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Cat. No. Product Name Information
PC-27127

GNE-2181

pan-TEAD inhibitor

GNE-2181 is a potent, selective, covalent, orally bioavailable and brain-penetrant pan-TEAD inhibitor, disrupts YAP-TEAD interaction with biochemical IC50s of 2/4/8/6 nM for TEAD1/2/3/4 in TR-FRET assays.
PC-26706

LC-TEAD01

TEAD inhibitor

LC-TEAD01 is a potent, selective and covalent TEAD inhibitor with IC50 of 116 nM for TEAD1, inhibits TEAD1-YAP peptide binding with IC50 of 48.29 nM.
PC-26510

TED-655

TEAD-YAP1 inhibitor

TED-655 is a small-molecule covalent inhibitor of TEAD-YAP1 transcription factor, reduces TEAD and YAP1 protein levels.
PC-26277

VT3989

YAP/TEAD inhibitor

VT3989 is a first-in-class, orally bioavailable, selective and potent inhibitor of YAP/TEAD inhibitor, inhibits TEAD autopalmitoylation and disrupts YAP transcriptional activity.
PC-26276

YAP1-TEAD inhibitor MRK-A

YAP/TEAD inhibitor

MRK-A is a highly potent, selective, orally bioavailable inhibitor of YAP1/TEAD with EC50 of 3.4 nM in cellular MCF7 assay expressing TEAD-reporter luciferase, inhibits TEAD palmitoylation that leads to allosteric YAP1/TEAD complex disruption.
PC-25992

MSC-4070

TEAD inhibitor

MSC-4070 is a selective, brain-penetrant TEAD1/2/4 inhibitor with IC50 of 14 nM in TEAD reporter assays in SK-HEP-1 cells, with selectivity for TEAD1, 2, 4 over TEAD3, has IC50 of 30 nM in NCI-H226 viability assays.
PC-24744

Cyclovirobuxine D

YAP inhibitor

Cyclovirobuxine D (CVB-D) is a naturally alkaloid, induces autophagy and attenuates the phosphorylation of Akt and mTOR, exerts its anti-cancer effects by directly binding to YAP, inhibits the nuclear translocation of YAP/TAZ and suppresses the transcription of downstream oncogenic target genes.
PC-24521

TJ-M11

YAP/TAZ inhibitor

TJ-M11 is a synthesized peptide inhibitor of YAP/TAZ transactivation domain (TAD), specifically blocks YAP transactivation (IC50=5.96 uM, NCI-H1299 cells) by disrupting its TAD interactions with the cofactors MED15 and TAF4.
PC-24392

GL-V9

YAP1 inhibitor

GL-V9 is synthetic flavonoid derivative that possess an antitumor effect, effectively promotes the degradation of YAP1, reduces YAP1 nuclear localization, and induces mitochondrial apoptosis in PDAC cells, also induce apoptosis of CML cells via MAPK signaling pathway.
PC-23670

M3686

TEAD1 inhibitor

M3686 is a potent, selective TEAD1 inhibitor with IC50 of 51 nM in TEAD reporter assay, shows weaker binding to TEAD3, and negligible activity on TEAD2 and TEAD4.
PC-23232

MSC-1254

TEAD1 inhibitor

MSC-1254 is a potent, selective, reversible TEAD1 inhibitor with EC50 of 1 uM in TEAD-reporter assay in SK-Hep-1 cells, shows viability affect in NCI-H226 cell line with EC50 of 0.04 uM.
PC-23231

MSC-5046

TEAD1 inhibitor

MSC-5046 is a potent, selective, reversible TEAD1 inhibitor with EC50 of 58 nM in TEAD-reporter assay in SK-Hep-1 cells, shows viability affect in NCI-H226 cell line with EC50 of 12 nM.

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