CAS 123970-01-4

7-Undeculo-7,3-pyranoside-1,4-furanuronicacid, 1-(6-amino-9H-purin-9-yl)-6,10-anhydro-1,5-dideoxy- (9CI)

Description:

7-Undeculo-7,3-pyranoside-1,4-furanuronic acid, 1-(6-amino-9H-purin-9-yl)-6,10-anhydro-1,5-dideoxy- (9CI), identified by CAS number 123970-01-4, is a complex organic compound that features a unique combination of a furanuronic acid structure and a purine derivative. This compound is characterized by its glycosidic linkage, which connects a sugar moiety to a purine base, contributing to its potential biological activity. The presence of the undecyloxy group suggests that it may exhibit amphiphilic properties, which can influence its solubility and interaction with biological membranes. The compound's structural features may also impart specific reactivity and stability under various conditions. Its potential applications could span fields such as biochemistry and pharmacology, particularly in the development of nucleoside analogs or as a tool in molecular biology. However, detailed studies on its biological activity, toxicity, and pharmacokinetics would be necessary to fully understand its characteristics and potential uses.

Formula: C₁₆H₁₉N₅O₉

Synonyms:

• 7-Undeculo-7,3-pyranoside-1,4-furanuronicacid, 1-(6-amino-9H-purin-9-yl)-6,10-anhydro-1,5-dideoxy- (9CI)
• D-arabino-α-L-ido-7-Undeculo-7,3-pyranoside-1,4-furanuronic acid, 1-(6-amino-9H-purin-9-yl)-6,10-anhydro-1,5-dideoxy-, (7S)-

Aureonuclemycin

CAS: 123970-01-4

Aureonuclemycin, isolated from Staphylococcus aureus to obtain its biosynthetic gene cluster, exists in two forms: Type A and Type B. Aureonuclemycin A is a nucleoside antibiotic structurally similar to herbicides and contains adenine, while Aureonuclemycin B contains 5′-deoxyadenosine and exhibits antibacterial activity. Aureonuclemycin can be used in research on bacterial leaf blight in rice, citrus canker, and bacterial leaf spot in rice. [1] [2]

Formula: C₁₆H₁₉N₅O₉

Color and Shape: Solid

Molecular weight: 425.35

Ref: TM-TN7636