CAS 59920-31-9
:2,5-Didesoxi-2,5-imino-D-manitol
- (2R,3R,4R,5R)-2,5-bis(hydroxymethyl)pyrrolidine-3,4-diol
- (2R,3R,4R,5R)-3,4-Dihydroxy-2,5-pyrrolidinedimethanol
- 2(R),5(R)-Bis(hydroxymethyl)-3(R),4(R)-dihydroxypyrrolidine
- 2,5-Bis(Hydroxymethyl)Pyrrolidine-3,4-Diol
- 2,5-Dideoxy-2,5-imino-<span class="text-smallcaps">D</span>-mannitol
- 2,5-Dideoxy-2,5-imino-D-mannitol
- 2,5-Pyrrolidinedimethanol, 3,4-dihydroxy-, (2R,3R,4R,5R)-
- 2,5-Pyrrolidinedimethanol, 3,4-dihydroxy-, [2R-(2α,3β,4α,5β)]-
- Dmdp
- α-Glucosidase
(2R,3R,4R,5R)-2,5-Bis(hydroxymethyl)pyrrolidine-3,4-diol
CAS:Fórmula:C6H13NO4Pureza:98%Forma y color:SolidPeso molecular:163.17172,5-Dideoxy-2,5-imino-D-mannitol
CAS:Producto controladoStability Hygroscopic
Applications A glucosidase inhibitor.
References Fellows, L.E.: Pestic. Sci., 17, 602 (1986)Fórmula:C6H13NO4Forma y color:Off White SolidPeso molecular:163.172,5-Dideoxy-2,5-imino-D-mannitol
CAS:2,5-Dideoxy-2,5-imino-D-mannitol is an iminosugar compound, which is a synthetic derivative with potent glycosidase inhibitory properties. The compound, typically synthesized through complex organic processes, acts by mimicking the transition state of natural substrates in glycosidases, thereby inhibiting their enzymatic activity. This mode of action involves binding to the active site of glycosidase enzymes, preventing the normal hydrolysis of glycosidic bonds.
Fórmula:C6H13NO4Pureza:Min. 95%Forma y color:PowderPeso molecular:163.17 g/mol2,5-Anhydro-2,5-imino-D-mannitol
CAS:Producto controladoApplications Many pyrrolidines are powerful inhibitors of glycohydrolases, enzymes responsible for cleavage of glycosidic bonds, glycoprotein processing and the gastrointestinal breakdown of dietary carbohydrates. These compounds are charged at physiological pH and are believed to associate with acidic amino acids at the active site. Inhibition of glycohydrolases could be of therapeutic value for the treatment of viral infections, cancer, diabetes, and obesity.
References Fellows, L.E., et al.: J. Chem. Brit., 287, (1987), Elbein, A.D.: Annu. Rev. Biochem., 56, 497 (1987), Fleet, G.W., et al.: J. Chem. Brit., 287, (1989) Baxter, E.W., et al.: J. Org. Chem., 59, 3175 (1994); Tyms, A.S. et al. Lancet 1025, (1987); Spearman, M.A. et al. Expt. Cell Res. 168, 116 (1987); Horii, S. et al. J. Med. Chem. 29, 1038 (1986), Minami, Y., et al.: Bioorg. Med. Chem., 16, 2734 (2008),Fórmula:C6H13NO4Forma y color:NeatPeso molecular:163.17



