Comando Vermelho
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Terpenes
Comando Vermelho effects are mostly calming.
Comando Vermelho
Comando Vermelho is a modern, auto-flowering strain derived from a genetic lineage of Ruderalis and Brazilian Sativa. Due to the limited documentation surrounding its development, the specific origins and the identity of its original breeder remain unknown. Designed for versatility, this cultivar thrives in both indoor and outdoor environments and maintains an easy difficulty level for cultivators. It completes its flowering cycle in 65 days, yielding a low-volume harvest at the end of its growth period.
The chemical profile of Comando Vermelho represents a complex assembly of compounds, anchored by myrcene as the primary terpene. Following this are caryophyllene, limonene, pinene, terpinolene, and linalool, with beta-pinene, humulene, nerolidol, ocimene, bisabolol, guaiol, camphene, caryophyllene-oxide, and p-cymene present in descending concentrations. This confirmed terpene sequence suggests a diverse olfactory experience that balances earthy and peppery base notes with subtler floral and woodsy nuances.
As a THC-dominant variety, Comando Vermelho produces consistent physiological effects, leaving users feeling relaxed, happy, and uplifted. These characteristics make it a functional choice for those managing stress, pain, or insomnia-related sleep difficulties. Despite its unique genetic composition, there are currently no recorded offspring linked to this strain.
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 |
| limonene | ~12% | citrus | social · creative |
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.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
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
Autoflower
Photoperiod-independent. Flowers based on age, not light cycle. Compact and fast.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Comando Vermelho.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parents ruderalis / brazil sativa
Composite Traits
Where to buy Comando Vermelho
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
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What would Comando Vermelho × ? 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 Comando Vermelho indica or sativa?
Comando Vermelho is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Comando Vermelho?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Comando Vermelho good for daytime use?
Comando Vermelho 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.