Australian Dead Head
16.4%
THC
Top flavors
Terpenes
Australian Dead Head effects are mostly calming.
Australian Dead Head potency is average.
Australian Dead Head
16.4%
THC
Top flavors
Terpenes
Australian Dead Head effects are mostly calming.
Australian Dead Head potency is average.
Australian Dead Head is a modern hybrid cannabis strain created through the crossing of Neville's Haze and Grateful Casey. This controlled breeding process results in a plant that requires moderate difficulty to cultivate in both indoor and outdoor environments. Growers can expect a high yield from this variety, which reaches maturity after a 63-day flowering period.
The chemical profile of Australian Dead Head is dominated by myrcene, followed by caryophyllene and limonene. These terpenes dictate the sensory experience, providing a distinct aromatic and flavorful nuance inherent to the strain’s specific genetic makeup.
Consumers of Australian Dead Head typically report feeling relaxed, happy, and uplifted following use. Due to these primary effects, the strain is frequently selected as a functional option for addressing stress, pain, and sleep difficulties. With a THC content of approximately 16.4 percent, the strain serves as a THC-dominant option for those seeking consistent therapeutic applications, though there are currently no notable offspring recorded for this variety.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| caryophyllene | ~28% | spicy | relaxing · social |
| 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.
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.
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 Australian Dead Head.
Ancestry
Grandparents
Siblings
Share parents nevilles haze / grateful casey
Composite Traits
Where to buy Australian Dead Head
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
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What would Australian Dead Head × ? 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 Australian Dead Head →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Australian Dead Head indica or sativa?
Australian Dead Head is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Australian Dead Head?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Australian Dead Head good for daytime use?
Australian Dead Head 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.