Blue Bear OG
Top flavors
Terpenes
Blue Bear OG effects are mostly calming.
Blue Bear OG
Top flavors
Terpenes
Blue Bear OG effects are mostly calming.
Blue Bear OG is a modern, autoflowering cultivar developed by crossing Blue Streak and Lowryder. As an easy-to-grow variety suitable for both indoor and outdoor environments, it completes its flowering lifecycle in approximately 90 days. While the plant offers a low yield, it has established its genetic legacy through notable offspring, including Creature Bear OG and Teddy Gramz.
The chemical profile of this strain is defined by a complex arrangement of terpenes, led by myrcene, terpinolene, and caryophyllene. These primary aromatics are complemented by a tertiary array that includes limonene, ocimene, linalool, humulene, pinene, beta-pinene, bisabolol, guaiol, alpha-terpinene, nerolidol, and camphene. This specific combination creates a nuanced sensory profile that reflects the depth of its inherited genetic traits.
As a THC-dominant cultivar, Blue Bear OG produces effects characterized primarily by a sense of relaxation, happiness, and an uplifted mood. These properties make it a frequent choice for users seeking support in navigating stress, managing pain, and facilitating sleep. Through its documented lineage and subsequent progeny, the strain remains a consistent contributor to the modern autoflowering landscape.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| terpinolene | ~28% | herbal | creative · social |
| 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.
~28%
herbal
●○○○
PMC11060501: antinociception via NO/PGE2/TNF-α inhibition; associated with cerebral sativa profiles; least clinically characterised of major terpenes.
~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
Autoflower
Photoperiod-independent. Flowers based on age, not light cycle. Compact and fast.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Blue Bear OG.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parents blue streak / lowryder
Offspring — 2 strains bred from Blue Bear OG
Composite Traits
Where to buy Blue Bear OG
No verified dispensaries on file — find it on Leafly.
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What would Blue Bear OG × ? 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 Blue Bear OG →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Blue Bear OG indica or sativa?
Blue Bear OG is modeled here as a autoflower (photoperiod-independent).
What terpene is dominant in Blue Bear OG?
Myrcene is shown as the dominant terpene at approximately ~60%. Terpinolene follows as the secondary terpene.
Is Blue Bear OG good for daytime use?
Blue Bear OG 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.