The chemical substance with the name "(4S)-4,4aα,7,7aα,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 "69176-72-3" is a complex organic compound characterized by its intricate polycyclic structure, which includes multiple fused rings and functional groups. The presence of hydroxyl (-OH) groups indicates potential for hydrogen bonding, which may influence its solubility and reactivity. The compound features a unique arrangement of stereocenters, contributing to its chirality and potentially affecting its biological activity. The inclusion of sulfur atoms in the form of an epidithio group suggests that it may exhibit specific chemical properties, such as increased reactivity or unique interactions with biological targets. Overall, this compound's structural complexity and functional groups suggest potential applications in medicinal chemistry or as a bioactive agent, although specific biological activities would require further investigation.

(4S)-4,4aα,7,7aα,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

69176-72-3: The chemical substance with the name "(4S)-4,4aα,7,7aα,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 "69176-72-3" is a complex organic compound characterized by its intricate polycyclic structure, which includes multiple fused rings and functional groups. The presence of hydroxyl (-OH) groups indicates potential for hydrogen bonding, which may influence its solubility and reactivity. The compound features a unique arrangement of stereocenters, contributing to its chirality and potentially affecting its biological activity. The inclusion of sulfur atoms in the form of an epidithio group suggests that it may exhibit specific chemical properties, such as increased reactivity or unique interactions with biological targets. Overall, this compound's structural complexity and functional groups suggest potential applications in medicinal chemistry or as a bioactive agent, although specific biological activities would require further investigation.

<p>Epicorazine B 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, with an MIC of 25 μg/mL.</p>

CAS 69176-72-3

(4S)-4,4aα,7,7aα,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 B

Ref: TM-TN10003