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Cat. No. Product Name Information
PC-23289

C071-0684

CHD1L inhibitor

C071-0684 is a potent small molecule inhibitor of CHD1L targeting ATP catalytic activity of chromodomain helicase CHD1L (IC50=17.36 uM, KD=0.5 uM), shows IC50 of 13.0 uM against human HCT116 colorectal cancer cells.
PC-23287

HKi6

HEG1-KRIT1 inhibitor

HKi6 is a specific small-molecule HEG1-KRIT1 inhibitor (IC50=1.5 uM) by competing orthosterically with HEG1 for binding to the KRIT1 FERM domain, elevates KLF4 and KLF2 gene expression and increases Akt phosphorylation.
PC-23286

HKi2

HEG1-KRIT1 inhibitor

HKi2 is a specific small-molecule HEG1-KRIT1 inhibitor (IC50=3.5 uM) by competing orthosterically with HEG1 for binding to the KRIT1 FERM domain, elevates KLF4 and KLF2 gene expression and increases Akt phosphorylation.
PC-23282

Malabaricone C

Sphingomyelin synthase inhibitor

Malabaricone C is a natural sphingomyelin synthase (SMS) inhibitor with IC50 values of 3 uM and 1.5 μM for SMS1 and SMS2, respectively.
PC-23260

Migalastat hydrochloride

α-Gal A inhibitor

Migalastat hydrochloride (GR181413A) is a potent and competitive inhibitor of alpha-galactosidase A (α-Gal A) with IC50 of 0.04 uM (human α-Gal A).
PC-23220

VPS18 inhibitor RDN

VPS18 inhibitor

VPS18 inhibitor RDN is a specific lysosomotropic agent that targeting vacuole protein sorting 18 (VPS18), binds to the RING domain of VPS18, leading to disruption of the VPS-C core complex and lysosomal function.
PC-23217

Steroid sulfatase inhibitor DU-14

Steroid sulfatase inhibitor

Steroid sulfatase inhibitor DU-14 is a hihly potent steroid sulfatase inhibitor with IC50 of 55.8 nM, inhibits inhibits the MCF-7 cell proliferation with IC50 of 38.7 nM.
PC-23216

hPIF1 inhibitor 6

PIF1 inhibitor

hPIF1 inhibitor 6 is a specific small molecule inhibitor targeting the helicase activity of human PIF1 with IC50 of 36 uM for inhibition of FLhPIF1 helicase activity, 22-fold selective over hUPF1, inhibits hPIF1 DNA-binding and helicase activity in vitro.
PC-23192

Swainsonine

Golgi α-mannosidase inhibitor

Swainsonine (Tridolgosir) is a natural product indolizidine alkaloid and an inhibitor of the human Golgi α-mannosidase, hGMII (MAN2A1), induces apoptosis and cell cycle arrest at G2/M phase, shows anti-tumor activity.
PC-23190

NB-115

FOXM1 inhibitor

NB-115 is a small molecule FOXM1 inhibitor with Ki of 40 nM and IC50 of 216 nM, suppresses TNBC progression and tumor metastasis.
PC-23178

SCR-7952

MAT2A inhibitor

SCR‐7952 is a potent, highly selective methionine adenosyltransferase 2A (MAT2A) inhibitor with IC50 of 18.7 nM, Ki of 14.49 nM, shows MTAP‐null selective antiproliferative activity.
PC-23153

GSD-16-24

α-synuclein inhibitor

GSD-16-24 is a small molecule inhibitor of amyloid fibrils of α-synuclein (α-syn), binds directly to the C-terminal IDR of α-syn monomer and fibril, preventing the fibril from binding to the receptors.

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