α-Glycosidase-IN-1 

α-Glycosidase-IN-1 (compound MZ7) is a potent α-GLY (α-Glycosidase) inhibitor, with an IC₅₀ of 44.72 nM and a K_I of 41.74 nM. α-Glycosidase-IN-1 also shows inhibition profile against human carbonic anhydrase isoenzymes I and II (hCA I and hCA II), and acetylcholinesterase (AChE), with IC₅₀ values of 104.87, 100.04, and 654.87 nM, respectively. α-Glycosidase-IN-1 can be used for the research of many diseases such as diabetes, Alzheimer’s disease, heart failure, ulcer, and epilepsy^[1].

IC₅₀: 44.72 ± 0.9964 nM (α-GLY), 100.04 ± 0.9688 nM (hCA II), 104.87 ± 0.9920 nM (hCA I), 654.87 ± 0.9383 nM (AChE); K_I: 41.74 ± 8.08 nM (α-GLY), 114.78 ± 20.33 nM (hCA I), 114.78 ± 9.54 nM (hCA II), 597.33 ± 100.56 nM (AChE)^[1]

557.56

C₂₁H₁₉N₉O₆S₂

2428389-66-4

O=[N+](C1=CC(NC2=NC(NC3=CC=C(S(=O)(N)=O)C=C3)=NC(NC4=CC=C(S(=O)(N)=O)C=C4)=N2)=CC=C1)[O-]

Room temperature in continental US; may vary elsewhere.

Please store the product under the recommended conditions in the Certificate of Analysis.

• [1]. Lolak N, et al. Synthesis, characterization, inhibition effects, and molecular docking studies as acetylcholinesterase, α-glycosidase, and carbonic anhydrase inhibitors of novel benzenesulfonamides incorporating 1,3,5-triazine structural motifs. Bioorg Ch  [Content Brief]