Sweet Tooth Auto
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Terpenes
Sweet Tooth Auto effects are mostly calming.
Sweet Tooth Auto
Sweet Tooth Auto is a modern, autoflowering variety developed from a genetic lineage of Ruderalis and Indica. As an autoflowering strain, it is designed for ease of cultivation, reaching maturity with a sixty-three-day flowering period. It is suitable for both indoor and outdoor environments, though growers should be aware that the plant produces a low yield regardless of the setting.
The terpene profile of this strain is complex and dominated by myrcene as the primary compound, followed by caryophyllene and limonene as the secondary and tertiary contributors. Further analysis of the chemical structure reveals the presence of pinene, terpinolene, linalool, beta-pinene, humulene, nerolidol, ocimene, bisabolol, guaiol, camphene, caryophyllene-oxide, and p-cymene. This specific arrangement of terpenes defines the sensory experience, balancing the earthy and herbal base notes against sharper, more citric, and woody undertones.
As a THC-dominant variety, Sweet Tooth Auto primarily produces effects categorized as relaxed, happy, and uplifted. These characteristics make it a functional choice for users seeking support with stress, pain, or sleep. The genetic legacy of this strain is evidenced by its role in the development of notable offspring, specifically the cultivar known as Black Chere.
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
Autoflower
Photoperiod-independent. Flowers based on age, not light cycle. Compact and fast.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Sweet Tooth Auto.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Offspring — 1 strains bred from Sweet Tooth Auto
Composite Traits
Where to buy Sweet Tooth Auto
No verified dispensaries on file — find it on Leafly.
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What would Sweet Tooth Auto × ? produce?
Predict the terpene profile, effects, and growing traits of a cross. Our gene weaver engine votes on dominant traits from both parents.
Build a cross with Sweet Tooth Auto →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Sweet Tooth Auto indica or sativa?
Sweet Tooth Auto is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Sweet Tooth Auto?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Sweet Tooth Auto good for daytime use?
Sweet Tooth 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.