Zombie D.F.
21.8%
THC
Top flavors
Terpenes
Zombie D.F. has balanced effects.
Zombie D.F. potency is average.
Zombie D.F.
21.8%
THC
Top flavors
Terpenes
Zombie D.F. has balanced effects.
Zombie D.F. potency is average.
Zombie D.F. is a modern hybrid-sativa strain that emerges from a lineage consisting of LA Pure Kush and an unknown strain. This genetic combination requires moderate cultivation experience to manage successfully in both indoor and outdoor environments. Growers can expect a high yield from this variety following a flowering period that typically spans 64 days.
The terpene profile of Zombie D.F. is led by terpinolene, followed by myrcene and caryophyllene. These compounds combine to provide a distinct aromatic and flavor experience defined by this specific dominant-to-tertiary hierarchy. The complex interplay of terpinolene, myrcene, and caryophyllene creates a nuanced sensory profile that informs the overall character of the plant.
With a THC-dominant profile testing at approximately 21.8%, the effects of Zombie D.F. are characterized by sensations of creativity, uplift, and general happiness. These traits make the strain well-suited for social circumstances, tasks requiring sustained focus, or projects that benefit from a creative boost. Currently, there are no recorded notable offspring for this strain, marking Zombie D.F. as a distinct entry in modern cannabis genetics.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| caryophyllene | ~60% | spicy | relaxing · social |
| limonene | ~28% | citrus | social · creative |
| myrcene | ~12% | earthy | relaxing · solo |
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.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
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 Zombie D.F..
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parents la pure kush / unknown strain
Composite Traits
Where to buy Zombie D.F.
No verified dispensaries on file — find it on Leafly.
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What would Zombie D.F. × ? 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 Zombie D.F. →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Zombie D.F. indica or sativa?
Zombie D.F. is modeled here as a sativa-dominant (primarily sativa with indica grounding).
What terpene is dominant in Zombie D.F.?
Caryophyllene is shown as the dominant terpene at approximately ~60%. Limonene follows as the secondary terpene.
Is Zombie D.F. good for daytime use?
Zombie D.F. 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.