Hula Girl
Top flavors
Terpenes
Hula Girl has balanced effects.
Hula Girl
Hula Girl is a modern hybrid-sativa variety resulting from the specific crossing of Larry OG and Iris. This strain is designed to balance the structural characteristics of its parentage, performing well in both indoor and outdoor cultivation environments. Growers can expect a moderate level of difficulty when managing this plant, which reaches maturity after a 65-day flowering period and is noted for producing a high overall yield.
The chemical profile of Hula Girl is defined by a complex, layered array of terpenes. Caryophyllene acts as the primary influence, followed by significant concentrations of myrcene and limonene, with humulene and linalool providing secondary aromatic notes. The lower-tier terpene profile includes nerolidol, bisabolol, beta-pinene, pinene, valencene, caryophyllene-oxide, isopulegol, camphene, borneol, and guaiol. This intricate combination creates a specific flavor and aroma nuance driven by these fifteen distinct compounds.
As a THC-dominant cultivar, Hula Girl is primarily utilized for its creative, uplifted, and euphoric effects. It is frequently selected as a functional strain for social engagements, tasks requiring concentrated focus, and individual creative pursuits. The genetic legacy of this strain is marked by its notable offspring, which includes the derivative cultivar known as La Hula, also referred to as MLI.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| caryophyllene | ~60% | spicy | relaxing · social |
| myrcene | ~28% | earthy | relaxing · solo |
| 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.
~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.
Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
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.
creative
morningAssociated with terpinolene/limonene profiles; dopaminergic and serotonergic modulation via limonene 5-HT1A supports divergent thinking.
uplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
happy
anytimeGenetic Profile
Sativa-dominant
Primarily sativa with indica grounding. Uplifting with body relaxation.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Hula Girl.
Ancestry
Great-grandparents
Grandparents
Offspring — 1 strains bred from Hula Girl
Composite Traits
Where to buy Hula Girl
No verified dispensaries on file — find it on Leafly.
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What would Hula Girl × ? 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 Hula Girl →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Hula Girl indica or sativa?
Hula Girl is modeled here as a sativa-dominant (primarily sativa with indica grounding).
What terpene is dominant in Hula Girl?
Caryophyllene is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.
Is Hula Girl good for daytime use?
Hula Girl 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.