London Poundcake
27.8%
THC
Top flavors
Terpenes
London Poundcake effects are mostly energizing.
London Poundcake potency is higher THC than average.
London Poundcake
27.8%
THC
Top flavors
Terpenes
London Poundcake effects are mostly energizing.
London Poundcake potency is higher THC than average.
London Poundcake is a modern hybrid-indica variety resulting from indica lineage. This strain has established a notable presence in the industry for its consistent performance and reliable botanical characteristics. Cultivators can expect a moderate difficulty level when growing the plant in either indoor or outdoor environments, with a flowering time of approximately 60 days and a high harvest yield.
The terpene profile is headlined by limonene, followed by myrcene, caryophyllene, linalool, beta-pinene, and humulene, which collectively shape its aromatic and sensory expression. This specific chemical composition defines the experience, balancing the citrus qualities of its primary terpene with the herbal and spicy undertones of the profile. As a THC-dominant variety with 27.8% THC and 0% CBD, it delivers a consistent profile that translates directly into its reported effects.
In practice, this strain is utilized to promote feelings of relaxation and focus, making it a functional choice for those seeking relief from pain, stress, or sleep-related issues. Its genetic influence has extended significantly, serving as a foundational parent for a wide array of subsequent varieties. This extensive lineage includes offspring such as Offshore Account, Swooner, Gary Payton X London Poundcake, Cheetah Piss, London Poundcake x F1 Durb x Gushers, Bubble Buzz, Candy Rain, Canoleez, Diepsloot Koek, Gas Works, Krumpets, and LPC X Kushmints F2.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| limonene | ~60% | citrus | social · creative |
| 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.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
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.
Genetic Profile
Indica-dominant
Primarily indica with sativa influence. Relaxing body with some cerebral lift.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of London Poundcake.
Siblings
Share parent indica
Offspring — 30 strains bred from London Poundcake
Composite Traits
Where to buy London Poundcake
No verified dispensaries on file — find it on Leafly.
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What would London Poundcake × ? 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 London Poundcake →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is London Poundcake indica or sativa?
London Poundcake is modeled here as a indica-dominant (primarily indica with sativa influence).
What terpene is dominant in London Poundcake?
Limonene is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.
Is London Poundcake good for daytime use?
London Poundcake 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.