197013-82-4

Basic information

• Product Name: 7-α-glucosyloxyacetyl paclitaxel
• Synonyms: 7-α-glucosyloxyacetyl paclitaxel
• CAS NO: 197013-82-4
• Molecular Weight: 1074.1
• Mol File: 197013-82-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7-α-glucosyloxyacetyl paclitaxel(CAS DataBase Reference)
• NIST Chemistry Reference: 7-α-glucosyloxyacetyl paclitaxel(197013-82-4)
• EPA Substance Registry System: 7-α-glucosyloxyacetyl paclitaxel(197013-82-4)

Safety Data

• Hazardous Substances Data: 197013-82-4(Hazardous Substances Data)

Upstream product

• 195455-06-2 2,3,4,6-tetra-O-benzylglucosyloxyacetic acid 

Downstream Products

• 32981-86-5 10-deacetylbaccatin III 
• 78432-77-6 10-deacetylpaclitaxel 
• 33069-62-4 taxol 
• 105454-04-4 7-epipaclitaxel 
• 27548-93-2 baccatin III 
• 71629-92-0 10-deacetyl-7-epi-baccatin III 
• 31077-81-3 7-epi-baccatine III 

Relevant articles and documents

Biological degradation of taxol by action of cultured cells on 7-acetyltaxol-2″-yl glucoside

Biodegradation pathways of taxol in cultured cells of Synechocystis sp. PCC 6803, Synechococcus sp. PCC 7942, Marchantia polymorpha, Nicotiana tabacum, and Glycine max were investigated using a water-soluble taxol derivative, 7-ace-tyltaxol-2″-yl glucoside, as the substrate. Although cyanobacteria, Synechocystis sp. PCC 6803 and Synechococcus sp. PCC 7942, and a lower plant, M. polymorpha, catalyzed the epimerization at 7-position of taxol skeleton, no epimerization occurred with higher plants, N. tabacum and G. max. On the other hand, Synechocystis sp. PCC 6803, Synechococcus sp. PCC 7942, M. polymorpha, and N. tabacum catalyzed hydrolysis at 13-position of taxol to give baccatin III and 10-deacetyl baccatin III. Both cyanobacteria cells also deacetylated 7-epi-baccatin III at its 10-position. M. polymorpha and G. max deacetylated at 10-position of taxol. Copyright