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| Product | Description | |
|---|---|---|
| 2-Acetamido-2-deoxy-D-glucuronic acid | 2-Acetamido-2-deoxy-D-glucuronic acid, an indispensable compound in the biomedical sector, plays a pivotal role in tackling a myriad of ailments such as urinary tract infections, bacterial endocarditis, and sepsis. Efficacious in its inhibition of bacterial enzymes, it remarkably impedes their proliferation and viability. Besides, this acid showcases remarkable anti-inflammatory attributes, thereby presenting itself as a promising candidate for combating autoimmune disorders and inflammatory conditions. Synonyms: D-Glucuronic acid, 2-(acetylamino)-2-deoxy-;(2S,3S,4R,5R)-5-acetamido-2,3,4-trihydroxy-6-oxohexanoic acid; N-Acetylglucosaminuronic acid;(2S,3S,4R,5R)-5-acetamido-2,3,4-trihydroxy-6-oxo-hexanoic acid. CAS No. 34047-66-0. Molecular formula: C8H13NO7. Mole weight: 235.19. |  |
| 2-Acetamido-2-deoxy-D-glucuronic Acid | 2-Acetamido-2-deoxy-D-glucuronic Acid is used as a reagent in the synthesis of N-acetyl-D-glucosaminuronic acid-based sialylmimetics which can be used as potential sialidase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 34047-66-0. Pack Sizes: 250mg, 2.5g. Molecular Formula: C8H13NO7, Molecular Weight: 235.19. US Biological Life Sciences. |  Worldwide |
| N-Acetyl-D-mannosaminuronic acid sodium | N-Acetyl-D-mannosaminuronic acid sodium, a fundamental component of hyaluronic acid, is widely applied in biomedicine. This versatile compound exhibits remarkable potential in the management of joint pathologies, skin senescence, and tissue regeneration via its moisture-attracting properties. Moreover, it emulates antibacterial interventions, providing a potential antidote to varying microbial pathogens. Synonyms: 5-acetamido-2,3,4-trihydroxy-6-oxohexanoic acid; 2-Acetamido-2-deoxy-D-glucuronicAcid; 34047-66-0; 32452-11-2; NSC256961; SCHEMBL23933730; NSC-256961. Grades: 95%. CAS No. 32452-11-2. Molecular formula: C8H12NO7Na. Mole weight: 257.17. | |
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