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首页-小分子抑制剂&激动剂-Others-Other Targets

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Cat. No. Product Name Information
PC-26717

HF-125

TRIB2 inhibitor

HF-125 is a potent, selective small molecule inhibitor of Tribbles 2 (TRIB2), directly binds to destabilize and degrade TRIB2 proteins involving proteasomes and is effective both in vitro and in vivo.
PC-26684

LMT328

Sulfiredoxin inhibitor

LMT328 (LMT-328) is a potent inhibitor of sulfiredoxin (Srx) with IC50 of 6.7 uM.
PC-26649

mtCI modulator C273

Mitochondrial complex I inhibitor/modulator

mtCI modulator C273 is a selective, brain-penetrant, orally bioavailable small molecule modulator/ weak inhibitor of mitochondrial complex I (mtCI) with IC50 of 201.5 uM, protects against Aβ toxicity through mtCI modulation.
PC-26615

ERG245

BCAT1 inhibitor

ERG245 is a potent, selective BCAT1 inhibitor with IC50 of 0.5 nM for recombinant human BCAT1 (rhBCAT1), >2000-fold selectivity for BCAT1 over BCAT2.
PC-26613

ERG240

BCAT1 inhibitor

ERG240 (ERG-240) is a potent, selective, orally active branched-chain amino acid aminotransferase 1 (BCAT1) inhibitor, inhibits recombinant BCAT1 with an IC50 of 0.1-1 nM, with no inhibition on BCAT2.
PC-26553

ZNF281 inhibitor ZIM

ZNF281 inhibitor

ZNF281 inhibitor ZIM (ZNF281 Interfering Molecule) is a specific small molecule inhibitor of transcription factor ZNF281, prevents anthracycline-mediated cardiotoxicity (AIC), enhances lung tumor regression, and prevents lung metastasis in a metastatic melanoma model.
PC-26548

SOD1 stabilizer C7

SOD1 binder

SOD1 stabilizer C7 is a SOD1-stabilizing small molecule preferentially bound the native-like conformation of SOD1, inhibits irreversible apo-SOD1 misfolding in vitro.
PC-26506

CCF0054500

OR2L13 agonist

CCF0054500 is a specific small molecule agonist of orphan GPCR OR2L13, inhibits platelet aggregation in platelet-rich plasma (PRP) with EC50 of 14 uM.
PC-26503

Z1149421873

NAP1L1 inhibitor

Z1149421873 (Z11) is a small-molecule inhibitor of NAP1L1 with SPR Kd value of 7.86 nM, inhibits its protein expression in vitro and exerts anti-fibrotic effects in PMCFs.
PC-26468

NCGC00238624

GALK1 inhibitor

NCGC00238624 is a highly selective galactokinase (GALK1) inhibitor with IC50 of 7.69 and 13.67 uM against the human and mouse recombinant GALK1, respectively, lowers gal-1P levels in primary fibroblast cells derived from patients with classic galactosemia.
PC-26467

GALK1-IN-1

GALK1 inhibitor

GALK1-IN-1 is an effective ATP-competitive galactokinase 1 (GALK1) inhibitor with IC50 of 1 uM in luminescence GALK-ATP-depletion assay.
PC-26445

PON2 inhibitor 2

PON2 inhibitor

PON2 inhibitor 2 is a potent, specific small molecule inhibitor of paraxonase 2 (PON2) with IC50 of 56 nM, inhibits the lactonase activity of PON2.

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