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Cat. No. Product Name Information
PC-27635

MAT2A inhibitor ZS97

MAT2A inhibitor

MAT2A inhibitor ZS97 is a potent, selective and orally bioavailable methionine adenosyltransferase 2A (MAT2A) inhibitor, demonstrates potent enzymatic inhibition, effectively depleting intracellular SAM and suppressing downstream PRMT5-mediated methylation.
PC-27632

TTBK1 inhibitor 62

TTBK1 inhibitor

TTBK1 inhibitor 62 is a potent, selective, brain-penetrant ATP-competitive Tau tubulin kinase 1 (TTBK1) inhibitor with IC50 of 0.89 uM, >100-fold selective over TTBK2.
PC-27619

Latrunculin B

Actin polymerization inhibitor

Latrunculin B is an antimicrobial marine alkaloid and actin polymerization inhibitor, disrupts microfilament organization and affects cell growth, sequesters monomeric G-actin, leading to the disassembly of actin filaments in cells.
PC-27618

Latrunculin A

Actin polymerization inhibitor

Latrunculin A (LAT-A) is a natural compound isolated from red sea sponge Latrunculia magnifica, is a G-actin polymerization inhibitor, binds to actin monomers and inhibits polymerization of actin with Kd of 0.1, 0.4, 4.7 and 0.19 uM for ATP-actin, ADP-Pi-actin, ADP-actin and G-actin, respectively.
PC-27617

ABT-E79

PGK1 inhibitor

ABT-E79 is a highly potent and selective PGK1 inhibitor, significantly inhibits TNBC cell proliferation.
PC-27604

OMDM-1

Anandamide uptake inhibitor

OMDM-1 is a potent, selective inhibitor of anandamide cellular uptake (ACU) with Ki of 2.4 uM, inhibits anandamide transport.
PC-27596

Isofagomine

Glycosidase inhibitor

Isofagomine (Afegostat) is a broad spectrum inhibitor of glycosidases, inhibits beta-glucosidase, glucoamylase, isomaltase, and alpha-glucosidase, specifically and reversibly binds lysosomal hydrolase acid β-glucosidase (GCase) in the ER with high affinity.
PC-27582

dPTBD

Cuproptosis inducer

dPTBD is a copper ionophore and cuproptosis inducer, promotes intracellular copper accumulation particularly in the mitochondria, leading to metabolic disruption and cuproptotic cell death, exhibits significant antitumor efficacy in KRAS-driven cancers both in vitro and in vivo.
PC-27579

K303MP20

GPRC5B/C inhibitor

K303MP20 (MP20) is a small molecule inhibitor of orphan GPCR GPRC5B and GPRC5C dimerization, inhibits GPRC5B/C-mediated modulation of EP2, IP, and AT1 signaling in vitro and in vivo.
PC-27512

MAT2A inhibitor ZS34

MAT2A inhibitor

MAT2A inhibitor ZS34 is a potent, selective, and orally bioavailable MAT2A inhibitor with IC50 of 13.7 nM.
PC-27508

Tazbentetol

Synaptic regenerative agent

Tazbentetol (SPG302) is a pegylated benzothiazole derivative and synaptic regenerative small molecule, targets the cytoskeleton and induces the formation of new glutamatergic synapses.
PC-27505

JXL069

MPC inhibitor

Suvomipic (JXL069) is a potent, small molecule mitochondrial pyruvate carrier (MPC) inhibitor with IC50 of 42.8 nM.

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