Auto CBDV 1:1
Top flavors
Terpenes
Auto CBDV 1:1 effects are mostly calming.
Auto CBDV 1:1
Auto CBDV 1:1 is a modern, auto-flowering hybrid derived from Asian genetics. Designed for simplicity, this strain is well-regarded for its ease of cultivation, reaching maturity with a 67-day flowering cycle. It is suitable for both indoor and outdoor growing environments, though cultivators should note that the plants yield a low output. As an established genetic line, it also serves as a notable parent for subsequent Asia hybrids.
The aromatic and flavor profile of Auto CBDV 1:1 is defined by a complex sequence of fifteen terpenes. Myrcene leads the profile, followed by caryophyllene, limonene, and pinene, which are complemented by terpinolene, linalool, beta-pinene, and humulene. The secondary nuances are provided by nerolidol, ocimene, bisabolol, guaiol, and camphene, with trace influences from caryophyllene-oxide and p-cymene. This diverse chemical arrangement creates a distinct sensory experience that reflects its specific terpene dominance.
This THC-dominant cultivar is engineered to induce effects characterized by feelings of being relaxed, happy, and uplifted. Because of these primary effects, the strain is specifically utilized for the management of stress, pain, and sleep-related concerns. Beyond its immediate user applications, the plant continues to influence the genetic landscape as a verified ancestor for modern hybrid breeding programs.
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.
Balanced THC:CBD
Roughly equal THC and CBD. CBD moderates THC psychoactivity — smoother, less anxious.
Genealogy
Parentage, ancestry, and genetic relatives of Auto CBDV 1:1.
Ancestry
Great-great-grandparents
Siblings
Share parent asia hybrid
Offspring — 1 strains bred from Auto CBDV 1:1
Composite Traits
Where to buy Auto CBDV 1:1
No verified dispensaries on file — find it on Leafly.
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What would Auto CBDV 1:1 × ? 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 CBDV 1:1 indica or sativa?
Auto CBDV 1:1 is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Auto CBDV 1:1?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Auto CBDV 1:1 good for daytime use?
Auto CBDV 1:1 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.