For research use only. Not for therapeutic Use.
<p style=/line-height:25px/>PF-543 is a novel cell-permeant inhibitor of SphK1 with a Ki of 3.6 nM, PF-543 is sphingosine-competitive and is more than 100-fold selective for SphK1 over the SphK2 isoform.<br>IC50 value: 3.6 nM (Ki)<br>Target: SphK1<br>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.</p>
Catalog Number | I001588 |
CAS Number | 1415562-82-1 |
Synonyms | [(2R)-1-[[4-[[3-(benzenesulfonylmethyl)-5-methylphenoxy]methyl]phenyl]methyl]pyrrolidin-2-yl]methanol |
Molecular Formula | C27H31NO4S |
Purity | ≥95% |
Target | S1P receptor |
Solubility | 10 mM in DMSO |
Storage | 3 years -20C powder |
IC50 | 3.6 nM (Ki) |
InChIKey | NPUXORBZRBIOMQ-RUZDIDTESA-N |
Reference | <p style=/line-height:25px/> |