CBG-Force Auto
Top flavors
Terpenes
CBG-Force Auto effects are mostly calming.
CBG-Force Auto
CBG-Force Auto is a modern hybrid strain derived from genetics involving Ruderalis. Developed for its specific chemical composition, it serves as the progenitor for the notable offspring strain known as CBG-Force. With a 74-day flowering cycle, this variety requires moderate cultivation skill and is suitable for both indoor and outdoor growing environments, consistently providing high yields for the grower.
The aromatic and flavor profile of this strain is defined by a complex sequence of terpenes, led by the dominant myrcene, followed by caryophyllene, limonene, pinene, and terpinolene. The secondary and tertiary layers of the profile include linalool, beta-pinene, humulene, nerolidol, and ocimene, with trace contributions from bisabolol, guaiol, camphene, caryophyllene-oxide, and p-cymene. This diverse chemical arrangement provides a distinct sensory experience shaped by the synergy of these aromatic compounds.
As a THC-dominant variety, CBG-Force Auto produces effects characterized as relaxed, happy, and uplifted. These qualities make it a functional choice for users seeking support with stress, pain, or sleep-related concerns. Through its established lineage and its role as the parent of the CBG-Force strain, it remains a recognized example of modern genetic stabilization in the cannabis industry.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| caryophyllene | ~28% | spicy | relaxing · social |
| limonene | ~12% | citrus | social · creative |
Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.
Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
~28%
spicy
●●○○
Russo 2011: only terpene that is a selective full CB2 agonist (100 nM); Gertsch et al. 2008: acts as dietary cannabinoid; unique anti-inflammatory and gastric cytoprotective properties.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
Effects
Reported effects — derived from terpene chemistry and cannabinoid profile.
relaxed
eveningPrimary endpoint of myrcene+linalool sedating combinations; GABA modulation is the dominant mechanistic driver.
happy
anytimeuplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
Genetic Profile
Balanced Hybrid
Equal indica and sativa genetics. Balanced body and mind effects.
CBG-Dominant
Rare CBG profile. "Mother cannabinoid." Antibacterial, anti-inflammatory, neuroprotective.
Genealogy
Parentage, ancestry, and genetic relatives of CBG-Force Auto.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parent ruderalis
Offspring — 1 strains bred from CBG-Force Auto
Composite Traits
Where to buy CBG-Force Auto
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
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What would CBG-Force Auto × ? produce?
Predict the terpene profile, effects, and growing traits of a cross. Our gene weaver engine votes on dominant traits from both parents.
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Frequently Asked Questions
Is CBG-Force Auto indica or sativa?
CBG-Force Auto is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in CBG-Force Auto?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is CBG-Force Auto good for daytime use?
CBG-Force Auto is versatile and works across different times of day depending on dose and individual response.
How accurate is this data?
See the "Data confidence" card in the sidebar. Terpene profiles and effects are chemistry-informed estimates — individual responses depend on phenotype, source, and personal chemistry.