DC07090
DC07090 is a potent, reversible and competitive non-peptidyl human enterovirus 71 3C protease inhibitor with an IC50 and a Ki value for 21.72 μM and 23.29 μM. DC07090 could also inhibit coxsackievirus A16 (CVA16) replication with an EC50 value of 27.76 μM.
For research use only. We do not sell to patients.
- CAS No.: 879070-72-1
- Formula: C18H14N4O
- Molecular Weight:302.33
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
IC50: 21.72 μM (EV71 3C protease)[1].
Ki: 23.29 μM (EV71 3C protease)[1].
EC50: 27.76 μM (coxsackievirus A16)[1]
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| RD | CC50 |
>200 μM
Compound: DC07090
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Cytotoxicity against human RD cells after 48 hrs by CellTiter-glo luminescent cell viability assay
Cytotoxicity against human RD cells after 48 hrs by CellTiter-glo luminescent cell viability assay
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[PMID: 27776325] |
DC07090 forms stable hydrogen-bonding interactions with the main chains of S128, G145, G164 and hydrophobic interactions with F25, L125, L127 and F170. DC07090 (0.01~10 μM) shows micromolar potency against EV71 3Cpro. DC07090 exhibits a highly inhibitory potency on EV71 replication with an EC50 value of 22.09 μM. DC07090 inhibits CVA16 with an EC50 value of 27.76 μM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 879070-72-1
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Molecular Weight 302.33
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Formula C18H14N4O
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SMILES
C1(C(C=C2)=CC=C2NCC3=NC=CC=C3)=NC(N=CC=C4)=C4O1
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)