Northern Lights
47d · easy
Seeds availableTop flavors
Terpenes
Grape Ape effects are mostly calming.
Grape Ape is a modern hybrid-indica cultivar derived from Haze genetics. It is a reliable choice for cultivators of moderate experience, thriving in both indoor and outdoor environments. This strain is characterized by a high yield and reaches maturity after a 60-day flowering period. Its genetic influence is extensive, having served as a parent to notable offspring including Purple Jello Pie, Strawberry Pines, Cherry Chardonnay, F.I.G., Hot Wax, Purple Passion, Alien Grapevine, Alien Tits, Ape Pie, Blue Cake, Cherry OG Kush, and Colorado Grapes.
The chemical profile of Grape Ape is defined by a complex sequence of terpenes, led by terpinolene, myrcene, and ocimene. These primary constituents are complemented by significant levels of caryophyllene, beta-pinene, and limonene. The secondary aromatic structure is rounded out by pinene, alpha-terpinene, gamma-terpinene, humulene, eucalyptol, and nerolidol. This diverse combination creates a nuanced sensory experience driven by this specific chemical hierarchy rather than any single dominant compound.
As a THC-dominant cultivar, Grape Ape is primarily utilized to promote states of relaxation and mental focus. These therapeutic qualities make it a common choice for managing symptoms related to pain, stress, and sleep difficulties. Given its consistent performance and widespread genetic impact, it remains a foundational hybrid for both breeders and those seeking specific functional outcomes from their cannabis consumption.
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
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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 Grape Ape.
Ancestry
Grandparents
Siblings
Share parent haze
Offspring — 30 strains bred from Grape Ape
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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 Grape Ape →Same primary terpene with overlapping effects.
47d · easy
Seeds available60d · easy
Seeds available56d · moderate
Seeds available56d · moderate
Seeds available60d · moderate
Seeds available47d · easy
Seeds availableGrape Ape 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.
Grape Ape 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.