Inhibitor of H5N1 avian influenza A virus infection

Negative control for CK156

Natural Dual Inhibitor for Wild Type and D816V Mutant of c-KIT Kinase

Inhibitor of vascular adhesion molecule-1 (VCAM-1), HMGB1 phosphorylation, iNOS expression, NFkB activation; Antiinflammatory

Novel inhibitor of CK2α, binding in the ATP pocket

Novel cell-permeable and selective inhibitor of human protein kinase CK2, inducing apoptosis in the prostate cancer cell line LNCaP

Novel potent and selective inhibitor of CK2. modulating the aforementioned signaling cascades and counteracting 17-AAG-mediated up-regulation of HSP70 in brain cancer cells

Novel CK2 inhibitor, targeting an allosteric pocket, exhibiting an IC50 of 3.4 μM against purified CK2α in combination with a favorable selectivity profile

Novel potent CK2 inhibitor

Potent, reversible, and ATP-competitive inhibitor of casein kinase-2 (CK2)

Novel selective allosteric modulator of the protein kinase CK2, inducing apoptosis and cell death in 786-O renal cell carcinoma cells (EC50 = 5 µM) and inhibiting STAT3 activation even more potently than the ATP-competitive drug candidate CX-4945

Novel potent PfNDH2 inhibitor

Novel CK2 inhibitor, showing potent CSC inhibitory effects in A549 cells

Long-lasting stimulator of the production of growth hormone (GH) from the pituitary gland

Stimulator of the production of growth hormone (GH) from the pituitary gland

Novel inhibitor of STAT3 activation and dimerization through targeting the phosphotyrosine binding site within the SH2 domain

Anti-HIF-1alpha agent, inhibiting HIF-1alpha and cellular VEGF proteins

Novel non-ATP competitive allosteric inhibitor of Aurora B kinase, binding in the allosteric site F

SecA inhibitor, showing antiprotozoal, antibacterial and antifungal effects, inhibiting post-translational protein transport into the endoplasmic reticulum. also Inhibiting ATP-dependant translocation of precursor proteins acrossing a bacterial cell membr

Novel potent muscarinic antagonist wirh antimuscarinic antidepressant-like activities, showing modest affinity across the mAChRs when compared to L-687306 and scopolamine

Potent and competitive antagonist at the human D3 receptor

Biological Active Reagents

Novel Cell-Permeable STAT3 Inhibitor, targeting the SH2 domain

Polo-like kinase 1 (Plk1) inhibitor

Negative control for VZ185

Novel, natural auxin efflux inhibitor, promoting lateral root formation

JBP923 analog, exerting potent therapeutic effect on inflammatory bowel disease (IBD)

Potent inhibitor of MRSA PK

Positive modulator of GABA A receptors

Non-Specific Anticoagulant Reversal Agent