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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC2781 Iy-iy-das Novel potent noncleavable proteolysis targeting chimeric (PROTAC) for TrkC degradation in metastatic breast cancer cells
DCC2782 Iy-iy-ss-das Novel potent and cleavable proteolysis targeting chimeric (PROTAC) for TrkC degradation in metastatic breast cancer cells
DCC2783 J-2156 Tfa Salt Potent and selective agonist of human somatostatin receptor 4 (sst4), reducing mechanosensitivity of peripheral nerve afferents and spinal neurons in an inflammatory pain model
DCC2784 Jak1-in-38a Novel highly potent JAK1-selective inhibitor, exhibiting excellent selectivity over JAK2, JAK3, and TYK2 (IC 50 : JAK1 0.145 nM; JAK2 2.94 nM; JAK3 2.31 nM; TYK2 8.17 nM)
DCC2785 Jak1-in-b61 Novel JAK1 inhibitor
DCC2786 Jak2-in-7j Novel selective Jak2 inhibitor, demonstrating a time-dependent knock-down of pSTAT5, a downstream target of Jak2
DCC2787 Jak3-in Tricyclic-1 Novel irreversible selective JAK3 inhibitor through the covalent interaction with a Jak3 active-site cysteine
DCC2788 Jak3-in Tricyclic-2 Novel irreversible selective JAK3 inhibitor through the covalent interaction with a Jak3 active-site cysteine
DCC2789 Jak3-in Tricyclic-3 Novel irreversible selective JAK3 inhibitor through the covalent interaction with a Jak3 active-site cysteine
DCC2790 Jak3-in-4 Novel Selective JAK3 Inhibitor with a Covalent Reversible Binding Mode Targeting a New Induced Fit Binding Pocket
DCC2791 Jak3-in-5 Novel Selective JAK3 Inhibitor with a Covalent Reversible Binding Mode Targeting a New Induced Fit Binding Pocket
DCC2792 Jak-in-1 Novel potent JAK1/2/3 inhibitor
DCC2793 Jak-in-3 Novel potent JAK1/3 inhibitor, targeting JAK3 and JAK1 with IC 50 at 3nM and 5nM, respectively
DCC2794 Jami1001a Novel positive allosteric modulator of AMPA receptor
DCC2795 Jamunone M Novel anti-triple-negative breast cancer (anti-TNBC) agent with a high selectivity against BC cells over normal human cells, downregulating phosphatidylinositide 3-kinase (PI3K)/Akt pathway by suppressing protein-tyrosine phosphatase 1B (PTP1B) expression
DCC2796 Janelia Fluor 526, Se Novel fluorogenic yellow fluorescent dye for use in self-labeling tag systems
DCC2797 Jar1.39 Novel mitophagy inducer with therapeutic potential for Parkinson's disease, acting as light chain 3 (LC3) interactors, similar to cardiolipin or ceramide, triggering mitophagy via Pink1/Parkin
DCC2798 jarid1b Demethylase Inhibitor Novel Inhibitor of Jumonji AT-Rich Interactive Domain 1B (JARID1B) Histone Demethylase
DCC2799 Jasminine Natural naphthyridine alkaloid
DCC2800 Jasplakinolide Potent inhibitor of the proliferation of PC3 prostate carcinoma cells
DCC2801 Jbir-22 Natural Inhibitor for Protein−Protein Interaction of the Homodimer of Proteasome Assembly Factor 3
DCC2802 Jbir-59 Natural radical scavenger, inhibiting L-glutamate toxicity in neuronal hybridoma N18-RE-105 cells
DCC2803 Jbp485 Inhibitor of renal transporters OAT1 and OAT3; Antihepatitis agent as a substrate for intestinal PEPT1
DCC2804 Jbp923 Natural anti-inflammatory agent, showing potential for the treatment of inflammatory bowel disease (IBD)
DCC2805 Jbsnf-000567 Metabolite of JBSNF-000088
DCC2806 Jc1-40 Novel RORα activator, diminishing diethylnitrosamine-induced acute liver injury and repressing transcriptional expression of APPs such as CXCL1 and LCN2 in mice
DCC2807 Jcp-170 Novel dose-dependent inhibitor of ABHD6
DCC2808 jcp174-alk JCP174 analog used for affinity purification of labeled targets
DCC2809 jcp174-ia Negative control of JCP174
DCC2810 Jcp-265 Novel dose-dependent inhibitor of ABHD6

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