Shark Shock
7.4%
THC
0.08%
CBD
0.05%
CBG
Top flavors
Terpenes
Shark Shock effects are mostly calming.
Shark Shock is lower THC than average.
Shark Shock
7.4%
THC
0.08%
CBD
0.05%
CBG
Top flavors
Terpenes
Shark Shock effects are mostly calming.
Shark Shock is lower THC than average.
Shark Shock is a modern hybrid strain derived from Skunk No. 1. Developed to maximize production, this plant thrives in both indoor and outdoor environments, offering a high yield potential after a relatively short flowering period of 50 days. While the cultivation process is considered of moderate difficulty, the strain has proven itself a reliable genetic foundation, serving as a primary component in the creation of notable offspring such as CBD Shark and Kripple Shock.
The sensory profile of Shark Shock is defined by a specific hierarchy of terpenes, led by myrcene, followed by caryophyllene and limonene. This chemical combination creates a distinct aromatic expression, characterized by the dominant earthy influence of myrcene balanced by the spicy notes of caryophyllene and the bright, citrus-forward qualities of limonene.
As a THC-dominant variety, Shark Shock typically induces effects described as relaxed, happy, and uplifted. These properties make the strain a frequent choice for users seeking support in the management of stress, pain, and sleep difficulties. Its consistent physical and cerebral profile has established it as a versatile cultivar within the modern secondary market, both for its therapeutic utility and its efficacy in subsequent breeding programs.
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 Shark Shock.
Siblings
Share parent skunk no 1
Offspring — 2 strains bred from Shark Shock
Composite Traits
Where to buy Shark Shock
No verified dispensaries on file — find it on Leafly.
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What would Shark Shock × ? 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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Frequently Asked Questions
Is Shark Shock indica or sativa?
Shark Shock is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Shark Shock?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Shark Shock good for daytime use?
Shark Shock 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.