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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| 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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