(-)-Codonopsine
(-)-Codonopsine is an alkaloid with antibacterial activity. (-)-Codonopsine can be used in research related to Staphylococcus aureus and Escherichia coli infections.
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- CAS. Nr.: 26989-20-8
- Formel: C14H21NO4
- Molecular Weight:267.32
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biologische Aktivität
Beschreibung
In Vitro
(-)-Codonopsine (0.5-1024 μg/mL; 18 h) inhibits Staphylococcus aureus (ATCC 29213) with a MIC of 32 μg/mL, Escherichia coli (ATCC 25922) with a MIC of 64 μg/mL[1].
(-)-Codonopsine (0.5-1024 μg/mL; 18 h) shows no activity (MIC >1024 μg/mL) against Klebsiella pneumoniae (ATCC 700603), Proteus mirabilis (ATCC 14153), Pseudomonas aeruginosa (ATCC 27853), Acinetobacter baumannii (clinical isolate), and Candida albicans (ATCC 10231)[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. Nr. 26989-20-8
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Molecular Weight 267.32
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Formel C14H21NO4
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SMILES
O[C@@H]1[C@H](N([C@@H]([C@H]1O)C)C)C2=CC(OC)=C(C=C2)OC
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Structure Classification
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Initial Source
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Protokoll
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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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Bacterial live/dead nucleic-acid viability staining
The LIVE/DEAD bacterial viability staining method is based on differential permeability of nucleic-acid-binding fluorescent dyes, most commonly SYTO 9 and propidium iodide (PI), which enables discrimination of bacterial populations with intact versus compromised cytoplasmic membranes. SYTO 9 penetrates both intact and damaged bacterial membranes and binds nucleic acids to produce green fluorescence, whereas propidium iodide penetrates only cells with compromised membranes and fluoresces red while also reducing SYTO 9 signal through competitive binding and fluorescence interactions. The resulting fluorescence pattern is interpreted as a proxy for membrane integrity, which is widely used as an indicator of bacterial viability in microscopy, flow cytometry, and spectroscopic platforms. However, mechanistic studies show that SYTO 9 and PI interactions involve displacement and fluorescence resonance energy transfer effects, which can influence signal interpretation depending on dye ratios a
Reinheit & Dokumentation
Verweise
[1]. El-Nezhawy AOH, et al. Design and total synthesis of (-)-codonopsinine, (-)-codonopsine and codonopsinine analogues by O-(2-oxopyrrolidin-5-yl)trichloroacetimidate as amidoalkylating agent with improved antimicrobial activity via solid lipid nanoparticle formulations. Bioorg Med Chem. 2019;27(7):1263-1273. [Content Brief]
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)
Keywords
- (-)-Codonopsine
- 26989-20-8
- Bacterial
- Proteus mirabilis (ATCC 14153)
- Staphylococcus aureus (ATCC 29213)
- solid lipid nanoparticle formulations
- Candida albicans
- bacterial infection
- Codonopsis clematidea
- Staphylococcus aureus
- Escherichia coli (ATCC 25922)
- Klebsiella pneumoniae (ATCC 700603)
- central nervous system
- Inhibitor
- inhibitor
- inhibit