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Cat. No. Product Name Information
PC-22161

Triacsin C

ACSL inhibitor

Triacsin C (WS 1228A) is an inhibitor of long fatty acid acyl-CoA synthetase (ACSL) with IC50 of 6.3 μM in Raji cells, inhibits TAG accumulation into lipid droplets (LD).
PC-22160

KML110

NUCB1 ligand

KML110 is a selective ligand for the lipid-binding protein nucleobindin-1 (NUCB1) with IC50 of 9.6 uM.
PC-22154

OU749

GGT inhibitor

OU749 is a potent, species-specific inhibitor of human gamma-glutamyl transpeptidase (GGT) with Ki of 17.6 uM.
PC-22145

WX-02-23

FOXA1 ligand

WX-02-23 is a covalent small molecule ligand of transcription factor FOXA1 with EC50 of 2 uM in NanoBRET assay, binds cysteine (C258) and promotes the stereoselective and site-specific binding of FOXA1 to DNA.
PC-22076

Sulfopin

Pin1 inhibitor

Sulfopin is a potent, selective and covalent inhibitor of Pin1 with Ki of 17 nM in FP assay, targets Pin1's active site Cys113, blocks Myc-driven tumors.
PC-22060

Ternatin-4

eEF1A inhibitor

Ternatin-4 is a small molecule elongation factor-1alpha (eEF1A) inhibitor, triggers the ubiquitination and degradation of eEF1A on stalled ribosomes, targets the complex of eEF1A bound to aminoacyl-tRNAs (aa-tRNA).
PC-21999

N-chloroacetyltryptamine

AANAT inhibitor

N-chloroacetyltryptamine is a potent in vitro and in vivo AANAT acetyltransferase inhibitor with IC50 of 5.2 uM.
PC-21998

AANAT inhibitor 1

AANAT inhibitor

AANAT inhibitor 1 is a highly potent arylalkylamine N-acetyltransferase (AANAT) inhibitor with IC50 of 500 nM, covalently reacts with AANAT product CoASH.
PC-21975

Canlitinib

Canlitinib is a tyrosine kinase inhibitor, extracted from patent WO2018072614 (IV-2).
PC-21972

Bezisterim

Bezisterim (HE3286) is an orally bioavailable synthetic analogue of an active DHEA metabolite, displays both glucose-lowering and cholesterol-lowering effects.
PC-21959

Tunicamycin

N-glycosylation inhibitor

Tunicamycin is a homologous nucleoside antibiotic and GlcNAc phosphotransferase (GPT) inhibitor, inhibits N-glycosylation and induces ER-stress, inhibits gram-positive bacteria, yeasts, fungi, and viruses and has anti-cancer activity.
PC-21945

EBP inhibitor 11

EBP inhibitor

EBP inhibitor 11 is a potent, selective, brain-penetrant, orally bioavailable inhibitor of emopamil binding protein (EBP) with mGCMS zymo EC50 of 8 nM, and OPC differentiation EC50 of 44 nM.

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