Kak'Nasty
Top flavors
Terpenes
Kak'Nasty effects are mostly calming.
Kak'Nasty
Kak'Nasty is a modern hybrid cannabis strain derived from a genetic cross of Medicine Man and White Widow. The specific origins and history of this strain remain undocumented, with no definitive records regarding its original breeder or regional development timeline. As a result, its historical context remains limited to the known lineage provided by its parentage.
The terpene profile of Kak'Nasty is led by myrcene, followed by limonene, caryophyllene, isopulegol, beta-pinene, linalool, pinene, nerolidol, humulene, bisabolol, caryophyllene-oxide, camphene, eucalyptol, terpinolene, ocimene, guaiol, gamma-terpinene, p-cymene, and alpha-terpinene. Cultivators can expect a consistent sensory experience defined by this chemical structure, which contributes to the strain's specific aroma and flavor characteristics. Growers should note that the plant reaches maturity after a 70-day flowering period, performing well in both indoor and outdoor environments while offering a high yield.
As a THC-dominant hybrid, Kak'Nasty produces effects described as relaxed, happy, and uplifted. These properties make the strain a suitable option for users seeking relief from symptoms associated with stress, pain, and sleep difficulties. Despite its status as a distinct modern hybrid, there are currently no recorded notable offspring linked to this variety in the StrainWeaver database. Due to its moderate cultivation difficulty, it remains a manageable inclusion for both new and experienced growers focused on high-output production.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| limonene | ~28% | citrus | social · creative |
| caryophyllene | ~12% | spicy | relaxing · social |
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.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
~12%
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.
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 Kak'Nasty.
Ancestry
Grandparents
Siblings
Share parents medicine man / white widow
Composite Traits
Where to buy Kak'Nasty
No verified dispensaries on file — find it on Leafly.
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What would Kak'Nasty × ? 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 Kak'Nasty indica or sativa?
Kak'Nasty is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Kak'Nasty?
Myrcene is shown as the dominant terpene at approximately ~60%. Limonene follows as the secondary terpene.
Is Kak'Nasty good for daytime use?
Kak'Nasty 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.