Deep in Paradise
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Terpenes
Deep in Paradise effects are mostly calming.
Deep in Paradise
Deep in Paradise is a modern hybrid whose precise origins remain obscure, as its exact lineage is undocumented beyond its parentage to Pirate Booty. Because at least one parent remains unnamed, breeders have not publicly confirmed the full genetic cross, leaving the history of this strain largely a mystery. It is categorized as a modern hybrid and does not possess ties to landrace or heirloom varieties.
The terpene profile of Deep in Paradise follows a complex, confirmed hierarchy dominated by myrcene, followed by caryophyllene and limonene. Secondary and tertiary compounds include pinene, nerolidol, beta-pinene, linalool, humulene, ocimene, guaiol, p-cymene, bisabolol, caryophyllene-oxide, camphene, geraniol, and isopulegol. This array of aromatic compounds provides a distinct sensory profile, though specific flavor nuances are not detailed in the verified data.
Users of this THC-dominant strain report feeling relaxed, happy, and uplifted. These effects make it a common selection for those seeking relief from stress, pain, and sleep-related difficulties. Cultivators can expect a moderate level of grow difficulty with this hybrid, which reaches maturity after a 56-day flowering period and is capable of thriving in both indoor and outdoor environments. The plant is noted for producing high yields, though there are currently no recorded offspring in the strain’s genetic legacy.
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 |
| limonene | ~12% | citrus | social · 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: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
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 Deep in Paradise.
Ancestry
Great-great-grandparents
Great-grandparents
Grandparents
Siblings
Share parents unknown strain / pirate booty
Composite Traits
Where to buy Deep in Paradise
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
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What would Deep in Paradise × ? produce?
Predict the terpene profile, effects, and growing traits of a cross. Our gene weaver engine votes on dominant traits from both parents.
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Frequently Asked Questions
Is Deep in Paradise indica or sativa?
Deep in Paradise is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Deep in Paradise?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Deep in Paradise good for daytime use?
Deep in Paradise 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.