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AutoflowerModernTHC-Dominantevening

Lele da Cuca

Top flavors

earthyspicycitrus
CalmingEnergizing

Lele da Cuca effects are mostly calming.

Lele da Cuca is a modern, autoflowering variety derived from a genetic foundation of Brazilian Sativa crossed with Ruderalis. The specific breeding history and origin of this strain remain undocumented, with no clear record regarding its breeder or the timeline of its development. As a modern autoflower, it is designed for accessibility, maintaining an easy difficulty level for growers that allows it to thrive in both indoor and outdoor environments. Despite its ease of cultivation, the strain is characterized by a low yield and a short flowering cycle that completes in exactly 55 days.

The terpene profile for Lele da Cuca is confirmed to be highly complex, led by a dominant inclusion of myrcene, followed by caryophyllene, limonene, pinene, and terpinolene. The remaining secondary and tertiary compounds, in descending order of presence, include linalool, beta-pinene, humulene, nerolidol, ocimene, bisabolol, guaiol, camphene, caryophyllene-oxide, and p-cymene. This diverse chemical arrangement contributes to a nuanced sensory experience, dictated by a rich intersection of herbal, spicy, and citrus-forward notes that stem directly from this confirmed distribution of aromatic compounds.

As a THC-dominant variety, Lele da Cuca is primarily sought for its ability to induce effects that are consistently described as relaxed, happy, and uplifted. These qualities make it a practical choice for consumers addressing issues related to stress, pain, or the need for sleep. At present, there is no recorded list of offspring for this strain, confirming it as a unique entry in the modern autoflower market that currently stands without documented genetic progeny.

Terpene Profile

Synergies (+) and conflicts (−) are relative to each other within this profile.

myrcene ~60%caryophyllene ~28%limonene ~12%
TerpeneShare
myrcene~60%
caryophyllene~28%
limonene~12%

Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.

~60%

earthy

●●●○

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.

~12%

citrus

●●○○

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.

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 Lele da Cuca.

Ancestry

Lele da CucaFull tree →
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Composite Traits

Use caution if

daytime-productivitymorning-useevening-wind-down

Where to buy Lele da Cuca

No verified dispensaries on file — find it on Leafly.

Dispensary Locator

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What would Lele da Cuca × ? 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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Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Lele da Cuca indica or sativa?

Lele da Cuca is modeled here as a autoflower (photoperiod-independent).

What terpene is dominant in Lele da Cuca?

Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.

Is Lele da Cuca good for daytime use?

Lele da Cuca 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.