Bubba D
20.2%
THC
Top flavors
Terpenes
Bubba D effects are mostly energizing.
Bubba D potency is average.
Bubba D
20.2%
THC
Top flavors
Terpenes
Bubba D effects are mostly energizing.
Bubba D potency is average.
Bubba D is a modern hybrid strain derived from Sour Diesel IBL. Cultivated to deliver a high yield, this variety thrives in both indoor and outdoor environments with a flowering period of 63 days and a moderate growing difficulty rating. Its genetic influence is evident in the development of several notable offspring, including Aconcagua Haze, Double Purple Bubba Diesel, Forest Queen, Pirate Sweat, and White Bubba Haze.
The chemical composition of Bubba D is defined by a complex terpene profile led by terpinolene, followed closely by myrcene and caryophyllene. This dominant expression transitions into humulene, bisabolol, and limonene, with secondary notes provided by beta-pinene, nerolidol, pinene, linalool, caryophyllene-oxide, camphene, p-cymene, and ocimene. As a THC-dominant cultivar, the interaction of these compounds shapes its unique sensory profile and overall potency.
Users typically report feeling relaxed, happy, and uplifted after consumption. Due to these primary effects, Bubba D is frequently utilized for managing stress, addressing pain, and assisting with sleep. Its legacy continues through its diverse genetic contributions to modern cannabis breeding, as seen in the wide array of established strains that claim Bubba D as a parent.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| terpinolene | ~60% | herbal | creative · social |
| myrcene | ~28% | earthy | relaxing · solo |
| 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.
~60%
herbal
●○○○
PMC11060501: antinociception via NO/PGE2/TNF-α inhibition; associated with cerebral sativa profiles; least clinically characterised of major terpenes.
Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
~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
Balanced Hybrid
Equal indica and sativa genetics. Balanced body and mind effects.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Bubba D.
Ancestry
Great-great-grandparents
Grandparents
Siblings
Share parent sour diesel ibl
Offspring — 4 strains bred from Bubba D
Composite Traits
Where to buy Bubba D
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
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What would Bubba D × ? 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 Bubba D →Similar strains
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Frequently Asked Questions
Is Bubba D indica or sativa?
Bubba D is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Bubba D?
Terpinolene is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.
Is Bubba D good for daytime use?
Bubba D 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.