Name | sclareol |
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Synonyms |
(1R,2R,4aS,8aS)-1-[(3R)-3-Hydroxy-3-methyl-4-penten-1-yl]-2,5,5,8a-tetramethyldecahydro-2-naphthalenol
(1R,2R,4aS,8aS)-1-[(3R)-3-Hydroxy-3-methylpent-4-en-1-yl]-2,5,5,8a-tetramethyldecahydronaphthalen-2-ol SCLAREOL(RG) EINECS 208-194-0 1-Naphthalenepropanol, α-ethenyldecahydro-2-hydroxy-α,2,5,5,8a-pentamethyl-, (αR,1R,2R,4aS,8aS)- Labd-14-ene-8,13-diol, (13R)- SCIADONIC ACID (1R,2R,8aS)-Decahydro-1-(3-hydroxy-3-methyl-4-pentenyl)-2,5,5,8a-tetramethyl-2-naphthol labd-14-ene-8,13(R)-diol MFCD00869558 SCLAREOL,NATURAL SCAREOL Sclareol (-)-sclareol SCLAREOL(P) (1R,2R,4aS,8aS)-1-[(3R)-3-Hydroxy-3-méthyl-4-pentèn-1-yl]-2,5,5,8a-tétraméthyldécahydro-2-naphtalénol |
Description | Sclareol is isolated from Salvia sclarea with anticarcinogenic activity. Sclareol shows strong cytotoxic activity against mouse leukemia (P-388), human epidermal carcinoma (KB) cells and human leukemia cell lines. Sclareol induces cell apoptosis[1]. |
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Related Catalog | |
In Vitro | Sclareol is cytotoxic to 13 of 14 human leukemia cell lines tested, with IC50 values ranging from 6.0–24.2 μg/mL, but is not cytotoxic to peripheral blood mononuclear leukocytes within the same dose range[1]. |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 398.3±15.0 °C at 760 mmHg |
Melting Point | 95-100 °C(lit.) |
Molecular Formula | C20H36O2 |
Molecular Weight | 308.499 |
Flash Point | 169.1±15.0 °C |
Exact Mass | 308.271515 |
PSA | 40.46000 |
LogP | 5.54 |
Vapour Pressure | 0.0±2.1 mmHg at 25°C |
Index of Refraction | 1.490 |
Storage condition | 2-8C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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RIDADR | NONH for all modes of transport |
WGK Germany | 2 |
RTECS | QK0301900 |
HS Code | 2906199090 |
~0% 515-03-7 |
Literature: Rogachev, Victor; Loehl, Thorsten; Markert, Thomas; Metz, Peter Arkivoc, 2012 , vol. 2012, # 3 p. 172 - 180 |
~% 515-03-7 |
Literature: Leite, Mary Ann F.; Sarragiotto, Maria Helena; Imamura, Paulo M.; Marsaioli, Anita J. Journal of Organic Chemistry, 1986 , vol. 51, # 26 p. 5409 - 5410 |
~% 515-03-7 |
Literature: Scheidegger,U. et al. Helvetica Chimica Acta, 1962 , vol. 45, p. 400 - 435 |
Precursor 3 | |
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DownStream 9 | |
HS Code | 2906199090 |
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Summary | 2906199090. cyclanic, cyclenic or cyclotherpenic alcohols. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |