The chemical substance with the name "(14E)-3-ethyl-7-hydroxy-2,8,10,12,16-pentamethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-9-yl 3,4,6-trideoxy-3-(dimethylamino)hexopyranoside" and CAS number "61417-47-8" is a complex organic compound characterized by its bicyclic structure and multiple functional groups. It features a dioxabicyclo framework, indicating the presence of ether linkages within its cyclic structure. The compound includes several methyl groups, contributing to its hydrophobic characteristics, and a hydroxy group, which can participate in hydrogen bonding, enhancing its solubility in polar solvents. The presence of a dimethylamino group suggests potential basicity and reactivity, which may influence its biological activity. Additionally, the trideoxyhexopyranoside moiety indicates that it is a glycoside, which may affect its interaction with biological systems. Overall, this compound's unique structural features suggest potential applications in pharmaceuticals or biochemistry, although specific biological activities would require further investigation.

(14E)-3-ethyl-7-hydroxy-2,8,10,12,16-pentamethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-9-yl 3,4,6-trideoxy-3-(dimethylamino)hexopyranoside

61417-47-8: The chemical substance with the name "(14E)-3-ethyl-7-hydroxy-2,8,10,12,16-pentamethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-9-yl 3,4,6-trideoxy-3-(dimethylamino)hexopyranoside" and CAS number "61417-47-8" is a complex organic compound characterized by its bicyclic structure and multiple functional groups. It features a dioxabicyclo framework, indicating the presence of ether linkages within its cyclic structure. The compound includes several methyl groups, contributing to its hydrophobic characteristics, and a hydroxy group, which can participate in hydrogen bonding, enhancing its solubility in polar solvents. The presence of a dimethylamino group suggests potential basicity and reactivity, which may influence its biological activity. Additionally, the trideoxyhexopyranoside moiety indicates that it is a glycoside, which may affect its interaction with biological systems. Overall, this compound's unique structural features suggest potential applications in pharmaceuticals or biochemistry, although specific biological activities would require further investigation.

<p>Juvenimicin A2 is effective against Gram-positive bacteria and certain Gram-negative bacteria.</p>

CAS 61417-47-8

(14E)-3-ethyl-7-hydroxy-2,8,10,12,16-pentamethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-9-yl 3,4,6-trideoxy-3-(dimethylamino)hexopyranoside

Juvenimicin A2

Ref: TM-TN10353