HLhybrid

Henkes Lolland

Top flavors

earthyspicycitrus
CalmingEnergizing

Henkes Lolland effects are mostly calming.

Henkes Lolland is a modern hybrid whose specific genetic origins remain undocumented and debated. While the lineage is recorded as Henkes Lolland crossed with Royal Dane, Royal Dane, and at least one unnamed parent, breeders have not publicly confirmed a definitive breeding history. Because documentation regarding its development is thin, the precise circumstances surrounding its creation lack official verification. This strain is cultivated in both indoor and outdoor environments, offering a high yield with a flowering time of 63 days and a moderate level of cultivation difficulty.

The chemical character of Henkes Lolland is defined by a complex range of terpenes, led by myrcene as the dominant compound, followed by caryophyllene and limonene as secondary and tertiary constituents. The profile further includes nerolidol, linalool, pinene, humulene, beta-pinene, ocimene, isopulegol, caryophyllene-oxide, camphene, guaiol, bisabolol, terpinolene, p-cymene, and eucalyptol. These compounds create a unique aromatic and flavor landscape, though the specific sensory intensity of individual notes tends to vary based on the cultivation environment.

As a THC-dominant hybrid, Henkes Lolland is characterized by effects that are relaxed, happy, and uplifted. These properties make the strain a common choice for individuals seeking support for stress, pain, and sleep-related concerns. While it serves as a versatile option for various use cases, there are no recorded instances of notable offspring produced from this specific genetic line to date.

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

Balanced Hybrid

■ Indica 50%■ Sativa 50%

Equal indica and sativa genetics. Balanced body and mind effects.

THC-Dominant

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

Genealogy

Parentage, ancestry, and genetic relatives of Henkes Lolland.

Ancestry

Henkes LollandFull tree →

Offspring — 1 strains bred from Henkes Lolland

name-inferred
View full lineage tree →

Composite Traits

Use caution if

daytime-productivitymorning-useevening-wind-down

Where to buy Henkes Lolland

No verified dispensaries on file — find it on Leafly.

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What would Henkes Lolland × ? 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 Henkes Lolland

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Henkes Lolland indica or sativa?

Henkes Lolland is modeled here as a balanced hybrid (equal indica and sativa genetics).

What terpene is dominant in Henkes Lolland?

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

Is Henkes Lolland good for daytime use?

Henkes Lolland 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.