CAS 172923-77-2

1,5,11-Trioxacyclohexadeca-7,13-diene-2,6,12-trione,9,15-dihydroxy-4,10,16-trimethyl-, (4S,7E,9R,10S,13E,15R,16S)-

Description:

1,5,11-Trioxacyclohexadeca-7,13-diene-2,6,12-trione,9,15-dihydroxy-4,10,16-trimethyl-, with the CAS number 172923-77-2, is a complex organic compound characterized by its unique cyclic structure and multiple functional groups. This compound features a trioxacyclohexadecane backbone, indicating the presence of three ether linkages within a 16-membered ring. The presence of diene and trione functionalities suggests that it has conjugated double bonds and multiple carbonyl groups, which can contribute to its reactivity and potential applications in organic synthesis or materials science. The specific stereochemistry, denoted by the (4S,7E,9R,10S,13E,15R,16S) configuration, indicates the spatial arrangement of atoms, which is crucial for determining the compound's biological activity and interaction with other molecules. Additionally, the presence of hydroxyl groups implies potential for hydrogen bonding, influencing solubility and reactivity. Overall, this compound's intricate structure and functional diversity make it a subject of interest in various fields, including medicinal chemistry and materials development.

Formula: C₁₆H₂₂O₈

Synonyms:

• (+)-MacrosphelideA
• Macrosphelide A

(+)-Macrosphelide A

CAS: 172923-77-2

(+)-Macrosphelide A, from Microsphaeropsis, thwarts HL-60 cell adhesion and SKOV3 cancer growth, fights Gram-positive bacteria, not Gram-negatives or fungi.

Formula: C₁₆H₂₂O₈

Color and Shape: Solid

Molecular weight: 342.344

Ref: TM-T37552

Macrosphelide A

CAS: 172923-77-2

Formula: C₁₆H₂₂O₈

Purity: ≥ 95.0%

Color and Shape: White solid

Molecular weight: 342.34

Ref: 7W-GA1224

Macrosphelide A

Controlled Product

CAS: 172923-77-2

Formula: C₁₆H₂₂O₈

Color and Shape: Neat

Molecular weight: 342.34

Ref: TR-M107520

Macrosphelide A

CAS: 172923-77-2

Macrosphelide A is a bioactive macrocyclic lactone, which is a secondary metabolite derived from the culture of certain fungal species. It functions primarily through the disruption of cell adhesion processes, which is facilitated by its ability to interfere with the function of specific cell surface receptors. This mode of action underlies its potential as an immunosuppressive agent, where it can inhibit the activities of immune cells by altering cellular communication and adhesion.

Formula: C₁₆H₂₂O₈

Purity: Min. 95%

Molecular weight: 342.34 g/mol

Ref: 3D-XGA92377