The chemical substance with the name "(2S,3S,4aR,12bR)-2,3,4a,8,12b-pentahydroxy-3-methyl-3,4,4a,5,6,12b-hexahydrotetraphene-1,7,12(2H)-trione" and CAS number "86413-77-6" is a complex organic compound characterized by multiple hydroxyl groups and a unique polycyclic structure. This compound features a stereochemistry denoted by specific configurations at several chiral centers, which significantly influence its chemical behavior and potential biological activity. The presence of hydroxyl groups suggests that it may exhibit strong hydrogen bonding capabilities, affecting its solubility and reactivity. Additionally, the polycyclic framework may contribute to its stability and potential interactions with other molecules. Such compounds are often of interest in medicinal chemistry and natural product synthesis due to their structural complexity and potential pharmacological properties. The specific arrangement of functional groups and stereochemistry can lead to diverse applications, including use as intermediates in organic synthesis or as bioactive agents in pharmaceutical research.

(2S,3S,4aR,12bR)-2,3,4a,8,12b-pentahydroxy-3-methyl-3,4,4a,5,6,12b-hexahydrotetraphene-1,7,12(2H)-trione

86413-77-6: The chemical substance with the name "(2S,3S,4aR,12bR)-2,3,4a,8,12b-pentahydroxy-3-methyl-3,4,4a,5,6,12b-hexahydrotetraphene-1,7,12(2H)-trione" and CAS number "86413-77-6" is a complex organic compound characterized by multiple hydroxyl groups and a unique polycyclic structure. This compound features a stereochemistry denoted by specific configurations at several chiral centers, which significantly influence its chemical behavior and potential biological activity. The presence of hydroxyl groups suggests that it may exhibit strong hydrogen bonding capabilities, affecting its solubility and reactivity. Additionally, the polycyclic framework may contribute to its stability and potential interactions with other molecules. Such compounds are often of interest in medicinal chemistry and natural product synthesis due to their structural complexity and potential pharmacological properties. The specific arrangement of functional groups and stereochemistry can lead to diverse applications, including use as intermediates in organic synthesis or as bioactive agents in pharmaceutical research.

<p>Sakyomicin D is a benzoquinone antibiotic with activity against Gram-positive bacteria.</p>

CAS 86413-77-6

(2S,3S,4aR,12bR)-2,3,4a,8,12b-pentahydroxy-3-methyl-3,4,4a,5,6,12b-hexahydrotetraphene-1,7,12(2H)-trione

Sakyomicin D

Ref: TM-TN9982