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865362-74-9

865362-74-9 Structure

865362-74-9 Structure
IdentificationBack Directory
[Name]

5-(2-Phenyl-pyrazolo[1,5-a]pyridin-3-yl)-1H-pyrazolo[3,4-c]pyridazin-3-ylamine
[CAS]

865362-74-9
[Synonyms]

CS-1137
FR 180204
LM-3319 FR 180204
ERK Inhibitor II, FR180204
FR 180204;FR-180204;FR180204
ERK Inhibitor II, FR180204 - CAS 865362-74-9 - Calbiochem
FR 180204, 98%, a potent and selective ATP-competitive inhibitor of ERK
5-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-1H-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-Phenyl-pyrazolo[1,5-a]pyridin-3-yl)-1H-pyrazolo[3,4-c]pyridazin-3-ylamine
5-(2-Phenyl-pyrazolo[1,5-a]pyridin-3-yl)-1H-pyrazolo[3,4-c]pyridazin-3-ylamine USP/EP/BP
5-(2-Phenyl-pyrazolo[1,5-a]pyridin-3-yl)-1H-pyrazolo[3,4-c]pyridazin-3-ylamine FR 180204
[Molecular Formula]

C18H13N7
[MDL Number]

MFCD14585805
[MOL File]

865362-74-9.mol
[Molecular Weight]

327
Chemical PropertiesBack Directory
[Melting point ]

267 °C
[density ]

1.55±0.1 g/cm3(Predicted)
[storage temp. ]

Store at +4°C
[solubility ]

DMSO: ≥10mg/mL
[form ]

Yellow solid
[pka]

7.19±0.50(Predicted)
[color ]

faint yellow to dark yellow
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-20
[Safety Statements ]

20/21
[WGK Germany ]

3
[HS Code ]

29339900
Hazard InformationBack Directory
[Uses]

FR180204 has been used as ERK inhibitor:
  • to block extracellular-signal-regulated kinase (ERK) in order to validate whether homeobox B7 (HOXB7) regulates the migration and proliferation process via AKT/mitogen-activated protein kinases (MAPK) signaling
  • of extracellular-signal-regulated kinase (ERK) to study the effects of signaling pathway inhibitors on differentiation and cell traction stress
  • to determine if phosphorylation of this signaling protein is essential for mesenchymal stromal cell (MSC) derived therapeutic efficacy

[Definition]

ChEBI: 5-(2-phenyl-3-pyrazolo[1,5-a]pyridinyl)-2H-pyrazolo[3,4-c]pyridazin-3-amine is a member of pyrazoles and a ring assembly.
[Biochem/physiol Actions]

FR180204 is a potent, cell-permeable, ATP-competitive inhibitor of ERK1 and ERK2 (mitogen-activated protein kinase (MAPK)/extracellular-signal-regulated kinases (ERK) 1/2).
[in vivo]

FR180204 (100 mg/kg, i.p., b.i.d.) significantly decreases the severity of symptoms and body weight loss in collagen-induced arthritis mice[2].?In a mouse model of dengue virus (DENV) infection, FR180204 limits hepatocyte apoptosis, reduces DENV-induced liver injury, and improves clinical parameters[4].

[IC 50]

ERK2: 0.14 μM (Ki); ERK1: 0.31 μM (Ki); ERK2: 0.33 μM (IC50); ERK1: 0.51 μM (IC50)
[storage]

Store at +4°C
Spectrum DetailBack Directory
[Spectrum Detail]

5-(2-Phenyl-pyrazolo[1,5-a]pyridin-3-yl)-1H-pyrazolo[3,4-c]pyridazin-3-ylamine(865362-74-9)1HNMR
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