CAS 168109-52-2
:Tricyclo[9.3.1.14,8]hexadeca-4,10-dien-2-one,3,6,9,14-tetrakis(acetyloxy)-12-hydroxy-1,5,16,16-tetramethyl-,(1S,3R,6S,8R,9S,10E,12S,14S)-
Description:
Tricyclo[9.3.1.14,8]hexadeca-4,10-dien-2-one,3,6,9,14-tetrakis(acetyloxy)-12-hydroxy-1,5,16,16-tetramethyl-, (1S,3R,6S,8R,9S,10E,12S,14S)- is a complex organic compound characterized by its intricate polycyclic structure and multiple functional groups. This compound features a tetracyclic framework with a conjugated diene system, which contributes to its potential reactivity and stability. The presence of multiple acetoxy groups indicates that it may exhibit significant solubility in organic solvents and could participate in various chemical reactions, such as esterification or hydrolysis. The hydroxyl group adds to its polarity, potentially influencing its biological activity and interactions with other molecules. The specific stereochemistry, denoted by the (1S,3R,6S,8R,9S,10E,12S,14S) configuration, suggests that the compound may exhibit chiral properties, which can affect its pharmacological profile. Overall, this compound's unique structural features and functional groups make it of interest in fields such as medicinal chemistry and organic synthesis.
Formula:C28H38O10
Synonyms:- Tricyclo[9.3.1.14,8]hexadeca-4,10-dien-2-one,3,6,9,14-tetrakis(acetyloxy)-12-hydroxy-1,5,16,16-tetramethyl-,[1S-(1R*,3S*,6R*,8S*,9R*,10E,12R*,14R*)]-
- Taxin B
- [(1E,3S,4R,6S,9R,11S,12S,14S)-3,9,12-triacetyloxy-14-hydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.1^{4,8}]hexadeca-1,7-dienyl] acetate
- Tricyclo[9.3.1.14,8]hexadeca-4,10-dien-2-one, 3,6,9,14-tetrakis(acetyloxy)-12-hydroxy-1,5,16,16-tetramethyl-, (1S,3R,6S,8R,9S,10E,12S,14S)-
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Found 4 products.
Taxin B
CAS:Taxin B has toxic effects.Formula:C28H38O10Purity:98%Color and Shape:SolidMolecular weight:534.6Taxin B
CAS:<p>Taxin B is a fungal metabolite, which is derived from endophytic fungi associated with plants, particularly within the Taxus species. It exerts its effects through disruption of microtubule dynamics, interfering with cell division and leading to cytotoxic effects in cancer cells. The mode of action involves binding to tubulin, thereby inhibiting microtubule assembly and destabilizing existing microtubules, crucial for mitotic spindle formation during cell division.</p>Formula:C28H38O10Purity:Min. 95%Molecular weight:534.6 g/mol




