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ChemicalBook--->CAS DataBase List--->84545-30-2

84545-30-2

84545-30-2 Structure

84545-30-2 Structure
IdentificationBack Directory
[Name]

ICI 162,846
[CAS]

84545-30-2
[Synonyms]

846
ICI 162
ICI 162,846
3-((imino((2,2,2-trifluoroethyl)amino)methyl)amino)-1h-pyrazole-1-pentanamid
3-[[Imino[(2,2,2-trifluoroethyl)amino]methyl]amino]-1H-pyrazole-1-pentanamide
N-[1-(4-CARBOXAMIDOBUTYL)-1H-PYRAZOL-3-YL]-N'-(2,2,2-TRIFLUOROETHYL)GUANIDINE
1H-Pyrazole-1-pentanamide, 3-[[imino[(2,2,2-trifluoroethyl)amino]methyl]amino]-
[Molecular Formula]

C11H17F3N6O
[MDL Number]

MFCD01310549
[MOL File]

84545-30-2.mol
[Molecular Weight]

306.29
Chemical PropertiesBack Directory
[Boiling point ]

180°C (rough estimate)
[density ]

1.3025 (estimate)
[storage temp. ]

Store at RT
[solubility ]

Soluble in ethanol and to 100 mM in DMSO
[form ]

Powder
Hazard InformationBack Directory
[Uses]

ICI 162846 is a histamine H2-receptor antagonist.
[Definition]

ChEBI: 5-[3-[[amino(2,2,2-trifluoroethylimino)methyl]amino]-1-pyrazolyl]pentanamide is a fatty amide.
[Biological Activity]

A potent histamine H 2 receptor antagonist.
[in vivo]

ICI 162846 (10 mg/kg, p.o., twice daily for 5 days) reduces the incidence of CDU and inhibits acid production accompanied by an increase in the secretion of histamine in induced CDU models of CFLP mice[2].

Animal Model:CFLP mice were irradiated to the lower mediastinum to induce CDU[2].
Dosage:10 mg/kg, twice daily for 5 days
Administration:Oral gavage (p.o.)
Result:Reduced the incidence of CDU.
Inhibited gastric acid secretion about 50% or more in the basal and the stimulated periods.
Induced massive rises in basal (12-fold) and stimulated (9-fold) luminal histamine.
[IC 50]

H2 Receptor
[storage]

Store at RT
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