| Name | manool | 
|---|---|
| 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]. | 
|---|---|
| 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 | 
|---|---|
| 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; | 
|---|---|
| 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 | 
| ~% 
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| Literature: Justus Liebigs Annalen der Chemie, , vol. 617, p. 134 Journal of the Chemical Society, , p. 2187,2189 | 
| Precursor 7 | |
|---|---|
| DownStream 6 | |