NFPhybrid

Nona F1 Project

Top flavors

spicycitrusearthy
CalmingEnergizing

Nona F1 Project has balanced effects.

Nona F1 Project is a modern hybrid cannabis strain derived from a genetic cross of Girl Scout Cookies and Sour Tangie. Its specific origins remain undocumented, with no definitive record detailing who first bred the strain or the precise timeframe of its development. As a project strain, it reflects the combination of its well-known parents, blending the structural traits associated with its lineage into a balanced cultivar. It is suitable for cultivation in both indoor and outdoor environments, with a flowering time of 70 days and a high yield potential for growers of moderate experience.

The terpene profile for Nona F1 Project is confirmed, with caryophyllene appearing as the dominant component, followed by limonene, myrcene, linalool, humulene, beta-pinene, bisabolol, pinene, and terpinolene. This complex arrangement suggests a sensory experience anchored by the spicy, peppery notes of caryophyllene, which are rounded out by the citrus-forward influence of limonene and the herbal, earthy undercurrents of myrcene and linalool. The secondary presence of humulene and pinene provides depth and nuance to the aroma, consistently delivering a layered profile that reflects the distinct chemical contributions of its parentage.

As a THC-dominant cultivar, Nona F1 Project is frequently chosen for its reliable therapeutic applications, including the management of stress, pain, and sleep difficulties. Users consistently report experiencing a sense of relaxation combined with a happy and uplifted mood, making it a versatile option for those seeking symptomatic relief. While the strain remains a focused project, there are currently no recorded notable offspring, leaving it as a singular entry in its genetic lineage.

Terpene Profile

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

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

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.

~28%

citrus

●●○○

Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.

~12%

earthy

●●●○

Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.

Effects

Reported effects — derived from terpene chemistry and cannabinoid profile.

Genetic Profile

Balanced Hybrid

■ Indica 50%■ Sativa 50%

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 Nona F1 Project.

Composite Traits

Use caution if

daytime-productivitymorning-use

Where to buy Nona F1 Project

No verified dispensaries on file — find it on Leafly.

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What would Nona F1 Project × ? 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 Nona F1 Project indica or sativa?

Nona F1 Project is modeled here as a balanced hybrid (equal indica and sativa genetics).

What terpene is dominant in Nona F1 Project?

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

Is Nona F1 Project good for daytime use?

Nona F1 Project 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.