CAS 73590-06-4

Glycinamide, (2R)-2-(4-hydroxyphenyl)glycyl-(2S)-2-[(2R,4S)-4-carboxy-5,5-dimethyl-2-thiazolidinyl]glycyl-N-[(2S,5R,6R)-2-carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-6-yl]-2-(4-hydroxyphenyl)-, (2R)-

Description:

Glycinamide, with the CAS number 73590-06-4, is a complex organic compound characterized by its multi-functional structure, which includes amino acids and thiazolidine derivatives. This substance features a glycine backbone, which is an amino acid known for its simple structure and role as a building block in proteins. The presence of a 4-hydroxyphenyl group suggests potential for hydrogen bonding and interactions with biological targets, enhancing its solubility and reactivity. Additionally, the thiazolidine ring contributes to its stereochemistry and may influence its biological activity, particularly in pharmaceutical applications. Glycinamide's intricate structure indicates potential for various interactions in biological systems, making it of interest in medicinal chemistry. Its properties, such as solubility, stability, and reactivity, are influenced by the functional groups present, which can affect its behavior in different environments. Overall, glycinamide is a noteworthy compound in the realm of organic chemistry and biochemistry, with implications for drug design and development.

Formula: C₃₂H₃₈N₆O₁₀S₂

InChI: InChI=1S/C32H38N6O10S2/c1-31(2)21(29(45)46)37-26(49-31)19(35-23(41)17(33)13-5-9-15(39)10-6-13)25(43)34-18(14-7-11-16(40)12-8-14)24(42)36-20-27(44)38-22(30(47)48)32(3,4)50-28(20)38/h5-12,17-22,26,28,37,39-40H,33H2,1-4H3,(H,34,43)(H,35,41)(H,36,42)(H,45,46)(H,47,48)/t17-,18-,19-,20-,21+,22+,26-,28-/m1/s1

InChI key: InChIKey=GERXQFMVSQUXHT-BOUYBQKTSA-N

SMILES: N(C([C@H](NC([C@@H](NC([C@H](N)C1=CC=C(O)C=C1)=O)[C@@]2(N[C@@H](C(O)=O)C(C)(C)S2)[H])=O)C3=CC=C(O)C=C3)=O)[C@H]4[C@@]5(N([C@@H](C(O)=O)C(C)(C)S5)C4=O)[H]

Synonyms:

• Glycinamide, (2R)-2-(4-hydroxyphenyl)glycyl-(2S)-2-[(2R,4S)-4-carboxy-5,5-dimethyl-2-thiazolidinyl]glycyl-N-[(2S,5R,6R)-2-carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-6-yl]-2-(4-hydroxyphenyl)-, (2R)-
• Amoxicillin dimer
• Glycinamide, D-2-(4-hydroxyphenyl)glycyl-L-2-(4-carboxy-5,5-dimethyl-2-thiazolidinyl)glycyl-N-(2-carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-6-yl)-D-2-(4-hydroxyphenyl)-, [2(2R-trans),3[2S-(2α,5α,6β)]]-

Amoxicillin EP Impurity J Disodium Salt (Amoxicillin USP Related Compound J Disodium Salt, Amoxicillin Dimer Impurity Disodium Salt) (Mixture of Diastereomers)

CAS: 2088960-43-2, 73590-06-4

Formula: C₃₂H₃₈N₆O₁₀S₂·2Na

Molecular weight: 728.79 2*22.99

Ref: 4Z-A-2319

Amoxicillin related compound J

CAS: 73590-06-4

Amoxicillin related compound J is a synthetic beta-lactam antibiotic that is synthesized by the reaction of amoxicillin sodium and potassium clavulanate. It has antimicrobial activity against Gram-positive bacteria, Gram-negative bacteria, and anaerobic bacteria. This drug binds to penicillin binding proteins in bacterial cell walls, inhibiting the formation of an enzyme-inhibitor complex with bacterial cell wall synthesis. This inhibits protein synthesis and cell division. Amoxicillin related compound J has been shown to be effective for the treatment of infectious diseases caused by ampicillin-resistant Staphylococcus aureus, Streptococcus pyogenes, and Chlamydia pneumoniae.

Formula: C₃₂H₃₈N₆O₁₀S₂

Purity: 90%

Color and Shape: Powder

Molecular weight: 730.81 g/mol

Ref: 3D-FA63615

Amoxicillin dimer sodium

CAS: 73590-06-4

Please enquire for more information about Amoxicillin dimer sodium including the price, delivery time and more detailed product information at the technical inquiry form on this page

Formula: C₃₂H₃₈N₆O₁₀S₂•(Na)x

Purity: 90%

Ref: 3D-FA183830