The chemical substance known as "2-(2-Methyl-1-oxopropoxy)ethyl 6,8-dideoxy-7-O-methyl-6-[[[(2S)-1-methylpyrrolidin-2-yl]carbonyl]amino]-1-thio-D-erythro-α-D-galacto-octopyranoside," with the CAS number 42715-01-5, is a complex organic compound characterized by its intricate structure, which includes multiple functional groups such as an ether, amide, and thioether. This compound features a pyrrolidine moiety, indicating potential biological activity, possibly related to its interaction with biological systems. The presence of deoxy sugars suggests that it may play a role in glycosylation processes or serve as a glycoside. Its specific stereochemistry, particularly the (2S) configuration, is crucial for its biological function and interaction with enzymes or receptors. The compound's solubility, stability, and reactivity would depend on its functional groups and overall molecular structure, making it of interest in medicinal chemistry and pharmacology. Further studies would be necessary to elucidate its precise biological activities and potential applications in drug development or therapeutic interventions.

2-(2-Methyl-1-oxopropoxy)ethyl 6,8-dideoxy-7-O-methyl-6-[[[(2S)-1-methylpyrrolidin-2-yl]carbonyl]amino]-1-thio-D-erythro-α-D-galacto-octopyranoside

42715-01-5: The chemical substance known as "2-(2-Methyl-1-oxopropoxy)ethyl 6,8-dideoxy-7-O-methyl-6-[[[(2S)-1-methylpyrrolidin-2-yl]carbonyl]amino]-1-thio-D-erythro-α-D-galacto-octopyranoside," with the CAS number 42715-01-5, is a complex organic compound characterized by its intricate structure, which includes multiple functional groups such as an ether, amide, and thioether. This compound features a pyrrolidine moiety, indicating potential biological activity, possibly related to its interaction with biological systems. The presence of deoxy sugars suggests that it may play a role in glycosylation processes or serve as a glycoside. Its specific stereochemistry, particularly the (2S) configuration, is crucial for its biological function and interaction with enzymes or receptors. The compound's solubility, stability, and reactivity would depend on its functional groups and overall molecular structure, making it of interest in medicinal chemistry and pharmacology. Further studies would be necessary to elucidate its precise biological activities and potential applications in drug development or therapeutic interventions.

<p>Celesticetin B is an antibiotic primarily exhibiting antibacterial activity against Gram-positive microorganisms.</p>

CAS 42715-01-5

2-(2-Methyl-1-oxopropoxy)ethyl 6,8-dideoxy-7-O-methyl-6-[[[(2S)-1-methylpyrrolidin-2-yl]carbonyl]amino]-1-thio-D-erythro-α-D-galacto-octopyranoside

Celesticetin B

Ref: TM-TN10200