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Cat. No. Product Name Information
PC-49075

SLP9101555

SphK2 inhibitor

SLP9101555 is a potent, selective sphingosine kinase SphK2 with Ki of 90 nM (hSphK2), 200-fold selectivity over SphK1.
PC-35529

RB-005

SphK1 inhibitor

RB-005 (RB-005) is a potent, selective inhibitor of sphingosine kinase SphK1 (SK1) with IC50 of 3.6 uM, displays 15-fold selectivity over SphK2.
PC-35528

PF-543

SphK1 inhibitor

PF-543 (PF543) is a potent, specific, cell-permeant inhibitor of SphK1 with Ki of 3.6 nM, displays >100-fold selectivity over the SphK2 isoform.
PC-61768

SKI-178

SphK1 inhibitor

SKI-178 is a potent, specific, non-lipid SphK1 inhibitor with Ki of 1.33 uM, displays no significant activity for SphK2 (IC50>25 uM).
PC-60525

ABC 294640 hydrochloride

SphK2 inhibitor

ABC 294640 (ABC294640, Opaganib) is a is a selective, competitive and orally bioavailable sphingosine kinase-2 (SphK-2) inhibitor with IC50 of 60 uM, Ki of 9.8 uM.
PC-60524

Opaganib

SphK2 inhibitor

Opaganib (ABC-294640, ABC294640) is a selective, competitive and orally bioavailable sphingosine kinase-2 (SphK-2) inhibitor with IC50 of 60 uM, Ki of 9.8 uM.
PC-45716

MP-A08

SphK inhibitor

MP-A08 is a first-in-class, highly selective, ATP competitive sphingosine kinase (SphK) inhibitor (Ki of 6.9/27 uM for SK2/SK1).
PC-49708

HWG-35D

SphK2 inhibitor

HWG-35D is a potent, selective sphingosine kinase 2 (SphK2, SK2) with IC50 of 41 nM, 100-fold selectivity for SK2 over SK1.
PC-49707

SLM6071469

SphK2 inhibitor

SLM6071469 (SLM 6071469) is a potent, highly selective sphingosine kinase 2 (Sphk2) inhibitor with Ki value of 89 nM (hSphk2), 73-fold selectivity over hSphk1.
PC-49706

SLM6031434

SphK2 inhibitor

SLM6031434 (SLM 6031434) is a potent, highly selective sphingosine kinase 2 (Sphk2) inhibitor with Ki value of 340 nM (hSphk2), 23-fold selectivity over hSphk1.
PC-49431

K6PC-5

SphK1 activator

K6PC-5 is a synthetic ceramide derivative, selective and direct sphingosine kinase 1 (SphK1) activator.
PC-47034

SLL3071511

CHIKV inhibitor

SLL3071511 is a novel potent inhibitor of Chikungunya virus (CHIKV) infection with EC50 of 2.91 uM, inhibits sphingosine kinase SK1 and SK2 with Ki values of 0.27 and 0.66 uM, respectively.

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