KOhybrid-indica
Hybrid-IndicaModernTHC-Dominantevening

KnightsBridge OG

Top flavors

earthyspicypine
CalmingEnergizing

KnightsBridge OG effects are mostly calming.

KnightsBridge OG is a modern hybrid-indica strain derived from the genetics of SFV OG Kush. As a direct descendant, it reflects the specialized lineage of its predecessor, and it is widely credited with establishing a stable foundation for further breeding projects. Cultivators can expect this strain to reach maturity with a 60-day flowering period. KnightsBridge OG is considered a moderate challenge to grow, though it remains a versatile choice that performs well in both indoor and outdoor environments while consistently providing high yields.

The chemical character of KnightsBridge OG is defined by a terpene profile dominated by myrcene, followed by secondary caryophyllene and tertiary pinene. This specific arrangement suggests a complex sensory experience that balances earthy, musky undertones with the spicy notes of caryophyllene and sharp, pine-forward highlights. These compounds interact to create a nuanced aromatic and flavor profile that reflects the lineage of its SFV OG Kush parentage.

The effects of KnightsBridge OG are primary THC-dominant, resulting in a state characterized by feeling relaxed, calm, and focused. These properties make the strain a functional option for users seeking support for pain, stress, or sleep-related concerns. The genetic legacy of this strain is evidenced by its notable offspring, which include Kensington Kush and KnightsBridge OG Haze, both of which demonstrate the enduring influence of these specific hybrid-indica genetics within modern breeding.

Terpene Profile

Synergies (+) and conflicts (−) are relative to each other within this profile.

myrcene ~60%caryophyllene ~28%pinene ~12%
TerpeneShare
myrcene~60%
caryophyllene~28%
pinene~12%

Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.

~60%

earthy

●●●○

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.

~12%

pine

●●○○

Russo 2011: acetylcholinesterase inhibitor (IC50 0.44 mM) counteracting THC-induced short-term memory deficits; most widely encountered terpenoid in nature; anti-inflammatory via PGE-1.

Effects

Reported effects — derived from terpene chemistry and cannabinoid profile.

Genetic Profile

Indica-dominant

■ Indica 70%■ Sativa 30%

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 KnightsBridge OG.

Composite Traits

Use caution if

daytime-productivitymorning-useevening-wind-down

Where to buy KnightsBridge OG

No verified dispensaries on file — find it on Leafly.

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What would KnightsBridge 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 KnightsBridge OG

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is KnightsBridge OG indica or sativa?

KnightsBridge OG is modeled here as a indica-dominant (primarily indica with sativa influence).

What terpene is dominant in KnightsBridge OG?

Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.

Is KnightsBridge OG good for daytime use?

KnightsBridge 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.