G#hybrid-indica
Hybrid-IndicaModernTHC-Dominantevening

Gonzo #2

Top flavors

earthyspicypine
CalmingEnergizing

Gonzo #2 effects are mostly calming.

Gonzo #2 manifests as a modern hybrid-indica cultivar of largely undocumented lineage. As a result of its obscure genetic origins, the precise history of its development remains unverified. Cultivators categorize this strain as a moderate-difficulty plant that performs successfully in both indoor and outdoor environments. With a flowering cycle of 63 days, it is recognized for producing a high yield, and its genetic impact on the modern market is evidenced by notable offspring such as BlueG and CnlpGonzo WhOgV2 x DC.

The chemical expression of Gonzo #2 is defined by a specific hierarchy of terpenes, led by myrcene as the primary aromatic compound. This is followed by secondary notes of caryophyllene and tertiary undertones of pinene, contributing to the distinct olfactory profile of this THC-dominant variety. The olfactory experience is intrinsically linked to this terpene arrangement, as the interaction between these dominant and trace constituents shapes the sensory delivery of the flower.

Clinically, the primary effects of Gonzo #2 are characterized by a sense of relaxation, calm, and focus. These properties inform its common use cases, which include the management of pain, stress, and sleep cycles. By providing a balanced experience that leans into its indica-dominant heritage while maintaining mental clarity, the strain functions as a versatile option for those seeking consistent therapeutic relief. Through its legacy in hybrids like BlueG and CnlpGonzo WhOgV2 x DC, the strain continues to exert a measurable influence on contemporary breeding programs.

Terpene Profile

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

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

pine

●●○○

Russo 2011: acetylcholinesterase inhibitor (IC50 0.44 mM) counteracting THC-induced short-term memory deficits; most widely encountered terpenoid in nature; anti-inflammatory via PGE-1.

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

Parent data not yet recorded for Gonzo #2.

Gonzo #2

Offspring — 1 strains bred from Gonzo #2

View full lineage tree →

Composite Traits

Use caution if

daytime-productivitymorning-useevening-wind-down

Where to buy Gonzo #2

No verified dispensaries on file — find it on Leafly.

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What would Gonzo #2 × ? 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 Gonzo #2

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Gonzo #2 indica or sativa?

Gonzo #2 is modeled here as a indica-dominant (primarily indica with sativa influence).

What terpene is dominant in Gonzo #2?

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

Is Gonzo #2 good for daytime use?

Gonzo #2 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.