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Cat. No. Product Name Information
PC-23517

ATX968

DHX9 inhibitor

ATX968 is a potent and selective inhibitor of DHX9 helicase activity with DHX9 unwinding IC50 of 8 nM, SPR Kd value of 1.3 nM.
PC-23494

Ibetazol

Importin β inhibitor

Ibetazol is novel specific small molecule inhibitor of importin β1 (KPNB1)-mediated nuclear import with EC50 of 6.3 uM in phenotypic importin α1 translocation assays , binds to cysteine 585 of importin β1.
PC-23451

PF-07328948

BDK inhibitor

PF-07328948 is the first potent, selective branched-chain ketoacid dehydrogenase kinase (BDK or BCKDK) with in vitro IC50 of 15 nM, and cellular IC50 of 46 nM in human skeletal muscle BDK activity assay.
PC-23439

KB-151

Phagocytosis inhibitor

KB-151 is a small molecule phagocytosis inhibitor with IC50 of 2.7 uM in human PBMCs, shows no significant toxicity.
PC-23438

KB-208

Phagocytosis inhibitor

KB-208 is a small molecule phagocytosis inhibitor with IC50 of 4.2 uM in human PBMCs, shows no significant toxicity.
PC-23404

NAC1 inhibitor NIC3

NAC1 inhibitor

NAC1 inhibitor NIC3 is a specific small molecule inhibitor of oncogenic nucleus accumbens-associated protein-1 (NAC1), inhibits NAC1 homodimerization, leading to proteasomal NAC1 degradation.
PC-23378

GQ262

Gαq/11 inhibitor

GQ262 is a small molecule Gαq/11 protein inhibitor with IC50 of <10 uM, inhibits MP41 cell proliferation with IC50 of 5.1 uM.
PC-23327

8-Prenylnaringenin

CDCP1 inhibitor

8-Prenylnaringenin (8PN) is a prenylflavonoid isolated from hop cones Humulus lupulus with cytotoxicity, is a small molecule inhibitor of CUB domain-containing protein 1 (CDCP1) and reduces CDCP1 protein levels in cancer cells.
PC-23325

Stomidazolone

Stomatal differentiation inhibitor

Stomidazolone is a doubly-sulfonylated imidazolone that inhibits stomatal differentiation, tightly binds to C-terminal ACT-Like (ACTL) domain of MUTE (Kd=8.9 uM) and perturbs the SCRM-MUTE heterodimerization.
PC-23304

PGMI-004A

PGAM1 inhibitor

PGMI-004A is a specific small molecule inhibitor of glycolytic enzyme phosphoglycerate mutase 1 (PGAM1) with IC50 of 13.1 uM, Ki of 3.91 uM.
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-23286

HKi2

HEG1-KRIT1 inhibitor

HKi2 (HEG1-KRIT1 inhibitor 2) 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.

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