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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2833 | Jnj-17148066 |
Estrogen receptor ESR1 agonist
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| DCC2832 | Jnj-17029259 |
Vascular endothelial growth factor receptor-2 (VEGF-2) kinase inhibitor
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| DCC2831 | Jnj-10311795 |
Novel, potent dual inhibitor of the leukocyte proteases cathepsin G and chymase
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| DCC2830 | Jnj-1013 |
Novel potent and selective IRAK1 degrader, effectively degraded cellular IRAK1 protein with a DC50 of 3 nM in HBL-1 cells
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| DCC2829 | Jmx0510-2 |
Novel Potent Human Adenovirus Inhibitor, showing improved anti-HAdV activity (IC50 = 0.27 μM), significantly decreasing cytotoxicity (CC50 = 156.8 μM), and lowering in vivo toxicity (maximum tolerated dose = 150 mg/kg in hamster) as compared with niclosam
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| DCC2828 | Jmx0254 |
Novel Potent NS4B Inhibitor for the Treatment of Dengue Virus Infection
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| DCC2827 | Jmx0207 |
Novel inhibitor of viral protease function, suppressing Zika virus Infection both In vitro and In vivo
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| DCC2826 | Jmv4484 |
Novel partial inverse agonist of GHS-R1a (K i = 3 nM, EC 50 = 70 nM, Emax = −37%)
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| DCC2825 | Jmv3168 |
Novel ghrelin receptor (GHS-R1a) antagonist [IC 50 (affinity): 5 nM IC 50 (Ca ): 60 nM]
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| DCC2824 | Jmv2951 |
Novel potent GHS-R1a agonist (EC50 (Ca ): 1.6 nM), significantly stimulating GH secretion
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| DCC2823 | Jlj-334 |
Potent non-nucleoside inhibitor of HIV-1 reverse transcriptase (NNRTIs)
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| DCC2822 | Jk-31 (vegfr2/cdk1 Inhibitor) |
Novel specific dual inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2) and cyclin-dependent kinase 1 (CDK1), targeting cell cycle progression and angiogenesis
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| DCC2821 | Jk-136 |
Novel Ras homologous A (RHOA) inhibitor, potently inhibiting cell viability and migration/invasion of gastric cancer (GC) cell lines, and mouse xenografts, diversely expressing RHOA, binding affinity for RHOA was >140-fold greater than Rhosin, a nonclinic
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| DCC2820 | Jh-i-25 |
Novel Interleukin-1 receptor-associated kinase 4 (IRAK4) inhibitor, binding preferentially to unphosphorylated IRAK4
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| 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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