CAS 149466-04-6

6,16-Epoxy-14H-anthra[2,3-d][1]benzoxocin-14-one,6,7,9,16-tetrahydro-3,11,13,15-tetrahydroxy-1,6,9,9-tetramethyl- (9CI)

Description:

6,16-Epoxy-14H-anthra[2,3-d][1]benzoxocin-14-one, 6,7,9,16-tetrahydro-3,11,13,15-tetrahydroxy-1,6,9,9-tetramethyl- (9CI) is a complex organic compound characterized by its polycyclic structure, which includes an anthraquinone core fused with a benzoxocin moiety. This compound features multiple hydroxyl groups, contributing to its potential reactivity and solubility in polar solvents. The presence of an epoxy group indicates that it may participate in various chemical reactions, including ring-opening reactions under appropriate conditions. Its tetrahydroxy and tetramethyl substitutions suggest that it may exhibit significant steric hindrance, influencing its biological activity and interactions with other molecules. The compound's intricate structure may confer unique properties, making it of interest in fields such as medicinal chemistry and materials science. Additionally, its CAS number, 149466-04-6, allows for precise identification and retrieval of information regarding its synthesis, applications, and safety data in chemical databases.

Formula: C₂₇H₂₄O₇

Synonyms:

• AntibioticBE 24566B
• Be 24566B
• L 755805
• 6,16-Epoxy-14H-anthra[2,3-d][1]benzoxocin-14-one, 6,7,9,16-tetrahydro-3,11,13,15-tetrahydroxy-1,6,9,9-tetramethyl-, (6S,16S)-

BE-24566B

CAS: 149466-04-6

Formula: C₂₇H₂₄O₇

Purity: 98.84%

Color and Shape: Green. Solid

Molecular weight: 460.0

Ref: 8R-CL0186

BE-24566B

CAS: 149466-04-6

BE-24566B, a polyketide from S. violaceusniger, inhibits various bacteria and blocks ET receptors (ETA IC50=11 μM, ETB=3.9 μM).

Formula: C₂₇H₂₄O₇

Color and Shape: Solid

Molecular weight: 460.482

Ref: TM-T38167

(-)-Anthrabenzoxocinone

CAS: 149466-04-6

(-)-Anthrabenzoxocinone is a type of polyketide compound, which is a natural product derived from microbial sources, specifically Streptomyces species. This compound is characterized by its complex aromatic structure, which is a hallmark of polyketides known for their diverse biological activities. The mode of action of (-)-anthrabenzoxocinone primarily involves the inhibition of bacterial RNA synthesis, reflecting its role as an antibiotic. Additionally, it exhibits potential antitumor activity, possibly through the inhibition of topoisomerase enzymes that are crucial for DNA replication and transcription.

Formula: C₂₇H₂₄O₇

Purity: Min. 95%

Molecular weight: 460.5 g/mol

Ref: 3D-ZFA46604