Antiviral agent 23
Antiviral agent 23 (compound 11b) is an antiviral agent to enterovirus 71 (EV71) with an EC50 value of 94 nM. Antiviral agent 23 effectively suppresses the activity of METTL3/METTL14. Antiviral agent 23 can be used for the research of infection.
For research use only. We do not sell to patients.
- CAS No.: 35940-03-5
- Formula: C18H21N5O4
- Molecular Weight:371.39
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| B16 | IC50 |
>166.7 μM
Compound: 12
|
Antitumor activity against mouse B16 cells after 72 hrs by Calcein AM assay
Antitumor activity against mouse B16 cells after 72 hrs by Calcein AM assay
|
[PMID: 17418578] |
| CCRF-CEM | IC50 |
19.1 μM
Compound: 12
|
Antitumor activity against human CEM cells after 72 hrs by Calcein AM assay
Antitumor activity against human CEM cells after 72 hrs by Calcein AM assay
|
[PMID: 17418578] |
| G-361 | IC50 |
>166.7 μM
Compound: 12
|
Antitumor activity against human G361 cells after 72 hrs by Calcein AM assay
Antitumor activity against human G361 cells after 72 hrs by Calcein AM assay
|
[PMID: 17418578] |
| HeLa | CC50 |
>100 μM
Compound: 11b
|
Cytotoxicity against human HeLa cells by MTS assay
Cytotoxicity against human HeLa cells by MTS assay
|
[PMID: 36455356] |
| HL-60 | IC50 |
6.4 μM
Compound: 12
|
Antitumor activity against human HL60 cells after 72 hrs by Calcein AM assay
Antitumor activity against human HL60 cells after 72 hrs by Calcein AM assay
|
[PMID: 17418578] |
| HOS | IC50 |
>166.7 μM
Compound: 12
|
Antitumor activity against human HOS cells after 72 hrs by Calcein AM assay
Antitumor activity against human HOS cells after 72 hrs by Calcein AM assay
|
[PMID: 17418578] |
| K562 | IC50 |
>166.7 μM
Compound: 12
|
Antitumor activity against human K562 cells after 72 hrs by Calcein AM assay
Antitumor activity against human K562 cells after 72 hrs by Calcein AM assay
|
[PMID: 17418578] |
| NIH3T3 | IC50 |
>166.7 μM
Compound: 12
|
Cytotoxicity against mouse NIH 3T3 cells after 72 hrs by Calcein AM assay
Cytotoxicity against mouse NIH 3T3 cells after 72 hrs by Calcein AM assay
|
[PMID: 17418578] |
| RD | CC50 |
>100 μM
Compound: 11b
|
Cytotoxicity against human RD cells by MTS assay
Cytotoxicity against human RD cells by MTS assay
|
[PMID: 36455356] |
| Vero | CC50 |
>100 μM
Compound: 11b
|
Cytotoxicity against african green monkey Vero cells by MTS assay
Cytotoxicity against african green monkey Vero cells by MTS assay
|
[PMID: 36455356] |
| Vero C1008 | CC50 |
>100 μM
Compound: 11b
|
Cytotoxicity against african green monkey Vero E6 cells by MTS assay
Cytotoxicity against african green monkey Vero E6 cells by MTS assay
|
[PMID: 36455356] |
In Vitro
Antiviral agent 23 (0-100 μM) inhibits CVA21 and EV68 replication in HeLa cells with EC50 values of 36.4 and 8.9 μM, respectively[1]. Antiviral agent 23 (100 μM) inhibits the enzymatic activity of METTL3/METTL14 of 74.45%[1]. Antiviral agent 23 (0-100 μM) shows antiviral effect to EV71 and inhibits the replication of the EV71 strain BrCr in RD cells with an EC50 value of 94 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
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CAS No. 35940-03-5
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Molecular Weight 371.39
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Formula C18H21N5O4
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SMILES
OC[C@@H]1[C@@H](O)[C@@H](O)[C@H](N2C(N=CN=C3NCC4=CC=CC(C)=C4)=C3N=C2)O1
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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.
Protocols
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Research Protocol for Infectious Diseases
Infectious-disease experiments test how pathogens interact with host barriers, innate immune receptors, inflammatory signaling, pathogen replication, and tissue injury; pattern-recognition receptors such as TLRs, RIG-I-like receptors, NOD-like receptors, and inflammasomes detect microbial molecules and activate NF-κB, interferon, and cytokine responses. The central hypothesis is that infection severity reflects the balance between pathogen burden and host response: protective inflammation restricts pathogen growth, whereas excessive or mislocalized inflammation contributes to tissue damage and disease phenotype. Unresolved questions include which host pathways are protective versus pathogenic, why some infection models fail to translate to human disease, and which combined readouts best predict clinically relevant infection outcomes.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)