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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC3861 Nystatin-3
Novel water-soluble nystatin derivative, being fully water-soluble (up to 1 g/mL) with the same potency of Nystatin but with 13.5 times lower toxicity
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DCC3860 Ny-eso-1
Cancer-testis antigen (CTA) with re-expression in numerous cancer types, eliciting spontaneous humoral and cellular immune responses, restricting expression pattern, being a good candidate target for cancer immunotherapy
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DCC3859 Nybomycin
Anti-microbial agent against Mycobacterium smegmatis and Mycobacterium bovis BCG, binding to DNA and inducing a unique morphological change to mycobacterial bacilli leading the bacterial cell death
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DCC3858 nxn-188
Selective nNOS inhibitor and a5-HT1B/1D receptor agonist
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DCC3857 Nxd30001
Novel potent Hsp90 inhibitor, inducing tumor regression in a genetically engineered mouse model of glioblastoma multiforme
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DCC3856 Nw-1772
Highly potent, selective, reversible, and orally active monoamine oxidase B inhibitor
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DCC3855 Nvx-108
Exceptional oxygen transporter, increasing brain tissue oxygen tension (PbtO2) when administered soon after traumatic brain injury (TBI)
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DCC3854 Nvs-sm2
Potent, orally active, small-molecule enhancer of SMN2 splicing, binding to and stabilizing the U1 snRNP:5′ss RNA complex
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DCC3853 Nvs-pak1-c
Negative control for NVS-PAK1-1 (8778)
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DCC3852 Nvs-mllt-1
Novel Potent and Selective inhibitor of YEATS proteins
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DCC3851 Nvs-bet-2
Novel selective bromodomain and extra-terminal domain (BET) protein family inhibitor (BETi ), inducing an ‘activated’ keratinocyte transcriptional profile with reversal of chronic wound biomarkers in human skin ex vivo
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DCC3850 Nvp-xaa228
Novel potent PKCθ inhibitor
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DCC3849 Nvp-vid400
Specific inhibitor of the 25-hydroxyvitamin D(3)-24-hydroxylase (24-hydroxylase)
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DCC3848 Nvp-tac544
Novel focal adhesion kinase (FAK) inhibitor, potently blocking kinase activity of FAK along with Aurora A, activated Cdc42-associated kinase 1 (ACK1), Met, insulin receptor (IR), TrkA, and IGF-1R
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DCC3847 Nvp-sra880
The first non-peptide somatostatin sst(1) receptor antagonist
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DCC3846 Nvp-saa164
Novel nonpeptide bradykinin B1 receptor antagonist
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DCC3845 Nvp-qab205
Novel Syk inhibitor
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DCC3844 Nvp-lbm415
Novel peptide deformylase (PDF) inhibitor; Antibacterial
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DCC3843 Nvp-dpp728
Potent, orally active dipeptidyl peptidase (DPP)-IV inhibitor
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DCC3842 Nvp-cfc218
Novel potent and selective p53-HDM2 inhibitor
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DCC3841 Nvp-bvb808
Novel potent Jak2 type 1 inhibitor
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DCC3840 Nvp-bhs345
Novel dual inhibitor of TORC1 and TORC2
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DCC3839 Nvp-aht202
Novel BCR-ABL Kinase Inhibitor
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DCC3838 Nvp-acq090
Novel potent and selective antagonist of somatostatin receptor subtype SST(3)
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DCC3837 Nvp-abj688
Novel Inhibitor of the Cysteine Protease Cathepsin K
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DCC3836 Nvp-abe171
Novel phosphodiesterase 4D (PDE4D) inhibitor
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DCC3835 Nvp Cxcr2 Antagonist 24
Novel potent, orally bioavailable CXCR2 receptor antagonist
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DCC3834 Nvp Cxcr2 Antagonist 14
Novel potent, orally bioavailable CXCR2 receptor antagonist
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DCC3833 Nv2913
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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DCC3832 Nv2909
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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