Conduritol B

CAS : 25348-64-5

Ref. 3D-FC20549

Informations sur le produit

• Nom: Conduritol B
• Synonymes: (1R,2S,3S,4R)-rel-5-cyclohexene-1,2,3,4-tetrol, (1S,2R,3R,4S)-cyclohex-5-ene-1,2,3,4-tetrol, 5-Cyclohexene-1,2,3,4-tetrol, 5-Cyclohexene-1,2,3,4-tetrol, (1R,2S,3S,4R)-rel-, 5-Cyclohexene-1,2,3,4-tetrol, (1alpha,2beta,3alpha,4beta)-(+-)-, 5-Cyclohexene-1,2,3,4-tetrol, (1α,2β,3α,4β)-, 5-Cyclohexene-1,2,3,4-tetrol, trans-1,2,cis-1,3,trans-1,4-(+-)-, rel-(1R,2S,3S,4R)-5-Cyclohexene-1,2,3,4-tetrol

Description

Conduritol B is a chiral, l-quebrachitol that is chemically synthesized. Conduritol B has been shown to be an effective inhibitor of beta-glucosidase, which is an enzyme involved in the hydrolysis of glycosides and the release of sugar monomers. Conduritol B selectively inhibits beta-glucosidase by binding to its active site and blocking access to the substrate. This inhibition prevents the hydrolysis of glycosides and yields a higher concentration of sugars. Conduritol B also has demethylation activity mediated by alcohols, with hydroxyl groups as moieties. The vicinal d-mannitol ring system facilitates this process.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 146.14 g/mol
• Formule: C₆H₁₀O₄
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C6H10O4/c7-3-1-2-4(8)6(10)5(3)9/h1-10H
• Code InChI: InChIKey=LRUBQXAKGXQBHA-UHFFFAOYSA-N
• SMILES: OC1C=CC(O)C(O)C1O