Description
This compound is a taxol derivative that may exhibit antiviral and anticancer chemotherapeutic activities.
| Product Unit Size | Cost | Quantity | Stock |
|---|
This compound is a taxol derivative that may exhibit antiviral and anticancer chemotherapeutic activities.
| Cas No. | 115437-18-8 |
|---|---|
| Purity | ≥97% |
| Formula | C35H50O10Si |
| Formula Wt. | 658.85 |
| IUPAC Name | [(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4-acetyloxy-1,12,15-trihydroxy-10,14,17,17-tetramethyl-11-oxo-9-triethylsilyloxy-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate |
| Appearance | White Powder |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Krawczyk E, Luczak M, Kniotek M, et al. Cytotoxic, antiviral (in-vitro and in-vivo), immunomodulatory activity and influence on mitotic divisions of three taxol derivatives: 10-deacetyl-baccatin III, methyl (N-benzoyl-(2'R,3'S)-3'-phenylisoserinate) and N-benzoyl-(2'R,3'S)-3'-phenylisoserine. J Pharm Pharmacol. 2005 Jun;57(6):791-7. PMID: 15969936.
Samaranayake G, Neidigh KA, Kingston DG. Modified taxols, 8. Deacylation and reacylation of baccatin III. J Nat Prod. 1993 Jun;56(6):884-98. PMID: 8102392.
NLRP3 and caspase-1 inhibitor.
BH3 mimetic; Bcl-2 and Bcl-xl inhibitor.
Inhibitor of FAK and ALK.
Proteinase subtrate.
β2-adrenergic agonist, BChE inhibitor.
HDAC6/10 inhibitor.
Ca2+ sensitizer; ATP-sensitive K+ channel activ...
Fluoroquinolone; topoisomerase IV and bacterial...
CB1 inverse agonist.
ATR inhibitor.
Naphthodianthrone found in Hypericum; dopamine ...
PKC and S6 kinase substrate.
Folate analog; thymidylate synthase inhibitor.<...
Staurosporine analog; PKC and PKA inhibitor.
Paclitaxel derivative
Prostacyclin analog
KRAS inhibitor
Inhibitor of Monoacyglycerol lipase (MAGL).
Cysteine-ITC conjugate, antioxidant.
Unlikely to reverse Alzheimer’s