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PRGL493

Cat. No. M55207
PRGL493 Structure
Size Price Availability
1mg USD 80  USD80 4-7 Days
5mg USD 180  USD180 4-7 Days
10mg USD 290  USD290 4-7 Days
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Quality Control & Documentation
Biological Activity

PRGL493 is a potent and selective long-chain acyl-CoA synthetase 4 (ACSL4) inhibitor. PRGL493 blocks cell proliferation and tumor growth in both breast and prostate cellular and animal models.

PRGL493 inhibits formation of arachidonoyl-CoA (AA-CoA) from arachidonic acid in, as well as the proliferation and migration of, PC3 and MDA-MB-231 cancer cells when used at a concentration of 50 μM. PRGL493 (5 μM) reduces production of progesterone induced by 8-Br-cyclic AMP (8-Br-cAMP) in MA-10 Leydig tumor cells.

PRGL493 inhibits tumor growth in a PC3 mouse xenograft model when administered at a dose of 0.25 mg/kg.

Chemical Information
Molecular Weight 451.48
Formula C25H21N7O2
CAS Number 2479378-45-3
Form Solid
Solubility (25°C) DMSO 4 mg/mL
Chloroform 1 mg/mL
Storage -20°C, sealed
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

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