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Chemical Structure| 366017-09-6 Chemical Structure| 366017-09-6

Structure of Mubritinib
CAS No.: 366017-09-6

Chemical Structure| 366017-09-6

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Mubritinib (TAK-165) is an effective and selective EGFR2/HER2 inhibitor with an IC50 value of 6 nM.

Synonyms: TAK-165

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Product Details of Mubritinib

CAS No. :366017-09-6
Formula : C25H23F3N4O2
M.W : 468.47
SMILES Code : FC(F)(C1=CC=C(/C=C/C2=NC(COC3=CC=C(C=C3)CCCCN4C=CN=N4)=CO2)C=C1)F
Synonyms :
TAK-165
MDL No. :MFCD09954135
InChI Key :ZTFBIUXIQYRUNT-MDWZMJQESA-N
Pubchem ID :6444692

Safety of Mubritinib

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H320-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Related Pathways of Mubritinib

RTK

Isoform Comparison

Biological Activity

Target
  • HER2

    HER2/ErbB2, IC50:6.0 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
Asthmatic human airway epithelial cells (Asthmatic HAECs) 100 nM 16 h Inhibition of ErbB2 phosphorylation had minimal effect on wound closure and CCND1 expression in asthmatic HAECs, indicating lower ErbB2 activity in these cells. PMC6556416
Healthy human airway epithelial cells (HC HAECs) 100 nM 16 h Inhibition of ErbB2 phosphorylation significantly reduced wound closure and CCND1 expression in healthy HAECs, but had less impact on asthmatic HAECs. PMC6556416
BTSC147 500 nM 24 h Measure basal oxygen consumption rate (OCR), results showed Mubritinib significantly reduced basal mitochondrial respiration in BTSC147 PMC11903783
BTSC73 100 nM 24 h Measure basal oxygen consumption rate (OCR), results showed Mubritinib significantly reduced basal mitochondrial respiration in BTSC73 PMC11903783
BTSC53 20 nM 24 h Measure basal oxygen consumption rate (OCR), results showed Mubritinib significantly reduced basal mitochondrial respiration in BTSC53 PMC11903783
OCI-AML3 cells 125 nM 24 h TAK-165 in combination with AC220 significantly reduced the viability of OCI-AML3 cells PMC5833862
HEL cells 125 nM 24 h TAK-165 in combination with AC220 significantly reduced the viability of HEL cells PMC5833862
Sum159 cells 125 nM 24 h TAK-165 in combination with AC220 significantly reduced the viability of Sum159 cells PMC5833862
ES-2 cells 125 nM 24 h TAK-165 in combination with AC220 significantly reduced the viability of ES-2 cells PMC5833862
SNU-16R cells 1 µM 72 h To evaluate the effect of Mubritinib on the growth of SNU-16R cells, the results showed that SNU-16R cells were sensitive to Mubritinib PMC4688307
BT474 cells 10 µM 24 h Selective inhibition of HER2 significantly reduced the mitochondrial metabolic rate of BT474 cells, but the effect was less pronounced than in SK-BR3 cells. PMC6107558
SK-BR3 cells 10 µM 24 h Selective inhibition of HER2 significantly reduced the mitochondrial metabolic rate of SK-BR3 cells by ~40%. PMC6107558
BC1 cells 15 nM 72 h To investigate the effect of Mubritinib on the cell cycle of PEL cells, Mubritinib reduced S and G2 populations and increased the sub-G1 population in BC1 cells. PMC7679036
BCBL1 cells 15 nM 72 h To investigate the effect of Mubritinib on the cell cycle of PEL cells, Mubritinib reduced S and G2 populations and increased the sub-G1 population in BCBL1 cells. PMC7679036
BC3 cells 10 µM 72 h To screen for drugs that selectively inhibit the growth of KSHV+ PEL cells, Mubritinib showed growth inhibition in BC3 cells. PMC7679036
Rat brain endothelial cells (RBECs) 1 µM 18 h To evaluate the protective effect of Mubritinib on the blood-spinal cord barrier function under oxygen-glucose deprivation and reoxygenation stress, results showed that Mubritinib significantly increased TEER and reduced Na-F permeability. PMC9723073
HCMEC/D3 cells 10 µM 24 h To evaluate the protective effect of Mubritinib on hCMEC/D3 cells under oxidative stress, results showed that Mubritinib protected cells from H2O2-induced oxidative stress damage. PMC9723073

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice GBM model Intraperitoneal injection 6 mg/kg 3 times per week for 40 days Evaluate the effect of Mubritinib on GBM tumor growth, results showed Mubritinib significantly delayed tumor growth and extended animal survival PMC11903783
Mice PEL mouse models Oral 25 mg/kg Once daily for 34 days To evaluate the inhibitory effect of Mubritinib on PEL cell growth in vivo, Mubritinib significantly slowed tumor growth in BCBL1 and BC1 mice. PMC7679036
Mice Spinal cord injury model Intraperitoneal injection 1 mg/kg Once daily for one day To evaluate the protective effect of Mubritinib on the blood-spinal cord barrier after spinal cord injury, results showed that Mubritinib significantly reduced IgG and Alb leakage. PMC9723073

Clinical Trial:

NCT Number Conditions Phases Recruitment Completion Date Locations
NCT00034281 Breast Neoplasm|Pancreatic Neo... More >>plasm|Lung Neoplasm|Ovarian Neoplasm|Renal Neoplasm Less << PHASE1 COMPLETED 2025-09-03 Arizona Cancer Center, Scottsd... More >>ale, Arizona, 85258, United States|The Institute for Drug Development, San Antonio, Texas, 78229, United States|Brooke Army Medical Center/Drug Development Unit, San Antonio, Texas, 78234, United States|South Texas VA, Audie Murphy Division, San Antonio, Texas, 78284, United States Less <<

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.13mL

0.43mL

0.21mL

10.67mL

2.13mL

1.07mL

21.35mL

4.27mL

2.13mL

 

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