The chemical substance known as "(5R,6R)-3-[(Carboxymethyl)sulfinyl]-7-oxo 6-[(S)-1-(sulfooxy)ethyl]-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid," with the CAS number 82138-65-6, is a complex bicyclic compound characterized by its unique structural features. It contains a bicyclo[3.2.0]heptane framework, which is notable for its fused ring system. The presence of multiple functional groups, including carboxylic acid and sulfinyl groups, contributes to its potential reactivity and solubility in polar solvents. The stereochemistry indicated by the (5R,6R) and (S) designations suggests specific spatial arrangements of atoms, which can influence the compound's biological activity and interactions. This compound may exhibit properties relevant to medicinal chemistry, particularly in the development of antibiotics or other therapeutic agents, due to its structural similarity to known bioactive molecules. Its sulfooxy and carboxymethyl substituents may enhance its solubility and bioavailability, making it a candidate for further research in pharmaceutical applications.

(5R,6R)-3-[(Carboxymethyl)sulfinyl]-7-oxo 6-[(S)-1-(sulfooxy)ethyl]-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid

82138-65-6: The chemical substance known as "(5R,6R)-3-[(Carboxymethyl)sulfinyl]-7-oxo 6-[(S)-1-(sulfooxy)ethyl]-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid," with the CAS number 82138-65-6, is a complex bicyclic compound characterized by its unique structural features. It contains a bicyclo[3.2.0]heptane framework, which is notable for its fused ring system. The presence of multiple functional groups, including carboxylic acid and sulfinyl groups, contributes to its potential reactivity and solubility in polar solvents. The stereochemistry indicated by the (5R,6R) and (S) designations suggests specific spatial arrangements of atoms, which can influence the compound's biological activity and interactions. This compound may exhibit properties relevant to medicinal chemistry, particularly in the development of antibiotics or other therapeutic agents, due to its structural similarity to known bioactive molecules. Its sulfooxy and carboxymethyl substituents may enhance its solubility and bioavailability, making it a candidate for further research in pharmaceutical applications.

<p>Pluracidomycin B, a carbapenem antibiotic, exhibits activity against both Gram-positive and Gram-negative bacteria and also functions as an inhibitor of β-lactamase enzymes.</p>

CAS 82138-65-6

(5R,6R)-3-[(Carboxymethyl)sulfinyl]-7-oxo 6-[(S)-1-(sulfooxy)ethyl]-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid

Pluracidomycin B

Ref: TM-TN10485