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ChemicalBook--->CAS DataBase List--->1345614-59-6

1345614-59-6

1345614-59-6 Structure

1345614-59-6 Structure
IdentificationBack Directory
[Name]

AM-095
[CAS]

1345614-59-6
[Synonyms]

AM-095
AM095 sodium
AM095 >=98% (HPLC)
AM095 (Sodium Salt)
AM095 hydrochloride
AM-095;AM095;AM 095
sodium,2-[4-[4-[3-methyl-4-[[(1R)-1-phenylethoxy]carbonylamino]-1,2-oxazol-5-yl]phenyl]phenyl]acetate
(2-[4-[4-[3-methyl-4-[[(1R)-1-phenylethoxy]carbonylamino]-1,2-oxazol-5-yl]phenyl]phenyl]acetic acid) sodium salt
4'-[3-Methyl-4-[[[(1R)-1-phenylethoxy]carbonyl]amino]-5-isoxazolyl]-[1,1'-biphenyl]-4-acetic acid sodium salt (1:1)
[Molecular Formula]

C27H24N2O5.Na
[MDL Number]

MFCD23380594
[MOL File]

1345614-59-6.mol
[Molecular Weight]

480.5
Chemical PropertiesBack Directory
[storage temp. ]

room temp
[solubility ]

≥23.9 mg/mL in DMSO; insoluble in H2O; ≥16.77 mg/mL in EtOH with ultrasonic
[form ]

powder
[color ]

white to beige
Spectrum DetailBack Directory
[Spectrum Detail]

AM-095(1345614-59-6)MS
AM-095(1345614-59-6)1HNMR
Hazard InformationBack Directory
[Biological Activity]

am095 is a novel, potent and orally bioavailable antagonist of lysophosphatidic acid type 1 receptor (lpa1) with ic50 values of 0.73 and 0.98 μm for mouse or recombinant human lpa1, respectively [1].
[in vitro]

am095 has shown to inhibit lpa1-induced chemotaxis of both mouse lpa1/cho cells and human a2058 melanoma cells with ic50 values of 0.78 μm and 0.23μm [1].
[in vivo]

am095 could dose-dependently block lpa-induced histamine release with an ed50 value of 8.3 mg/kg in mice. additionally, am095 has been revealed to remarkably reduce the balf collagen and protein with an ed50 value of 10 mg/kg in lungs. am095 has also shown to decrease both macrophage and lymphocyte infiltration induced by bleomycin in mice [1].
[target]

LPA1 receptor
[References]

[1] swaney js1, chapman c, correa ld, stebbins kj, broadhead ar, bain g, santini am, darlington j, king cd, baccei cs, lee c, parr ta, roppe jr, seiders tj, ziff j, prasit p, hutchinson jh, evans jf, lorrain ds. pharmacokinetic and pharmacodynamic characterization of an oral lysophosphatidic acid type 1 receptor-selective antagonist. j pharmacol exp ther. 2011 mar;336(3):693-700.
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