Cannabichromene (CBC): Understanding its Biosynthesis, Pharmacology, and Effects

The compound cannabichromene (CBC), also known as cannabichrome, cannanbichromene, pentylcannabichromene, or cannabinochromene, has been shown in vitro to have anti-inflammatory characteristics. These features may, in theory, be a factor in the analgesic effects of cannabis. Among the hundreds of cannabinoids included in the Cannabis plant, it is a phytocannabinoid. The other naturally occurring cannabinoids, such as tetrahydrocannabinol (THC), tetrahydrocannabivarin (THCV), cannabidiol (CBD), and cannabinol (CBN), among others, share structural similarities with it. 

Cannabis contains cannabinols and CBC. A nonpsychotropic phytocannabinoid with anti-inflammatory and antibacterial qualities, CBC has been demonstrated to be a strong TRPA1 agonist. Preclinical research (unpublished) showed that CBC and CBG both have antitumor effects on cells that cause stomach cancer.

Earlier Researches

In 1966, two groups reported isolating cannabichromene (CBC) by either a benzene percolation of hemp or a hexane/florisil extraction method from hashish (Claussen, Von Spulak, & Korte, 1966; Gaoni & Mechoulam, 1966). This cannabinoid makes up approximately 0.3% of the components of cannabis that has been seized. It is noteworthy that there are commercial and medical cannabis preparations and varieties with much higher content available (de Meijer & Limited, 2011; Mehmedic et al., 2010; Meijer, Hammond, & Micheler, 2008; Swift, Wong, Li, Arnold, & McGregor, 2013). 

Biosynthesis of CBC

Cannabichromene (CBC) is synthesized within the cannabis plant through a complex biosynthetic pathway. It begins with the enzymatic conversion of cannabigerolic acid (CBGA), a precursor molecule abundant in cannabis, into cannabichromenic acid (CBCA). This acidic form of CBC is the initial stage of its biosynthesis and serves as the precursor for the active form of the cannabinoid. Through decarboxylation, which can occur naturally over time or through external factors such as heat, CBCA is converted into CBC, the neutral and pharmacologically active form of the cannabinoid.

Enzymatic Pathways

Cannabichromene (CBC) biosynthesis within the cannabis plant involves a series of enzymatic reactions orchestrated by specialized enzymes encoded by specific genes. These enzymes facilitate the conversion of precursor molecules, such as cannabigerolic acid (CBGA), into CBCA, the acidic precursor of CBC. Key enzymes involved in this process include geranyl pyrophosphate (GPP) synthase, olivetolic acid cyclase (OAC), and cannabichromenic acid synthase (CBCAS). GPP synthase catalyzes the formation of GPP, a precursor molecule for cannabinoids, while OAC and CBCAS are responsible for the cyclization and prenylation of CBGA to form CBCA. Subsequent decarboxylation of CBCA yields CBC, the neutral and pharmacologically active form of the cannabinoid.

Environmental Influences

The biosynthesis of CBC is influenced by various environmental factors, including light, temperature, humidity, and nutrient availability. Light intensity and spectrum play a crucial role in regulating the expression of genes involved in cannabinoid biosynthesis, with certain wavelengths of light known to enhance cannabinoid production. Temperature fluctuations and humidity levels also impact enzyme activity and metabolic processes within the plant, affecting the rate and efficiency of CBC biosynthesis. Additionally, nutrient availability, particularly nitrogen, phosphorus, and potassium, influences plant growth and cannabinoid production, with optimal nutrient levels essential for maximizing CBC yields. By understanding the intricate interplay between genetic, biochemical, and environmental factors, researchers can optimize cultivation techniques and breeding strategies to enhance CBC production and harness its therapeutic potential.

Pharmacology of CBC

CBC interacts with the endocannabinoid system (ECS), a network of receptors, endocannabinoids, and enzymes that regulate various physiological processes in the human body. Unlike tetrahydrocannabinol (THC), CBC does not bind directly to cannabinoid receptors CB1 and CB2. Instead, it modulates the ECS by inhibiting the reuptake of the endocannabinoid anandamide (AEA), thereby prolonging its presence in the body and enhancing its effects. Additionally, CBC interacts with other receptors and molecular targets, including transient receptor potential (TRP) channels and non-cannabinoid receptors, contributing to its diverse pharmacological effects.

Interaction with Endocannabinoid System (ECS)

Cannabichromene (CBC) exerts its pharmacological effects primarily through interaction with the endocannabinoid system (ECS), a complex network of receptors, endogenous ligands, and enzymes involved in regulating various physiological processes. Unlike THC, which predominantly binds to cannabinoid receptor type 1 (CB1) and cannabinoid receptor type 2 (CB2), CBC exhibits low affinity for these receptors. Instead, CBC is believed to modulate the ECS indirectly by inhibiting the enzymatic degradation of endocannabinoids, such as anandamide and 2-arachidonoylglycerol (2-AG). By inhibiting the activity of enzymes like fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL), which hydrolyze endocannabinoids, CBC enhances endocannabinoid tone and prolongs their activity, leading to downstream effects on neurotransmission, inflammation, and pain perception.

Pharmacokinetics and Metabolism

Following administration, CBC undergoes absorption, distribution, metabolism, and elimination within the body, collectively referred to as pharmacokinetics. Absorption of CBC occurs primarily through oral and inhalation routes, with peak plasma concentrations achieved within hours of administration. Once absorbed, CBC is distributed throughout various tissues and organs, where it interacts with target receptors and mediates its pharmacological effects. Metabolism of CBC occurs primarily in the liver, where it undergoes enzymatic transformation into metabolites that are subsequently eliminated from the body via urine and feces. The pharmacokinetic profile of CBC may vary depending on factors such as route of administration, dose, and individual differences in metabolism, highlighting the need for further research to elucidate its pharmacokinetic properties and optimize therapeutic dosing regimens.

Psychedelic Effects of CBC

Despite its therapeutic potential, CBC is known to exhibit mild psychoactive effects, although significantly less pronounced than THC. Some users report feelings of relaxation, euphoria, and mild sedation after consuming CBC-rich cannabis strains. These psychedelic effects are believed to result from CBC's interaction with the ECS and its modulation of neurotransmitter systems in the brain. However, it's important to note that CBC's psychoactive effects are generally milder and less pronounced compared to THC, making it a potentially safer option for individuals seeking therapeutic relief without experiencing intense psychoactive effects.

CBC's Effects in the Human Body

Research suggests that CBC may offer a wide range of potential therapeutic benefits, including anti-inflammatory, analgesic, and neuroprotective properties. Preclinical studies have demonstrated CBC's ability to reduce inflammation and pain by inhibiting the production of pro-inflammatory molecules and modulating pain perception pathways in the central nervous system. Furthermore, CBC exhibits neuroprotective effects by promoting the growth of new brain cells and enhancing brain function, suggesting potential applications in the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's.

While CBC's therapeutic potential and pharmacological effects are promising, further research is needed to fully understand its mechanisms of action and clinical applications. As scientific investigations into CBC continue to expand, its role in cannabis pharmacology and its potential impact on human health are poised to be further elucidated. With ongoing research and growing interest in cannabis-based medicine, CBC holds the promise of offering new insights into the therapeutic potential of cannabinoids and contributing to the development of novel treatments for various medical conditions.