CAS 210241-65-9

(3R,4R)-1-ethyl-2-(hydroxymethyl)piperidine-3,4,5-triol hydrochloride

Description:

(3R,4R)-1-ethyl-2-(hydroxymethyl)piperidine-3,4,5-triol hydrochloride is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. The compound features multiple hydroxyl groups, specifically at the 3, 4, and 5 positions of the piperidine ring, contributing to its hydrophilicity and potential for forming hydrogen bonds. The presence of the ethyl group at the 1-position and the hydroxymethyl group at the 2-position further influence its solubility and reactivity. As a hydrochloride salt, it is typically more stable and soluble in aqueous solutions compared to its free base form. This compound may exhibit biological activity, making it of interest in medicinal chemistry and pharmacology. Its stereochemistry, indicated by the (3R,4R) configuration, suggests specific spatial arrangements that can affect its interaction with biological targets. Overall, this compound's unique structural features and functional groups make it a subject of interest for research in various chemical and pharmaceutical applications.

Formula: C₈H₁₈ClNO₄

InChI: InChI=1/C8H17NO4.ClH/c1-2-9-3-6(11)8(13)7(12)5(9)4-10;/h5-8,10-13H,2-4H2,1H3;1H/t5?,6?,7-,8-;/m1./s1

SMILES: CCN1CC([C@H]([C@@H](C1CO)O)O)O.Cl

N-Ethyldeoxynojirimycin Hydrochloride

CAS: 210241-65-9

Formula: C₈H₁₈ClNO₄

Color and Shape: Solid

Molecular weight: 227.6858

Ref: IN-DA002KNX

N-Ethyldeoxynojirimycin Hydrochloride

Controlled Product

CAS: 210241-65-9

Applications An inhibitor of HIV cytopathicity. A Moranoline derivative as thrombolytics.
References Wisselaar, H., et al.: J. Biol. Chem., 268, 2223 (1993), Andersson, U., et al.: Biochem. Pharmacol., 67, 697 (2004), Ernst, H., et al.: J. Mol. Biol., 358, 1106 (2006), Parenti, G., et al.: Molec. Ther., 15, 508 (2007),

Formula: C₈H₁₇NO₄·ClH

Color and Shape: Neat

Molecular weight: 227.69

Ref: TR-E915000

N-Ethyldeoxynojirimycin hydrochloride

CAS: 210241-65-9

N-Ethyldeoxynojirimycin hydrochloride is a mutant of the natural compound, deoxynojirimycin. The chemical structure of this compound is similar to that of the natural product and its molecular weight is 547.7 g/mol. N-Ethyldeoxynojirimycin hydrochloride has been shown to interact with the bacterial chaperone GroEL and enhance the activity of this protein. Further study has shown that this agent binds to GroEL in a manner that allows it to bind directly to ATPase domains I and II, leading to an increase in ATPase activity.

Formula: C₈H₁₇NO₄·HCl

Purity: (%) Min. 95%

Color and Shape: White Off-White Powder

Molecular weight: 227.69 g/mol

Ref: 3D-ME05155