10-Deacetylbaccatin
Names | |
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IUPAC name
(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 10-Deacetylbaccatine III | |
Identifiers | |
32981-86-5 | |
ChEBI | CHEBI:18193 |
ChEMBL | ChEMBL393912 |
ChemSpider | 135935 |
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Jmol-3D images | Image |
PubChem | 154272 |
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Properties | |
C29H36O10 | |
Molar mass | 544.59 g/mol |
Appearance | colorless solid |
Melting point | 234 °C (453 °F; 507 K) |
insoluble | |
Solubility | soluble in methanol |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
verify (what is: / ?) | |
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).
10-deacetylbaccatin III 10-O-acetyltransferase converts 10-Deacetylbaccatin to baccatin III. (acetyl-CoA + 10-deacetylbaccatin III CoA + baccatin III)
External links
- PubChem 6712096 - 7-Epi-10-Deacetylbaccatin III
- PubChem 9872117 - 10-Deacetylbaccatin V
- PubChem 5316348 - 10-Deacetylbaccatin VI
- PubChem 5317065 - 13-Epi-10-Deacetylbaccatin III
- PubChem 15957452 - 13-[3-(2-Naphthyl)prop-2-enoyl]-2-debenzoyl-2-(4-methoxybenzoxyl)-10-deacetylbaccatin III
- PubChem 15957458 - 10-N,N-Dimethylglycyl-13-[3-(2-Naphthyl)prop-2-enoyl]-10-deacetylbaccatin III