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FR 180204
Cat. No.:
OB0225WX-2362
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, HPLC, and LC-MS.
Size:
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Product Overview
Description:
FR 180204 is a potent, ATP-competitive inhibitor characterized by its high selectivity for the ERK1 and ERK2 kinase isoforms.
Synonym:
FR180204; 865362-74-9; FR-180204; ERK inhibitor II; 5-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-2H-pyrazolo[3,4-c]pyridazin-3-amine; 1H-Pyrazolo(3,4-C)pyridazin-3-amine, 5-(2-phenylpyrazolo(1,5-a)pyridin-3-yl)-; 5-(2-Phenylpyrazolo(1,5-a)pyridin-3-yl)-2H-pyrazolo(3,4-C)pyridazin-3-amine; 5-{2-phenylpyrazolo[1,5-a]pyridin-3-yl}-1H-pyrazolo[3,4-c]pyridazin-3-amine; 5-{2-phenylpyrazolo[1,5-a]pyridin-3-yl}-2H-pyrazolo[3,4-c]pyridazin-3-amine; MFCD14585805; 3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-7H-pyrazolo[3,4-c]pyridazin-5-amine; 5-(2-Phenyl-pyrazolo[1,5-a]pyridin-3-yl)-1H-pyrazolo[3,4-c]pyridazin-3 -ylamine; 5-(2-phenylH-pyrazolo[1,5-a]pyridin-3-yl)-1H-pyrazolo[3,4-c]pyridazin-3-amine
CAS No.:
865362-74-9
Compound CID:
11493598
Formula:
C18H13N7
Formula Weight:
327.34
Specification
Targets&IC50:
ERK1: 0.31 μM(Ki); ERK2: 0.14 μM(Ki)
Relative Density:
1.55 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
FR 180204 is used in neuropharmacology and inflammation research as a selective, ATP-competitive ERK1/2 inhibitor to investigate the role of MAPK signaling in nociception and inflammatory responses.
Library Information
Target:
ERK
Receptor:
ERK1; ERK2
Pathways:
Apoptosis; MAPK
Plate Number:
AOCL-31
Plate Location:
c4
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
32.7 mg/mL; 100 mM
ALogP:
2.969
HBA_Count:
4
HBD_Count:
2
Rotatable Bond:
2





