AKAauto
AutoflowerModernTHC-Dominantevening

Afghan Kush Auto

Top flavors

earthyspicycitrus
CalmingEnergizing

Afghan Kush Auto effects are mostly calming.

Afghan Kush Auto is a modern, auto-flowering variety derived from the integration of Ruderalis genetics. Engineered for accessibility, this strain is well-suited for cultivation in both indoor and outdoor environments, maintaining an easy difficulty level despite its low yield output. Growers can expect a 74-day flowering period for this specific cultivar. Notably, this strain has served as a genetic foundation for other varieties, including its offspring Afberry Auto and EazyDaze Ryder.

The chemical expression of Afghan Kush Auto is defined by a complex terpene profile led by myrcene, followed by caryophyllene, limonene, pinene, and terpinolene. The secondary aromatic notes include linalool, beta-pinene, humulene, and nerolidol, while the nuanced background is rounded out by ocimene, bisabolol, guaiol, camphene, caryophyllene-oxide, and p-cymene. This diverse range of compounds creates a distinct olfactory and gustatory experience that reflects the strain's specific chemical composition.

As a THC-dominant variety, Afghan Kush Auto is recognized for producing effects that are primarily characterized as relaxed, happy, and uplifted. These physiological and psychological outcomes make the strain a frequent choice for individuals seeking support with stress, physical pain, and sleep difficulties. Through its role in developing subsequent strains like Afberry Auto and EazyDaze Ryder, Afghan Kush Auto remains a functional contributor to modern breeding programs.

Terpene Profile

Synergies (+) and conflicts (−) are relative to each other within this profile.

myrcene ~60%caryophyllene ~28%limonene ~12%
TerpeneShare
myrcene~60%
caryophyllene~28%
limonene~12%

Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.

~60%

earthy

●●●○

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.

~12%

citrus

●●○○

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

Autoflower

Photoperiod-independent. Flowers based on age, not light cycle. Compact and fast.

THC-Dominant

High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.

Genealogy

Parentage, ancestry, and genetic relatives of Afghan Kush Auto.

Ancestry

Afghan Kush AutoFull tree →

Offspring — 2 strains bred from Afghan Kush Auto

View full lineage tree →

Composite Traits

Use caution if

daytime-productivitymorning-useevening-wind-down

Where to buy Afghan Kush Auto

No verified dispensaries on file — find it on Leafly.

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What would Afghan Kush Auto × ? 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 Afghan Kush Auto

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Afghan Kush Auto indica or sativa?

Afghan Kush Auto is modeled here as a autoflower (photoperiod-independent).

What terpene is dominant in Afghan Kush Auto?

Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.

Is Afghan Kush Auto good for daytime use?

Afghan Kush Auto 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.