10-Deacetylbaccatin
10-Deacetylbaccatin III | |
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(2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)- 12b-(Acetyloxy)-12-(benzoyloxy)- 1,2a,3,4,4a,6,9,10,11,12,12a,12b- dodecahydro-4,6,9,11-tetrahydroxy- 4a,8,13,13-tetramethyl-7,11-methano- 5H-cyclodeca(3,4)benz(1,2-b) oxet-5-one | |
Other names 10-Deacetylbaccatin III | |
Identifiers | |
CAS number | 32981-86-5 |
PubChem | 154272 |
ChemSpider | 135935 |
ChEBI | CHEBI:18193 |
ChEMBL | CHEMBL393912 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C29H36O10 |
Molar mass | 544.59 g/mol |
Appearance | colorless solid |
Melting point | 234 °C; 453 °F; 507 K |
Solubility in water | insoluble |
Solubility | soluble in methanol |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
Infobox references | |
10-Deacetylbaccatins are a series of closely related natural organic compounds isolated from the Pacific yew tree (Taxus brevifolia) and related species. 10-Deacetylbaccatin III is a precursor to the anti-cancer drug docetaxel (Taxotere).