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Cat. No. Product name CAS No.
DCC1434 Ciraparantag Acetate

Non-Specific Anticoagulant Reversal Agent

1644388-83-9
DCC1435 Cis,cis-2,6-dimethylcyclohexanol

Positive modulator of GABA A receptors

39170-84-8
DCC1436 Cis-3-4-dihydrohamacanthin B

Potent inhibitor of MRSA PK

264624-39-7
DCC1437 Cis-4-d-hyp-d-ser Hydrochloride

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

DCC1438 Cis-cinnamic Acid

Novel, natural auxin efflux inhibitor, promoting lateral root formation

102-94-3
DCC1439 Cis-vz185

Negative control for VZ185

2306193-98-4
DCC1440 Cj-054

Polo-like kinase 1 (Plk1) inhibitor

DCC1441 Cj-1383

Novel Cell-Permeable STAT3 Inhibitor, targeting the SH2 domain

DCC1442 Cj-15208

Biological Active Reagents

210236-47-8
DCC1443 Cj-1882

Potent and competitive antagonist at the human D3 receptor

DCC1444 Cj2100

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

DCC1445 Cj-21058

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

405072-57-3
DCC1446 Cj2-150

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

DCC1447 Cj-3-60

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

1798328-35-4
DCC1448 Cj-887 Sodium Salt

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

1220952-08-8
DCC1449 Cjc-1293 Tfa Salt

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

446262-89-1
DCC1450 Cjc-1295

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

446262-90-4
DCC1451 Ck2 Inhibitor Hy1

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

DCC1452 Ck-2-68

Novel potent PfNDH2 inhibitor

1361004-87-6
DCC1453 Ck2-in-27

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

DCC1454 Ck2-in-3b

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

1361229-76-6
DCC1455 Ck2-in-4p

Novel potent CK2 inhibitor

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