Auto AK Mir
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Terpenes
Auto AK Mir effects are mostly calming.
Auto AK Mir
Auto AK Mir is a modern auto-flowering cultivar developed by crossing AK47 with Ruderalis genetics. This breeding lineage was designed to produce an accessible, easy-to-grow plant capable of reaching harvest in 63 days. The strain performs well in both indoor and outdoor environments, although growers should anticipate a low yield compared to photoperiod counterparts. Its genetic influence is notable for producing the offspring strain Auto Maxi Goom Tupolev.
The chemical profile of Auto AK Mir is complex and anchored by a high concentration of myrcene, followed by caryophyllene and limonene as secondary and tertiary terpenes. This foundation is further nuanced by a wide spectrum of additional compounds, including pinene, terpinolene, linalool, beta-pinene, humulene, nerolidol, ocimene, bisabolol, guaiol, camphene, caryophyllene-oxide, and p-cymene. These terpenes combine to define the sensory experience of the plant, reflecting the varied aromatic contributions of its extensive chemical range.
As a THC-dominant variety, Auto AK Mir is characterized by effects that are primarily relaxed, happy, and uplifted. These traits make the strain a functional choice for users seeking relief from stress and pain, or aid for sleep. Its balance of physiological and cerebral effects establishes its utility in therapeutic applications, while its specific lineage continues to impact modern breeding programs through its direct descendants.
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 AK Mir.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Composite Traits
Where to buy Auto AK Mir
No verified dispensaries on file — find it on Leafly.
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What would Auto AK Mir × ? 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 Auto AK Mir →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Auto AK Mir indica or sativa?
Auto AK Mir is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Auto AK Mir?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Auto AK Mir good for daytime use?
Auto AK Mir 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.