The chemical substance known as 4,17-Dioxabicyclo[14.1.0]heptadeca-6-ene-5,13-dione, with the CAS number 11011-06-6, is a complex organic compound characterized by its bicyclic structure and multiple functional groups. This compound features a dioxabicyclo framework, indicating the presence of two ether linkages within its cyclic structure. The presence of diketone functionalities (5,13-dione) suggests it has significant reactivity, particularly in condensation and oxidation reactions. Additionally, the molecule contains multiple methyl groups, which can influence its steric properties and solubility. The presence of sugar moieties, specifically a 6-deoxy-2,3-di-O-methyl-b-D-allopyranosyl group, indicates potential biological activity, possibly enhancing its interaction with biological systems. The stereochemistry of the compound, denoted by the specific configuration at various chiral centers, suggests that it may exhibit unique optical properties and reactivity patterns. Overall, this compound's intricate structure and functional diversity make it a subject of interest in both synthetic and medicinal chemistry.

4,17-Dioxabicyclo[14.1.0]heptadeca-6-ene-5,13-dione,2-[[(6-deoxy-2,3-di-O-methyl-b-D-allopyranosyl)oxy]methyl]-9-[[(4S,5R,6R,7S,9R)-6-hydroxy-4,9-dimethyl-2-oxo-1,3,8-trioxaspiro[4.5]dec-7-yl]oxy]-3,8,10,12-tetramethyl-,(1S,2R,3R,6E,8S,9S,10S,12R,16S)-

11011-06-6: The chemical substance known as 4,17-Dioxabicyclo[14.1.0]heptadeca-6-ene-5,13-dione, with the CAS number 11011-06-6, is a complex organic compound characterized by its bicyclic structure and multiple functional groups. This compound features a dioxabicyclo framework, indicating the presence of two ether linkages within its cyclic structure. The presence of diketone functionalities (5,13-dione) suggests it has significant reactivity, particularly in condensation and oxidation reactions. Additionally, the molecule contains multiple methyl groups, which can influence its steric properties and solubility. The presence of sugar moieties, specifically a 6-deoxy-2,3-di-O-methyl-b-D-allopyranosyl group, indicates potential biological activity, possibly enhancing its interaction with biological systems. The stereochemistry of the compound, denoted by the specific configuration at various chiral centers, suggests that it may exhibit unique optical properties and reactivity patterns. Overall, this compound's intricate structure and functional diversity make it a subject of interest in both synthetic and medicinal chemistry.

<p>Aldgamycin E is a neutral macrolide antibiotic agent from culture filtrates of Streptomyces lavendulae. Methanolysis produces methyl algarosides A &amp; B.</p>

CAS 11011-06-6

4,17-Dioxabicyclo[14.1.0]heptadeca-6-ene-5,13-dione,2-[[(6-deoxy-2,3-di-O-methyl-b-D-allopyranosyl)oxy]methyl]-9-[[(4S,5R,6R,7S,9R)-6-hydroxy-4,9-dimethyl-2-oxo-1,3,8-trioxaspiro[4.5]dec-7-yl]oxy]-3,8,10,12-tetramethyl-,(1S,2R,3R,6E,8S,9S,10S,12R,16S)-

Aldgamycin E

Ref: TM-T25038