Voglibose: Overview, Properties and Synthesis from Valiolamine

General Description

Voglibose, a pharmaceutical compound derived from valiolamine, exhibits potent inhibitory activity against α-glucosidases, making it effective in addressing hyperglycemia and related disorders. It demonstrates strong anti-obesity and anti-diabetic activities, with clinical trials highlighting its efficacy in reducing postprandial blood glucose levels. Voglibose also shows promising results in lowering triglyceride levels and elevating HDL cholesterol. Compared to acarbose, it has fewer adverse effects, positioning it as a valuable therapeutic option for individuals with diabetes and metabolic disorders. Voglibose's synthesis from valiolamine involves several key steps, showcasing its complex yet meticulously orchestrated process.

Figure 1. Voglibose

Overview

Voglibose is a pharmaceutical compound that has garnered significant attention due to its wide-ranging therapeutic and pharmacological properties. Structurally, it is an N-substituted derivative of valiolamine, a branched-chain aminocyclitol, with its N-substituted moiety derived from glycerol. Voglibose exhibits potent inhibitory activity against α-glucosidases, making it effective in addressing hyperglycemia and related disorders. Notably, voglibose demonstrates strong anti-obesity and anti-diabetic activities, positioning it as a potent glucosidase inhibitor and a valuable treatment option for non-insulin-dependent diabetes mellitus (NIDDM) in several Asian countries, including Japan, China, and Korea. Comparative studies have shown voglibose to be 20-30 times more potent in inhibiting semipurified porcine small intestine disaccharides compared to acarbose, a typical α-glucosidase inhibitor. Clinical trials have further highlighted the efficacy of voglibose in reducing postprandial blood glucose concentration in both animal models and human subjects with diabetes mellitus. Additionally, voglibose treatment has resulted in a significant decline in triglyceride levels and an elevation of high-density lipoprotein (HDL) cholesterol and apolipoprotein A-1. Importantly, compared to acarbose, voglibose has demonstrated fewer adverse symptoms, showing a promising safety profile in clinical trials. In summary, voglibose's multifaceted benefits, including its potent α-glucosidase inhibition, efficacy in managing postprandial blood glucose levels, and favorable safety profile make it a valuable therapeutic option for individuals with diabetes and related metabolic disorders. ¹

Properties

Voglibose is a compound with the molecular formula C10H21NO7 and a molecular weight of 267.28. It exhibits certain physico-chemical properties, such as being easily soluble in water and acetic acid, while it is not easily soluble in methanol and ethanol and almost insoluble in ether. With a melting point of about 166°C, voglibose has a sweet taste but no smell. The 1H NMR spectra of voglibose in both hydrochloride and non-hydrochloride forms reveal its structural characteristics. One of the key properties of voglibose lies in its ability to inhibit intestinal α-glucosidases, which play a role in the digestion of disaccharides like maltose and sucrose. This inhibitory effect makes voglibose significant for the treatment of NIDDM (non-insulin-dependent diabetes mellitus). Voglibose's inhibitory effects on porcine maltase and sucrase have been found to be higher compared to other related compounds, demonstrating its potential for therapeutic applications. The introduction of a hydroxyl group into specific positions on the alkyl unit has been observed to enhance the inhibitory activities of voglibose, particularly against porcine maltase. Furthermore, voglibose has shown strong inhibitory activity against disaccharidases, displaying no α-amylase and β-D-glucosidase inhibitory activity in vitro. This strong inhibitory activity can be attributed to the similar three-dimensional positioning of voglibose's structure to that of sucrose and maltose, as evidenced by NMR spectral data and the formation of an intramolecular hydrogen bond. Given its ease of synthesis and safety of potential metabolites in the body, voglibose was selected for further biological evaluation over other N-substituted valiolamine derivatives, making it a promising candidate for the treatment of NIDDM. ²

Synthesis from Valiolamine

The synthesis of Voglibose from Valiolamine involves several key steps. Valiolamine, a compound isolated from fermentation broth, serves as the starting material for the synthesis. Five total syntheses of valiolamine have been reported, with various approaches including starting from a Diels-Alder cycloadduct, D-glucose via Ferrier rearrangement, 2,3,4,6-tetra-Obenzyl-D-glucono-1,5-lactone using an aldol reaction, (-)-quinic acid via a novel acetyl migration, and validamine/valienamine via stereoselective conversion. In one method, valiolamine is oxidatively deamined to produce valiolone 27 using oxidizing agents in alcohol at 50°C such as Di-t-butyl-1,2-benzoquinone (DBQ), nicotinic aldehyde with a base, and benzothiazole-2-aldehyde. Subsequently, hydrolysis of the imine to a ketone is achieved using oxalic acid under specific pH conditions. Following the production of valiolone, the synthesis continues by reacting valiolone with 2-amino-1,3-propanediol (serinol) in the presence of a reducing agent, Na(CN)BH3, with or without an acid catalyst (e.g., acetic acid, HCl) to yield Voglibose. This multistep process involves careful control of reaction conditions and reagents to ensure the successful transformation of valiolamine into Voglibose. Each step demands precise manipulation and understanding of chemical properties to achieve the desired product. Overall, the synthesis of Voglibose from Valiolamine is a complex yet meticulously orchestrated process that necessitates expertise in organic chemistry and an in-depth understanding of reaction mechanisms and compound transformations. ²

Reference

1. Kaku K. Efficacy of voglibose in type 2 diabetes. Expert Opin Pharmacother. 2014;15(8):1181-1190.

2. Chen X, Zheng Y, Shen Y. Voglibose (Basen, AO-128), one of the most important alpha-glucosidase inhibitors. Curr Med Chem. 2006;13(1):109-116.