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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC3831 Nv2907
Novel translational readthrough-inducing drug (TRID), rescuing the functional full-length protein expression in genetic diseases, such as cystic fibrosis, caused by premature termination codons (PTCs)
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DCC3830 Nv2899
Novel translational readthrough-inducing drug (TRID), rescuing the functional full-length protein expression in genetic diseases, such as cystic fibrosis, caused by premature termination codons (PTCs)
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DCC3829 Nutlin-2
Potent and selective p53-MDM2 binding inhibitor
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DCC3828 Nutlin-1
p53-MDM2 binding inhibitor; p-Glycoprotein (p-gp) transport substrate; Antitumer agent
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DCC3827 Nusb-nuse Interaction Inhibitor-1
Novel modulator of the NusB-NusE interaction
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DCC3826 Nusb-nuse Inhibitor-22
Novel Inhibitor of the NusB-NusE Protein-Protein Interaction with Antibiotic Activity
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DCC3825 Nurf Inhibitor Bz1
Novel Potent Cell-Active Inhibitor of the Nucleosome Remodeling Factor (NURF) via BPTF Bromodomain Inhibition
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DCC3824 Nuod-in-25
Novel inhibitor of Helicobacter pylori , targeting H. pylori's respiratory complex I subunit NuoD
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DCC3823 Nucleocidin
Nucleosidic antibiotic
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DCC3822 Nucc-555
First-in-class activin antagonist, specifically binding to ALK4, which opens a completely new approach to inhibiting the activity of TGF-beta receptor superfamily members
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DCC3821 Nucc-474
Novel potent activin antagonist
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DCC3820 Nucc-201177
Novel highly potent and selective MEK4 inhibitor
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DCC3819 Nuc013
Novel DNA methytransferase inhibitor, be significantly safer and more effective than decitabine in xenograft models of human leukemia and colon cancer
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DCC3818 Nu6155
Novel potent CDK2 inhibitor
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DCC3817 Ntzdpa
Novel potent and selective non-thiazolidinedione partial Peroxisome_proliferator-activated_receptor>PPARγ agonist, acting as an antibiotic effectively against bacterial persisters
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DCC3816 Ntz-24
Novel potent STAT3 inhibitor
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DCC3815 Ntz-15
Novel potent STAT3 inhibitor, exhibiting much improved in vivo pharmacokinetic parameters in rats and efficacies against proliferations in multiple cancer cell lines
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DCC3814 Ntr-responsive Protac 17-1
The first NTR-responsive PROTAC, incorporating the caging group on the Von Hippel-Lindau (VHL) E3 ubiquitin ligase ligand, efficiently degrading the EGFR protein and subsequently exert antitumor efficacy
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DCC3813 Ntrd22
Novel Allosteric Modulator of RNA Binding Targeting the N-Terminal Domain of TDP-43
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DCC3812 Ntrc-808
Novel nonpeptide potent and selective partial agonist of the Neurotensin receptor type 2 (NTS2)
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DCC3811 Ntrc-739
Novel nonpeptide selective ligand for NTS2
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DCC3810 Nti-007
Potent anti-HBV agent, targeting the NTCP-APOA1-HBx-Beclin1-mediated autophagic pathway
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DCC3809 Nsp-116
Novel free radical scavenger, against light-induced photoreceptor cell damage
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DCC3808 Nsmase2-in-1
Novel inhibitor of neutral sphingomyelinase 2 (nSMase2) for the treatment of neurodegenerative diseases
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DCC3807 Nsi-189 Phosphate
Novel stimulator of neurogenesis of human hippocampus-derived neural stem cells in vitro and in vivo.
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DCC3806 nsc-96626
Novel B-Raf(V600E) inhibitor
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DCC3805 Nsc-9037
First-in-class probe of Rad6 function, inhibiting Rad6 function and Rad6-Rad18 interaction in the PCNA ubiquitination cascade
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DCC3804 Nsc-8891
Tyrosyl-DNA phosphodiesterase (Tdp1) inhibitor
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DCC3803 Nsc-84096
Potent inhibitor of endopeptidase activity of botulinum neurotoxin type A light chain (rBoNT/A-LC)
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DCC3802 Nsc-80141
Selective inhibitor of HsEg5
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