| Identification | Back Directory | [Name]
Cyclopropanecarboxylic acid, 1-[4'-[4-Methyl-5-[[[(1R)-1-phenylethoxy]carbonyl]aMino]-1H-1,2,3-triazol-1-yl][1,1'-biphenyl]-4-yl]- | [CAS]
1396006-71-5 | [Synonyms]
Ro 6842262 LPA1 antagonist 1 LPA1 receptor antagonist 1 PXQUHYSYFWQRMF-LJQANCHMSA-N LPA1 receptor antagonist 1,LPA-1 receptor antagonist 1 1-[4'-[4-Methyl-5-[[[(1R)-1-phenylethoxy]carbonylamino]-1H-1,2,3-triazol-1-yl][1,1'-biphenyl]-4-yl]cyclopropanecarboxylic acid Cyclopropanecarboxylic acid, 1-[4'-[4-Methyl-5-[[[(1R)-1-phenylethoxy]carbonyl]aMino]-1H-1,2,3-triazol-1-yl][1,1'-biphenyl]-4-yl]- | [Molecular Formula]
C28H26N4O4 | [MDL Number]
MFCD25976929 | [MOL File]
1396006-71-5.mol | [Molecular Weight]
482.53 |
| Chemical Properties | Back Directory | [density ]
1.31±0.1 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
Soluble in DMSO | [form ]
Solid | [pka]
4.15±0.20(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Uses]
Ro 6842262 is a potent lysophosphatidic acid receptor-1 (LPA1) antagonist. | [in vivo]
Oral dosing of LPA1 receptor antagonist 1 in mice causes a dose-dependent reduction in serum histamine levels induced following intravenous LPA stimulation. When mice are orally dosed with LPA1 antagonist 1 (100 mg/kg, aqueous suspension) prior to intravenous LPA injection, the LPA-induced histamine level is significantly blocked A clear PK/PD relationship is demonstrated by the correlation between the levels of LPA1 receptor antagonist 1 and LPA-induced histamine concentrations in plasma. Although AM095 almost completely blocks histamine release (100 mg/kg), analysis of plasma samples revealed more than 65-fold higher concentrations of AM095 than LPA1 receptor antagonist 1 (100 mg/kg). The ability of LPA1 receptor antagonist 1 to block histamine release at much lower plasma concentration suggests that further improvement of pharmacokinetic properties of this chemical class could lower the effective dose[1]. | [storage]
Store at -20°C |
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