A.A.A
Top flavors
Terpenes
A.A.A has balanced effects.
A.A.A
Top flavors
Terpenes
A.A.A has balanced effects.
A.A.A is a modern, autoflowering variety developed through the crossing of Amnesia Haze and Black Domina with Ruderalis genetics. The origins of this specific lineage are presented without official documentation regarding a precise breeder or developmental timeline, leaving its exact creation history obscure. As a modern hybrid, it is engineered for accessible cultivation, requiring an easy difficulty level in both indoor and outdoor environments, though growers should anticipate a low yield over its 67-day flowering cycle.
The aroma and flavor profile of A.A.A is anchored by a confirmed hierarchy of terpenes, beginning with caryophyllene and followed by myrcene, terpinolene, and limonene. The sensory nuance continues through pinene, linalool, humulene, beta-pinene, bisabolol, nerolidol, ocimene, and camphene. These compounds contribute to a complex aromatic expression that reflects the diversity of its haze and indica-dominant parentage.
A.A.A is a THC-dominant strain known to produce effects that are relaxed, happy, and uplifted. These characteristics make it a functional candidate for users seeking management of stress, pain, or difficulties with sleep. While it serves as a distinct modern addition to the cannabis landscape, there are currently no recorded notable offspring traced back to this particular genetic line.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| caryophyllene | ~60% | spicy | relaxing · social |
| myrcene | ~28% | earthy | relaxing · solo |
| terpinolene | ~12% | herbal | creative · social |
Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.
~60%
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: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
~12%
herbal
●○○○
PMC11060501: antinociception via NO/PGE2/TNF-α inhibition; associated with cerebral sativa profiles; least clinically characterised of major terpenes.
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 A.A.A.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Parents
Siblings
Share parents amnesia haze / black domina / ruderalis
Composite Traits
Where to buy A.A.A
No verified dispensaries on file — find it on Leafly.
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What would A.A.A × ? 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 A.A.A indica or sativa?
A.A.A is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in A.A.A?
Caryophyllene is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.
Is A.A.A good for daytime use?
A.A.A 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.