Purple Pakistani Chitral
Top flavors
Terpenes
Purple Pakistani Chitral effects are mostly calming.
Purple Pakistani Chitral
Top flavors
Terpenes
Purple Pakistani Chitral effects are mostly calming.
Purple Pakistani Chitral is a modern hybrid-indica cultivar developed from the Pakistan Chitral Kush. According to lore, the original genetics emerged from the rugged terrain of the Hindu Kush mountain range, though this specific iteration is maintained as a modern breeding project. It is a moderately difficult plant to cultivate, performing well in both indoor and outdoor environments. Growers can expect a high yield from this variety, which reaches maturity after a flowering period of exactly 63 days.
The chemical profile of this strain is defined by a dominant presence of myrcene, followed by secondary concentrations of caryophyllene and tertiary notes of pinene. This terpene profile dictates a specific sensory experience, balancing earthy undertones with spicy, herbaceous, and crisp aromatic qualities. As a THC-dominant cultivar, the aromatic output is consistent and pronounced throughout the entirety of the flowering stage and following the curing process.
The physiological profile of Purple Pakistani Chitral provides users with effects described as relaxed, calm, and focused. These qualities make the strain a suitable candidate for managing pain, stress, and sleep-related concerns. The genetic lineage of this hybrid has proven influential in the development of subsequent varieties, serving as a foundational parent for notable offspring such as Berry Potpourri and Double Dalai.
Terpene Profile
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.
Effects
Reported effects — derived from terpene chemistry and cannabinoid profile.
Genetic Profile
Indica-dominant
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 Purple Pakistani Chitral.
Siblings
Share parent pakistan chitral kush
Offspring — 1 strains bred from Purple Pakistani Chitral
Composite Traits
Dispensary Locator
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What would Purple Pakistani Chitral × ? 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 Purple Pakistani Chitral →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is Purple Pakistani Chitral indica or sativa?
Purple Pakistani Chitral is modeled here as a indica-dominant (primarily indica with sativa influence).
What terpene is dominant in Purple Pakistani Chitral?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Purple Pakistani Chitral good for daytime use?
Purple Pakistani Chitral 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.