CAS 87139-37-5

(5R,6R)-3-{(R)-[2-(acetylamino)ethyl]sulfinyl}-7-oxo-6-[2-(sulfooxy)propan-2-yl]-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid

Description:

The chemical substance with the name "(5R,6R)-3-{(R)-[2-(acetylamino)ethyl]sulfinyl}-7-oxo-6-[2-(sulfooxy)propan-2-yl]-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid" and CAS number "87139-37-5" is a complex organic compound characterized by its bicyclic structure, which includes a nitrogen atom in the ring, indicating it is a bicyclic amine. The presence of functional groups such as sulfinyl, acetylamino, and sulfoxy suggests that this compound may exhibit significant biological activity, potentially as an antibiotic or in other therapeutic applications. The stereochemistry indicated by the (5R,6R) and (R) designations implies specific spatial arrangements of atoms, which can influence the compound's reactivity and interaction with biological targets. Additionally, the carboxylic acid group contributes to its acidity and solubility in polar solvents. Overall, this compound's unique structure and functional groups suggest potential utility in medicinal chemistry, although specific biological activities would require further investigation.

Formula: C₁₄H₂₀N₂O₉S₂

InChI: InChI=1/C14H20N2O9S2/c1-7(17)15-4-5-26(21)9-6-8-10(14(2,3)25-27(22,23)24)12(18)16(8)11(9)13(19)20/h8,10H,4-6H2,1-3H3,(H,15,17)(H,19,20)(H,22,23,24)/t8-,10+,26-/m1/s1

Carpetimycin D

CAS: 87139-37-5

Carpetimycin D exhibits potent activity against both Gram-positive and Gram-negative bacteria, including those that produce β-lactamase. Additionally, Carpetimycin D strongly inhibits β-lactamase.

Formula: C₁₄H₂₀N₂O₉S₂

Color and Shape: Solid

Molecular weight: 424.447

Ref: TM-TN10715