Kilimanjaro
66d · moderate
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Terpenes
Kahuna effects are mostly calming.
Kahuna is a modern indica-dominant cultivar bred from a complex genetic lineage consisting of Big Skunk Korean, Jack Herer, and Afghani Hawaiian. Designed for accessibility in a controlled environment, this strain is well-regarded for its straightforward cultivation process. Growers can expect a medium yield following a flowering cycle of approximately 67 days, with the plant proving resilient enough for success in both indoor and outdoor setups. Its genetic influence is notable in the industry, as it has served as a parent in the breeding of Big Skunk Korean.
The chemical profile of Kahuna is characterized by a sophisticated arrangement of ten distinct terpenes, led by a dominant concentration of terpinolene. This primary terpene is supported by secondary and tertiary notes of myrcene, caryophyllene, ocimene, and limonene, which blend with trailing traces of humulene, beta-pinene, linalool, pinene, and alpha-terpinene. This specific terpene hierarchy informs the strain's sensory expression, providing a nuanced aromatic and flavor profile maintained by the balance of these organic compounds.
As a THC-dominant cultivar, Kahuna produces subjective effects primarily described as relaxed, calm, and focused. These qualities make it a practical choice for consumers seeking relief from pain, stress, or difficulties with sleep. Beyond its immediate utility for the individual user, the strain maintains a clear genetic footprint in modern breeding cycles, reinforcing its position as a functional and reliable component within its category.
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 |
| pinene | ~12% | pine | focus · 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: acetylcholinesterase inhibitor (IC50 0.44 mM) counteracting THC-induced short-term memory deficits; most widely encountered terpenoid in nature; anti-inflammatory via PGE-1.
Reported effects — derived from terpene chemistry and cannabinoid profile.
Primary endpoint of myrcene+linalool sedating combinations; GABA modulation is the dominant mechanistic driver.
Linalool GABA-A modulation + caryophyllene CB2 agonism drive anxiolysis without heavy sedation; distinct from sleepy — supports sustained presence and mild focus.
Pinene acetylcholinesterase inhibition (IC50 0.44 mM per Russo 2011) sustains acetylcholine; counteracts THC-induced short-term memory deficits.
Body-heavy, relaxing genetics. Short stature, dense buds, broad leaves.
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Parentage, ancestry, and genetic relatives of Kahuna.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Parents
Siblings
Share parents big skunk korean / jack herer / afghani hawaiian
Offspring — 1 strains bred from Kahuna
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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 Kahuna →Same primary terpene with overlapping effects.
66d · moderate
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Seeds available56d · moderate
Seeds availableKahuna is modeled here as a pure indica (body-heavy, relaxing genetics).
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Kahuna is versatile and works across different times of day depending on dose and individual response.
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.