ChemicalBook--->CAS DataBase List--->339303-87-6

339303-87-6

339303-87-6 Structure

339303-87-6 Structure
IdentificationBack Directory
[Name]

N-(4-Fluorophenyl)-4-phenyl-2-thiazolamine
[CAS]

339303-87-6
[Synonyms]

GP130 receptor agonist-1
N-(4-Fluorophenyl)-4-phenyl-2-thiazolami
N-(4-Fluorophenyl)-4-phenylthiazol-2-amine
N-(4-Fluorophenyl)-4-phenyl-2-thiazolamine
2-Thiazolamine, N-(4-fluorophenyl)-4-phenyl-
GP130 receptor agonist-1,neuroprotective,Inhibitor,penetrant,NMDA,inhibit,GP-130 receptor agonist-1,brain,Interleukin Related,GP130 receptor agonist1,GP130,GP130 receptor agonist 1
[Molecular Formula]

C15H11FN2S
[MDL Number]

MFCD00784992
[MOL File]

339303-87-6.mol
[Molecular Weight]

270.32
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

A solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

N-(4-Fluorophenyl)-4-phenyl-1,3-thiazol-2-amine is a gp130 agonist. Protects against NMDA-induced toxicity in primary hippocampal neurons in vitro. Increases STAT3 phosphorylation in SH-SY5Y cells. Brain penetrant.
[in vivo]

For GP130 receptor agonist-1 (Compound 2), mice are dosed orally at 10 or 30 mg/kg, or injected subcutaneously (SQ) at 10 mg/kg, and euthanized after 1, 2, 4, 6, and 8 h post dose. At 2 h after SQ delivery at 10 mg/kg the brain Cmax is 161 ng/g while dosing at 30 mg/kg orally, results in the brain Cmax of 156 ng/g (0.57 μM). The brain to plasma ratio for 2 is ~4:1 for oral 30 mg/kg and ~7.5:1 for 10 mg/kg SQ injection[1].

[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

N-(4-Fluorophenyl)-4-phenyl-2-thiazolamine(339303-87-6)1HNMR
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