Auto Blue Amnesia
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Terpenes
Auto Blue Amnesia effects are mostly calming.
Auto Blue Amnesia
Auto Blue Amnesia is a modern auto-flowering variety resulting from a cross between Blueberry and Ruderalis. Due to the lack of detailed documentation regarding its specific breeding history, the exact origins of this strain remain varied and undocumented beyond its designated parentage. As an auto-flowering hybrid, it is engineered for accessible cultivation, requiring only 49 days of flowering time. It is classified as an easy strain to grow, performing well in both indoor and outdoor environments, though growers should be prepared for a low yield.
The chemical profile of this strain is defined by a broad spectrum of compounds. Its terpene profile is dominated by myrcene, followed by caryophyllene, limonene, pinene, beta-pinene, terpinolene, humulene, linalool, bisabolol, nerolidol, ocimene, guaiol, and camphene. Because these constituents serve to shape the aromatic and flavor characteristics of the plant, the sensory experience of Auto Blue Amnesia is likely influenced by this specific hierarchy, contributing to a complex olfactory presentation.
As a THC-dominant variety, Auto Blue Amnesia produces effects that are characterized as relaxed, happy, and uplifted. These qualities make the strain a common choice for users seeking relief from stress and pain, or support for improved sleep. While it remains a distinct cross in the current cannabis market, there are currently no recorded offspring associated with this variety in the strain genealogy.
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 Blue Amnesia.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Composite Traits
Where to buy Auto Blue Amnesia
No verified dispensaries on file — find it on Leafly.
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What would Auto Blue Amnesia × ? 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 Blue Amnesia indica or sativa?
Auto Blue Amnesia is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Auto Blue Amnesia?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Auto Blue Amnesia good for daytime use?
Auto Blue Amnesia 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.