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Cat. No. Product Name Information
PC-21207

Ticlopidine

CD39 inhibitor

Ticlopidine (PCR 5332) is an allosteric, noncompetitive inhibitor of CD39 with the IC50 of 81.7 μM, shows antithrombotic effect.
PC-21205

ARL67156

ecto-ATPase inhibitor

ARL67156 (FPL 67156) is a selective inhibitor of ecto-ATPase, ARL67156 is a competitive inhibitor of NTPDase1 (CD39), NTPDase3 and NPP1, with Kis of 11, 18 and 12 μM, respectively.
PC-21193

Gliotoxin

LTA4 hydrolase inhibitor

Gliotoxin (Aspergillin) is a virulence factor of Aspergillus fumigatus, functions as a potent and selective inhibitor of the epoxide hydrolase activity of LTA4 hydrolase (LTA4H), selectively inhibits LTB4 biosynthesis.
PC-21176

GPR54 antagonist 9l

GPR54 inhibitor

GPR54 antagonist 9l is a potent, selective, small molecule antagonist of GPR54 with IC50 of 3.7 nM (human GPR54) in receptor binding assays.
PC-21175

GPR54 antagonist 15a

GPR54 inhibitor

GPR54 antagonist 15a is a potent, selective, small molecule antagonist of GPR54 with IC50 of 3.6/15 nM (human/rat GPR54) in receptor binding assays.
PC-21149

25-Hydroxycholesterol

SREBP-1 inhibitor

25-Hydroxycholesterol (25-HC) is a specific sterol regulatory element-binding proteins (SREBP-1) inhibitor, decreases SREBP-1 protein level in cells.
PC-21144

4-ABAH

MPO inhibitor

4-ABAH is a specific irreversible inhibitor of myeloperoxidase (MPO) activity.
PC-21100

DSHN

NR0B2 agonist

DSHN is a small molecule activator of small heterodimer partner (SHP, NR0B2), functions as a transcriptional activator of SHP, inhibits HCC metastasis via SHP-mediated repression of Ccl2 signaling.
PC-21096

PSB-KD477

GPR18 agonist

PSB-KD477 is a potent, selective GPR18 agonist with EC50 of 454 nM, shows no activity against GPR55.
PC-21071

BDP-13176

Fascin-1 inhibitor

BDP-13176 is a small molecule inhibitor of actin-bundling protein Fascin-1 (Fscn1) with SPR and ITC Kd values of 85 and 50 nM, respectively, inhibits fascin-mediated actin bundling with IC50 of 240 nM.
PC-21057

C10M

CRP inhibitor

C10M is a small molecule inhibitor of C-reactive protein (CRP), inhibits the binding of pCRP to the physiological ligand phosphocholine (PC) with IC50 of 1.5 mM in ELISA assays.
PC-21028

PIP-199

RMI-MM2 inhibitor

PIP-199 is a small-molecule inhibitor of the Fanconi anemia complementation group M-RecQ-mediated genome instability protein (FANCM-RMI) protein-protein interaction, inhibits RMI core complex with Kd of 3.4 uM.

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