CAS 210174-73-5

3,4,5-Piperidinetriol,2-methyl-, hydrochloride (1:1), (2S,3R,4S,5R)-

Description:

3,4,5-Piperidinetriol, 2-methyl-, hydrochloride (1:1), with the CAS number 210174-73-5, is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. This compound features three hydroxyl (-OH) groups at the 3, 4, and 5 positions of the piperidine ring, contributing to its hydrophilicity and potential for hydrogen bonding. The presence of a methyl group at the 2-position adds to its steric properties. As a hydrochloride salt, it is typically more soluble in water than its free base form, enhancing its utility in various applications, including pharmaceuticals. The specific stereochemistry indicated by the (2S,3R,4S,5R) configuration suggests that the compound has defined spatial arrangements, which can influence its biological activity and interactions. Overall, this compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug development.

Formula: C₆H₁₃NO₃・ClH

Synonyms:

• 3,4,5-Piperidinetriol,2-methyl-, hydrochloride, (2S,3R,4S,5R)- (9CI)

Deoxyfuconojirimycin hydrochloride

CAS: 210174-73-5

Formula: C₆H₁₄ClNO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 183.6333

Ref: IN-DA00C32U

(2S,3R,4S,5R)-2-Methyl-3,4,5-trihydroxypiperidine hydrochloride

CAS: 210174-73-5

(2S,3R,4S,5R)-2-Methyl-3,4,5-trihydroxypiperidine hydrochloride

Formula: C₆H₁₃NO₃·ClH

Purity: ≥95%

Color and Shape: light brown solid

Molecular weight: 183.63g/mol

Ref: 54-OR3600T

Deoxyfuconojirimycin, Hydrochloride

Controlled Product

CAS: 210174-73-5

Applications A powerful and specific inhibitor of several alpha-L-fucosidases.
References Winchester, B., et al.: Biochem. J., 265, 277 (1990)

Formula: C₆H₁₃NO₃·ClH

Color and Shape: Neat

Molecular weight: 183.63

Ref: TR-D236000

1-Deoxyfuconojirimycin HCl

CAS: 210174-73-5

Specific, potent and competitive inhibitor of α-L-fucosidase with Ki of 10 nM. In human breast cancer cells, it causes increase of fucosylation on cell surface molecules such as Lewis X antigen (CD15) and CD44 glycoprotein. The 1-deoxyfuconojirimycin treatment increases invasiveness of cancer cells.

Formula: C₆H₁₃NO₃·HCl

Purity: Min. 95%

Color and Shape: Off-White Powder

Molecular weight: 183.63 g/mol

Ref: 3D-MD06117

Deoxyfuconojirimycin hydrochloride

CAS: 210174-73-5

Deoxyfuconojirimycin hydrochloride acts as a specific competitive inhibitor targeting human liver α-L-fucosidase.

Formula: C₆H₁₄ClNO₃

Color and Shape: Solid

Molecular weight: 183.63

Ref: TM-T72106