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Cat. No. Product Name Information
PC-22326

E745-0011

TIPE3 inhibitor

E745-0011 is a small molecule inhibitor of tumor necrosis factor-α-induced protein 8-like 3 (TNFAIP8L3, TIPE3), exhibits potent anti-tumor activities.
PC-22325

K784-8160

TIPE3 inhibitor

K784-8160 is a small molecule inhibitor of tumor necrosis factor-α-induced protein 8-like 3 (TNFAIP8L3, TIPE3), exhibits potent anti-tumor activities.
PC-22324

OR51E2 antagonist C80

OR51E2 inhibitor

OR51E2 antagonist C80 (Compound 80) is an allosteric antagonist and inverse agonist of olfactory receptor OR51E2 with IC50 of 5.2 uM, acts as a negative allosteric modulator (NAM) by significantly decreasing the agonist efficacy.
PC-22305

JYQ-164

DJ-1/PARK7 inhibitor

JYQ-164 (JYQ164) is a potent, highly selective Parkinson disease protein 7 (PARK7/DJ-1) inhibitor with IC50 of 21 nM, binds covalently and selectively to PARK7 Cys106.
PC-22304

JYQ-173

DJ-1/PARK7 inhibitor

JYQ-173 (JYQ173) is a potent, highly selective Parkinson disease protein 7 (PARK7/DJ-1) inhibitor with IC50 of 19 nM, binds covalently and selectively to PARK7 Cys106.
PC-22302

α-chlorofluoroacetamide

α-chlorofluoroacetamide (CFA) is a novel warhead of targeted covalent inhibitor (TCI), shows high reactivity toward Cys797 of epidermal growth factor receptor (EGFR).
PC-22299

MTOB sodium

CtBP inhibitor

MTOB sodium is a potent C-terminal binding protein (CtBP) inhibitor, inhibits the transactivation activity of CtBP1 and CtBP2.
PC-22298

CtBP1/BARS inhibitor Comp.11

CtBP1/BARS inhibitor

CtBP1/BARS inhibitor Comp.11 is a potent, selective inhibitor targeting the C-terminal-binding protein 1/brefeldin A ADP-ribosylation substrate (CtBP1/BARS), directly binds and inhibits the CtBP1/BARS protein-partners interaction with Kd of 0.66 uM.
PC-22285

MS-L6

OXPHOS inhibitor

MS-L6 is a novel small molecule OXPHOS inhibitor, exerts dual mitochondrial effects: mitochondrial electron transport chain complexe ETC-I inhibition and uncoupling of OXPHOS.
PC-22262

Fatostatin

SREBP inhibitor

Fatostatin is a small molecule sterol regulatory element binding protein (SREBP) inhibitor, impairs the activation process of SREBPs, thereby decreasing the transcription of lipogenic genes in cells.
PC-22255

SC26196

D6D inhibitor

SC26196 (SC-26196) is a potent, selective delta6 desaturase (Δ6 desaturase, D6D, FADS2) inhibitor with IC50 of 0.2 uM in rat liver microsomal assay.
PC-22249

PRDX1 inhibitor 15

PRDX1 inhibitor

PRDX1 inhibitor 15 is a potent, selective and covalent peroxiredoxin (PRDX1) inhibitor with IC50 of 0.35 uM, covalently binds to Cys-173 of PRDX1 with KD of 0.37 uM, shows antiproliferative potency against colon cancer cells.

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