10-Deacetylbaccatin III structure
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Common Name | 10-Deacetylbaccatin III | ||
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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 |
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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 |
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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 |
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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 | |
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DownStream 10 | |
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)- |