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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC2819 | Jh-i-17 |
Novel type I Interleukin-1 receptor-associated kinase 4 (IRAK4) inhibitor, binding preferentially to unphosphorylated IRAK4
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| DCC2818 | Jg2-38 |
Novel inhibitor of the heat shock protein 70 (Hsp70) with anti-proliferative activity in breast and prostate cancer cells
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| DCC2817 | Jfd00950 |
Novel human flap endonuclease 1 (FEN1) inhibitor with in vitro inhibition of flap cleavage activity as well as cytotoxic activity against a colon cancer cell line, DLD-1
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| DCC2816 | Jesridonin |
Novel apoptosis inducer, significantly inhibiting tumor growth in the xenograft model
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| DCC2815 | jd-5006 |
Peripheral Selective CB1 Receptor Antagonist
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| DCC2814 | Jcp678 |
Novel irriversable serine hydrolases inhibitor
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| DCC2813 | Jcp474 |
Novel potent inhibitor of Mpro
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| DCC2812 | Jcp410 |
Covalent dual inhibitor of DPAP1 and DPAP3
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| DCC2811 | Jcp405 |
Covalent dual inhibitor of DPAP1 and DPAP3
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| DCC2810 | Jcp-265 |
Novel dose-dependent inhibitor of ABHD6
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| DCC2809 | jcp174-ia |
Negative control of JCP174
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| DCC2808 | jcp174-alk |
JCP174 analog used for affinity purification of labeled targets
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| DCC2807 | Jcp-170 |
Novel dose-dependent inhibitor of ABHD6
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| 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
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| DCC2805 | Jbsnf-000567 |
Metabolite of JBSNF-000088
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| DCC2804 | Jbp923 |
Natural anti-inflammatory agent, showing potential for the treatment of inflammatory bowel disease (IBD)
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| DCC2803 | Jbp485 |
Inhibitor of renal transporters OAT1 and OAT3; Antihepatitis agent as a substrate for intestinal PEPT1
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| DCC2802 | Jbir-59 |
Natural radical scavenger, inhibiting L-glutamate toxicity in neuronal hybridoma N18-RE-105 cells
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| DCC2801 | Jbir-22 |
Natural Inhibitor for Protein−Protein Interaction of the Homodimer of Proteasome Assembly Factor 3
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| DCC2800 | Jasplakinolide |
Potent inhibitor of the proliferation of PC3 prostate carcinoma cells
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| DCC2799 | Jasminine |
Natural naphthyridine alkaloid
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| DCC2798 | jarid1b Demethylase Inhibitor |
Novel Inhibitor of Jumonji AT-Rich Interactive Domain 1B (JARID1B) Histone Demethylase
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| 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
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| DCC2796 | Janelia Fluor 526, Se |
Novel fluorogenic yellow fluorescent dye for use in self-labeling tag systems
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| 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
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| DCC2794 | Jami1001a |
Novel positive allosteric modulator of AMPA receptor
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| DCC2793 | Jak-in-3 |
Novel potent JAK1/3 inhibitor, targeting JAK3 and JAK1 with IC 50 at 3nM and 5nM, respectively
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| DCC2792 | Jak-in-1 |
Novel potent JAK1/2/3 inhibitor
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| DCC2791 | Jak3-in-5 |
Novel Selective JAK3 Inhibitor with a Covalent Reversible Binding Mode Targeting a New Induced Fit Binding Pocket
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| DCC2790 | Jak3-in-4 |
Novel Selective JAK3 Inhibitor with a Covalent Reversible Binding Mode Targeting a New Induced Fit Binding Pocket
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