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PF-8380

SIGMA/SML0715 - ≥98% (HPLC)

Synonym: 4-[3-(2,3-Dihydro-2-oxo-6-benzoxazolyl)-3-oxopropyl]-1-piperazinecarboxylic acid (3,5-dichlorophenyl)methyl ester; 4-[3-Oxo-3-(2-oxo-2,3-dihydrobenzoxazol-6-yl)propyl]piperazine-1-carboxylic acid 3,5-dichlorobenzyl ester

CAS Number: 1144035-53-9
Empirical Formula (Hill Notation): C22H21Cl2N3O5
Molecular Weight: 478.33
Linear Formula: C22H21Cl2N3O5
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML0715-5MG 5 mg
$125.00
1/EA
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45-SML0715-25MG 25 mg
$478.00
1/EA
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assay ≥98% (HPLC)
color white to beige
form powder
Quality Level 100 
solubility DMSO: 5 mg/mL, clear (warmed)
storage temp. −20°C
Application: PF-8380 has been used in biological assays. It has also been used to estimate the role of intestinally-derived lysophosphatidic acid in dyslipidemia and atherosclerosis.
Biochem/physiol Actions: PF-8380 is a potent orally bioavailable inhibitor of autotaxin (ATX), the enzyme that synthesize lysophosphatidic acid (LPA) from lysophosphatidyl choline, and is an emerging target for treatment of inflammatory conditions, including cancer, arthritis and multiple sclerosis. PF-8380 blocks inflammation-induced LPA synthesis. PF-8380 works both in vitro and in vivo through direct inhibition of autotaxin. In human whole blood PF-8380 inhibited autotaxin with an IC50 of 101 nM.
Biochem/physiol Actions: PF-8380 [6-(3-(piperazin-1-yl)propanoyl)benzo[d]oxazol-2(3H)-one] has the ability to change the resistant and invasive features of glioblastoma and helps to improve the response to radiation therapy.
Packaging: 5, 25 mg in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. −20°C
UNSPSC 12352200

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