The chemical substance with the name "(4bS,8aS,9S,10S)-9-(Acetyloxy)-4b,5,6,7,8,8a,9,10-octahydro-3,10-dihydroxy-4b,8,8-trimethyl-2-(1-methylethyl)-1,4-phenanthrenedione" and CAS number "71539-83-8" is a complex organic compound characterized by its multi-ring structure, specifically a phenanthrene derivative. It features multiple functional groups, including hydroxyl (-OH) and acetoxy (-OCOCH3) groups, which contribute to its reactivity and potential biological activity. The presence of several methyl groups indicates a degree of hydrophobicity, while the hydroxyl groups can enhance solubility in polar solvents. This compound may exhibit interesting pharmacological properties due to its structural features, which could influence interactions with biological targets. Its stereochemistry, indicated by the specific configuration at multiple chiral centers, is crucial for its biological activity and potential applications in medicinal chemistry. Overall, this substance represents a unique class of organic compounds with potential implications in various fields, including pharmaceuticals and biochemistry.

(4bS,8aS,9S,10S)-9-(Acetyloxy)-4b,5,6,7,8,8a,9,10-octahydro-3,10-dihydroxy-4b,8,8-trimethyl-2-(1-methylethyl)-1,4-phenanthrenedione

71539-83-8: The chemical substance with the name "(4bS,8aS,9S,10S)-9-(Acetyloxy)-4b,5,6,7,8,8a,9,10-octahydro-3,10-dihydroxy-4b,8,8-trimethyl-2-(1-methylethyl)-1,4-phenanthrenedione" and CAS number "71539-83-8" is a complex organic compound characterized by its multi-ring structure, specifically a phenanthrene derivative. It features multiple functional groups, including hydroxyl (-OH) and acetoxy (-OCOCH3) groups, which contribute to its reactivity and potential biological activity. The presence of several methyl groups indicates a degree of hydrophobicity, while the hydroxyl groups can enhance solubility in polar solvents. This compound may exhibit interesting pharmacological properties due to its structural features, which could influence interactions with biological targets. Its stereochemistry, indicated by the specific configuration at multiple chiral centers, is crucial for its biological activity and potential applications in medicinal chemistry. Overall, this substance represents a unique class of organic compounds with potential implications in various fields, including pharmaceuticals and biochemistry.

<p>GZN39838, a natural Kv1.2 blocker, induces C-type inactivation without blocking the outer pore.</p>

CAS 71539-83-8

(4bS,8aS,9S,10S)-9-(Acetyloxy)-4b,5,6,7,8,8a,9,10-octahydro-3,10-dihydroxy-4b,8,8-trimethyl-2-(1-methylethyl)-1,4-phenanthrenedione

GZN39838

Ref: TM-T68814