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Chemical Structure| 1094614-85-3 Chemical Structure| 1094614-85-3

Structure of (E/Z)-BIX02189
CAS No.: 1094614-85-3

Chemical Structure| 1094614-85-3

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BIX-02189(Random Configuration) is a selective and potent inhibitor of both MEK5 and ERK5 with IC50 values of 1.5 and 59 nM, respectively.

Synonyms: BIX 02189

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Product Details of (E/Z)-BIX02189

CAS No. :1094614-85-3
Formula : C27H28N4O2
M.W : 440.54
SMILES Code : O=C(C1=CC(NC/2=O)=C(C=C1)C2=C(NC3=CC=CC(CN(C)C)=C3)/C4=CC=CC=C4)N(C)C
Synonyms :
BIX 02189
MDL No. :MFCD18074528
InChI Key :ZGXOBLVQIVXKEB-UHFFFAOYSA-N
Pubchem ID :135659062

Safety of (E/Z)-BIX02189

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of (E/Z)-BIX02189

MAPK

Isoform Comparison

Biological Activity

Target
  • MEK5

    MEK5, IC50:1.5 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
neonatal rat cardiomyocytes (NRCMs) 10μM 2 h Inhibited ERK5 phosphorylation, attenuated MEF2 transcriptional activity, and blunted the hypertrophic response in cardiomyocytes Circ Res. 2010 Mar 19;106(5):961-70.
Human umbilical vein endothelial cells (HUVECs) 10 μM 16–24 h To investigate the role of ERK5 in laminar flow-induced Nrf2 nuclear translocation. Results showed that BIX02189 inhibited laminar flow-induced Nrf2 nuclear translocation. J Biol Chem. 2012 Nov 23;287(48):40722-31.
PC12 cells 30 μM 30 min To investigate the role of ERK5 signaling in PC12 cells, results showed that BIX02189 selectively inhibited ERK5 phosphorylation without affecting ERK1/2 phosphorylation status. J Biol Chem. 2009 Aug 28;284(35):23564-73.
INS-1 cells 2 μM 9 h To evaluate the role of ERK5 in STZ-induced apoptosis in INS-1 cells. Results showed that BIX02189 pretreatment significantly increased the cleavage levels of PARP-1 and caspase-3 induced by STZ, indicating that ERK5 inhibition exacerbated STZ-induced apoptosis. Mol Cells. 2017 Jul 31;40(7):457-465
Rat superior cervical ganglion neurons 10 μM 48 h To evaluate the selective inhibition of MEK5-ERK5 signaling by BIX02189, results showed that BIX02189 alone or in combination with PD184352 had no significant effect on WldS-mediated axon protection. PLoS One. 2013 Oct 4;8(10):e76505
C2C12 myoblasts 10 μM 20 min To investigate the role of MEK5/ERK5 pathway in PMA-induced mTORC1 signaling activation. BIX-02189 partially prevented PMA-induced phosphorylation of S6K1 (41% decrease in Thr389 phosphorylation and 29% decrease in Ser421/Thr424 phosphorylation) and completely blocked ERK5 phosphorylation. FEBS Open Bio. 2017 Jan 30;7(3):424-433

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 mice Pregnant mouse model Intraperitoneal injection 10 mg/kg Once daily from gestational day 1 to day 15 To suppress ERK5 activation and study its effect on beta-cell proliferation in pregnant mice, results showed that BIX02189 significantly reduced beta-cell proliferation, leading to increased blood glucose levels and impaired glucose response Cell Prolif. 2018 Jun;51(3):e12410
C57BL/6 mice Nrf2 nuclear translocation model in aortic endothelial cells Intraperitoneal injection 10 mg/kg Single dose To investigate the effect of ERK5 on Nrf2 nuclear translocation in vivo. Results showed that BIX02189 inhibited Nrf2 nuclear translocation in aortic endothelial cells of mice. J Biol Chem. 2012 Nov 23;287(48):40722-31.
C57BL/6J mice STZ-induced type 1 diabetes model Intraperitoneal injection 10 mg/kg Every 2 days for 6 days To evaluate the effect of ERK5 inhibition on STZ-induced hyperglycemia and pancreatic β-cell apoptosis. Results showed that co-treatment with BIX02189 and STZ significantly exacerbated hyperglycemia and pancreatic β-cell apoptosis, indicating that ERK5 inhibition aggravated diabetic symptoms. Mol Cells. 2017 Jul 31;40(7):457-465

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.27mL

0.45mL

0.23mL

11.35mL

2.27mL

1.13mL

22.70mL

4.54mL

2.27mL

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