IDX-320
IDX-320 is a Pipecolic acid (HY-Y0669) derivative. IDX-320 inhibits NS3/4a proteases across genotypes 1a, 1b, 2a, and 4a with an IC50 0.8-1.9 nM. IDX-320 can be used in the research of HCV infection.
For research use only. We do not sell to patients.
- CAS No.: 1251165-81-7
- Formula: C37H43F3N6O7S2
- Molecular Weight:804.90
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
IC50: 0.8-1.9 nM (NS3/4a proteases across genotypes 1a, 1b, 2a, and 4a)[1].
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| Hepatocyte | CC50 |
>10 μM
Compound: 8; IDX320
|
Cytotoxicity against human hepatocytes
Cytotoxicity against human hepatocytes
|
[PMID: 26410074] |
| Huh-7 | CC50 |
52.78 μM
Compound: 8; IDX320
|
Cytotoxicity against human HuH7 cells by colorimetric proliferation assay
Cytotoxicity against human HuH7 cells by colorimetric proliferation assay
|
[PMID: 26410074] |
| Huh-7 | EC50 |
0.7 nM
Compound: 8; IDX320
|
Antiviral activity against HCV genotype 1b infected in human HuH7 cells after 3 days by luciferase assay
Antiviral activity against HCV genotype 1b infected in human HuH7 cells after 3 days by luciferase assay
|
[PMID: 26410074] |
Clinical Trial
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
Chemical Information
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CAS No. 1251165-81-7
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Molecular Weight 804.90
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Formula C37H43F3N6O7S2
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SMILES
O=C(NS(=O)(C1(CC1)C)=O)[C@]23NC([C@@](C[C@@H](OC4=CC(C5=NC(C(F)(F)F)=CS5)=NC6=C(C)C(OC)=CC=C46)CC7)([H])N7C(N(C)CCCC/C=C\[C@]2([H])C3)=O)=O
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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.
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)