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XMD8-92
Cat. No.:
OB0225WX-2171
Appearance:
Solid
Purity:
≥98%
Identity:
Confirmed by NMR, HPLC, and LC-MS.
Size:
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Product Overview
Description:
XMD8-92 functions as a highly specific and effective inhibitor of the BMK1/ERK5 pathway, with a binding dissociation constant (Kd) of 80 nM.
Synonym:
1234480-50-2; XMD 8-92; 2-[[2-Ethoxy-4-(4-hydroxy-1-piperidinyl)phenyl]amino]-5,11-dihydro-5,11-dimethyl-6H-pyrimido[4,5-B][1,4]benzodiazepin-6-one; MFCD18782742; 2-{[2-ethoxy-4-(4-hydroxypiperidin-1-yl)phenyl]amino}-5,11-dimethyl-5,11-dihydro-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one; XMD 8-92 (free base); 2-[2-ethoxy-4-(4-hydroxypiperidin-1-yl)anilino]-5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one; 2-((2-ethoxy-4-(4-hydroxypiperidin-1-yl)phenyl)amino)-5,11-dimethyl-5,11-dihydro-6H-benzo[e]pyrimido[5,4-b][1,4]diazepin-6-one; 6H-Pyrimido[4,5-b][1,4]benzodiazepin-6-one, 2-[[2-ethoxy-4-(4-hydroxy-1-piperidinyl)phenyl]amino]-5,11-dihydro-5,11-dimethyl-; 2-((2-ethoxy-4-(4-hydroxypiperidin-1-yl)phenyl)amino)-5,11-dimethyl-5H-benzo[e]pyrimido[5,4-b][1,4]diazepin-6(11H)-one
CAS No.:
1234480-50-2
Compound CID:
46843772
Formula:
C26H30N6O3
Formula Weight:
474.55
Specification
Targets&IC50:
BMK1: 80 nM(Kd)
Relative Density:
1.301 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
XMD8-92 is utilized in molecular biology and oncology research as a potent and selective inhibitor of BMK1 (ERK5) to investigate the regulation of cell proliferation and the suppression of tumor growth.
Library Information
Target:
BMI-1; ERK; Epigenetic reader domain
Receptor:
BMI-1; ERK; Epigenetic reader domain
Pathways:
DNA damage/DNA repair; Cell cycle/Checkpoint; MAPK; Chromatin/Epigenetic
Plate Number:
AOCL-28
Plate Location:
g6
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
19 mg/mL; 40 mM
ALogP:
3.505
HBA_Count:
4
HBD_Count:
2
Rotatable Bond:
5





