Norbatzelladine L
Norbatzelladine L (Compound 2) is an inhibitor of the catalytic and functional activity of Pdr5p transporter. Norbatzelladine L inhibits Pdr5p ATPase activity with an IC50 of 3.8 µM. Norbatzelladine L shows antifungal, antiparasitic, antiviral, antibacterial and antitumoral activities.
For research use only. We do not sell to patients.
- CAS No.: 1187954-93-3
- Formula: C38H66N6O2
- Molecular Weight:638.97
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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
IC50: 3.8 µM (Pdr5p ATPase)[1]
Chemical Information
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CAS No. 1187954-93-3
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Molecular Weight 638.97
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Formula C38H66N6O2
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SMILES
C[C@@H]1NC2=N[C@@H](C[C@@]3([H])N2[C@@](CC3)([H])C1)CCCCCCC[C@@H](C)OC([C@@H]4[C@@]5([H])N6C(N[C@@H](C[C@]6([H])CC5)CCCCCCCC)=N[C@@H]4C)=O
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Structure Classification
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Initial Source
Monanchora arbuscula
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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)