Description
Taxol C is an intermediate in taxane synthesis. Like other taxanes, this compound may also promote microtubule polymerization and prevent microtubule depolymerization, exhibiting anticancer potential, although research is limited.
| Product Unit Size | Cost | Quantity | Stock |
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Taxol C is an intermediate in taxane synthesis. Like other taxanes, this compound may also promote microtubule polymerization and prevent microtubule depolymerization, exhibiting anticancer potential, although research is limited.
| Cas No. | 153415-45-3 |
|---|---|
| Purity | ≥95% |
| Formula | C46H57NO14 |
| Formula Wt. | 847.94 |
| IUPAC Name | [(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-diacetyloxy-15-[(2R,3S)-3-(hexanoylamino)-2-hydroxy-3-phenylpropanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate |
| Synonym | Paclitaxel C, -Pentyl Analog of Paclitaxel; N-Debenzoyl-N-hexanoylpaclitaxel; Taxuyunnanine;Taxuyunnanine A;(-)-Taxuyunnanine;Paclitaxel EP Impurity C. |
| Appearance | White Powder |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
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| Info Sheet |
Slichenmyer WJ, Von Hoff DD. New natural products in cancer chemotherapy. J Clin Pharmacol. 1990 Sep;30(9):770-88. PMID: 1980498.
Shen YC, Chen YJ, Chen CY. Taxane diterpenoids from the seeds of Chinese yew Taxus chinensis. Phytochemistry. 1999 Dec;52(8):1565-9. PMID: 10647221.
Synthesis impurity
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