The chemical substance known as Glycine, N-((5-((6-deoxy-beta-D-galactopyranosyl)oxy)-5,6,8,13-tetrahydro-1,6,9,14-tetrahydro-3-methyl-8,13-dioxo-11-(beta-L-xylopyranosyloxy)benzo(a)naphthacen-2-yl)carbonyl)-, (5S-trans)-, with CAS number 149598-63-0, is a complex organic compound characterized by its intricate molecular structure that includes multiple sugar moieties and a naphthacene backbone. This compound features a glycine moiety, which is an amino acid known for its role in protein synthesis and various metabolic processes. The presence of sugar units, specifically 6-deoxy-beta-D-galactopyranosyl and beta-L-xylopyranosyl, suggests potential biological activity, possibly related to glycosylation processes. The tetrahydro and dioxo groups indicate that the compound may exhibit unique chemical reactivity and stability. Its stereochemistry, denoted by (5S-trans)-, implies specific spatial arrangements that could influence its interactions in biological systems. Overall, this compound may have applications in medicinal chemistry or biochemistry, particularly in the development of glycosylated drugs or therapeutic agents.

Glycine, N-((5-((6-deoxy-beta-D-galactopyranosyl)oxy)-5,6,8,13-tetrahy dro-1,6,9,14-tetrahydro-3-methyl-8,13-dioxo-11-(beta-L-xylopyranosylox y)benzo(a)naphthacen-2-yl)carbonyl)-, (5S-trans)-

149598-63-0: The chemical substance known as Glycine, N-((5-((6-deoxy-beta-D-galactopyranosyl)oxy)-5,6,8,13-tetrahydro-1,6,9,14-tetrahydro-3-methyl-8,13-dioxo-11-(beta-L-xylopyranosyloxy)benzo(a)naphthacen-2-yl)carbonyl)-, (5S-trans)-, with CAS number 149598-63-0, is a complex organic compound characterized by its intricate molecular structure that includes multiple sugar moieties and a naphthacene backbone. This compound features a glycine moiety, which is an amino acid known for its role in protein synthesis and various metabolic processes. The presence of sugar units, specifically 6-deoxy-beta-D-galactopyranosyl and beta-L-xylopyranosyl, suggests potential biological activity, possibly related to glycosylation processes. The tetrahydro and dioxo groups indicate that the compound may exhibit unique chemical reactivity and stability. Its stereochemistry, denoted by (5S-trans)-, implies specific spatial arrangements that could influence its interactions in biological systems. Overall, this compound may have applications in medicinal chemistry or biochemistry, particularly in the development of glycosylated drugs or therapeutic agents.

Pradimicin T2 is an antibiotic with activity against filamentous fungi and yeast-like fungi.

CAS 149598-63-0

Glycine, N-((5-((6-deoxy-beta-D-galactopyranosyl)oxy)-5,6,8,13-tetrahy dro-1,6,9,14-tetrahydro-3-methyl-8,13-dioxo-11-(beta-L-xylopyranosylox y)benzo(a)naphthacen-2-yl)carbonyl)-, (5S-trans)-

Pradimicin T2

Ref: TM-TN10083