Holy Nana Crack
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Terpenes
Holy Nana Crack effects are mostly calming.
Holy Nana Crack
Holy Nana Crack is a modern hybrid strain derived from the crossbreeding of Green Crack and Big Sur Holy Weed. The history and specific breeding origin of this variety remain undocumented, as there is no provided information regarding the breeder or the specific intent behind its creation. As a modern hybrid, it is suited for both indoor and outdoor cultivation environments, where it typically requires a 63-day flowering period to reach maturity. Growers can expect a high yield from this strain, which presents a moderate level of difficulty for those maintaining it.
The chemical profile of Holy Nana Crack is complex, featuring a dominant presence of myrcene, followed by caryophyllene, camphene, terpinolene, humulene, linalool, limonene, pinene, bisabolol, beta-pinene, caryophyllene-oxide, and nerolidol. Because this exact terpene hierarchy is confirmed, these compounds serve as the foundation for the strain's sensory profile. Consumers often experience a diverse bouquet that shifts through these various aromatic notes, ranging from the earthy influence of myrcene to the lighter, cleaner nuances provided by the inclusion of pinene and nerolidol at the end of the spectrum.
As a THC-dominant hybrid, Holy Nana Crack produces effects that are characterized as relaxed, happy, and uplifted. These traits make it a frequent choice for users seeking relief from stress, pain, or difficulties with sleep. While the strain is widely recognized for these therapeutic applications, there are currently no recorded notable offspring descending from this genetic line.
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 |
| camphene | ~12% | earthy | focus · relaxing |
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.
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
Parentage, ancestry, and genetic relatives of Holy Nana Crack.
Ancestry
Great-grandparents
Grandparents
Siblings
Share parents green crack / big sur holy weed
Composite Traits
Where to buy Holy Nana Crack
No verified dispensaries on file — find it on Leafly.
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What would Holy Nana Crack × ? produce?
Predict the terpene profile, effects, and growing traits of a cross. Our gene weaver engine votes on dominant traits from both parents.
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Frequently Asked Questions
Is Holy Nana Crack indica or sativa?
Holy Nana Crack is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Holy Nana Crack?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is Holy Nana Crack good for daytime use?
Holy Nana Crack 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.