PF-543 HCl
CAS No. | 1706522-79-3 | Cat. No. | BCP26198 |
Name | PF-543 HCl | ||
Synonyms | PF-543 hydrochloride; PF543 hydrochloride; PF 543 hydrochloride; | ||
Formula | C27H32ClNO4S | M. Wt | 502.06 |
Description | PF-543 HCl is the hydrochloride salt form of PF-543.PF-543 is a novel selective SK-1 inhibitor which inhibited SK-1 activity in a competitive manner with sphingosine. PF-543 inhibits SphK1 with a K(i) of 3.6 nM, is sphingosine-competitive and is more than 100-fold selective for SphK1 over the SphK2 isoform. PF-543 was effective as a potent inhibitor of S1P formation in whole blood, indicating that the SphK1 isoform of sphingosine kinase is the major source of S1P in human blood. PF-543 is the most potent inhibitor of SphK1 described to date and it will be useful for dissecting specific roles of SphK1-driven S1P signalling. | ||
Pathways | GPCR/G Protein | ||
Targets | S1P Receptor |
Structure
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