| Cat. No. |
Product Name |
Information |
| PC-21786 |
UT-59
Scap inhibitor
|
UT-59 is a specific inhibitor of cholesterol-sensing membrane protein Scap, binds to Scap's cholesterol-binding site, blocks SREBP activation and inhibits lipid synthesis. |
| PC-21752 |
DHC-156
Brachyury inhibitor
|
DHC-156 is a covalent small molecule inhibitor of oncogenic transcription factor brachyury, selectively binds to brachyury, DHC-156 is potent brachyury downmodulator with DC50 of 4.1 uM. |
| PC-21744 |
G3BP inhibitor a
G3BP inhibitor
|
G3BP inhibitor a (G3Ia) is a specific, peptide mimetic inhibitor of RNA-binding proteins G3BP1/2 with SPR Kd value of 0.54 uM, blcoks the association of G3BP with its binding partners and inhibits condensation of G3BP both in vitro and in live cells. |
| PC-21742 |
Cypin inhibitor B9
Cypin inhibitor
|
Cypin inhibitor B9 is a small molecule cypin (cytosolic postsynaptic density protein 95 interactor) inhibitor, attenuates SCI-induced neuropathic pain, potentially by interfering with uric acid (UA) production. |
| PC-21741 |
GPR31 antagonist SAH2
GPR31 inhibitor
|
GPR31 antagonist SAH2 (SLU-0011371) is the first highly potent and selective small molecule GPR31 antagonist, antagonizes 12(S)-HETE-induced β-arrestin recruitment with IC50 of 1.09 uM. |
| PC-21728 |
Plitidepsin
eEF1A inhibitor
|
Plitidepsin (Aplidine) is a potent anti-cancer agent by targeting eEF1A2 with KD value of 80 nM, shows antiviral activity against SARS-CoV-2 with IC90 of 0.88 nM. |
| PC-21727 |
Didemnin B
eEF1A inhibitor
|
Didemnin B is selective eukaryotic elongation factor 1A1 (EEF1A1) inhibitor, Didemnin B is a depsipeptide extracted from the marine tunicate Trididemnin cyanophorum. |
| PC-21725 |
A71915
NPRA inhibitor
|
A71915 is a highly potent and competitive natriuretic peptide receptor A (ANP, NPRA) antagonist with pKi of 9.18. |
| PC-21724 |
L6H21
MD-2 inhibitor
|
L6H21 is an orally active, potent and specific myeloid differentiation 2 (MD-2) inhibitor with binding KD value of 33.3 uM, blocks the formation of the LPS-TLR4/MD-2 complex. |
| PC-21705 |
KVS0001
SMG1 inhibitor
|
KVS0001 is a specific and bioavailable small molecule inhibitor of SMG1 kinase, disrupts nonsense mediated decay (NMD). |
| PC-21701 |
SKOG102
OLIG2 inhibitor
|
SKOG102 is a specific, brain penetrant small molecule inhibitor of protein transcription factor OLIG2 with IC50 of 1.04 uM, impacts OLIG2 DNA binding ability, inhibits human GBM4 and GBM8 cells with IC50 of 1-2 uM. |
| PC-21687 |
BCL3ANT
Bcl-3 inhibitor
|
BCL3ANT (NSC-659509) is a small molecule inhibitor of Bcl-3-mediated cyclin D1 expression, reduces cyclin D1 luciferase activity in Bcl-3-overexpressing melanoma cells with IC50 of 40.4 uM. |
