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1-(4,6-dimethylpyrimidin-2-yl)-3-[2-(trifluoromethyl)phenyl]guanidine

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1-(4,6-dimethylpyrimidin-2-yl)-3-[2-(trifluoromethyl)phenyl]guanidine Basic information

Product Name:
1-(4,6-dimethylpyrimidin-2-yl)-3-[2-(trifluoromethyl)phenyl]guanidine
Synonyms:
  • 1-(4,6-dimethylpyrimidin-2-yl)-3-[2-(trifluoromethyl)phenyl]guanidine
  • ZINC69391
  • Guanidine, N-(4,6-dimethyl-2-pyrimidinyl)-N'-[2-(trifluoromethyl)phenyl]-
  • N'-(4,6-dimethylpyrimidin-2-yl)-N-[2-(trifluoromethyl)phenyl]guanidine
  • ZINC69391, 10 mM in DMSO
CAS:
303094-67-9
MF:
C14H14F3N5
MW:
309.29
Mol File:
303094-67-9.mol
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1-(4,6-dimethylpyrimidin-2-yl)-3-[2-(trifluoromethyl)phenyl]guanidine Chemical Properties

Melting point:
149-151 °C
Boiling point:
404.3±55.0 °C(Predicted)
Density 
1.35±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
DMSO : 25 mg/mL (80.83 mM; ultrasonic and warming and heat to 60°C)
pka
4.69±0.70(Predicted)
form 
Solid
color 
White to off-white
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1-(4,6-dimethylpyrimidin-2-yl)-3-[2-(trifluoromethyl)phenyl]guanidine Usage And Synthesis

Uses

ZINC 69391 is a novel specific Rac1 inhibitor, interferring with the interaction of Rac1 with Dock180, a relevant Rac1 activator in glioma invasion, and to reduce Rac1-GTP levels.

in vivo

ZINC69391 (25 mg/kg; i.p; daily for 21 days) impairs metastatic lung colonization in a syngeneic animal model[3].

Animal Model:Specific pathogen-free female BALB/c inbred mice (bearing F3II cells)[3]
Dosage:25 mg/kg body weight
Administration:I.p; daily for 21 days
Result:Significantly reduced by about 60% the formation of total metastatic lung colonies.

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