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Cat. No. Product Name Information
PC-21277

MSN-CD44 inhibitor 1

CD44-MSN inhibitor

MSN-CD44 inhibitor 1 is a small molecule FERM domain protein-protein interaction inhibitor for moesin (MSN) and CD44 with SPR KD of 4.2 uM, is a potent inhibitor of CD44-MSN interaction in live cells with IC50 of 600 nM.
PC-21265

Feeblin

IRF5 inhibitor

Feeblin (SLC15A4 inhibitor C5) is a small molecule inhibitor of the proinflammatory TLR7/8/9-IRF5 pathway (IC50=1.6 uM) by disrupting the SLC15A4-TASL adapter module, Feeblin is an IRF5 pathway-specific inhibitor.
PC-21240

NOX-6-7

GPR132 agonist

NOX-6-7 is a potent, selective GPR132 agonist with EC50 of 44 nM.
PC-21239

NOX-6-18

GPR132 inhibitor

NOX-6-18 is a potent, selective GPR132 antagonist with IC50 of 17 nM.
PC-21213

YL-365

GPR34 inhibitor

YL-365 (YL365) is a highly potent, selective and competitive antagonist of GPR34.
PC-21184

UGT8 inhibitor 19

UGT8 inhibitor

UGT8 inhibitor 19 is a highly potent, selective and orally active ceramide galactosyltransferase enzyme UGT8 inhibitor with IC50 of 0.2 nM.
PC-21142

(3S) ALG-05

TILs inhibitor

(3S) ALG-05 is a potent pan-inhibitor of gut microbia tryptophan-indole-lyases (TILs, E.C. 4.1.99.1), exhibits inhibitory activity across TILs with Ki of 7-11 uM.
PC-21113

VJDT

TREM1 inhibitor

VJDT (TREM1 inhibitor) is a novel small molecule inhibitor of triggering receptor expressed on myeloid cell 1 (TREM1), effectively blocks TREM1 signaling.
PC-21097

PSB-KK1415

GPR18 agonist

PSB-KK1415 is a selective GPR18 agonist with EC50 of 19.1 nM (hGPR18) in β-arrestin recruitment assays, shows no activity against GPR55.
PC-21076

JSD26

SCoR2 inhibitor

JSD26 is a selective S-nitroso-coenzyme A reductase 2 (SCoR2; AKR1A1) inhibitor with Ki of 93 nM, 10-fold selectivity over AKR1B1.
PC-21070

NP-G2-044

Fascin inhibitor

NP‐G2‐044 is a small molecule inhibitor of actin-bundling protein Fascin-1 (Fscn1), inhibits fascin-mediated actin bundling with IC50 of 0.2 uM.
PC-21054

SOFTI

SPINDLY inhibitor

SOFTI is a small molecule inhibitor of O-fucosyltransferase SPINDLY (SPY) with IC50 of 13.32 uM, binds to the GDP-fucose-binding pocket of SPY and competitively inhibits GDP-fucose binding.

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