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My Cart> Small Molecule Compounds > Inhibitors & Antagonists & Agonists > Metabolic Enzyme & Protease > CedrolCAS：77-53-2
Molecular Formula：C15H26O
Molecular Weight：222.37
Storage：Powder:2-8℃，2 years;Insolvent(Mother Liquid):-20℃，6 months;-80℃，1 year
Purity：GC≥98%
Appearance：White to off-white Solid
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| CAS | 77-53-2 |
| Name | Cedrol |
| Molecular Formula | C15H26O |
| Molecular Weight | 222.37 |
| Solubility | Soluble in DMSO ≥5mg/mL |
| Purity | GC≥98% |
| Appearance | White to off-white Solid |
| Storage | Powder:2-8℃，2 years;Insolvent(Mother Liquid):-20℃，6 months;-80℃，1 year |
| EC | EINECS 201-035-6 |
| MDL | MFCD00062952 |
| SMILES | O[C@]1(C)CC[C@@]23[C@H](C)CC[C@@]2([H])C(C)(C)[C@@]1([H])C3 |
| Target Point | Cytochrome P450 |
| Passage | Metabolic Enzyme&Protease |
| Background | Cedrol is a biologically active sesquiterpene, a potent cytochrome P-450 (CYP) enzyme competitive inhibitor. |
| Biological Activity | Cedrol is bioactive sesquiterpenes found in cedar essential oil and exert antiseptic, anti-inflammatory, antispasmodic, tonic, astringent, diuretic, sedative, insecticidal, and antifungal activities. Cedrol was found to be potent competitive inhibitors of CYP2B6-mediated bupropion hydroxylase . [1-3] |
| Data Literature Source | [1] Chen SS，et al. Environ Toxicol Pharmacol. 2016，46:270-276. [2] Jeong HU，et al. J Toxicol Environ Health A. 2014，77(22-24):1522-32. [3] Jin MH，et al. Ann Dermatol. 2012，24(1):16-21. |
| Unit | Piece |
| Specification | 20mg 50mg 100mg |
Remark：These protocols are for reference only. Solarbio does not independently validate these methods.
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