CAS 57672-78-3

1β－Dehydroxybaccatin IV

CAS: 57672-78-3

Formel: C₃₂H₄₄O₁₃

Reinheit: 98.0%

Molekulargewicht: 636.684

Ref: IN-DA00ELMM

1-Dehydroxybaccatin IV

CAS: 57672-78-3

1-Dehydroxybaccatin IV is a natural product from Taxus mairei.

Formel: C₃₂H₄₄O₁₃

Reinheit: 98%

Farbe und Form: Solid

Molekulargewicht: 636.691

Ref: TM-TN2530

1-Dehydroxybaccatin IV

CAS: 57672-78-3

Formel: C₃₂H₄₄O₁₃

Reinheit: 95%~99%

Molekulargewicht: 636.691

Ref: BP-SBP04214

[(1R,2R,3R,4S,7R,9S,10S,11R,12R,15S)-2,4,9,11,12-Pentaacetyloxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-1 3-en-15-yl] acetate

CAS: 57672-78-3

[(1R,2R,3R,4S,7R,9S,10S,11R,12R,15S)-2,4,9,11,12-Pentaacetyloxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-1 3-en-15-yl] acetate is a diterpene ester compound, which is derived from certain species in the Euphorbiaceae family, such as the Croton plant. It acts primarily by interfering with biological membranes and proteins, often inhibiting specific enzymes or interrupting cellular processes. The mode of action may involve binding to protein kinase C, leading to alterations in cell signaling pathways and resulting in various biological effects, including anti-inflammatory and antiproliferative activities. This compound has been of scientific interest for its potential applications in pharmacology, particularly in designing new drugs targeting inflammatory diseases and cancer. Its role in modulating cellular processes makes it a valuable candidate for biochemical research, offering insights into cellular mechanisms and potential therapeutic uses. Further studies are required to fully elucidate its mechanisms and explore its biocompatibility and efficacy in clinical settings.

Formel: C₃₂H₄₄O₁₃

Reinheit: Min. 95%

Molekulargewicht: 636.7 g/mol

Ref: 3D-HCA67278