Antimalarial agent 8
Antimalarial agent 8 (Compound 7e) is a novel orally active class of antimalarials. Antimalarial agent 8 is potent in vitro against P. falciparum and is orally efficacious (40 mg/kg) in an in vivo mouse model of malaria.
For research use only. We do not sell to patients.
- CAS No.: 2715222-97-0
- Formula: C22H21Cl3N4O
- Molecular Weight:463.79
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All Parasite Isoforms
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Biological Activity
Description
IC50 & Target
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Plasmodium |
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| HEK293 | CC50 |
32 μM
Compound: 7e.HCl
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Cytotoxicity against human HEK293 cells by resazurin based cell viability assay
Cytotoxicity against human HEK293 cells by resazurin based cell viability assay
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[PMID: 35300096] |
| Hepatocyte | CC50 |
8500 nM
Compound: 7e.HCl
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Cytotoxicity against human hepatocytes measured after 96 hrs by DAPI staining based fluroscence assay
Cytotoxicity against human hepatocytes measured after 96 hrs by DAPI staining based fluroscence assay
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[PMID: 35300096] |
Chemical Information
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CAS No. 2715222-97-0
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Molecular Weight 463.79
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Formula C22H21Cl3N4O
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SMILES
O=C(C1=CC2=C(NC3=C2C=CC=C3C)C(C4=CC(Cl)=C(Cl)C=C4)=N1)NCCNC.Cl
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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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How to Choose the Right Model Animal
Choosing the right model animal is a validity-driven decision in which the species, strain, sex, age, genetic background, disease-induction method, outcome measures, and welfare burden must match the scientific question rather than laboratory tradition or convenience. A model should be selected by judging face validity, construct validity, and predictive validity: whether it resembles the human phenotype, whether it reproduces relevant mechanisms, and whether results are likely to predict human biology or treatment response. Animal studies often fail to translate because of species differences, weak disease resemblance, poor experimental design, inadequate reporting, publication bias, and underuse of randomization, blinding, and sample-size justification. Unresolved questions include how to rank competing models objectively, how much human-disease complexity must be reproduced for a given objective, and when non-animal systems such as organoids, ex vivo tissue, or computational models
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)