LSD Poison
Top flavors
Terpenes
LSD Poison effects are mostly calming.
LSD Poison
LSD Poison is a modern hybrid-sativa strain developed from a cross between Skunk and Lavender. Its specific origin and breeding history remain undocumented, providing little information beyond its genetic components. The strain reaches maturity after a flowering period of 65 days and is considered to be of moderate cultivation difficulty. It is suitable for both indoor and outdoor environments and offers a high yield to the grower.
The aromatic and flavor profile of this strain is defined by a complex array of terpenes, an estimated order of which begins with myrcene, followed by pinene, caryophyllene, humulene, terpinolene, linalool, beta-pinene, limonene, and bisabolol. Due to the diverse nature of these volatile compounds, the user experience is characterized by a nuanced sensory interaction that likely leans on the earthy and pine-forward properties established in this specific order. These terpenes contribute to the unique organoleptic qualities that differentiate the strain within a modern cannabis collection.
LSD Poison is a THC-dominant cultivar known for producing effects that are creative, uplifted, and happy. It is frequently utilized in settings that demand creativity, social engagement, or sustained focus. Currently, there are no recorded notable offspring derived from this lineage, as it remains a standalone variety in its functional application.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| pinene | ~28% | pine | focus · creative |
| 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.
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%
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 LSD Poison.
Ancestry
Great-grandparents
Composite Traits
Where to buy LSD Poison
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
Find which dispensaries near you currently stock LSD Poison.
or enter a city / postcode
Community Reviews
No reviews yet — be the first!
No reviews yet for LSD Poison.
What would LSD Poison × ? 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 LSD Poison →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is LSD Poison indica or sativa?
LSD Poison is modeled here as a sativa-dominant (primarily sativa with indica grounding).
What terpene is dominant in LSD Poison?
Myrcene is shown as the dominant terpene at approximately ~60%. Pinene follows as the secondary terpene.
Is LSD Poison good for daytime use?
LSD Poison 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.