The chemical substance with the name "(4S)-4,4aα,7,7aβ,11,11aα,14,14aβ-Octahydro-4α,11α-dihydroxy-8H,13H-6aβ,13aβ-epidithio-1H,6H-pyrazino[1,2-a:4,5-a']diindole-1,6,8,13-tetrone" and CAS number "62256-05-7" is a complex organic compound characterized by its multi-ring structure and multiple functional groups. It features a pyrazino-diindole framework, which is indicative of its potential biological activity. The presence of hydroxyl groups suggests it may exhibit hydrogen-bonding capabilities, influencing its solubility and reactivity. The compound's stereochemistry, denoted by the specific configuration at various chiral centers, may play a crucial role in its interaction with biological targets. Additionally, the presence of sulfur atoms in the form of an epidithio group could impart unique electronic properties and reactivity. Such compounds are often of interest in medicinal chemistry due to their potential pharmacological properties, including antimicrobial or anticancer activities. However, detailed studies would be necessary to elucidate its specific biological effects and applications.

(4S)-4,4aα,7,7aβ,11,11aα,14,14aβ-Octahydro-4α,11α-dihydroxy-8H,13H-6aβ,13aβ-epidithio-1H,6H-pyrazino[1,2-a:4,5-a']diindole-1,6,8,13-tetrone

62256-05-7: The chemical substance with the name "(4S)-4,4aα,7,7aβ,11,11aα,14,14aβ-Octahydro-4α,11α-dihydroxy-8H,13H-6aβ,13aβ-epidithio-1H,6H-pyrazino[1,2-a:4,5-a']diindole-1,6,8,13-tetrone" and CAS number "62256-05-7" is a complex organic compound characterized by its multi-ring structure and multiple functional groups. It features a pyrazino-diindole framework, which is indicative of its potential biological activity. The presence of hydroxyl groups suggests it may exhibit hydrogen-bonding capabilities, influencing its solubility and reactivity. The compound's stereochemistry, denoted by the specific configuration at various chiral centers, may play a crucial role in its interaction with biological targets. Additionally, the presence of sulfur atoms in the form of an epidithio group could impart unique electronic properties and reactivity. Such compounds are often of interest in medicinal chemistry due to their potential pharmacological properties, including antimicrobial or anticancer activities. However, detailed studies would be necessary to elucidate its specific biological effects and applications.

<p>Epicorazine A exhibits activity against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE), with a minimum inhibitory concentration (MIC) of 12.5-25 μg/mL. It is also effective against Candida albicans, showing an MIC of 25 μg/mL.</p>

CAS 62256-05-7

(4S)-4,4aα,7,7aβ,11,11aα,14,14aβ-Octahydro-4α,11α-dihydroxy-8H,13H-6aβ,13aβ-epidithio-1H,6H-pyrazino[1,2-a:4,5-a']diindole-1,6,8,13-tetrone

Epicorazine A

Ref: TM-TN9989