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Cat. No. Product Name Field of Application Chemical Structure
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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