PF-543 Citrate is a novel cell-permeant inhibitor of SphK1 with a K(i) of 3.6 nM, PF-543 is sphingosine-competitive and is more than 100-fold selective for SphK1 over the SphK2 isoform.
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.
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名称 | PF-543 Citrate |
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Iupac 化学名称 | PF-543 Citrate |
同义词 | PF543 Citrate; PF 543 Citrate |
英文同义词 | PF543 Citrate; PF 543 Citrate |
分子式 | C33H39NO11S |
分子量 | 657.73 |
Smile | Cc1cc(cc(c1)OCc2ccc(cc2)CN3CCC[C@@H]3CO)CS(=O)(=O)c4ccccc4.C(C(=O)O)C(CC(=O)O)(C(=O)O)O |
InChiKey | PWXXWUWKNPXSGW-VQIWEWKSSA-N |
InChi | InChI=1S/C27H31NO4S.C6H8O7/c1-21-14-24(20-33(30,31)27-7-3-2-4-8-27)16-26(15-21)32-19-23-11-9-22(10-12-23)17-28-13-5-6-25(28)18-29;7-3(8)1-6(13,5(11)12)2-4(9)10/h2-4,7-12,14-16,25,29H,5-6,13,17-20H2,1H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/t25-;/m1./s1 |
Cas号 | 1415562-83-2 |
MDL | MFCD23098795 |
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