Guatemala Pot
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Terpenes
Guatemala Pot has balanced effects.
Guatemala Pot
Guatemala Pot is a modern hybrid created through the crossing of Hindu Kush, Super Skunk, and Bubba 76. The specific origins and history of this cross remain largely undocumented, as there is no provided record regarding the breeder or the specific circumstances surrounding its initial development. As a project of unknown provenance, it persists in the archive as a distinct genetic collaboration of these three specific parent strains.
The sensory profile of Guatemala Pot is defined by a diverse array of chemical compounds, led by dominant caryophyllene followed by myrcene, linalool, nerolidol, limonene, humulene, camphene, pinene, terpinolene, beta-pinene, bisabolol, guaiol, caryophyllene-oxide, and geraniol. This complex composition contributes to the strain's nuanced aroma and flavor, which shift between the spicy notes of its primary terpene and the subtle floral or woody undertones provided by the range of secondary and tertiary constituents.
As a THC-dominant hybrid, Guatemala Pot produces effects consisting of relaxation, happiness, and an uplifted mood. These traits make it a frequent selection for users managing stress, pain, or sleep-related issues. Cultivators can expect a moderate difficulty level when growing the plant in either indoor or outdoor environments, with a flowering phase lasting 77 days and a consistently high yield. There are currently no recorded offspring for this variety.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| caryophyllene | ~60% | spicy | relaxing · social |
| myrcene | ~28% | earthy | relaxing · solo |
| linalool | ~12% | floral | 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: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
Russo 2011: local anesthetic equal to procaine; anticonvulsant via glutamate/GABA modulation; reduces morphine tolerance via multisite opioid/GABAergic/cannabinoid action.
Effects
Reported effects — derived from terpene chemistry and cannabinoid profile.
relaxed
eveningPrimary endpoint of myrcene+linalool sedating combinations; GABA modulation is the dominant mechanistic driver.
happy
anytimeuplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
Genetic Profile
Balanced Hybrid
Equal indica and sativa genetics. Balanced body and mind effects.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Guatemala Pot.
Ancestry
Parents
Siblings
Share parents hindu kush / super skunk / bubba 76
Composite Traits
Where to buy Guatemala Pot
No verified dispensaries on file — find it on Leafly.
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What would Guatemala Pot × ? 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 Guatemala Pot →Similar strains
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Frequently Asked Questions
Is Guatemala Pot indica or sativa?
Guatemala Pot is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Guatemala Pot?
Caryophyllene is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.
Is Guatemala Pot good for daytime use?
Guatemala Pot 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.