DR OG
10.2%
THC
Top flavors
Terpenes
DR OG effects are mostly calming.
DR OG is lower THC than average.
DR OG
10.2%
THC
Top flavors
Terpenes
DR OG effects are mostly calming.
DR OG is lower THC than average.
DR OG is a modern hybrid-sativa strain derived directly from its parent, Em-Dog. As a cultivar developed for specific traits, it requires moderate attention throughout its growth cycle, which reaches completion after a flowering period of 68 days. Adaptable to both indoor and outdoor environments, the strain is recognized for its ability to produce high yields.
The chemical profile of DR OG is led by a terpene complex dominated by terpinolene, followed in intensity by myrcene and caryophyllene. This specific arrangement of terpenes dictates the strain’s distinct sensory profile, balancing sharp, aromatic notes with deeper, earthy undertones. These compounds define the character of the plant, ensuring a consistent aromatic experience for the user.
In terms of therapeutic and recreational application, DR OG provides consistent effects that are primarily creative, uplifted, and happy. Because of this profile, the strain is frequently selected for activities that require heightened creativity, social interaction, and mental focus. With a THC-dominant composition averaging approximately 10.2 percent, it functions as a functional hybrid, though there are currently no notable offspring recorded in its genetic lineage.
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 |
| nerolidol | ~12% | floral | sleep · relaxing |
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: sedative properties; enhances transdermal pharmaceutical penetration; antimalarial; PMC11060501: GABAergic-mediated antinociception.
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 DR OG.
Ancestry
Great-great-grandparents
Great-grandparents
Siblings
Share parent em dog
Composite Traits
Where to buy DR OG
No verified dispensaries on file — find it on Leafly.
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What would DR 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 DR OG →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is DR OG indica or sativa?
DR OG is modeled here as a sativa-dominant (primarily sativa with indica grounding).
What terpene is dominant in DR OG?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is DR OG good for daytime use?
DR 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.