Katie Crippin
Top flavors
Terpenes
Katie Crippin effects are mostly calming.
Katie Crippin
Katie Crippin is a modern, hybrid-sativa cultivar bred from the crossing of Blue Dream and Blues Bx1. The origins of the strain remain grounded in this specific lineage, with no further historical records provided regarding its development. Cultivation of this hybrid is considered of moderate difficulty, requiring a 70-day flowering period to reach its full potential. The plant thrives in both indoor and outdoor environments, and growers can expect a high yield from this genetic combination.
The chemical profile of Katie Crippin is confirmed to feature a primary concentration of myrcene, followed by pinene, caryophyllene, limonene, terpinolene, beta-pinene, humulene, linalool, and ocimene. This diverse terpene arrangement creates a nuanced sensory experience, though its specific aromatic intensity and flavor notes are an estimated outcome of this complex chemical sequence. THC-dominant by nature, the strain presents a profile defined by these nine specific compounds, which contribute to its distinct character.
Users typically report effects characterized by feelings of being creative, uplifted, and happy. Due to these qualities, the strain is well-suited for use cases involving creativity, social interaction, and focus. No notable offspring have been recorded in the genetic registry for Katie Crippin at this time.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| pinene | ~28% | pine | focus · 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: acetylcholinesterase inhibitor (IC50 0.44 mM) counteracting THC-induced short-term memory deficits; most widely encountered terpenoid in nature; anti-inflammatory via PGE-1.
~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.
creative
morningAssociated with terpinolene/limonene profiles; dopaminergic and serotonergic modulation via limonene 5-HT1A supports divergent thinking.
uplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
happy
anytimeGenetic Profile
Sativa-dominant
Primarily sativa with indica grounding. Uplifting with body relaxation.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Katie Crippin.
Ancestry
Great-grandparents
Grandparents
Siblings
Share parents blue dream / blues bx1
Composite Traits
Where to buy Katie Crippin
No verified dispensaries on file — find it on Leafly.
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What would Katie Crippin × ? 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 Katie Crippin →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Katie Crippin indica or sativa?
Katie Crippin is modeled here as a sativa-dominant (primarily sativa with indica grounding).
What terpene is dominant in Katie Crippin?
Myrcene is shown as the dominant terpene at approximately ~60%. Pinene follows as the secondary terpene.
Is Katie Crippin good for daytime use?
Katie Crippin 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.