Cap-dependent endonuclease-IN-27
Cap-dependent endonuclease-IN-27 (Compound 8) is an orally active potent cap-dependent endonuclease (CEN) inhibitor. Cap-dependent endonuclease-IN-27, an antiviral agent, shows activity against influenza B virus. Cap-dependent endonuclease-IN-27 has inhibitory activity against IFV A/WSN/33 (H1N1) polymerase (EC50 = 12.26 nM).
For research use only. We do not sell to patients.
- CAS No.: 2741952-21-4
- Formula: C23H19F2N3O4
- Molecular Weight:439.41
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A-375 | CC50 |
13.3 μM
Compound: 8
|
Cytotoxicity against human A-375 cells incubated for 3 days by CellTiter-Glo assay
Cytotoxicity against human A-375 cells incubated for 3 days by CellTiter-Glo assay
|
[PMID: 38301207] |
| CCRF-CEM | CC50 |
6.48 μM
Compound: 8
|
Cytotoxicity against human CCRF-CEM cells incubated for 3 days by CellTiter-Glo assay
Cytotoxicity against human CCRF-CEM cells incubated for 3 days by CellTiter-Glo assay
|
[PMID: 38301207] |
| COLO 205 | CC50 |
7.04 μM
Compound: 8
|
Cytotoxicity against human COLO 205 cells incubated for 3 days by CellTiter-Glo assay
Cytotoxicity against human COLO 205 cells incubated for 3 days by CellTiter-Glo assay
|
[PMID: 38301207] |
| H1-HeLa | CC50 |
9.77 μM
Compound: 8
|
Cytotoxicity against human H1-HeLa cells incubated for 3 days by CellTiter-Glo assay
Cytotoxicity against human H1-HeLa cells incubated for 3 days by CellTiter-Glo assay
|
[PMID: 38301207] |
| HEK293 | CC50 |
20.3 μM
Compound: 8
|
Cytotoxicity against HEK293 cells incubated for 3 days by CellTiter-Glo assay
Cytotoxicity against HEK293 cells incubated for 3 days by CellTiter-Glo assay
|
[PMID: 38301207] |
| HEp-2 | CC50 |
12.45 μM
Compound: 8
|
Cytotoxicity against human HEp-2 cells incubated for 3 days by CellTiter-Glo assay
Cytotoxicity against human HEp-2 cells incubated for 3 days by CellTiter-Glo assay
|
[PMID: 38301207] |
| HepG2 | CC50 |
5.19 μM
Compound: 8
|
Cytotoxicity against human HepG2 cells incubated for 3 days by CellTiter-Glo assay
Cytotoxicity against human HepG2 cells incubated for 3 days by CellTiter-Glo assay
|
[PMID: 38301207] |
| MOLT-4 | CC50 |
4.13 μM
Compound: 8
|
Cytotoxicity against human MOLT-4 cells incubated for 3 days by CellTiter-Glo assay
Cytotoxicity against human MOLT-4 cells incubated for 3 days by CellTiter-Glo assay
|
[PMID: 38301207] |
| MRC5 | CC50 |
19.95 μM
Compound: 8
|
Cytotoxicity against human MRC5 cells incubated for 3 days by CellTiter-Glo assay
Cytotoxicity against human MRC5 cells incubated for 3 days by CellTiter-Glo assay
|
[PMID: 38301207] |
Chemical Information
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CAS No. 2741952-21-4
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Molecular Weight 439.41
-
Formula C23H19F2N3O4
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SMILES
O=C1N(C)[C@@]2([H])N(N3C1=C(O)C(C=C3)=O)[C@H](C4=CC=CC=C4)C5=CC(F)=C(F)C=C5OCC2
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Shipping
Room temperature in continental US; may vary elsewhere.
-
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)