Messagenin–based Chalcones: Synthesis, Modification and Perspectives of Antidiabetic Potency

Author:

Galimova Zarema1ORCID,Khusnutdinova Elmira1ORCID,Smirnova Irina1ORCID,Poptsov Alexander1ORCID,Spirikhin Leonid1ORCID,Gabdrakhmanova Svetlana1ORCID,Makara Nina1ORCID,Nguyen Thi Thu Ha2ORCID,Thi Tu Anh Le2ORCID,Thanh Tra Nguyen2ORCID,Thi Cham Ba2ORCID,Kazakova Oxana1ORCID

Affiliation:

1. Ufa Institute of Chemistry, UFRC RAS 71, pr. Oktyabrya Ufa 450054 Russian Federation

2. Institute of Chemistry Vietnamese Academy of Science and Technology 18 Hoang Quoc Viet Str., Cau Giay Dist. Hanoi Vietnam

Abstract

AbstractA series of messagenin–based chalcones has been synthesized by Claisen‐Schmidt condensation and screened for in vitro α‐glucosidase inhibitory activity. The heterocyclization of 30‐(3‐pyridinylidene)‐messagenin led to syn/anti N‐acetyl‐pyrazoles in a ratio of 2 : 1 that were isolated by HPLC. Messagenin chalcones act as α‐glucosidase inhibitors with IC50 range from 0.055 to 80.70 μM. The lead nanomolar level α‐glucosidase inhibitor 30‐(4‐hydroxymethyl‐benzylidene)‐messagenin 10 was studied for antihyperglycemic activity on streptozotocin–induced diabetic animal models using in vivo mechanism–based assays. In a rat model of STZ‐induced T1DM, compound 10 (20 mg/kg, orally) exhibited antihyperlipidemic activity, reducing AIP (p>0.05) and CRI (p<0.05) compared to control. Compound 10 improved diabetic nephropathy, locomotor activity in rats, and reduced diabetes–related mortality.

Publisher

Wiley

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