HHhybrid-indica
Hybrid-IndicaModernTHC-Dominantevening

Huckleberry Hound

Top flavors

earthyspicysweet
CalmingEnergizing

Huckleberry Hound effects are mostly calming.

Huckleberry Hound is a modern, hybrid-indica strain derived from its parent, TreStarDawg. This cultivar serves as the genetic foundation for several notable offspring, including Huckleberry Soda, Pink Dream, Pink LemonAid, Purple Pineapple Express, and Purple Pleiades. Cultivators can expect a moderate growth difficulty, with plants reaching harvest after a 60-day flowering period. Suitable for both indoor and outdoor environments, the strain is recognized for producing a high yield.

The chemical complexity of Huckleberry Hound is defined by a diverse terpene profile led by myrcene, caryophyllene, and ocimene. These primary constituents are supported by pinene, nerolidol, limonene, humulene, and linalool, with trace amounts of beta-pinene, bisabolol, guaiol, camphene, eucalyptol, p-cymene, caryophyllene-oxide, and terpinolene rounding out the composition. This specific arrangement of terpenes dictates the strain's sensory profile, which is inherently linked to its THC-dominant cannabinoid structure.

When consumed, Huckleberry Hound provides users with effects that are consistently relaxed, calm, and focused. These characteristics make it a functional choice for addressing physical pain and mitigating high levels of stress, while also being well-suited for individuals seeking assistance with sleep. As a verified hybrid-indica, the strain remains a consistent tool for therapeutic applications and a significant contributor to the lineage of its various progeny.

Terpene Profile

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

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

sweet

●○○○

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.

Genetic Profile

Indica-dominant

■ Indica 70%■ Sativa 30%

Primarily indica with sativa influence. Relaxing body with some cerebral lift.

THC-Dominant

High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.

Genealogy

Parentage, ancestry, and genetic relatives of Huckleberry Hound.

Composite Traits

Use caution if

daytime-productivitymorning-use

Where to buy Huckleberry Hound

No verified dispensaries on file — find it on Leafly.

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What would Huckleberry Hound × ? 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 Huckleberry Hound

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Huckleberry Hound indica or sativa?

Huckleberry Hound is modeled here as a indica-dominant (primarily indica with sativa influence).

What terpene is dominant in Huckleberry Hound?

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

Is Huckleberry Hound good for daytime use?

Huckleberry Hound 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.