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Cat. No. Product Name Information
PC-26013

GPR83 agonist CPD1

GPR83 agonist

GPR83 agonist CPD1 is a potent, selective small molecule GPR83 agonist with binding IC50 of 10 nM, induces dose-dependent increases in intracellular Ca+2 release in CHO cells expressing mouse GPR83 with EC50 of 74 nM.
PC-26000

Iodomethylcholine

CutC/D inhibitor

Iodomethylcholine (IMC) is a highly potent non-lethal, irreversible and non-competitive TMA-generating enzyme CutC/D inhibitor with IC50 of 1.2 nM against Proteus mirabilis CutC/D, reduces TMAO levels in vivo.
PC-25999

Fluoromethylcholine

TMA Lyase inhibitor

Fluoromethylcholine (FMC) is a highly potent TMA Lyase inhibitor in Escherichia coli (IC50 = 900 pM against Proteus mirabilis CutC/D) and in a polymicrobial human fecal culture (IC50 = 7.9 nM).
PC-25996

ADAR1i-124

ADAR1 inhibitor

ADAR1i-124 is a selective inhibitor of the ADAR1 A-to-I RNA editing activity with in vitro editing IC50 values of 10-30 uM, inhibits the catalytic activities of both ADAR1p150 and ADAR1p110.
PC-25994

LP-856866

ACSL5 inhibitor

LP-856866 (ACSL5i) is a potent, selective inhibitor of Acyl-CoA Synthetase 5 (ACSL5) with IC50 of 4 nM and 8 nM for huamn and mouse ACSL5 in acyl-CoA synthetase (ACS) assays, highly selective against ACSL3.
PC-25980

AVIL inhibitor Compound A

Advillin inhibitor

AVIL inhibitor Compound A (PLH1215) is a specific small molecule actin-binding protein advillin (AVIL)-interacting compound with MST Kd of 6 uM, also blocks AVIL binding to its substrate actin.
PC-25859

Lysosome inhibitor LLAD

SLC38A9 inhibitor

LLAD is a long-term lysosome-targeting anticancer drug, inhibits SLC38A9 in lysosomes and alkalinizes lysosomes, induces apoptosis through long-term lysosomal damage in vivo and in vitro.
PC-25818

DS89092425

PUF60-UHM inhibitor

DS89092425 is a small molecule RNA splicing factor PUF60-UHM inhibitor with ITC KD of 83 uM.
PC-25817

Claudin 5 binder CL5B

CLDN5 binder

Claudin 5 binder CL5B is a small molecule binder of Claudin 5 (CLDN5), binds directly to hCLDN5 with KD of 31.7 uM, opens the blood-brain barrier and safely enhances brain drug delivery.
PC-25807

Ciliogenesis inhibitor Nao-3

Ciliogenesis inhibitor

Ciliogenesis inhibitor Nao-3 (Naonedin-3) is specific small-molecule inhibitor of ciliogenesis, represses primary ciliogenesis and induces the death of chemoresistant ciliated stem-like cells.
PC-25797

JPC0661

ΔFOSB inhibitor

JPC0661 is a specific small molecule direct inhibitor of AP1 transcription factor ΔdeltaFOSB (ΔFOSB), inhibits FOSB/JUND and ΔFOSB DNA-binding biochemically with IC50 of 9 uM and 52 uM respectively.
PC-25682

Ferovicin

FERONIA receptor inhibitor

Ferovicin is a specific small molecule inhibitor FERONIA (FER) receptor kinase with IC50 of 70 nM, selectively binds to the ATP-binding pocket of the kinase domain of FER and inhibits its kinase activity.

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