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ETC-206
Cat. No.:
OB0225WX-1630
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, HPLC, and LC-MS.
Size:
Add to basket
Product Overview
Description:
ETC-206 is a selective kinase inhibitor that targets the MNK1 and MNK2 isoforms with IC50 values measured at 64 nM and 86 nM.
Synonym:
1464151-33-4; Tinodasertib; 4-(6-(4-(morpholine-4-carbonyl)phenyl)imidazo[1,2-a]pyridin-3-yl)benzonitrile; AUM001; AUM-001; 4-[6-[4-(morpholine-4-carbonyl)phenyl]imidazo[1,2-a]pyridin-3-yl]benzonitrile; 4-{6-[4-(morpholine-4-carbonyl)phenyl]imidazo[1,2-a]pyridin-3-yl}benzonitrile; Benzonitrile, 4-(6-(4-(4-morpholinylcarbonyl)phenyl)imidazo(1,2-a)pyridin-3-yl)-; MFCD31692387; 4-{6-[4-(morpholin-4-ylcarbonyl)phenyl]imidazo[1,2-a]pyridin-3-yl}benzonitrile; 4-{6-[4-(morpholine-4-carbonyl)phenyl]imidazo[1,2- a]pyridin-3-yl}benzonitrile
CAS No.:
1464151-33-4
Compound CID:
71766360
Formula:
C25H20N4O2
Formula Weight:
408.45
Specification
Targets&IC50:
MNK2: 86 nM; MNK1: 64 nM
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
ETC-206 is applied in medicinal chemistry research as a targeted kinase inhibitor to explore its pharmacodynamic profile and its potential for modulating specific intracellular signaling cascades.
Library Information
Target:
MNK
Receptor:
MNK; MNK1; MNK2
Pathways:
MAPK
Plate Number:
AOCL-21
Plate Location:
h5
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
55 mg/mL; 134.66 mM





