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Cedrol

Cat. No. M17603

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Cedrol Structure
Size Price Availability Quantity
500mg USD 40 In stock
1g USD 60 In stock
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Quality Control & Documentation
Biological Activity

Cedrol is a potent competitive inhibitor of cytochrome P-450 (CYP) enzymes. Cedrol inhibits CYP2B6-mediated bupropion hydroxylase and CYP3A4-mediated midazolam hydroxylation with Ki of 0.9 μM and 3.4 μM, respectively. Cedrol also has weak inhibitory effect on CYP2C8, CYP2C9, and CYP2C19 enzymes. Cedrol is found in cedar essential oil and poetesses anti-septic, anti-inflammatory, anti-spasmodic, tonic, astringent, diuretic, insecticidal, and anti-fungal activities.

Chemical Information
Molecular Weight 222.37
Formula C15H26O
CAS Number 77-53-2
Solubility (25°C) DMSO 90 mg/mL
Storage 4°C, protect from light
References

[1] Gulmira zek, et al. Molecules. Innate Immunomodulatory Activity of Cedrol, a Component of Essential Oils Isolated from Juniperus Species

[2] Wangchao Dong, et al. In Vitro Cell Dev Biol Anim. Cedrol alleviates the apoptosis and inflammatory response of IL-1β-treated chondrocytes by promoting miR-542-5p expression

[3] Kai-Fu Chang, et al. Cancer Lett. Cedrol suppresses glioblastoma progression by triggering DNA damage and blocking nuclear translocation of the androgen receptor

[4] Kai-Fu Chang, et al. J Nat Prod. Cedrol, a Sesquiterpene Alcohol, Enhances the Anticancer Efficacy of Temozolomide in Attenuating Drug Resistance via Regulation of the DNA Damage Response and MGMT Expression

[5] Mohammad Hossein Sakhaee, et al. Metab Brain Dis. Cedrol protects against chronic constriction injury-induced neuropathic pain through inhibiting oxidative stress and inflammation

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Keywords: Cedrol supplier, Cytochrome P450 (e.g. CYP17), inhibitors, activators

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