Pandora
Top flavors
Terpenes
Pandora effects are mostly calming.
Pandora
Pandora is a modern, autoflowering variety developed using Ruderalis genetics, designed to offer a streamlined growth cycle that accommodates both indoor and outdoor cultivation environments. This strain presents an accessible option for cultivators, characterized by a 68-day flowering period and a low total yield. Its history is cemented through its role as a parent for several significant cultivars, as it is the genetic contributor to Auto Kong #4 and Blue Haze Auto 2.0.
The sensory profile of Pandora is defined by an extensive terpene hierarchy, led primarily by myrcene, caryophyllene, and limonene. Following these primary notes, the strain features a complex secondary and tertiary profile including pinene, terpinolene, linalool, beta-pinene, humulene, and nerolidol. The chemistry is further rounded out by trace amounts of ocimene, bisabolol, guaiol, camphene, caryophyllene-oxide, and p-cymene, which coalesce to create its distinct aromatic and flavor characteristics.
As a THC-dominant variety, Pandora delivers effects that users frequently report as relaxed, happy, and uplifted. These qualities make the strain a functional choice for those seeking relief from stress and pain, or looking for assistance in achieving sleep. Beyond these therapeutic applications, the strain remains a notable component of the modern cannabis gene pool, specifically due to the successful progeny it has produced in contemporary 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.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Pandora.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parent ruderalis
Offspring — 2 strains bred from Pandora
Composite Traits
Where to buy Pandora
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
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Community Reviews
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What would Pandora × ? 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 Pandora indica or sativa?
Pandora is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Pandora?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Pandora good for daytime use?
Pandora 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.