Euphoscopin H
Euphoscopin H is a diterpenoid compound found in the fresh leaves and roots of Euphorbia helioscopia. Euphoscopin H shows weak inhibitory activity against LPS-induced NO production and no obvious cytotoxicity in the mouse microglial BV-2 cell model.
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- CAS. Nr.: 126239-88-1
- Formel: C31H40O8
- Molecular Weight:540.64
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Biologische Aktivität
Beschreibung
In Vitro
Euphoscopin H (compound 6) exhibits weak inhibitory activity against LPS-induced NO production in the mouse microglial BV-2 cell model, with an IC50 ＞ 100 μM, and shows no obvious cytotoxicity to BV-2 cells at this effective concentration[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. 126239-88-1
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Molecular Weight 540.64
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Formel C31H40O8
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SMILES
O=C1C(C)(C)/C=C/[C@@H](C)[C@@H](OC(C)=O)[C@](C[C@@H](C)[C@@H]2OC(C3=CC=CC=C3)=O)(O)[C@@]2([H])/C=C(C)/[C@H](OC(C)=O)C1
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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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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.
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Mammalian live/dead viability and cytotoxicity staining
Live/dead viability and cytotoxicity staining assays are based on the simultaneous detection of intracellular esterase activity in metabolically active (viable) cells and membrane integrity loss in non-viable cells. In commonly used dual-staining approaches, membrane-permeant fluorogenic substrates are converted by intracellular esterases into fluorescent products in live cells, while impermeant DNA-binding dyes selectively enter cells with compromised plasma membranes and label nucleic acids in dead or dying cells, enabling discrimination between viable and non-viable populations by fluorescence microscopy or flow cytometry.
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Cell Viability Determination by MTT Colorimetric Assay
The following protocol uses the MTT colorimetric assay as a classic literature-established method for assessing cell viability/metabolic activity in cultured mammalian cells. MTT[3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] is reduced by metabolically active cells to a colored formazan product; the amount of formazan is quantified spectrophotometrically and provides an indirect measure of metabolically active viable cells. Importantly, MTT reduction reflects cellular oxidoreductase/metabolic activity rather than an absolute direct count of living cells, so changes in cellular metabolism can alter the signal independently of cell number.
Reinheit & Dokumentation
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Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)
Euphoscopin H Related Classifications
HY-N21923 Related Classifications
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