Jota Mayúscula Purple Auto
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Terpenes
Jota Mayúscula Purple Auto has balanced effects.
Jota Mayúscula Purple Auto
Jota Mayúscula Purple Auto is a modern, auto-flowering cultivar derived from the crossbreeding of Purple Kush and Ruderalis. Developed for growers seeking an accessible cultivation experience, this strain is well-suited for both indoor and outdoor environments. It maintains a short 50-day flowering cycle and is characterized by a low yield, making it an appropriate choice for those prioritizing an easy cultivation process over high-volume output.
The sensory profile of this strain is defined by a complex, diverse range of terpenes, led by the dominant influence of caryophyllene. This base is supported by pinene and humulene, followed by myrcene, limonene, and bisabolol. Moving further into the profile, the composition includes beta-pinene, linalool, guaiol, and terpinolene, with trace contributions from caryophyllene-oxide, camphene, ocimene, nerolidol, and borneol. This intricate chemical structure dictates the aromatic and flavorful nuance of the plant.
As a THC-dominant variety, Jota Mayúscula Purple Auto produces effects that are typically described as relaxed, happy, and uplifted. These characteristics make the strain a functional option for users managing stress, pain, or difficulties with sleep. Beyond its individual therapeutic utility, the strain has secured a position in its genetic legacy as the parent to the notable Dark Purple Auto.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| caryophyllene | ~60% | spicy | relaxing · social |
| pinene | ~28% | pine | focus · creative |
| humulene | ~12% | earthy | focus · solo |
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: acetylcholinesterase inhibitor (IC50 0.44 mM) counteracting THC-induced short-term memory deficits; most widely encountered terpenoid in nature; anti-inflammatory via PGE-1.
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 Jota Mayúscula Purple Auto.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parents purple kush / ruderalis
Offspring — 1 strains bred from Jota Mayúscula Purple Auto
Composite Traits
Where to buy Jota Mayúscula Purple Auto
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What would Jota Mayúscula Purple Auto × ? 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 Jota Mayúscula Purple Auto indica or sativa?
Jota Mayúscula Purple Auto is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Jota Mayúscula Purple Auto?
Caryophyllene is shown as the dominant terpene at approximately ~60%. Pinene follows as the secondary terpene.
Is Jota Mayúscula Purple Auto good for daytime use?
Jota Mayúscula Purple 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.