Description
2-Debenzoyl Paclitaxel-2-(2-Methyl-2-Butenoate) is an impurity of the chemotherapy drug paclitaxel. Is also known as paclitaxel impurity A or iso-cephalomannine.
2-Debenzoyl Paclitaxel-2-(2-Methyl-2-Butenoate)
Product ID T1002
Cas No. 173101-54-7
Purity ≥95%
| Product Unit Size | Cost | Quantity | Stock |
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Product Info
| Cas No. | 173101-54-7 |
|---|---|
| Purity | ≥95% |
| Formula | C45H53NO14 |
| Formula Wt. | 831.9 |
| Chemical Name | 2-Debenzoyl Paclitaxel-2-(2-Methyl-2-Butenoate) |
| IUPAC Name | [(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-diacetyloxy-15-[(2R,3S)-3-benzamido-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] (E)-2-methylbut-2-enoate |
| Synonym | Paclitaxel 2-debenzoyl-2-(2-methyl-2-butenoate); Paclitaxel 2-debenzoyl pentenoate; iso-cephalomannine; paclitaxel impurity A |
Shipping and Storage
| Store Temp | -20°C |
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| Ship Temp | Ambient |
Downloads
| MSDS | |
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| Info Sheet |
References
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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.