The chemical substance known as "6-Oxabicyclo[11.3.1]heptadeca-1(17),13,15-trien-5-one, 3,4,11-trihydroxy-7-[(1Z,3R)-3-(hydroxymethyl)-1-methyl-1-penten-1-yl]-9-methoxy-12,12-dimethyl-, (3R,4S,7S,9S,11S)-" with CAS number 1784751-83-2 is a complex organic compound characterized by its bicyclic structure and multiple functional groups. It features a bicyclo[11.3.1] framework, which contributes to its unique three-dimensional shape and potential reactivity. The presence of hydroxyl groups indicates that it may exhibit hydrogen bonding capabilities, influencing its solubility and interaction with biological systems. The methoxy group suggests potential for methylation reactions, while the triene system implies the presence of conjugated double bonds, which can affect its electronic properties and reactivity. This compound's stereochemistry, denoted by the specific configurations at various chiral centers, is crucial for its biological activity and interaction with enzymes or receptors. Overall, this substance may have applications in medicinal chemistry or as a synthetic intermediate due to its intricate structure and functional diversity.

6-Oxabicyclo[11.3.1]heptadeca-1(17),13,15-trien-5-one, 3,4,11-trihydroxy-7-[(1Z,3R)-3-(hydroxymethyl)-1-methyl-1-penten-1-yl]-9-methoxy-12,12-dimethyl-, (3R,4S,7S,9S,11S)-

1784751-83-2: The chemical substance known as "6-Oxabicyclo[11.3.1]heptadeca-1(17),13,15-trien-5-one, 3,4,11-trihydroxy-7-[(1Z,3R)-3-(hydroxymethyl)-1-methyl-1-penten-1-yl]-9-methoxy-12,12-dimethyl-, (3R,4S,7S,9S,11S)-" with CAS number 1784751-83-2 is a complex organic compound characterized by its bicyclic structure and multiple functional groups. It features a bicyclo[11.3.1] framework, which contributes to its unique three-dimensional shape and potential reactivity. The presence of hydroxyl groups indicates that it may exhibit hydrogen bonding capabilities, influencing its solubility and interaction with biological systems. The methoxy group suggests potential for methylation reactions, while the triene system implies the presence of conjugated double bonds, which can affect its electronic properties and reactivity. This compound's stereochemistry, denoted by the specific configurations at various chiral centers, is crucial for its biological activity and interaction with enzymes or receptors. Overall, this substance may have applications in medicinal chemistry or as a synthetic intermediate due to its intricate structure and functional diversity.

<p>JC168 is a phenyl analog of peloruside and functions as a microtubule inhibitor with antiproliferative and anticancer properties. It enhances tubulin polymerization, thereby disrupting microtubule dynamics, making it a useful agent in the study of microtubule-associated diseases.</p>

CAS 1784751-83-2

6-Oxabicyclo[11.3.1]heptadeca-1(17),13,15-trien-5-one, 3,4,11-trihydroxy-7-[(1Z,3R)-3-(hydroxymethyl)-1-methyl-1-penten-1-yl]-9-methoxy-12,12-dimethyl-, (3R,4S,7S,9S,11S)-

JC168

Ref: TM-T204381