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Cat. No. Product Name Information
PC-42293

EC330

LIF inhibitor

EC330 (EC-330, EC 330) is a first-in-class, orally bioavailable LIF (leukemia inhibitory factor, LIFR) inhibitor.
PC-45088

SP-420

Iron chelating agent

Petadeferitrin (SP-420) is a desferrithiocin analogue and iron chelating agent that has iron-clearing efficiency with ICE value of 26.7, SP-420 is more potent than desferrithiocin.
PC-45513

HQ-415

Metal chelator, TDP-43 modulator

HQ-415 is a derivative of 8-hydroxyquinoline that has selectivity for rescuing the distinct toxicities caused by the expression of TDP-43 with EC50 of 15 uM, α-synuclein or polyglutamine proteins.
PC-45271

Pramiracetam

Cognitive activator

Pramiracetam (CI-879) is a central nervous system stimulant and nootropic agent and PREP (prolyl endopeptidase) inhibitor, shows cognition-restoring and neuroprotective properties.
PC-42072

BAPTA

Mg2+ chelator

BAPTA is a cell-permeant, calcium-specific chelator with high selectivity over Mg2+.
PC-45623

GW4869

nSMase inhibitor

GW-4869 (GW4869, GW 4869) is a cell-permeable, potent, specific, non-competitive inhibitor of neutral sphingomyelinase (nSMase) with IC50 of 1 uM.
PC-42082

TPEN

LIN28 inhibitor

TPEN (TPEDA) is a potent, cell-permeable inhibitor of LIN28 that abolishes LIN28-mediated oligouridylation with IC50 of 2.5 uM, also is a specific cell-permeable heavy metal chelator.
PC-42281

GGTI298

GGTase I inhibitor

GGTI298 (GGTI-298) is a CAAZ peptidomimetic geranylgeranyltransferase I (GGTase I) inhibitor that inhibits the processing of geranylgeranylated Rap1A with little effect on processing of farnesylated Ha-Ras (IC50s are 3 and >10 uM respectively).
PC-28707

CINS-1

RIOK1 inhibitor

CINS-1 is a potent, specific RIO Kinase 1 (RIOK1) inhibitor with high binding affinity (ITC Kd=97 nM, AfRIOK1), binds to human RIOK1 with a Kd of 176 nM, exhibits antiproliferative activity against CRC cell lines HCT116 with IC50 of 7.81 uM.
PC-28703

CDD-3155

STK33 inhibitor

CDD-3155 is a potent, selective Serine/threonine kinase 33 (STK33) inhibitor with IC50 of 1.83 uM and Kd of 0.863 nM, 446-fold selective over CLK4 (based on Kd value).
PC-28702

CDD-3094

STK33 inhibitor

CDD-3094 is a potent, selective Serine/threonine kinase 33 (STK33) inhibitor with IC50 of 56.3 nM and Kd of 0.087 nM, 21-fold selective over CLK4 (based on Kd value).
PC-28697

ATF4/CHOP inhibitor T-22

ATF4/CHOP inhibitor

ATF4/CHOP inhibitor T-22 is a potent, specific CHOP/ATF4 inhibitor, inhibits CHOP expresion with IC50 of 1.41 uM in CHOP-Luc assay under ER stress conditions, significantly inhibits ATF4 mRNA expression.

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