Vitafoods Insights is part of the Informa Markets Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

Hobamine: Can supplementation slow down the ageing process?

Article-Hobamine: Can supplementation slow down the ageing process?

In addition to diet, fasting, exercise, stress reduction, and sleep, hobamine has the potential to slow down the ageing process.

The ageing process exerts significant changes in the way the body’s cells function, which alters outward appearance and levels of activity. During old age, this manifests itself externally through slower functioning, decreased mobility, and reduced levels of fitness. There are many factors that can rapidly increase the ageing process of cells, including exposure to UV light, hot weather, infections, and bacteria.  

In a recent press release, Greg Macpherson, a biotechnologist, pharmacist and founder of SRW Laboratories stated, “by using the nine hallmarks of aging, or identified causes of aging, we can literally reprogram our cells to function at a much younger biological age than our current chronological age.” One nutraceutical that Macpherson states has a profound impact on slowing the ageing process is SRW’s supplement, Cel1 Stability. This is due to one of the molecules used in the formulation, hobamine (2-HOBA), which was discovered by Vanderbilt University scientists through research led by Naji Abumrad, M.D. 

Discovered in the early 2000s, hobamine is an extract from Himalayan Tartary buckwheat. In a recent interview with Macpherson and Dr. Abumrad, they described the benefits Cel1 and hobamine provide the consumer as well as its current market position. 

Benefits and risks 

According to Macpherson: “DNA damage is the primary driver of the speed at which we age. Cel1 has been designed to support healthy DNA. The formula is designed to lower the impact of oxidative stress and isolevuglandins on DNA, to support healthy telomere lengths and to support regular methylation processes to regulate gene expression.” 

Hobamine is a new class of molecule referred to as a reactive carbonyl species scavenger. A byproduct of free radical damage to cell lipids, Reactive Carbonyl Species (RCS) come in a variety of forms, the most reactive being isolevuglandins. These isolevuglandins react almost instantly with proteins, DNA, and other cellular components to form Isolevuglandin-protein/DNA adducts that are associated with pathophysiological changes to the cell. As stated by Macpherson, hobamine reacts with isolevuglandins, preventing damage to cell components. Additionally, it supports a stable immune system1,2,4 and helps fight against the effects of oxidative stress without interfering with healthy free radical signaling, a common downside of traditional antioxidants.3,5 

The benefits of consuming Cel1 are not age-dependent; however, it is designed to be taken daily over the course of a lifetime to limit the impact of chronic free radical damage to the cells, organs, and body. Apart from hobamine, Cel1’s formulation includes well-established ingredients in the natural health space such as curcumin, Astragaloside A, rutin, vitamin C, Levometholic acid, vitamin B12, zinc and selenium. Hobamine is the newcomer and has been self-affirmed GRAS. 

Hobamine is available in the USA, New Zealand, and China with plans to expand availability across Europe, South America, North America, and Asia; however, this is dependent on regional approval processes.  



1. Davies SS, May-Zhang LS, Boutaud O, Amarnath V, Kirabo A, Harrison DG. Isolevuglandins as mediators of disease and the development of dicarbonyl scavengers as pharmaceutical interventions. Pharmacol Ther. 2020;205:107418. doi:10.1016/j.pharmthera.2019.107418 

2. Davies SS, Zhang LS. Reactive Carbonyl Species Scavengers-Novel Therapeutic Approaches for Chronic Diseases. Curr Pharmacol Rep. 2017;3(2):51-67. doi:10.1007/s40495-017-0081-6 

3. Mayorov V, Uchakin P, Amarnath V, et al. Targeting of reactive isolevuglandins in mitochondrial dysfunction and inflammation. Redox Biol. 2019;26:101300. doi:10.1016/j.redox.2019.101300 

4. McMaster WG, Kirabo A, Madhur MS, Harrison DG. Inflammation, immunity, and hypertensive end-organ damage. Circ Res. 2015;116(6):1022-1033. doi:10.1161/CIRCRESAHA.116.303697 

5. Ngwenyama N, Kirabo A, Aronovitz M, et al. Isolevuglandin-Modified Cardiac Proteins Drive CD4+ T-Cell Activation in the Heart and Promote Cardiac Dysfunction [published correction appears in Circulation. 2021 Mar 23;143(12):e794]. Circulation. 2021;143(12):1242-1255. doi:10.1161/CIRCULATIONAHA.120.051889 

TAGS: Ingredients