The chemical substance with the name "(3R,4aS,5R,6R,6aR,10R,10aS,10bR)-3-ethenyl-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxododecahydro-1H-benzo[f]chromen-5-yl 4-(4-methylpiperazin-1-yl)butanoate" and CAS number "110452-75-0" is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a benzochromene core structure, which is a fused ring system that contributes to its potential biological activity. The presence of multiple hydroxyl groups indicates that it may exhibit significant polarity and potential for hydrogen bonding, which can influence its solubility and reactivity. The ethylene group suggests potential for further chemical reactivity, while the piperazine moiety may enhance its pharmacological properties, possibly contributing to its interaction with biological targets. Overall, this compound's unique structural features suggest it may have applications in medicinal chemistry, particularly in the development of therapeutic agents. However, specific biological activities and properties would require empirical investigation.

(3R,4aS,5R,6R,6aR,10R,10aS,10bR)-3-ethenyl-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxododecahydro-1H-benzo[f]chromen-5-yl 4-(4-methylpiperazin-1-yl)butanoate

110452-75-0: The chemical substance with the name "(3R,4aS,5R,6R,6aR,10R,10aS,10bR)-3-ethenyl-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxododecahydro-1H-benzo[f]chromen-5-yl 4-(4-methylpiperazin-1-yl)butanoate" and CAS number "110452-75-0" is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a benzochromene core structure, which is a fused ring system that contributes to its potential biological activity. The presence of multiple hydroxyl groups indicates that it may exhibit significant polarity and potential for hydrogen bonding, which can influence its solubility and reactivity. The ethylene group suggests potential for further chemical reactivity, while the piperazine moiety may enhance its pharmacological properties, possibly contributing to its interaction with biological targets. Overall, this compound's unique structural features suggest it may have applications in medicinal chemistry, particularly in the development of therapeutic agents. However, specific biological activities and properties would require empirical investigation.

<p>Adenylate cyclase activator; forskolin analogue</p>

L 858051

L 858051 activates adenylate cyclase. It also inhibits glucose transport in rat adipocytes.

CAS 110452-75-0

(3R,4aS,5R,6R,6aR,10R,10aS,10bR)-3-ethenyl-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxododecahydro-1H-benzo[f]chromen-5-yl 4-(4-methylpiperazin-1-yl)butanoate

L 858051

Ref: 3D-FL157044

L 858051

Ref: TM-T24365