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Hybrid-SativaModernTHC-Dominantafternoon

Evil Queen

Top flavors

spicypinecitrus
CalmingEnergizing

Evil Queen has balanced effects.

Evil Queen is a modern hybrid-sativa strain developed through the crossing of Cinderellas and Space Queen. Its precise origins remain undocumented, with no specific breeder information or historical records available to clarify the circumstances or timeline of its emergence. As a modern hybrid, the strain functions as a distinct genetic product rather than a landrace or heirloom variety, though its background reflects the common practice of combining established sativa-leaning genetics to reach a specific cannabinoid profile.

The aromatic and flavor profile of Evil Queen is defined by a complex chemical composition, led by caryophyllene, pinene, and limonene. Secondary notes in its terpene profile include myrcene, linalool, humulene, beta-pinene, terpinolene, bisabolol, and caryophyllene-oxide. This diverse combination suggests a nuanced sensory experience that balances spicy and woody notes with sharper, citrus-forward undertones. Consumers can expect a THC-dominant experience, though the potency level remains an estimated value based on general observations of similar hybrid-sativa profiles within this genetic lineage.

Reported effects of Evil Queen are centered on creative, uplifted, and happy states, making it a functional choice for social settings and tasks requiring focus. The cultivation of this strain is considered moderately difficult, requiring consistent management for both indoor and outdoor environments. Growers can expect a high yield from plants that complete a 56-day flowering cycle. At this time, no notable offspring have been recorded for Evil Queen, and it represents a standalone genetic entry in the current catalogue.

Terpene Profile

Synergies (+) and conflicts (−) are relative to each other within this profile.

caryophyllene ~60%pinene ~28%limonene ~12%
TerpeneShare
caryophyllene~60%
pinene~28%
limonene~12%

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.

~28%

pine

●●○○

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.

~12%

citrus

●●○○

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.

Genetic Profile

Sativa-dominant

■ Indica 30%■ Sativa 70%

Primarily sativa with indica grounding. Uplifting with body relaxation.

THC-Dominant

High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.

Genealogy

Parentage, ancestry, and genetic relatives of Evil Queen.

Composite Traits

Use caution if

sleep-seekingevening-wind-downappetite-boost

Where to buy Evil Queen

No verified dispensaries on file — find it on Leafly.

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What would Evil Queen × ? produce?

Predict the terpene profile, effects, and growing traits of a cross. Our gene weaver engine votes on dominant traits from both parents.

Build a cross with Evil Queen

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Evil Queen indica or sativa?

Evil Queen is modeled here as a sativa-dominant (primarily sativa with indica grounding).

What terpene is dominant in Evil Queen?

Caryophyllene is shown as the dominant terpene at approximately ~60%. Pinene follows as the secondary terpene.

Is Evil Queen good for daytime use?

Evil Queen 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.