- If we had asked any veteran grower or chemist just a decade ago if we knew all the secrets of Cannabis sativa, the answer would have been a resounding yes. After all, we isolated THC in 1964 and mapped the endocannabinoid system in the 90s.
- However, 2025 has arrived to prove just how wrong we were with a finding that has shaken the foundations of modern cannabis botany: the discovery of cannabizetol (CBGD).
- This is not simply cannabinoid number 150 on the list. We are not talking about a minor variant that appears timidly on a chromatogram.
Cannabizetol is a "super-molecule", a compound with a chemical architecture so unique and anti-inflammatory potency so promising that it forces us to rewrite what we thought we knew about the plant. But its appearance poses an uncomfortable question, almost a detective mystery: How is it possible that, after thousands of years of medicinal use and decades of modern science, we overlooked a compound of this calibre until the year 2025? The answer is a story of prohibition and misinterpreted forensic science.
What is Cannabizetol?
To understand why cannabizetol (CBGD) is so special, imagine classic cannabinoids (like THC, CBD, or CBG) as individual Lego bricks. Until recently, we thought the plant only built with these loose pieces (monomers). Cannabizetol breaks that rule: it is a dimer.
In simple terms, cannabizetol is the result of the fusion of two molecules of cannabigerol (CBG) joined by a chemical methylene bridge that acts as an indestructible hinge. This union creates a structure much larger and more complex than that of its solitary relatives.
Let's try to explain what makes cannabizetol so fascinating from a chemical point of view. Most cannabinoids we know (THC, CBD, CBG, CBN, and the rest) are monomeric molecules. They exist independently, synthesised through well-known biochemical pathways, starting with cannabigerolic acid (CBGA), which is converted into various cannabinoids by specific enzymes.
Dimeric cannabinoids are completely different beasts. They are formed when two cannabinoid molecules, whether identical or of different types, join via a methylene bridge, creating a single new molecule with properties that neither possessed individually. It is not a mixture nor a simple chemical reaction. It is a molecular fusion that creates something with completely new biological activity.
Only four dimeric cannabinoids have been identified in cannabis: cannabizetol (the new discovery), cannabitwinol, cannabitriol, and cannabiripsol. Four, in a plant that produces more than 100 known cannabinoids. This rarity tells us something important: either these compounds form in minuscule amounts, are chemically unstable and decompose quickly, or (and we suspect this is the true answer) we simply haven't looked for them properly.
That is why the discoverers, a team of scientists from the University of Milan and the Swiss company Linnea SA, did not choose its name at random. They named it after Zethus, a character from Greek mythology and son of Zeus, known for being the inseparable twin brother of Amphion. Just as Zethus stood out for his physical strength, cannabizetol stands out for a chemical and biological robustness that its monomer "brothers" do not possess.

Unexpected Potency for the Skin
What has really excited the scientific community is not just its strange shape, but what it is capable of doing. Preliminary trials have revealed that cannabizetol possesses "remarkable" anti-inflammatory and antioxidant properties, far surpassing other similar compounds discovered previously.
In tests carried out on human keratinocytes (the main cells of our epidermis), cannabizetol demonstrated a unique ability to "put out" cellular fires. It acts by blocking the NF-κB pathway, a master switch that our cells activate when stressed or attacked. By preventing this signal, cannabizetol stopped the production of Interleukin-8 (IL-8), one of the molecules responsible for chronic inflammation in diseases such as psoriasis or dermatitis, dead in its tracks.
This finding suggests that the future of cannabis cosmetics and dermatological treatments might not lie in the famous CBD, but in this new molecular giant that, until yesterday, we didn't even know existed.
The Scar of Prohibition
Here we return to the big unknown: Why now? Why in 2025? The reality is that the global prohibition of cannabis acted as a deep freeze for science. For more than half a century, chemical research was practically paralysed.
The few scientists who could study the plant often had to work with material seized by the police: old cannabis, poorly stored in evidence lockers, degraded by heat and time. This lack of access to fresh, quality plant material created a historical bias. When chemists of the past found strange signals in their analyses (peaks that did not correspond to THC or CBD), they assumed they were artefacts: impurities caused by degradation or poor preservation.
For years, it was believed that dimers (like cannabisol, discovered in 2012) were simply chemical "dirt" produced by ageing cannabis or even contamination with formaldehyde. The 2025 study has vindicated the plant. Thanks to the total synthesis of the compound in the laboratory, researchers have proven that cannabizetol is not an error or a product of decomposition. It is a natural metabolite, a phytochemical jewel that Cannabis sativa produces deliberately, perhaps as an advanced defence against UV radiation or pests. We have taken decades to see it because, for the first time, we are looking at the plant through the lens of cutting-edge botany and not criminalistics.
Cutting-Edge Technology to Hunt the Invisible
The discovery of cannabizetol is also a triumph of modern technology. Finding a needle in a haystack is easy compared to finding a trace molecule in the complex chemical soup of cannabis. To achieve this, the Italian-Swiss team not only isolated the compound from CBG-rich varieties (chemotype IV), but used flow chemistry.
This technique, more typical of aerospace engineering than classical botany, allows chemical reactions to be carried out in microscopic tubes at high pressures and controlled temperatures. This is how they managed to synthesise enough cannabizetol to confirm its identity and test its effects, a process that would have been slow and inefficient with traditional methods. It is a brilliant strategy: by creating analytical standards in the laboratory, they provide other researchers with the tools to identify if cannabizetol exists naturally in cannabis plants and, if so, under what conditions it forms.

A New Horizon for the Grower and the Patient
The discovery of cannabizetol is not the end of the road, but the starting gun for a new era. It confirms that the plant is much more complex than we imagined and that there are probably more dimeric "siblings" waiting to be discovered. Could there be dimers formed by the union of THC and CBD? What properties would they have? The door is now open.
For the cannabis community, this underscores the importance of genetic diversity. Those CBG-rich strains that were sometimes overlooked could be the natural factories of the next dermatological revolution. As legalisation advances and science makes up for lost time, we stop seeing cannabis as a simple source of THC and see it for what it really is: a pharmacological bio-factory whose instruction manual we are only just beginning to decipher.
But cannabizetol is not just a scientific curiosity. It is proof of the opportunity cost. Every compound we discover now represents decades of delayed research, wasted medical applications, and therapeutic potential that could have helped millions of people. And here is what is truly exciting: if we are still discovering new classes of compounds now, imagine what we would discover with full research funding, open institutional access, and the scientific resources we dedicate to pharmaceutical or agricultural development.
Because cannabizetol is living proof that, even in 2025, nature still keeps its best secrets for those who have the freedom and patience to look closely.
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