BPTQ
BPTQ is a potent inhibitor against VEGFR1 and CHK2 with IC50 values of 0.54 and 1.70 µmol/L, respectively. BPTQ is also an intercalator of DNA with anticancer activities. BPTQ inhibits the proliferation of HL-60 cells by arresting cells at S and G2/M phase with an IC50 value of 12 µmol/L. BPTQ also activates the mitochondria-mediated Apoptosis pathway by a decrease in mitochondrial membrane potential, increase in the Bax:Bcl-2 ratio and activation of caspases.
Para uso exclusivo en investigación. No vendemos a pacientes.
- No. CAS: 1802665-43-5
- Fòrmula: C17H16N4S
- Peso molecular:308.40
-
Almacenamiento:
Please store the product under the recommended conditions in the Certificate of Analysis.
Ver todos los productos específicos de isoformas VEGFR
MoreVer todos los productos específicos de isoformas Caspase
More
Actividad biológica
Descripciòn
Chemical Information
-
No. CAS 1802665-43-5
-
Peso molecular 308.40
-
Fòrmula C17H16N4S
-
SMILES
CCCCNC1=NC=NC2=C1SC3=C2C=C4C=CC=CC4=N3
-
Envío
Room temperature in continental US; may vary elsewhere.
-
Almacenamiento
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureza y Documentación
Referencias
[1]. RohitKumar HG, et al. DNA intercalative 4-butylaminopyrimido[4',5':4,5]thieno(2,3-b)quinoline induces cell cycle arrest and apoptosis in leukemia cells. Cancer Chemother Pharmacol. 2015 Jun;75(6):1121-33. [Content Brief]
[2]. Rohit Kumar H, et al. Inhibition of protein kinases by anticancer DNA intercalator, 4-butylaminopyrimido[4',5':4,5]thieno(2,3-b)quinoline. Acta Pharm Sin B. 2017 May;7(3):303-310. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)