Mindica

Mr. Nice G13 X Hash Plant

28.6%

THC

Top flavors

earthyspicycitrus
CalmingEnergizing

Mr. Nice G13 X Hash Plant effects are mostly calming.

Low THCHigh THC

Mr. Nice G13 X Hash Plant potency is higher THC than average.

Mr. Nice G13 X Hash Plant is a modern indica variety born from the crossing of Hash Plant and Chemdawg. This lineage combines two influential genetic lines to create a stable plant well-suited for cultivation by growers of any experience level. It thrives in both indoor and outdoor environments, offering a medium yield with a consistent flowering time of 60 days.

The chemical profile of this strain is defined by a complex sequence of terpenes, led by myrcene, caryophyllene, and limonene. Secondary contributions from humulene and linalool round out the profile, supported by minor traces of beta-pinene, bisabolol, pinene, camphene, nerolidol, and guaiol. This terpene composition dictates the sensory experience, providing a balanced aromatic profile that reflects its multi-faceted genetic background without leaning into a single dominant note.

As a THC-dominant cultivar with 28.6% THC, this strain is recognized for producing effects that are primarily relaxed and focused. These properties make it a frequent choice for users seeking support with pain management, stress relief, and sleep quality. The genetic utility of Mr. Nice G13 X Hash Plant is evidenced by its extensive list of notable offspring, which includes Xnine, G14, Jamaican Warlock, Juice WRLD, Kandahar Kreeper, Kuntry Gramma, Kush of Ra, Michigan Medicine, Rasah, Shakedown, Twisted HashPlant OG Kush, and Cosmic Lights.

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

Pure Indica

■ Indica 100%■ Sativa 0%

Body-heavy, relaxing genetics. Short stature, dense buds, broad leaves.

THC-Dominant

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

Genealogy

Parentage, ancestry, and genetic relatives of Mr. Nice G13 X Hash Plant.

View full lineage tree →

Composite Traits

Use caution if

daytime-productivitymorning-useevening-wind-down

Where to buy Mr. Nice G13 X Hash Plant

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What would Mr. Nice G13 X Hash Plant × ? 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 Mr. Nice G13 X Hash Plant

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Mr. Nice G13 X Hash Plant indica or sativa?

Mr. Nice G13 X Hash Plant is modeled here as a pure indica (body-heavy, relaxing genetics).

What terpene is dominant in Mr. Nice G13 X Hash Plant?

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

Is Mr. Nice G13 X Hash Plant good for daytime use?

Mr. Nice G13 X Hash Plant 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.