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Cat. No. Product Name Field of Application Chemical Structure
DCC3275 Mcule-5948770040
Novel SARS-CoV-2 Main Protease (Mpro) inhibitor, binding to Subsites S1 and S2 (Kd=1.3 µM)
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DCC3274 Mct4-in-18n
Novel highly selective inhibitor of monocarboxylate transporter 4 (MCT4/SLC16A3), resulting in lactate efflux inhibition and reduction of cellular viability in MCT4 high expressing cells
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DCC3272 Mcl1-in-1
Novel potent and selective inhibitor of the apoptosis regulating proteins Mcl-1
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DCC3271 Mcl-1 Inhibitor-5
The first reversible covalent inhibitor for Mcl-1, a protein-protein interaction (PPI) target
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DCC3270 Mcl-1 Inhibitor-39
Novel selective Mcl-1 inhibitor
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DCC3269 Mcl-1 Inhibitor-11
Novel reversible covalent inhibitor for Mcl-1 with improved water solubility than Mcl-1 Inhibitor-5
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DCC3268 Mcl-1 Degrader C3
Novel potent and selective degrader of Mcl-1
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DCC3267 Mcl0527-3
Novel inhibitor of p53-MDM2 interaction
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DCC3266 Mci-225
Selective NA reuptake inhibitor with 5-HT3 receptor antagonism
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DCC3265 Mcg315
Novel potent F508del-CFTR corrector, modulating poly-ADP ribose polymerase 3 and poly-ADP ribose polymerase 16 activities
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DCC3264 Mc-doxhzn
Albumin-binding prodrug of Doxorubicin
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DCC3262 Mcc-134
Novel inverse agonist for the pancreatic-type ATP-sensitive K channel as vascular relaxing agent
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DCC3261 Mcc1189
First-in-class inhibitor of MFS efflux pump CaMdr1p
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DCC3260 Mcc1019
Novel selective inhibitor of the Polo-box domain of Polo-like kinase 1 (PLK1)
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DCC3259 Mca-yvadapk(dnp)-oh
Specific and highly fluorescent substrate for caspase-1, also acting as a substrate for caspase-4
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DCC3258 Mca-13
Novel neurotropic agent
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DCC3257 Mc-70 Hydrochloride
Potent P-gp inhibitor with good selectivity towards BCRP pump (EC50 values 0.05 μM, 0.69 μM, 9.3 μM, and 73 μM for Caco-2, MDR1, MRP1, and BCRP inhibition, respectively)
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DCC3256 Mc2392
Novel hybrid retinoid-HDAC inhibitor
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DCC3255 Mc2050
Novel selective PARP1 inhibitor, inhibitng apoptosis and blocking poly ADP-ribosylation of histone H1 in hydrogen peroxide treated SH-SY5Y neuroblastoma cells
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DCC3254 Mc-1-f2
The first inhibitor of forkhead Box Protein C2 (FOXC2)
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DCC3253 Mc1420
Novel potent acetylcholinesterase (AChE) inhibitor
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DCC3252 Mc-1353
Potent and HDAC class I-selective inhibitor
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DCC3251 Mc1220
Topical nonnucleoside reverse transcriptase inhibitor, partially preventing vaginal RT-SHIV infection of macaques
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DCC3250 Mbx2546
Novel specific inhibitor of HA-mediated viral entry, inhibiting HPAI H5N1 virus strain A/Hong Kong/H5N1
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DCC3249 Mbx-1887
Antibacterial agent, with a relatively narrow spectrum against bacteria and a very high CC 50 value
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DCC3248 Mbx-1162
Novel antibacterial agent, remarkably potent against antibiotic-resistant bacterial strains such as MDR A. baumannii , ESBL-producing Klebsiella pneumoniae, VRE, and MRSA
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DCC3247 Mbx-1066
Potent antibacterial agent against a wide range of Gram-positive and Gram-negative bacteria
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DCC3246 Mbt-fh Inhibitor-7
The first selective small molecule inhibitor of the Mycobacterium tuberculosis fumarate hydratase
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DCC3245 Mbri-001
Deuterium-substituted anticancer agent, plinabulin, exhibiting better pharmacokinetic characteristics than that of plinabulin
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DCC3244 Mbp-c9
Novel detergent, showing enhanced stability to all tested proteins compared to a gold standard detergent (DDM)
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