Z-Up Auto
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Terpenes
Z-Up Auto effects are mostly calming.
Z-Up Auto
Z-Up Auto is a modern autoflowering variety developed through the crossing of Ruderalis, Happy Vibez, and Voilà. This strain is designed for efficient cultivation, maintaining a growth cycle of sixty days from flowering, which renders it an accessible option for growers of all skill levels. It thrives in both indoor and outdoor environments, though cultivators should anticipate a low yield from each harvest. Its genetic influence is notable in its role as a parent for subsequent strains, specifically Happy Vibez and Let's Get Fizzicle.
The complex organoleptic profile of Z-Up Auto is defined by a deep chemical hierarchy, led by dominant myrcene, followed by caryophyllene, limonene, and linalool. This foundational structure transitions into mid-tier notes of terpinolene, pinene, beta-pinene, humulene, and ocimene, while concluding with traces of nerolidol, bisabolol, guaiol, caryophyllene-oxide, and camphene. This specific combination creates a nuanced sensory experience that mirrors the biological diversity of its complex lineage.
As a THC-dominant cultivar, Z-Up Auto is primarily reported to produce effects characterized by a sense of relaxation, happiness, and an uplifted mood. These therapeutic attributes make it a frequent choice for users seeking to manage stress, alleviate pain, or improve sleep quality. By balancing its specific cannabinoid output with its extensive terpene profile, Z-Up Auto serves as a reliable genetic contributor to modern breeding projects.
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 Z-Up Auto.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Parents
Siblings
Share parents ruderalis / happy vibez / voil
Offspring — 1 strains bred from Z-Up Auto
Composite Traits
Dispensary Locator
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What would Z-Up 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 Z-Up Auto indica or sativa?
Z-Up Auto is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Z-Up Auto?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Z-Up Auto good for daytime use?
Z-Up 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.