Name | manool |
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Synonyms |
8,14-labdadien-13-ol
MFCD01310996 MANOOL |
Description | Manool is a diterpene from Salvia officinalis. Manool induces selective cytotoxicity in cancer cells. Manool arrests the cancer cells at the G(2)/M phase of the cell cycle[1][2]. |
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Related Catalog | |
In Vitro | Manool exhibits higher cytotoxic activity against HeLa (IC50=6.7 µg/mL) and U343 (IC50=6.7 µg/mL) cells[1]. Manool exhibits a protective effect against chromosome damage induced by MMS in HepG2 cells[3]. |
References |
[2]. Pratsinis H, et al. Antiproliferative activity of Greek propolis. J Med Food. 2010;13(2):286-290. |
Density | 0.93g/cm3 |
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Boiling Point | 368.2ºC at 760mmHg |
Melting Point | 49-52ºC(lit.) |
Molecular Formula | C20H34O |
Molecular Weight | 290.48300 |
Flash Point | 118.2ºC |
Exact Mass | 290.26100 |
PSA | 20.23000 |
LogP | 5.50240 |
Index of Refraction | 1.5 |
Hazard Codes | Xi: Irritant; |
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Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36 |
WGK Germany | 3 |
~91% 596-85-0 |
Literature: Rogachev, Victor; Loehl, Thorsten; Markert, Thomas; Metz, Peter Arkivoc, 2012 , vol. 2012, # 3 p. 172 - 180 |
~15% 596-85-0 596-85-0 |
Literature: Organic and Biomolecular Chemistry, , vol. 9, # 7 p. 2156 - 2165 |
~% 596-85-0 |
Literature: Arkivoc, , vol. 2012, # 3 p. 172 - 180 |
~% 596-85-0 |
Literature: Arkivoc, , vol. 2012, # 3 p. 172 - 180 |
~% 596-85-0 |
Literature: Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, , vol. 26, # 1-12 p. 453 - 458 |
~% 596-85-0 |
Literature: Agricultural and Biological Chemistry, , vol. 46, # 10 p. 2477 - 2484 |
~%
Detail
|
Literature: Justus Liebigs Annalen der Chemie, , vol. 617, p. 134 Journal of the Chemical Society, , p. 2187,2189 |
Precursor 7 | |
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DownStream 6 | |