Hilo Hammer
14.4%
THC
Top flavors
Terpenes
Hilo Hammer has balanced effects.
Hilo Hammer is lower THC than average.
Hilo Hammer
14.4%
THC
Top flavors
Terpenes
Hilo Hammer has balanced effects.
Hilo Hammer is lower THC than average.
Hilo Hammer is a modern hybrid cannabis strain resulting from the crossing of Moloka'i Frost and Face/Off OG BX1. Designed for cultivators seeking high output, this variety requires moderate growing expertise and is suitable for both indoor and outdoor environments. Growers can expect a 63-day flowering period, consistently culminating in high yields.
The chemical profile of Hilo Hammer is defined by a complex terpene hierarchy, led by caryophyllene and followed by myrcene, limonene, and humulene. The aromatic experience is further shaped by secondary notes of beta-pinene, linalool, pinene, and bisabolol. This specific combination of dominant and tertiary compounds dictates the strain’s distinct sensory profile, presenting a balanced chemical composition derived from its hybrid parentage.
With a THC-dominant profile testing at approximately 14.4% and negligible CBD, Hilo Hammer acts primarily as a tool for those seeking to feel relaxed, happy, and uplifted. These reported effects make it a functional choice for managing stress and pain, or for users looking to facilitate sleep. There are currently no recorded offspring for this strain, marking it as a distinct, standalone entry in modern hybrid genetics.
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.
relaxed
eveningPrimary endpoint of myrcene+linalool sedating combinations; GABA modulation is the dominant mechanistic driver.
happy
anytimeuplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
Genetic Profile
Balanced Hybrid
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 Hilo Hammer.
Ancestry
Siblings
Share parents molokai frost / face off og bx1
Composite Traits
Where to buy Hilo Hammer
No verified dispensaries on file — find it on Leafly.
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What would Hilo Hammer × ? 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 Hilo Hammer →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Hilo Hammer indica or sativa?
Hilo Hammer is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Hilo Hammer?
Caryophyllene is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.
Is Hilo Hammer good for daytime use?
Hilo Hammer 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.