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Cat. No. Product Name Information
PC-61554

ML154

NPSR antagonist

ML154 (NCGC00185684) is a potent, selective, brain penetrant NPSR (Neuropeptide S receptor, GPR154) antagonist with IC50 of 22.1 nM and 36.5 nM in Ca2+ assay and cAMP assay, respectively.
PC-61519

NPD926

ROS inducer

NPD926 is a small molecule ROS inducer that induces rapid cell death in cancer cells, induces reactive oxygen species via cellular glutathione depletion.
PC-61485

VJ115

ENOX1 inhibitor

VJ115 (VJ-115) is a small molecule inhibitor of NADH oxidase ENOX1 with IC50 of 10 uM, increases intracellular NADH in endothelial cells and inhibits endothelial cell tubule formation.
PC-61473

BI 1467335

VAP-1 inhibitor

BI 1467335 (PXS-4728A, PXS-4728) is a potent, selective, orally active SSAO/VAP-1 (AOC3) inhibitor with IC50 of 5 nM.
PC-61472

PXS-4681A

VAP-1 inhibitor

PXS-4681A is a potent, selective, and irreversible inhibitor of semicarbazide-sensitive amine oxidase (SSAO, VAP-1) with Ki of 37 nM, IC50 of <10 nM.
PC-61463

VPC-18005

ERG antagonist

VPC-18005 (VPC18005) is a novel small molecule ERG (ETS-related gene) antagonist that inhibits ERG-induced transcription and interacts directly with the ERG-ETS domain, disrupts the ERG binding to DNA (Kd=250 uM).
PC-61429

Lucerastat

GCS inhibitor

Lucerastat (NB-DGJ, ACT-434964) is a galactose analogue that is an UDP-glucose ceramide glucosyltransferase (UGCG/GCS) inhibitor (IC50=41.4 uM).
PC-61428

Ibiglustat

Glucosylceramide synthase inhibitor

Ibiglustat (Venglustat, Genz-682452) is an orally active, selective and potent Glucosylceramide synthase (GCS) inhibitor with central nervous system (CNS) access.
PC-61427

EXEL-0346

Glucosylceramide synthase inhibitor

EXEL-0346 (EXEL0346) is a novel potent, orally active Glucosylceramide synthase (GCS) inhibitor with IC50 of 2 nM.
PC-61426

CCG-203586

Glucosylceramide synthase inhibitor

CCG-203586 is a potent, CNS-active Glucosylceramide synthase (GCS) inhibitor with IC50 of 27 nM.
PC-61425

PDMP hydrochloride

Glucosylceramide synthase inhibitor

PDMP hydrochloride is a ceramide analog that inhibits glucosylceramide synthase (GCS), reduces the synthesis of sphingosine and its derivatives, increases cellular ceramide, and induces cell cycle arrest.
PC-61424

Fumonisin B1

Ceramide synthase inhibitor

Fumonisin B1 is a mycotoxin produced from F. moniliforme, and an inhibitor of ceramide synthase (sphingosine N-acyltransferase/CerS).

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