Bizarre
53d · moderate
Top flavors
Terpenes
Gorilla Grape effects are mostly calming.
Gorilla Grape is a modern hybrid-indica strain derived from the genetics of Double Purple Doja. Developed to offer a specific balance of traits, this strain thrives in both indoor and outdoor environments. Cultivators can expect a high yield from these plants, which reach maturity after a flowering cycle of 60 days. While the cultivation process is rated as moderate in difficulty, the strain remains a consistent choice for growers seeking reliable productivity.
The chemical profile of Gorilla Grape is defined by a distinct terpene arrangement, led by myrcene as the dominant compound, followed by caryophyllene and pinene. This specific combination creates a complex sensory experience, grounding the aromatic properties of the strain in its primary terpene base. The interplay between these three constituents defines the overarching profile, providing a consistent structural identity to the plant's scent and flavour.
Users typically experience effects that are relaxed and focused, making the strain well-suited for addressing symptoms of pain, stress, and sleep. As a THC-dominant cultivar, its influence on the user is primarily driven by its cannabinoid concentration. Beyond its immediate effects, Gorilla Grape has served as a foundational component in further breeding efforts, resulting in a diverse genetic legacy that includes offspring such as Phantom Cookie x Black Domina x Gorilla Grape, Chocolate Chunky Munky F2, Candy Magic, Magic Fire, Asshat, Big Laughing, Black Grapes, Buckeye Purple, Call Girl, Dr Grape, Dumpster Diver, and Generic Weed.
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 |
| pinene | ~12% | pine | focus · 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: acetylcholinesterase inhibitor (IC50 0.44 mM) counteracting THC-induced short-term memory deficits; most widely encountered terpenoid in nature; anti-inflammatory via PGE-1.
Reported effects — derived from terpene chemistry and cannabinoid profile.
Primary endpoint of myrcene+linalool sedating combinations; GABA modulation is the dominant mechanistic driver.
Linalool GABA-A modulation + caryophyllene CB2 agonism drive anxiolysis without heavy sedation; distinct from sleepy — supports sustained presence and mild focus.
Pinene acetylcholinesterase inhibition (IC50 0.44 mM per Russo 2011) sustains acetylcholine; counteracts THC-induced short-term memory deficits.
Primarily indica with sativa influence. Relaxing body with some cerebral lift.
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Parentage, ancestry, and genetic relatives of Gorilla Grape.
Siblings
Share parent double purple doja
Offspring — 27 strains bred from Gorilla Grape
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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 Gorilla Grape →Same primary terpene with overlapping effects.
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Seeds availableGorilla Grape is modeled here as a indica-dominant (primarily indica with sativa influence).
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Gorilla Grape is versatile and works across different times of day depending on dose and individual response.
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.