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Cat. No. Product name CAS No.
DCC5628 Zinc17043486

Novel CDK6 inhibitor

DCC5629 Zinc17167211

Potent and selective agonist of peroxisome proliferator activated receptors-α (PPAR-α)

592539-21-4
DCC5630 Zinc20531199

Novel EGFR triple mutant T790M/C797S allosteric inhibitor

DCC5631 Zinc27905174

Novel GDNF Family Receptor Agonist

DCC5632 Zinc32540717

Potent Ebolavirus (EBOV) Inhibitor

1010869-76-7
DCC5633 Zinc36617540

Novel Nef Protein Inhibitor; Anti-HIV

1174905-91-9
DCC5634 Zinc4085554

Novel blocker of AKT1-FAK interaction, reducing the stimulation of FAK phosphorylation in response to extracellular pressure in human SW620 colon cancer cells without affecting basal FAK phosphorylation

383147-92-0
DCC5635 Zinc50166190

Novel Zika virus RNA polymerase inhibitor

1455388-54-1
DCC5636 Zinc63908257

Novel CtpF inhibitor, inhibiting Ca -dependent ATPase activity in Mtb membrane vesicles

DCC5637 Zinc64700951

Novel gp120 of HIV-1 Antagonist

DCC5638 Zinc65022200

Novel potent and specific inhibitor of the UNC119-Src interaction, binding to UNC119 in cells, and inducing redistribution of Src to endomembranes and reduction of activating Src autophosphorylation on Y419

DCC5639 Zinc69811181

Novel ASCT2 inhibitor

DCC5640 Zinpyr-1

Cell-permeable fluorometric zinc sensor

288574-78-7
DCC5641 Zk187638

Non-competitive AMPA receptor antagonist

397298-63-4
DCC5642 Zk230211

Type III progesterone receptor antagonist with enhanced antiproliferative properties

211254-73-8
DCC5643 Zk-304709

Novel oral multitarget tumour growth inhibitor

1010440-84-2
DCC5644 Zk-806450

Novel potent inhibitor of factor Xa (FXa)

DCC5645 Zl006-05

Novel dual mordulator of nNOS-PSD-95 interaction and GABA A receptor

DCC5646 Zl0513

Novel potent and selective BRD4 bromodomain 1 (BD1) inhibitor

2230496-92-9
DCC5647 Zl0516

Novel potent and selective BRD4 bromodomain 1 (BD1) inhibitor

2230496-93-0
DCC5648 Zl3138

Novel β-catenin/B-cell lymphoma 9 (BCL9) inhibitor, disrupting the β-catenin/BCL9 protein-protein interaction (PPI) with a Ki of 0.96 μM and without affecting the β-catenin/E-cadherin interaction in living cells, displaying good selectivity for β-catenin/

DCC5649 Zld10a

Novel potent and highly selective inhibitor of wild-type and mutant versions of EZH2

1782064-91-8
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