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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC3788 | Nsc-689857 |
Novel inhibitor of the Skp2-Cks1 protein-protein interaction and p27Kip1 ubiquitination in vitro
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| DCC3787 | nsc-681152 |
Novel inhibitor of the Skp2-Cks1 protein-protein interaction and p27(Kip1) ubiquitination in vitro
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| DCC3786 | Nsc676914a |
Novel NF-κB inhibitor
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| DCC3785 | Nsc-674205 |
Potent and selective nociceptin opioid receptor (NOP) agonist
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| DCC3784 | Nsc-672121 |
Potent CDC25A>Cdc25A inhibitor; Vitamine K3 analogue
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| DCC3783 | Nsc-670224 |
Toxitant of Saccharomyces_cerevisiae>Saccharomyces cerevisiae
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| DCC3782 | Nsc663627 |
IκBα phosphorylation inhibitor
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| DCC3781 | Nsc66098 |
Novel potent inhibitor of Huntington's disease (HD) pathogenesis via targeting CAG repeats RNA and Poly Q protein
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| DCC3780 | Nsc65847 |
Novel dual inhibitor of viral and Streptococcus pneumoniae neuraminidase
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| DCC3779 | Nsc-657186 |
Novel selective non-zinc-binding MMP-2 inhibitor
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| DCC3778 | Nsc636795 |
Novel inhibitor of ABCG2 transporter function
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| DCC3777 | Nsc-627757 |
Novel DNA repair inhibitor
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| DCC3776 | Nsc61610 |
Novel activator of lanthionine synthetase C-like 2 (LANCL2), down-modulating pulmonary inflammation through the downregulation of TNF-α and MCP-1 and reduction in the infiltration of neutrophils, accelerating recovery and inducing IL-10-mediated regulator
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| DCC3775 | Nsc-60339 |
Novel efflux pump inhibitor (EPI)
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| DCC3774 | Nsc57971 |
Novel non-peptide disruptor of IKKß/NEMO complex
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| DCC3773 | Nsc-57774 |
Novel potent SHP2 Inhibitor with Anti-Proliferative Activity in Breast Cancer Cell Lines
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| DCC3772 | Nsc-57148 |
Novel antagonist of the Grb7 SH2 domain; Antitumor Agent
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| DCC3771 | Nsc56452 |
Novel specific inhibitor of EGF receptor autophosphorylation and cell proliferation in HeLa cells by disrupting allosteric activation of EGF-stimulated dimer
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| DCC3770 | Nsc-55158 |
Novel antagonist of the Grb7 SH2 domain; Antitumor Agent
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| DCC3769 | Nsc52101 |
Novel potent inhibitor of Huntington's disease (HD) pathogenesis via targeting CAG repeats RNA and Poly Q protein
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| DCC3768 | nsc48693 Dihydrochloride |
Potent apoptosis inducer in pancreatic cancer cells
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| DCC3767 | Nsc-4231 |
Novel Rho-Kinase-II Inhibitor with Vasodilatory Activity
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| DCC3766 | Nsc-347518 |
DT-diaphorase inhibitor
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| DCC3765 | Nsc339614 Potassium Salt |
Selective potentiator at GluN1/GluN2C and GluN1/GluN2D receptors
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| DCC3764 | Nsc-339579 |
Novel potent Mycobacterium tuberculosis DHFR inhibitor
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| DCC3763 | Nsc-33353 |
Potent inhibitor of the AcrAB-TolC efflux pump in Escherichia coli, potentiating the antibacterial activities of novobiocin and erythromycin upon binding to the membrane fusion protein AcrA
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| DCC3762 | Nsc-311068 |
Novel selective inhibitor of TET1 transcription and 5-hydroxymethylcytosine (5hmC) modification, effectively inhibiting cell viability in AML with high expression of TET1
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| DCC3761 | Nsc30049 |
Novel inhibitor of Chk1 pathway in 5-FU-resistant CRC bulk and stem cell populations
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| DCC3760 | Nsc-299202 |
Novel potent gonist of Human G Protein-Coupled Receptor-35 (hGPR35) (EC50 8 nM)
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| DCC3759 | Nsc-2888 |
Novel Rho-Kinase-II Inhibitor with Vasodilatory Activity
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