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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-28805

L759-0762

RBM41 inhibitor

L759-0762 is a small molecule RNA-binding motif protein 41 (RBM41) inhibitor, disrupts the interaction between RBM41 and CKMT1B mRNA, selectively sensitizes TSCC cells to disulfidptosis under glucose deprivation by abolishing the protective function of RBM41.
PC-28754

CHI3L1 inhibitor DELC2

CHI3L1 inhibitor

DELC2 is a brain-penetrant Chitinase-3-like protein 1 (CHI3L1) inhibitor with MST KD of 10.31 uM, SPR KD of 8.7 uM, inhibits CHI3L1-RAGE association with IC50 of 2.25 uM in ELISA assays, suppresses RAGE-linked inflammatory signaling.
PC-28750

ZINC00784494

LCN2 inhibitor

ZINC00784494 is a small molecule inhibitor of Lipocalin-2 (LCN2), significantly decreases cell proliferation, cell viability and the AKT phosphorylation levels in ectopically expressing LCN2 MCF7 cells.
PC-28749

ZINC00640089

LCN2 inhibitor

ZINC00640089 is a small molecule inhibitor of Lipocalin-2 (LCN2), significantly decreases cell proliferation, cell viability and the AKT phosphorylation levels in ectopically expressing LCN2 MCF7 cells.

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