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Cat. No. Product Name Information
PC-36130

Auxin agonist RN3

Auxin agonist

Auxin agonist RN3 (RubNeddin 3) is a potent, selective auxin agonist that induces specific AUX/IAA protein degradation to modulate plant development.
PC-36127

HlyU inhibitor CM14

HlyU inhibitor

HlyU inhibitor CM14 (1025E12) is a specifc, small-molecule inhibitor of transcriptional regulator HlyU activity with EC50 of 30.97 uM, inhibits HlyU from binding to target DNA by covalently modifying Cys30.
PC-36125

VK-1850

EBNA1 inhibitor

VK-1850 (VK1850) is a small-molecule inhibitor of the DNA binding activity of EBNA1 (Epstein-Barr nuclear antigen1).
PC-36124

VK-1727

EBNA1 inhibitor

VK-1727 (VK1727) is a small-molecule inhibitor of the DNA binding activity of EBNA1 (Epstein-Barr nuclear antigen1).
PC-36122

Z433927330

AQP7 inhibitor

Z433927330 (Z 433927330) is a potent and selective aquaporin-7 (AQP7) inhibitor, inhibits glycerol permeability in erythrocytes with IC50 of 0.6 uM.
PC-36121

DFP00173

AQP3 inhibitor

DFP00173 (DFP 00173) is a potent and selective aquaporin-3 (AQP3) inhibitor with IC50 of 0.9-1.4 uM for mouse and human AQP3, with low efficacy toward mouse AQP7 and AQP9.
PC-36108

Spastazoline

Spastin inhibitor

Spastazoline is a potent, selective, cell-permeable, ATP-competitive inhibitor of human Spastin, inhibits the steady-state ATPase activity of the Hs-spastin with IC50 of 99 nM.
PC-36092

Fadaltran

α2 adrenoceptor antagonist

Fadaltran is an α2-adrenoreceptor antagonist.
PC-36087

Berotralstat

Plasma kallikrein inhibitor

Berotralstat (BCX7353, BCX-7353) is a potent, highly selective, oral plasma kallikrein inhibitor.
PC-36076

FDI-6

FOXM1 inhibitor

FDI-6 (FOXM1 inhibitor FDI6, NCGC00099374) is a small molecule inhibitor of FOXM1 with IC50 of 22.5 uM (FOXM1 DNA binding inhibition).
PC-36073

AER-271

AQP4 inhibitor

AER-271 (AER271) is a selective, small molecule inhibitor of aquaporin-4 (AQP4), the prodrug of AER-270 with enhanced solubility.
PC-36065

SGC-GAK-1N

SGC-GAK-1N is the nagative control compound for SGC-GAK-1, which is a potent, selective, and cell-active inhibitor of cyclin G-associated kinase (GAK)..

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