Auto Kaya 47
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Terpenes
Auto Kaya 47 effects are mostly calming.
Auto Kaya 47
Auto Kaya 47 is a modern, auto-flowering variety derived from Ruderalis genetics, yielding a THC-dominant profile. Developed to offer a streamlined growth cycle, this cultivar completes its flowering phase in 75 days. Considered an easy strain to cultivate, it thrives in both indoor and outdoor environments, though growers should anticipate a low yield performance. Its genetic contributions to the broader cannabis landscape are evidenced by its status as a parent to the notable offspring Auto Skunk 47.
The organoleptic profile of this strain is defined by a complex, layered terpene expression. Myrcene leads the chemical composition, followed by caryophyllene and limonene, with secondary notes provided by pinene, terpinolene, and linalool. The tertiary range of the profile includes beta-pinene, humulene, nerolidol, ocimene, bisabolol, guaiol, camphene, caryophyllene-oxide, and p-cymene. This specific arrangement of compounds produces a nuanced, multi-faceted sensory experience that reflects the distinct chemical depth of the variety.
The primary effects of Auto Kaya 47 are characterized by sensations of being relaxed, happy, and uplifted. Due to this chemical synergy, it is frequently chosen by users seeking relief from stress and pain, as well as those attempting to assist with sleep. By combining a simplified cultivation cycle with a consistent, THC-dominant therapeutic profile, this strain remains a functional selection for those prioritizing ease of access and relaxation.
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 Auto Kaya 47.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parent ruderalis
Composite Traits
Where to buy Auto Kaya 47
No verified dispensaries on file — find it on Leafly.
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What would Auto Kaya 47 × ? 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 Auto Kaya 47 indica or sativa?
Auto Kaya 47 is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Auto Kaya 47?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Auto Kaya 47 good for daytime use?
Auto Kaya 47 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.