ChemicalBook--->CAS DataBase List--->162112-37-0

162112-37-0

162112-37-0 Structure

162112-37-0 Structure
IdentificationBack Directory
[Name]

RWJ 50271
[CAS]

162112-37-0
[Synonyms]

RWJ 50271
N-(3-hydroxypropyl)-5-methyl-1-[4-[3-(trifluoromethyl)phenyl]-1,3-thiazol-2-yl]pyrazole-4-carboxamide
N-(3-Hydroxypropyl)-5-methyl-1-[-4-[3-(trifluoromethyl)phenyl)]-2-thiazolyl]-1H-pyrazole-4-carboxamide
1H-Pyrazole-4-carboxamide, N-(3-hydroxypropyl)-5-methyl-1-[4-[3-(trifluoromethyl)phenyl]-2-thiazolyl]-
[Molecular Formula]

C18H17F3N4O2S
[MDL Number]

MFCD00938572
[MOL File]

162112-37-0.mol
[Molecular Weight]

410.41
Chemical PropertiesBack Directory
[density ]

1.44±0.1 g/cm3(Predicted)
[storage temp. ]

Store at RT
[solubility ]

<41.04mg/ml in DMSO
[form ]

Solid
[pka]

14.28±0.46(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Hazard InformationBack Directory
[Uses]

RWJ 50271 is an inhibitor of LFA-1/ICAM-1 mediated cell adhesion.
[in vivo]

RWJ 50271 (50 mg/kg; p.o.) is effective in animal model of inflammation[1].

Animal Model:Mice, the delayed-type hypersensitivity [DTH] reaction model[1]
Dosage:50 mg/kg
Administration:Oral administration
Result:Significantly reduced foot pad swelling (>50%) 48 h after the challenge.
Spectrum DetailBack Directory
[Spectrum Detail]

RWJ 50271(162112-37-0)1HNMR
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