The chemical substance with the name "(3aS,8R,10S,10aS,10bS,13R,13aR)-10-hydroxy-13-methoxy-1,1-dimethyl-7-methylidenedecahydro-5a,8-methanocyclohepta[c]furo[3,4-e]chromene-5,6(7H)-dione" and CAS number "84304-91-6" is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a fused ring system that includes a chromene moiety, which is indicative of its potential biological activity. The presence of hydroxyl and methoxy groups suggests that it may exhibit polar characteristics, influencing its solubility and reactivity. The compound's structure implies potential interactions with biological systems, making it of interest in medicinal chemistry and pharmacology. Its stereochemical configuration, denoted by the specific stereocenters, may play a crucial role in determining its biological activity and mechanism of action. Overall, this compound exemplifies the diversity and complexity found in natural products and synthetic organic chemistry, highlighting the importance of structural features in influencing chemical behavior and potential applications.

Rabdosin A is a antitumor constituent of Rabdosia japonica. It is a diterpenoid from Rabdosia Japonica.

(3aS,8R,10S,10aS,10bS,13R,13aR)-10-hydroxy-13-methoxy-1,1-dimethyl-7-methylidenedecahydro-5a,8-methanocyclohepta[c]furo[3,4-e]chromene-5,6(7H)-dione

84304-91-6: The chemical substance with the name "(3aS,8R,10S,10aS,10bS,13R,13aR)-10-hydroxy-13-methoxy-1,1-dimethyl-7-methylidenedecahydro-5a,8-methanocyclohepta[c]furo[3,4-e]chromene-5,6(7H)-dione" and CAS number "84304-91-6" is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a fused ring system that includes a chromene moiety, which is indicative of its potential biological activity. The presence of hydroxyl and methoxy groups suggests that it may exhibit polar characteristics, influencing its solubility and reactivity. The compound's structure implies potential interactions with biological systems, making it of interest in medicinal chemistry and pharmacology. Its stereochemical configuration, denoted by the specific stereocenters, may play a crucial role in determining its biological activity and mechanism of action. Overall, this compound exemplifies the diversity and complexity found in natural products and synthetic organic chemistry, highlighting the importance of structural features in influencing chemical behavior and potential applications.

<p>Rabdosin A is a diterpenoid antitumor constituent from Rabdosia japonica.</p>

CAS 84304-91-6

(3aS,8R,10S,10aS,10bS,13R,13aR)-10-hydroxy-13-methoxy-1,1-dimethyl-7-methylidenedecahydro-5a,8-methanocyclohepta[c]furo[3,4-e]chromene-5,6(7H)-dione

Rabdosin A

Ref: TM-T26029