2,5-Anhydro-2,5-imino-D-mannitol

CAS : 59920-31-9

Ref. TR-A648350

Informations sur le produit

• Nom: 2,5-Anhydro-2,5-imino-D-mannitol
• Synonymes: (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

Description

Applications 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),

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 163.17
• Formule: C₆H₁₃NO₄
• Couleur/Forme: Neat
• InChI: InChI=1S/C6H13NO4/c8-1-3-5(10)6(11)4(2-9)7-3/h3-11H,1-2H2/t3-,4-,5-,6-/m1/s1
• Code InChI: InChIKey=PFYHYHZGDNWFIF-KVTDHHQDSA-N
• SMILES: OC[C@H]1N[C@H](CO)[C@@H](O)[C@@H]1O