Egoloss
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Terpenes
Egoloss effects are mostly energizing.
Egoloss
Egoloss is a modern hybrid-sativa developed from a lineage of Memory Loss, Africa-Sativa, and NL5 x Haze. The specific origin story of this strain remains undocumented, offering no definitive information regarding the breeder or the timeline of its development. As a cultivation project, it maintains a moderate difficulty level and performs well in both indoor and outdoor environments. Growers can expect a high yield from this variety, which reaches maturity after a 67-day flowering period.
The sensory profile of Egoloss is defined by a broad spectrum of secondary metabolites. Its confirmed terpene profile is led by terpinolene, followed by limonene, nerolidol, caryophyllene, myrcene, humulene, beta-pinene, linalool, pinene, bisabolol, ocimene, caryophyllene-oxide, camphene, alpha-terpinene, and gamma-terpinene. This complex arrangement of compounds contributes to its distinct aromatic qualities, ensuring that the influence of its top-tier terpenes remains prominent in the final product.
As a THC-dominant cultivar, Egoloss is primarily associated with effects that are creative, uplifted, and happy. It is frequently utilized by consumers seeking to facilitate creative pursuits, enhance social interaction, or improve focus. There are currently no notable offspring recorded for this strain, leaving it as a singular entry in the contemporary cannabis landscape.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| terpinolene | ~60% | herbal | creative · social |
| limonene | ~28% | citrus | social · creative |
| nerolidol | ~12% | floral | sleep · relaxing |
Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.
~60%
herbal
●○○○
PMC11060501: antinociception via NO/PGE2/TNF-α inhibition; associated with cerebral sativa profiles; least clinically characterised of major terpenes.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
Russo 2011: sedative properties; enhances transdermal pharmaceutical penetration; antimalarial; PMC11060501: GABAergic-mediated antinociception.
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 Egoloss.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Parents
Siblings
Share parents memory loss / africa sativa / nl5 x haze
Composite Traits
Where to buy Egoloss
No verified dispensaries on file — find it on Leafly.
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What would Egoloss × ? 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 Egoloss →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Egoloss indica or sativa?
Egoloss is modeled here as a sativa-dominant (primarily sativa with indica grounding).
What terpene is dominant in Egoloss?
Terpinolene is shown as the dominant terpene at approximately ~60%. Limonene follows as the secondary terpene.
Is Egoloss good for daytime use?
Egoloss 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.