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Review
. 2020 Jun;81(4):390-401.
doi: 10.1002/ddr.21636. Epub 2020 Jan 9.

A review of phenformin, metformin, and imeglimin

Affiliations
Review

A review of phenformin, metformin, and imeglimin

Raghunandan Yendapally et al. Drug Dev Res. 2020 Jun.

Abstract

Diabetes mellitus is a serious metabolic disorder affecting millions of people worldwide. Phenformin and metformin are biguanide antidiabetic agents that are conveniently synthesized in a single-step chemical reaction. Phenformin was once used to lower blood glucose levels, but later withdrawn from the market in several countries because it was frequently associated with lactic acidosis. Metformin is still a widely prescribed medication for the treatment of type 2 diabetes despite the introduction of several newer antidiabetic agents. Metformin is administered orally and has desirable pharmacokinetics. Incidence of metformin-induced lactic acidosis is serious but very rare. Imeglimin, a novel molecule being investigated by Poxel and Sumitomo Dainippon Pharma in Japan, is currently in clinical trials for the treatment of type 2 diabetes. Unlike metformin, imeglimin is a cyclic molecule containing a triazine ring. However, like metformin, imeglimin is also a basic small molecule. Imeglimin is synthesized from metformin as a precursor via a single step chemical reaction. Recent mechanism of action studies suggests that imeglimin improves mitochondria function, when given in combination with metformin it helps achieve better glycemic control in patients with type 2 diabetes. We herein describe and compare the current status, synthesis, physicochemical properties, pharmacokinetic parameters, mechanism of action, and preclinical/clinical studies of metformin and imeglimin.

Keywords: diabetes; imeglimin; metformin; pharmacokinetics; phenformin; physicochemical properties; therapeutics.

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References

REFERENCES

    1. Abdul-Ghani, M., & DeFronzo, R. A. (2017). Is it time to change the type 2 diabetes treatment paradigm? Yes! GLP-1 RAs should replace metformin in the type 2 diabetes algorithm. Diabetes Care, 40(8), 1121-1127. https://doi.org/10.2337/dc16-2368
    1. ADA. (2010). American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care, 1(Suppl. 1), S62-S69. https://doi.org/10.2337/dc10-S062
    1. ADA. (2019). American Diabetes Association, pharmacologic approaches to glycemic treatment: Standards of medical care in diabetes-2019. Diabetes Care, 42(Suppl. 1), S90-S102. https://doi.org/10.2337/dc19-S009
    1. Alkalay, D., Khemani, L., Wagner, W. E., & Bartlett, M. F. (1975). Pharmacokinetics of phenformin in man. Journal of Clinical Pharmacology, 15(5-6), 446-448. https://doi.org/10.1002/j.1552-4604.1975.tb02367.x
    1. Al-Khalili, L., Forsgren, M., Kannisto, K., Zierath, J. R., Lonnqvist, F., & Krook, A. (2005). Enhanced insulin-stimulated glycogen synthesis in response to insulin, metformin or rosiglitazone is associated with increased mRNA expression of GLUT4 and peroxisomal proliferator activator receptor gamma co-activator 1. Diabetologia, 48(6), 1173-1179. https://doi.org/10.1007/s00125-005-1741-3

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