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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| DCC3243 | Mbp-c12 |
Novel detergent, showing enhanced stability to all tested proteins compared to a gold standard detergent (DDM)
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| DCC3242 | Mbls-in-5 |
Novel non-hemolytic and low toxic inhibitor of metallo-β-lactamases (MBLs), restoring the activity of meropenem against Escherichia coli, Citrobacter freundii, Proteus mirabilis and Klebsiella pneumonia, which carried resistance genes of blaNDM-1
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| DCC3241 | Mb-211 |
Novel inhibitor of dengue and West Nile virus NS2B-NS3 protease
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| DCC3240 | Mb16695 |
Novel Inhibitor of Mycobacterium tuberculosis α-1,4-Glucan Branching Enzyme (GlgB)
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| DCC3239 | Mb06322 |
Prodrug of MB05032, acting as potent and selective inhibitor of fructose 1,6-bisphosphatase for controlling gluconeogenesis in type 2 diabetes
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| DCC3238 | Mb-001 |
Novel potent inhibitor of the membrane-bound retinoid isomerase RPE65
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| DCC3237 | Maysin |
Natural Anti-inflammation Agent, Attenuating Amyloid Plaques by Inducing Humoral Immune Response with Th2 Skewed Cytokine Response in the Tg (APPswe, PS1dE9) Alzheimer's Mouse Model
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| DCC3236 | May1-in-13a |
Novel potent inhibitor of May1 with Ki = 12 ± 1 nM, also inhibiting wild-type HIV-1 protease with Ki = 32 ± 5 pM and three drug resistance-associated mutants with Ki values ranging from 24 to 320 pM
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| DCC3235 | Massiliamide |
Novel potent tyrosinase inhibitor from the Gram-negative bacterium Massilia albidiflava DSM 17472T
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| DCC3233 | Maritinone |
Novel, active, and less toxic anti-tuberculosis (anti-TB) agent
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| DCC3232 | Margatoxin |
Inhibitor of voltage-gated K(+) (Kv) channels Kv1.3 and Kv1.5
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