Deoxycaesaldekarin C
Deoxycaesaldekarin C (Methyl vouacapenate) is a naturally occurring, orally active cassane furanoditerpene with antibacterial, antioxidant, antiplasmodial, and analgesic effects. Deoxycaesaldekarin C inhibits bacterial growth and lipid peroxidation, and scavenges free radicals. Deoxycaesaldekarin C exhibits weak antiplasmodial activity and shows analgesic activity in mouse in vivo models. Deoxycaesaldekarin C can be used in research related to pain, bacterial infections, and Plasmodium infections.
For research use only. We do not sell to patients.
- CAS No.: 4614-50-0
- Formula: C21H30O3
- Molecular Weight:330.46
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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
[2]|
Plasmodium |
In Vitro
Deoxycaesaldekarin C (compound 1) (12.5-200 μg/mL; 20 min) exhibits antioxidant activity, with DPPH radical scavenging IC50 = 97.4 μM and TBA lipid peroxidation inhibition IC50 = 134.8 μM[1].
Deoxycaesaldekarin C (1000-7.8 μg/mL; 24 h) exhibits antibacterial activity against a panel of bacteria, with the strongest effect against Bacillus subtilis (MIC = 47 μM)[1].
Deoxycaesaldekarin C (cpd 5) exhibits low to moderate antimalarial activity against chloroquine-sensitive (D6) and chloroquine-resistant (W2) Plasmodium falciparum strains, with an IC50 of 25.67 μM against D6 and an IC50 of 30.33 μM against W2[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
Deoxycaesaldekarin C (100 mg/kg; i.p.; single administration) exhibits significant central antinociceptive activity in the hot-plate test[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Swiss albino mice (20-25 g; either sex)[2]
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Dosage:100 mg/kg
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Administration:i.p.; single dose; 60 min before acetic acid
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Result:Reduced the number of writhing episodes induced by Acetic acid by 77.59% compared to control.
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Animal Model:Swiss albino mice (17-30 g; either sex)[2]
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Dosage:100 mg/kg
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Administration:i.p.; single dose
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Result:Showed significant central antinociceptive activity in the hot-plate test at 60 min relative to control.
Chemical Information
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CAS No. 4614-50-0
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Molecular Weight 330.46
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Formula C21H30O3
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SMILES
C[C@@]12[C@]3([H])[C@](CC[C@@]1([H])[C@](C)(CCC2)C(OC)=O)([H])[C@H](C4=C(OC=C4)C3)C
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Synonyms
Methyl vouacapenate
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Structure Classification
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Initial Source
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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.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)