Afghani No.1
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Terpenes
Afghani No.1 effects are mostly calming.
Afghani No.1
Afghani No.1 is a modern hybrid with an undocumented lineage. According to lore, this strain is recognized for its stable genetic structure and consistent performance, which has allowed it to serve as a foundational building block in contemporary cultivation. Designed for versatility, the strain can be grown in both indoor and outdoor environments. It requires moderate cultivation skill and reaches maturity after a 63-day flowering period, consistently providing a high yield for the producer.
The olfactory experience of Afghani No.1 is defined by a primary concentration of myrcene, which provides the base of its aromatic profile. This is supported by secondary notes of caryophyllene, while a tertiary presence of limonene adds a nuanced finish to the overall terpene composition. This specific arrangement of compounds contributes to the strain's distinct sensory characteristics, appealing to those who appreciate a balanced aromatic profile driven by these three dominant terpenes.
As a THC-dominant variety, the effects of Afghani No.1 are characterized as relaxed, happy, and uplifted. These therapeutic attributes make it a frequent choice for users managing stress, pain, or difficulty with sleep. The genetic legacy of this strain is evidenced by its role in the development of notable offspring, including the SK1/A1 Hybrid, which reinforces its ongoing importance within the broader scope of modern hybrid cannabis genetics.
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 |
| limonene | ~12% | citrus | social · 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: 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.
relaxed
eveningPrimary endpoint of myrcene+linalool sedating combinations; GABA modulation is the dominant mechanistic driver.
happy
anytimeuplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
Genetic Profile
Balanced Hybrid
Equal indica and sativa genetics. Balanced body and mind effects.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parent data not yet recorded for Afghani No.1.
No parent or offspring records — similar strains
Same primary terpene with overlapping effects.
Browse more similar strains →Composite Traits
Where to buy Afghani No.1
No verified dispensaries on file — find it on Leafly.
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What would Afghani No.1 × ? 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 Afghani No.1 →Frequently Asked Questions
Is Afghani No.1 indica or sativa?
Afghani No.1 is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Afghani No.1?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Afghani No.1 good for daytime use?
Afghani No.1 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.