CAS 81703-56-2

(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)-2-piperidinesulfonic acid

Description:

The chemical substance known as (2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)-2-piperidinesulfonic acid, with the CAS number 81703-56-2, is a sulfonic acid derivative characterized by its piperidine ring structure. This compound features multiple hydroxyl groups, which contribute to its hydrophilicity and potential for forming hydrogen bonds, enhancing its solubility in water. The stereochemistry indicated by the (2S,3R,4S,5R,6R) configuration suggests specific spatial arrangements of its substituents, which can influence its biological activity and interactions with other molecules. As a sulfonic acid, it likely exhibits acidic properties, making it useful in various biochemical applications, including as a buffer or in the synthesis of other compounds. Its structural features may also suggest potential roles in biological systems, possibly as a metabolite or a precursor in metabolic pathways. Overall, this compound's unique characteristics make it of interest in both synthetic and biological chemistry contexts.

Formula: C₆H₁₃NO₇S

InChI: InChI=1S/C6H13NO7S/c8-1-2-3(9)4(10)5(11)6(7-2)15(12,13)14/h2-11H,1H2,(H,12,13,14)/t2-,3-,4+,5-,6+/m1/s1

InChI key: InChIKey=PLICPKOWHZITQE-DVKNGEFBSA-N

SMILES: S(=O)(=O)(O)[C@@H]1N[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

Synonyms:

• 2-Piperidinesulfonic acid, 3,4,5-trihydroxy-6-(hydroxymethyl)-, (2S,3R,4S,5R,6R)-
• (2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)-2-piperidinesulfonic acid
• 2-Piperidinesulfonic acid, 3,4,5-trihydroxy-6-(hydroxymethyl)-, [2S-(2α,3β,4α,5β,6α)]-

Nojirimycin bisulfite

CAS: 81703-56-2

Nojirimycin bisulfite is a potent glycosidase inhibitor, which is a derivative of nojirimycin known for its significant impact on carbohydrate metabolism. This compound originates from microorganisms, primarily isolated from the bacterium *Streptomyces* species. The mechanism through which Nojirimycin bisulfite exerts its effects involves the inhibition of glycosidases, enzymes responsible for breaking down complex carbohydrates into simpler sugars. By interfering with these enzymes, Nojirimycin bisulfite disrupts the normal processing of carbohydrates.

Formula: C₆H₁₃NO₇S

Purity: Min. 95%

Molecular weight: 243.24 g/mol

Ref: 3D-GDA70356

Nojirimycin Bisulfite

CAS: 81703-56-2

Nojirimycin Bisulfite is a potent inhibitor of protein synthesis. It is a receptor-selective ligand that binds to the extracellular domain of the epidermal growth factor (EGF) receptor, thereby inhibiting receptor signaling. Nojirimycin Bisulfite has also been shown to inhibit ion channels and ligand-gated ion channels. Nojirimycin Bisulfite has been shown to bind to both peptides and antibodies, which makes it a useful research tool for studying protein interactions.

Formula: C₆H₁₃NO₇S

Purity: Min. 95%

Molecular weight: 243.23 g/mol

Ref: 3D-CAR-24003-V