10-Deacetylbaccatin III structure 
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        Common Name | 10-Deacetylbaccatin III | ||
|---|---|---|---|---|
| CAS Number | 32981-86-5 | Molecular Weight | 544.590 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 716.8±60.0 °C at 760 mmHg | |
| Molecular Formula | C29H36O10 | Melting Point | 231-236 °C | |
| MSDS | Chinese USA | Flash Point | 233.5±26.4 °C | |
            Use of 10-Deacetylbaccatin III10-Deacetylbaccatin-III is an intermediate for taxol analog preparations. IC50 value:Target: Taxols have exhibit antitumor agents. Several of these taxols can be synthesized from 10- Deacetylbaccatin-III. 10-Deacetylbaccine III is the fifth intermediate of paclitaxel biosynthesis. The biosynthetic pathway consists of approximately 20 enzymatic steps but is not fully elucidated. 10-Deacetylbaccine III is an antineoplastic agent and an anti-cancer intermediate.  | 
    
| Name | 10-deacetylbaccatin III | 
|---|---|
| Synonym | More Synonyms | 
| Description | 10-Deacetylbaccatin-III is an intermediate for taxol analog preparations. IC50 value:Target: Taxols have exhibit antitumor agents. Several of these taxols can be synthesized from 10- Deacetylbaccatin-III. 10-Deacetylbaccine III is the fifth intermediate of paclitaxel biosynthesis. The biosynthetic pathway consists of approximately 20 enzymatic steps but is not fully elucidated. 10-Deacetylbaccine III is an antineoplastic agent and an anti-cancer intermediate. | 
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| Related Catalog | |
| References | 
| Density | 1.4±0.1 g/cm3 | 
|---|---|
| Boiling Point | 716.8±60.0 °C at 760 mmHg | 
| Melting Point | 231-236 °C | 
| Molecular Formula | C29H36O10 | 
| Molecular Weight | 544.590 | 
| Flash Point | 233.5±26.4 °C | 
| Exact Mass | 544.230835 | 
| PSA | 159.82000 | 
| LogP | 3.51 | 
| Vapour Pressure | 0.0±2.4 mmHg at 25°C | 
| Index of Refraction | 1.624 | 
| Water Solubility | INSOLUBLE | 
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter | 
|---|---|
| Hazard Codes | T:Toxic | 
| Risk Phrases | R23/24/25 | 
| Safety Phrases | S45-S38-S36/37/39-S28A | 
| RIDADR | 1544 | 
| WGK Germany | 3 | 
| Packaging Group | III | 
| Hazard Class | 6.1(b) | 
| Precursor 7 | |
|---|---|
| DownStream 10 | |
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                                    Disposition of [G-(3)H]paclitaxel and cremophor EL in a patient with severely impaired renal function.
                                    
                                    
                                     Drug Metab. Dispos. 27 , 1300, (1999) In the present work, we studied the pharmacokinetics and metabolic disposition of [G-(3)H]paclitaxel in a female patient with recurrent ovarian cancer and severe renal impairment (creatinine clearance...  | 
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                                    Molecular mechanisms of patupilone resistance.
                                    
                                    
                                     Cancer Res. 68 , 10197-10204, (2008) Patupilone is an epothilone in advanced clinical development that has shown promising efficacy in heavily pretreated patients. This study aimed at characterizing the mechanisms of patupilone activity ...  | 
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                                    Taxol biosynthesis: Molecular cloning of a benzoyl- CoA:taxane 2-O-benzoyltransferase cDNA from Taxus and functional expression in Escherichia coli Kevin Walker and Rodney Croteau PNAS
                                    
                                    
                                     Proc. 10th Am. Peptide Symp 97 , 13591-13596, (2000) 
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| 10-Dab | 
| 10-DAB (10-Deacetylbaccatin) | 
| MFCD00132913 | 
| EINECS 418-680-6 | 
| (2α,5β,7β,10α,13α)-4-Acetoxy-1,7,10,13-tetrahydroxy-9-oxo-5,20-epoxytax-11-en-2-yl benzoate | 
| (2α,5β,7β,10β,13α)-4-(acetyloxy)-1,7,10,13-tetrahydroxy-9-oxo-5,20-epoxytax-11-en-2-yl benzoate | 
| 10-Deacetylbaccatine | 
| 10-deacetylbaccatin11 | 
| 10-DAB-III | 
| 10DBA III | 
| 10-Deacetyl | 
| 10-DEACETYLBACCATIN | 
| 10-Deacetylbaccatin-III | 
| 10-desacetylbaccatin III | 
| 10-Deacetylbaccatin III | 
| DESACETYLBACCATINE | 
| Docetaxel impurity E | 
| 7,11-Methano-5H-cyclodeca[3,4]benz[1,2-b]oxet-5-one, 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-, (2aR,4S,4aS,6S,9S,11S,12S,12aR,12bS)- | 
| (2α,5β,7β,10β,13α)-4-Acetoxy-1,7,10,13-tetrahydroxy-9-oxo-5,20-epoxytax-11-en-2-yl benzoate | 
| 7,11-Methano-5H-cyclodeca[3,4]benz[1,2-b]oxet-5-one, 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-, (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)- |