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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC5659 | Zolantidine Dimaleate |
Potent, selective, and brain penetrating H2 receptor antagonist
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| DCC5658 | Zofenoprilat |
Inducer of functional angiogenesis through increased H 2 S availability
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| DCC5657 | Zn-htsm |
Novel antidiabetic agent for the treatment of type 2 diabetes mellitus (DM)
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| DCC5656 | Zm39923 Hydrochloride |
Potent, selective inhibitor of Janus tyrosine kinase 3 (JAK3)
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| DCC5655 | Zm-260384 |
Potassium channel opener
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| DCC5654 | zm-253270 |
Selective nonpeptide, NK-2 receptor (NK-2R) antagonist
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| DCC5653 | Zm-244085 |
K-Channel opener (PCO) activating predominantly KATP channels in vitro to relax bladder detrusors
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| DCC5652 | zm-230487 |
5-Lipoxygenase (5-LO) inhibitor
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| DCC5651 | zm-189154 |
Non-steroidal pure antioestrogen
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| DCC5650 | Zm-181037 |
ATP-sensitive potassium channel-blocker; Eukalemic diuretic
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| DCC5649 | Zld10a |
Novel potent and highly selective inhibitor of wild-type and mutant versions of EZH2
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| 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/
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| DCC5647 | Zl0516 |
Novel potent and selective BRD4 bromodomain 1 (BD1) inhibitor
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| DCC5646 | Zl0513 |
Novel potent and selective BRD4 bromodomain 1 (BD1) inhibitor
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| DCC5645 | Zl006-05 |
Novel dual mordulator of nNOS-PSD-95 interaction and GABA A receptor
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| DCC5644 | Zk-806450 |
Novel potent inhibitor of factor Xa (FXa)
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| DCC5643 | Zk-304709 |
Novel oral multitarget tumour growth inhibitor
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| DCC5642 | Zk230211 |
Type III progesterone receptor antagonist with enhanced antiproliferative properties
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| DCC5641 | Zk187638 |
Non-competitive AMPA receptor antagonist
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| DCC5640 | Zinpyr-1 |
Cell-permeable fluorometric zinc sensor
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| DCC5639 | Zinc69811181 |
Novel ASCT2 inhibitor
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| 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
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| DCC5637 | Zinc64700951 |
Novel gp120 of HIV-1 Antagonist
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| DCC5636 | Zinc63908257 |
Novel CtpF inhibitor, inhibiting Ca -dependent ATPase activity in Mtb membrane vesicles
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| DCC5635 | Zinc50166190 |
Novel Zika virus RNA polymerase inhibitor
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| 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
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| DCC5633 | Zinc36617540 |
Novel Nef Protein Inhibitor; Anti-HIV
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| DCC5632 | Zinc32540717 |
Potent Ebolavirus (EBOV) Inhibitor
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| DCC5631 | Zinc27905174 |
Novel GDNF Family Receptor Agonist
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| DCC5630 | Zinc20531199 |
Novel EGFR triple mutant T790M/C797S allosteric inhibitor
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