White OG
Modern
Hhybrid-indica
Harambe
14.9%
THC
Top flavors
floralearthycitrus
CalmingEnergizing
Harambe effects are mostly calming.
Low THCHigh THC
Harambe is lower THC than average.
Harambe is a modern hybrid-indica strain bred from Frost Berry Blast. The genetic lineage is characterized by this specific ancestry, which also serves as the parent to its notable offspring, Frost Berry Blast. This cultivar requires moderate cultivation experience and is suitable for both indoor and outdoor environments. Growers can expect a high yield from this plant, which reaches maturity after a 68-day flowering cycle.
The terpene profile of Harambe is dominated by nerolidol, followed by myrcene, limonene, beta-pinene, and pinene. The chemical sequence continues with isopulegol, camphene, terpinolene, and finally caryophyllene. This complex arrangement of secondary metabolites shapes the sensory experience, providing a distinct aromatic and flavor profile defined by this specific hierarchy of organic compounds.
As a THC-dominant strain, Harambe is primarily sought for its ability to induce states of relaxation, calmness, and mental focus. These effects make it a consistent choice for individuals managing pain, stress, or sleep-related difficulties. Beyond its immediate therapeutic utility, the strain maintains a clear genetic footprint through its documented role as both a descendant and a predecessor to the Frost Berry Blast variety.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
nerolidol ~60%myrcene ~28%limonene ~12%
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| nerolidol | ~60% | floral | sleep · relaxing |
| myrcene | ~28% | earthy | relaxing · solo |
| 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: sedative properties; enhances transdermal pharmaceutical penetration; antimalarial; PMC11060501: GABAergic-mediated antinociception.
Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
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.
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 Harambe.
Ancestry
Great-great-grandparents
Bubba Kush
limonene· relaxed· sleepy
Durban PoisonLandrace
terpinolene· energetic· uplifted
OG Kush
limonene· relaxed· creative
Skunk #1
pinene· relaxed· uplifted
Great-grandparents
AfghaniLandrace
myrcene· relaxed· sleepy
Girl Scout Cookies
caryophyllene· relaxed· creative
Green Crack
myrcene· energetic· uplifted
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Siblings
Share parent frost berry blast
Offspring — 1 strains bred from Harambe
Composite Traits
Where to buy Harambe
No verified dispensaries on file — find it on Leafly.
Dispensary Locator
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What would Harambe × ? 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 Harambe →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Harambe indica or sativa?
Harambe is modeled here as a indica-dominant (primarily indica with sativa influence).
What terpene is dominant in Harambe?
Nerolidol is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.
Is Harambe good for daytime use?
Harambe 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.