Brasil x K.C.
Top flavors
Terpenes
Brasil x K.C. effects are mostly calming.
Brasil x K.C.
Top flavors
Terpenes
Brasil x K.C. effects are mostly calming.
Brasil x K.C. is a modern hybrid-indica variety developed through the crossing of the Brasil landrace genetics. This hybrid produces a high yield and typically reaches harvest after a 63-day flowering period. It is regarded as a moderately difficult strain to cultivate, demonstrating reliable performance in both indoor and outdoor growing environments. The genetic stability of this hybrid is further evidenced by its role as a progenitor, most notably serving as a parent to the offspring known as KC 51.
The chemical profile of Brasil x K.C. is defined by a distinct dominance of myrcene, which provides the foundational aromatic qualities, followed by secondary notes of caryophyllene and a tertiary presence of pinene. These terpenes combine to define the strain's sensory character, balancing the earthy, musk-like profiles of the dominant myrcene with the spicy undertones of caryophyllene and the sharp, resinous notes contributed by pinene. The resulting bouquet remains consistent across varying cultivation methods, reflecting the specific chemical composition inherent to this hybrid-indica classification.
As a THC-dominant cultivar, Brasil x K.C. is primarily utilized for its therapeutic potential in addressing pain management, stress reduction, and sleep support. Consumers frequently report effects categorized as relaxed and focused, allowing for a balanced experience despite the strain's indica-leaning heritage. By providing a sedative physical sensation alongside a stable mental state, the strain serves as a functional tool for patients seeking relief, cementing its utility in both medicinal and recreational applications.
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 |
| 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.
Effects
Reported effects — derived from terpene chemistry and cannabinoid profile.
Genetic Profile
Indica-dominant
Primarily indica with sativa influence. Relaxing body with some cerebral lift.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Brasil x K.C..
Offspring — 1 strains bred from Brasil x K.C.
Composite Traits
Where to buy Brasil x K.C.
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What would Brasil x K.C. × ? 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 Brasil x K.C. →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Brasil x K.C. indica or sativa?
Brasil x K.C. is modeled here as a indica-dominant (primarily indica with sativa influence).
What terpene is dominant in Brasil x K.C.?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Brasil x K.C. good for daytime use?
Brasil x K.C. 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.