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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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