Mhybrid-indica
Hybrid-IndicaModernTHC-Dominantevening

Misty

36.4%

THC

1.94%

CBD

Top flavors

floralcitrusspicy
CalmingEnergizing

Misty effects are mostly calming.

Low THCHigh THC

Misty potency is higher THC than average.

Misty is a modern hybrid-indica cultivar derived from pure India Indica lineage. Developed for versatility in cultivation, this plant requires a moderate skill level and performs effectively in both indoor and outdoor environments. Growers can expect a high yield from this strain, which reaches maturity following a 63-day flowering cycle. Its genetic stability has allowed it to serve as a foundation for other notable cultivars, including Double Fun and Mayday Express.

The chemical profile of Misty is anchored by nerolidol, followed by limonene and caryophyllene. This dominant terpene chain continues with humulene, linalool, myrcene, bisabolol, and beta-pinene, rounded out by trace amounts of caryophyllene-oxide, camphene, terpinolene, and pinene. This complex arrangement of secondary metabolites dictates the specific sensory signature of the flower, ensuring a consistent chemical expression across harvests.

As a THC-dominant variety, Misty produces effects characterized primarily by a sense of relaxation, calm, and focus. These properties make it a frequent choice for users seeking support with pain, stress, and sleep management. Through its role as a parent strain, Misty has secured a verified legacy in the development of modern hybrids, maintaining its status as a functional component in the genetic history of its offspring.

Terpene Profile

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

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

floral

●●○○

Russo 2011: sedative properties; enhances transdermal pharmaceutical penetration; antimalarial; PMC11060501: GABAergic-mediated antinociception.

~28%

citrus

●●○○

Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.

~12%

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.

Effects

Reported effects — derived from terpene chemistry and cannabinoid profile.

Genetic Profile

Indica-dominant

■ Indica 70%■ Sativa 30%

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 Misty.

Composite Traits

Use caution if

daytime-productivitymorning-useappetite-boost

Where to buy Misty

No verified dispensaries on file — find it on Leafly.

Dispensary Locator

Find which dispensaries near you currently stock Misty.

or enter a city / postcode

Community Reviews

No reviews yet — be the first!

No reviews yet for Misty.

What would Misty × ? 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 Misty

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Misty indica or sativa?

Misty is modeled here as a indica-dominant (primarily indica with sativa influence).

What terpene is dominant in Misty?

Nerolidol is shown as the dominant terpene at approximately ~60%. Limonene follows as the secondary terpene.

Is Misty good for daytime use?

Misty 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.