Delhi Friend
11.4%
THC
Top flavors
Terpenes
Delhi Friend effects are mostly calming.
Delhi Friend is lower THC than average.
Delhi Friend
11.4%
THC
Top flavors
Terpenes
Delhi Friend effects are mostly calming.
Delhi Friend is lower THC than average.
Delhi Friend is a modern indica strain developed from Indian indica genetics. This cultivar is categorized as easy to grow, thriving in both indoor and outdoor environments with a moderate yield and a short flowering period of 49 days. Its distinct genetic lineage has contributed to the development of notable offspring, including Bud Bud Bling Tingz, Chemdog Millionaire, and Patel's Cornershop Surprise.
The chemical profile of Delhi Friend is defined by a complex arrangement of terpenes, led by the floral and woody notes of nerolidol, followed by the citrus-forward influence of limonene and the spicy warmth of caryophyllene. The secondary and tertiary layers of this strain feature humulene, linalool, myrcene, and bisabolol, with trace contributions from beta-pinene, caryophyllene-oxide, camphene, terpinolene, and pinene. This specific terpene hierarchy informs the strain's sensory expression, providing a structured aromatic profile that balances zest with deeper, grounding musk.
As a THC-dominant variety, Delhi Friend is primarily utilized for the induction of relaxed, calm, and focused states. Its therapeutic application is focused on the management of pain, stress, and sleep disturbances, making it a functional choice for those seeking relief without excessive sedation. Beyond its primary use cases, its impact on the modern market is evidenced by its role as a parent for multiple prominent offspring, solidifying its place within contemporary selective breeding programs.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| nerolidol | ~60% | floral | sleep · relaxing |
| limonene | ~28% | citrus | social · 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: sedative properties; enhances transdermal pharmaceutical penetration; antimalarial; PMC11060501: GABAergic-mediated antinociception.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
~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.
Genetic Profile
Pure Indica
Body-heavy, relaxing genetics. Short stature, dense buds, broad leaves.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of Delhi Friend.
Ancestry
Great-grandparents
Grandparents
Siblings
Share parent india indica
Offspring — 2 strains bred from Delhi Friend
Composite Traits
Where to buy Delhi Friend
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
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What would Delhi Friend × ? 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 Delhi Friend →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Delhi Friend indica or sativa?
Delhi Friend is modeled here as a pure indica (body-heavy, relaxing genetics).
What terpene is dominant in Delhi Friend?
Nerolidol is shown as the dominant terpene at approximately ~60%. Limonene follows as the secondary terpene.
Is Delhi Friend good for daytime use?
Delhi Friend 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.