Green Mountain Power
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Terpenes
Green Mountain Power effects are mostly calming.
Green Mountain Power
Green Mountain Power is a modern hybrid strain derived from its parent, Appalachia. Developed for consistent performance, this cultivar is capable of thriving in both indoor and outdoor growing environments. Cultivators should expect a moderate difficulty level during the 60-day flowering period, which ultimately rewards growers with a high yield. Its genetic potential is demonstrated by its role in producing the notable offspring Green Mountain Skunk #1.
The complex aromatic profile of Green Mountain Power is defined by a deep spectrum of twenty-one terpenes. The sensory experience is anchored by dominant notes of myrcene, caryophyllene, and ocimene, complemented by nuances of nerolidol, linalool, and limonene. Further layers of complexity are provided by the presence of pinene, humulene, guaiol, bisabolol, eucalyptol, beta-pinene, and p-cymene, which taper into subtle finishes of caryophyllene-oxide, terpinolene, camphene, isopulegol, valencene, borneol, sabinene, and gamma-terpinene.
As a THC-dominant variety, Green Mountain Power delivers effects reported by users as relaxed, happy, and uplifted. These characteristics make the strain a suitable choice for addressing symptoms related to stress, pain, and sleep. Beyond its immediate application, the strain continues to exert influence on the modern genetic landscape through its confirmed legacy in subsequent breeding projects.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| caryophyllene | ~28% | spicy | relaxing · social |
| ocimene | ~12% | sweet | energetic · 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%
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.
Antifungal, antiviral, decongestant; activates CB1/CB2 at 10–60% THC efficacy per Israeli receptor study (NORML 2025); highly volatile (bp 50–66°C); limited clinical data.
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 Green Mountain Power.
Ancestry
Great-great-grandparents
Great-grandparents
Siblings
Share parent appalachia
Composite Traits
Where to buy Green Mountain Power
No verified dispensaries on file — find it on Leafly.
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What would Green Mountain Power × ? 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 Green Mountain Power indica or sativa?
Green Mountain Power is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Green Mountain Power?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Green Mountain Power good for daytime use?
Green Mountain Power 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.