Us
5g$675Check With Us

Cat #: V4115 CAS #: 66592-89-0 Purity ≥ 98%

Description: Kevetrin hydrochloride (also known as thioureidobutyronitrile; 4-Isothioureidobutyronitrile hydrochloride; thioureidobutyronitrile hydrochloride; thioureido butyronitrile hydrochloride), is a water-soluble, small molecule activator of the tumor suppressor protein p53.

References: Napolitano R, et al. Kevetrin induces apoptosis in TP53 wildtype and mutant acute myeloid leukemia cells. Oncol Rep. 2020 Oct;44(4):1561-1573.

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Molecular Weight (MW)179.67
Molecular FormulaC5H10ClN3S
CAS No.66592-89-0
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 35 mg/mLr
Water: 36 mg/mLr
Ethanol: 20 mg/mL
SMILES CodeNC(SCCCC#N)=N.[H]Cl
SynonymsKevetrin; thioureidobutyronitrile; thioureido butyronitrile; 4-Isothioureidobutyronitrile hydrochloride; thioureidobutyronitrile hydrochloride; thioureido butyronitrile hydrochloride
ProtocolIn VitroKevetrin hydrochloride (100, 200, 400 µM; 48 h) increases the mRNA and protein level of p53 and induces p21 protein production in A2780 cells. Kevetrin hydrochloride (340 µM; 24 h) induces apoptosis on KASUMI-1 cell line, without leading cell cycle alteration. Kevetrin hydrochloride (340 µM; 6 h) induces metallothionein (MT) expression in acute myeloid leukemia (AML) cells, and also down-regulates genes in relation to p53 activity, the regulator of WNT/β-catenin signaling forkhead box K2 and the transcription factor signal transducer and activator of transcription 5A (STAT5A). Kevetrin hydrochloride (85, 170, 340 µM; 6 h) significantly inhibits KASUMI-1 cells growth in a dose-dependent manner, without affecting MOLM-13 cells.
In VivoKevetrin hydrochloride (150-200 mg/kg; i.p.; 20 d) induces ~40% cell death in OV-90 or OVCAR-3 xenograft tumors, also inhibits tumor growth and extents survival time of mice with tumor xenograft mode.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM5.5658 mL27.8288 mL55.6576 mL111.3152 mL
5mM1.1132 mL5.5658 mL11.1315 mL22.2630 mL
10mM0.5566 mL2.7829 mL5.5658 mL11.1315 mL
20mM0.2783 mL1.3914 mL2.7829 mL5.5658 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg Average weight of animals g Dosing volume per animal µL Number of animals
Step Two: Enter the in vivo formulation
%DMSO + % + %Tween 80 + %ddH2O

Calculation Results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in µL DMSO(Master liquid concentration mg/mL) ,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation: Take µL DMSO master liquid, next add µL PEG300, mix and clarify, next add µL Tween 80,mix and clarify, next add µL ddH2O,mix and clarify.
Note:
  • (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
  • (2) Be sure to add the solvent(s) in order.