CAS 77-53-2|(+)-Cedrol
| Common Name | (+)-Cedrol | ||
|---|---|---|---|
| CAS Number | 77-53-2 | Molecular Weight | 222.366 |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 277.2±8.0 °C at 760 mmHg |
| Molecular Formula | C15H26O | Melting Point | 55-59 °C(lit.) |
| MSDS | ChineseUSA | Flash Point | 115.5±10.9 °C |
Names
| Name | cedrol |
|---|---|
| Synonym | More Synonyms |
(+)-Cedrol BiologicalActivity
| Description | Cedrol is a bioactive sesquiterpene, 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[1]. Cedrol is found in cedar essential oil and poetesses anti-septic, anti-inflammatory, anti-spasmodic, tonic, astringent, diuretic, sedative, insecticidal, and anti-fungal activities[2]. |
|---|---|
| Related Catalog | Research Areas >>InfectionSignaling Pathways >>Metabolic Enzyme/Protease >>Cytochrome P450Research Areas >>Inflammation/Immunology |
| Target | CYP2B6; CYP3A4; CYP2C8; CYP2C9; CYP2C19[1] |
| References | [1]. Jeong HU, et al. Inhibitory effects of cedrol, β-cedrene, and thujopsene on cytochrome P450 enzyme activities in human liver microsomes. J Toxicol Environ Health A. 2014;77(22-24):1522-32. [2]. Jin MH, et al. Cedrol Enhances Extracellular Matrix Production in Dermal Fibroblasts in a MAPK-Dependent Manner. Ann Dermatol. 2012 Feb;24(1):16-21 |
Chemical & Physical Properties
| Density | 1.0±0.1 g/cm3 |
|---|---|
| Boiling Point | 277.2±8.0 °C at 760 mmHg |
| Melting Point | 55-59 °C(lit.) |
| Molecular Formula | C15H26O |
| Molecular Weight | 222.366 |
| Flash Point | 115.5±10.9 °C |
| Exact Mass | 222.198364 |
| PSA | 20.23000 |
| LogP | 4.77 |
| Vapour Pressure | 0.0±1.3 mmHg at 25°C |
| Index of Refraction | 1.519 |
| InChIKey | SVURIXNDRWRAFU-OGMFBOKVSA-N |
| SMILES | CC1CCC2C(C)(C)C3CC12CCC3(C)O |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Safety Phrases | S22-S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 2 |
| RTECS | PB7728666 |
| HS Code | 2906199090 |
Customs
| HS Code | 2906299090 |
|---|---|
| Summary | 2906299090 other aromatic alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0% |
Articles21
More Articles| Development and application of a non-targeted extraction method for the analysis of migrating compounds from plastic baby bottles by GC-MS. Food Addit. Contam. Part A. Chem. Anal. Control. Expo. Risk Assess. 31(12) , 2090-102, (2014) In 2011, the European Union prohibited the production of polycarbonate (PC) baby bottles due to the toxic effects of the PC monomer bisphenol-A. Therefore, baby bottles made of alternative materials, ... | |
| Discovery of an oviposition attractant for gravid malaria vectors of the Anopheles gambiae species complex. Malaria Journal 14 , 119, (2015) New strategies are needed to manage malaria vector populations that resist insecticides and bite outdoors. This study describes a breakthrough in developing 'attract and kill' strategies targeting gra... | |
| Fragrance material review on cedrol. Food Chem. Toxicol. 46 Suppl 11 , S100-2, (2008) A toxicologic and dermatologic review of cedrol when used as a fragrance ingredient is presented. |
Synonyms
| 8bH-Cedran-8-ol |
| EINECS 201-035-6 |
| Cedarwood oil alcohols |
| (8α)-Cedran-8-ol |
| Cedar camphor |
| (1S,2R,5S,7R,8R)-2,6,6,8-Tetramethyltricyclo[5.3.1.0]undecan-8-ol |
| 8betaH-Cedran-8-ol |
| EUDESMOL |
| 1H-3a,7-Methanoazulen-6-ol, octahydro-3,6,8,8-tetramethyl-, (3R,3aS,6R,7R,8aS)- |
| (1S,2R,5S,7R,8R)-2,6,6,8-Tétraméthyltricyclo[5.3.1.0]undécan-8-ol |
| Cypress camphor |
| 8βH-cedran-8-ol |
| [3R-(3a,3ab,6a,7b,8aa)]-Octahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-6-ol |
| Cedrol |
| MFCD00062952 |
