Description
N-Debenzoylpaclitaxel is a paclitaxel derivative that can be used as a starting material for the synthesis of other paclitaxel related compounds.
Product Unit Size | Cost | Quantity | Stock |
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N-Debenzoylpaclitaxel is a paclitaxel derivative that can be used as a starting material for the synthesis of other paclitaxel related compounds.
Cas No. | 133524-70-6 |
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Purity | ≥95% |
Formula | C40H47NO13 |
Formula Wt. | 749.80 |
Chemical Name | 3’-N-debenzoylpaclitaxel |
IUPAC Name | (2α,5β,7β,10β,13α)-4,10-bis(acetyloxy)-13-{[(2R,3S)-3-amino-2-hydroxy-3-phenylpropanoyl]oxy}-1,7-dihydroxy-9-oxo-5,20-epoxytax-11-en-2-yl benzoate |
Synonym | N-Debenzoyltaxol, 3’-N-debenzoyltaxol, 3'-debenzoylpaclitaxel, 13-O-3-Phenylisoserinoyl baccatin III, (2alpha,5beta,7beta,10beta,13alpha)-4,10-bis(acetyloxy)-13-{[(2R,3S)-3-amino-2-hydroxy-3-phenylpropanoyl]oxy}-1,7-dihydroxy-9-oxo-5,20-epoxytax-11-en-2-yl benzoate |
Appearance | White solid |
Store Temp | -20°C |
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Ship Temp | Ambient |
Info Sheet |
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Nicolaou K, Yang Z, Liu J, et al. Total synthesis of taxol. Nature. 1994 Feb 17;367(6464):630-634. PMID: 7906395.
Nicolaou K, Valiulin R. Synthesis and biological evaluation of new paclitaxel analogs and discovery of potent antitumor agents. Org Biomol Chem. 2013 Jul 7;11(25):4154-4163. PMID: 23685867.
Sanchez-Munoz R, Perez-Mata E, Almagro L, et al. A novel hydroxylation step in the taxane biosynthetic pathway: a new approach to paclitaxel production by synthetic biology. Front Bioeng Biotechnol. 2020 May 13;8::410. PMID: 32528936.
Guo B, Kai G, Jin H, et al. Taxol synthesis. African J Biotechnol. 2006 Jan 2;5(1):15-20.
Wang T, Chen Y, Zhuang W, et al. Transcriptome sequencing reveals regulatory mechanisms of taxol synthesis in Taxus wallichiana var. Mairei. Int J Genomics. 2019 May 2;2019:1596895. PMID: 31192250.
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