Deep Psychosis
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Terpenes
Deep Psychosis effects are mostly calming.
Deep Psychosis
Top flavors
Terpenes
Deep Psychosis effects are mostly calming.
Deep Psychosis is a modern hybrid-sativa cultivar derived from a Deep Purple lineage. Designed for versatility, this strain performs well in both indoor and outdoor environments, presenting a moderate cultivation difficulty and a high yield potential. Growers can expect a floral cycle that reaches maturity after 64 days of flowering.
The terpene profile of Deep Psychosis is complex, led by a dominant concentration of myrcene, followed by terpinolene, caryophyllene, and limonene. The secondary and tertiary chemical structure continues with ocimene, linalool, humulene, pinene, beta-pinene, bisabolol, guaiol, alpha-terpinene, nerolidol, and camphene. This broad spectrum of compounds contributes to a distinct aromatic profile that balances the earthy foundation of the primary myrcene with the lighter, nuanced notes of the subsequent terpene chain.
As a THC-dominant variety, Deep Psychosis is reported to produce creative, uplifted, and happy effects. These characteristics make it a functional choice for activities requiring focus or social interaction. The strain has served as a foundational genetic component for future breeding projects, resulting in a notable legacy that includes the offspring Deep Blue and Psycho Killer.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| terpinolene | ~28% | herbal | creative · social |
| caryophyllene | ~12% | spicy | relaxing · social |
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%
herbal
●○○○
PMC11060501: antinociception via NO/PGE2/TNF-α inhibition; associated with cerebral sativa profiles; least clinically characterised of major terpenes.
~12%
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.
Effects
Reported effects — derived from terpene chemistry and cannabinoid profile.
creative
morningAssociated with terpinolene/limonene profiles; dopaminergic and serotonergic modulation via limonene 5-HT1A supports divergent thinking.
uplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
happy
anytimeGenetic Profile
Sativa-dominant
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 Deep Psychosis.
Ancestry
Great-great-grandparents
Great-grandparents
Siblings
Share parent deep purple
Offspring — 2 strains bred from Deep Psychosis
Composite Traits
Where to buy Deep Psychosis
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
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What would Deep Psychosis × ? 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 Deep Psychosis indica or sativa?
Deep Psychosis is modeled here as a sativa-dominant (primarily sativa with indica grounding).
What terpene is dominant in Deep Psychosis?
Myrcene is shown as the dominant terpene at approximately ~60%. Terpinolene follows as the secondary terpene.
Is Deep Psychosis good for daytime use?
Deep Psychosis 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.