Alien Rock Candy
56d · moderate
Top flavors
Terpenes
Purple Tahoe Alien effects are mostly calming.
Purple Tahoe Alien is a modern hybrid-indica variety established through the genetic lineage of Tahoe Alien. As a descendant of this specific line, the strain has provided a foundation for further hybridization in modern breeding programs. Cultivators can expect a flowering period of 60 days, with the plant demonstrating a high yield potential that makes it suitable for both indoor and outdoor environments, though it is categorized as having a moderate growth difficulty.
The chemical profile of Purple Tahoe Alien is defined by a diverse array of compounds, starting with a dominant presence of myrcene, followed by caryophyllene and limonene. The secondary and tertiary layers of the profile include humulene, linalool, ocimene, beta-pinene, bisabolol, pinene, and camphene. This broad combination dictates the sensory experience, grounding the aromatic and flavor complexities in a specific sequence of these identified volatile organic compounds.
As a THC-dominant cultivar, Purple Tahoe Alien is utilized primarily for its capacity to induce effects of relaxation, calmness, and focus. These properties make it a frequent selection for the management of pain, stress, and sleep difficulties. The strain’s influence on the broader genetic landscape is evidenced by its role as a parent in the development of notable offspring, including Lavoo, MoJo, and Prometheus.
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 Purple Tahoe Alien.
Ancestry
Great-great-grandparents
Siblings
Share parent tahoe alien
Offspring — 3 strains bred from Purple Tahoe Alien
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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 Purple Tahoe Alien →Same primary terpene with overlapping effects.
56d · moderate
60d · moderate
56d · moderate
Seeds available56d · moderate
Seeds available60d · moderate
Seeds available47d · easy
Seeds availablePurple Tahoe Alien 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.
Purple Tahoe Alien 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.