Cedrol [CAS 77-53-2]

Cedrol is a potent competitive inhibitor of cytochrome P-450 (CYP) enzyme. Cedrol plays an anticancer role by inducing cell cycle arrest and Caspase-dependent apoptosis. Cedrol acts as a neutrophil agonist that can desensitize cells to subsequent stimulation of N-formyl peptides. Cedrol prevents neuropathic pain caused by chronic contractile injury by inhibiting oxidative stress and inflammation. In addition, Cedrol has antibacterial, hair loss prevention and anti-anxiety properties[1][2][3][4][5][6][7].

[77-53-2]

C15H26O

222.37

O[C@@]1(CC[C@]23[C@@H](CC[C@]2(C(C)([C@]1(C3)[H])C)[H])C)C

Apoptosis; Caspase; Cytochrome P450; Fungal; Platelet-activating Factor Receptor (PAFR)

CYP2; CYP3

99.76

DMSO : 110 mg/mL (ultrasonic) |H2O : < 0.1 mg/mL

4°C (Powder, protect from light)

Room Temperature

H315, H319, H320

H315, H319, H320