Auto Jack Hammer
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Terpenes
Auto Jack Hammer effects are mostly calming.
Auto Jack Hammer
Auto Jack Hammer is a modern, auto-flowering variety derived from Ruderalis genetics. Engineered for accessibility, this strain is categorized as easy to cultivate and thrives in both indoor and outdoor environments. Growers can expect a 74-day flowering cycle, which culminates in a low yield. Its genetic lineage has also proven influential in subsequent breeding projects, as it is the parent of the notable offspring known as Auto Big Angel.
The chemical profile of Auto Jack Hammer is complex, dominated by myrcene, caryophyllene, and limonene, followed by pinene, terpinolene, and linalool. The secondary and tertiary registers consist of beta-pinene, humulene, nerolidol, ocimene, bisabolol, guaiol, camphene, caryophyllene-oxide, and p-cymene. This specific chemical array defines the sensory experience of the plant, grounding the interplay between its primary and minor aromatic compounds.
As a THC-dominant variety, Auto Jack Hammer typically induces effects characterized by feelings of being relaxed, happy, and uplifted. These traits make the strain a suitable choice for users seeking relief from stress and pain, while others utilize the variety to assist with sleep. Its reliable phenotypic expression and functional chemical profile have solidified its role as a manageable, effective option within modern cannabis cultivation.
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
Autoflower
Photoperiod-independent. Flowers based on age, not light cycle. Compact and fast.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Auto Jack Hammer.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parent ruderalis
Offspring — 1 strains bred from Auto Jack Hammer
Composite Traits
Where to buy Auto Jack Hammer
No verified dispensaries on file — find it on Leafly.
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What would Auto Jack 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 Auto Jack Hammer →Similar strains
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Frequently Asked Questions
Is Auto Jack Hammer indica or sativa?
Auto Jack Hammer is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Auto Jack Hammer?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Auto Jack Hammer good for daytime use?
Auto Jack 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.