Dragons Blood Hashplant
Top flavors
Dragons Blood Hashplant effects are mostly calming.
Dragons Blood Hashplant is a modern hybrid developed from the 88 G-13 Hashplant. This strain is cultivated in both indoor and outdoor environments, requiring moderate growing expertise to reach its potential. Growers can anticipate a high yield from this variety, which reaches maturity after a 63-day flowering period. Its notable genetic legacy includes progeny such as Chamhaole, Dozer, Fina Dene, and Ice Keki.
The aromatic and flavor profile of this THC-dominant cultivar is defined by a complex chemical composition led by myrcene, followed by pinene, ocimene, and limonene. The secondary and tertiary terpene structure continues with caryophyllene, beta-pinene, linalool, humulene, guaiol, bisabolol, nerolidol, and camphene. This specific arrangement of aromatic compounds provides a nuanced sensory experience that reflects the strain's hash-focused heritage.
Reportedly valued for its specific therapeutic applications, Dragons Blood Hashplant is widely chosen by consumers to manage stress, alleviate pain, and encourage sleep. Users frequently report feelings of being relaxed, happy, and uplifted following consumption. Due to its balanced effects and reliable development, this hybrid continues to influence contemporary breeding programs through its prominent offspring.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| pinene | ~28% | pine | focus · creative |
| ocimene | ~12% | sweet | energetic · social |
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.
Russo 2011: acetylcholinesterase inhibitor (IC50 0.44 mM) counteracting THC-induced short-term memory deficits; most widely encountered terpenoid in nature; anti-inflammatory via PGE-1.
Antifungal, antiviral, decongestant; activates CB1/CB2 at 10–60% THC efficacy per Israeli receptor study (NORML 2025); highly volatile (bp 50–66°C); limited clinical data.
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 Dragons Blood Hashplant.
Ancestry
Siblings
Share parent 88 g 13 hashplant
Offspring — 4 strains bred from Dragons Blood Hashplant
Composite Traits
Where to buy Dragons Blood Hashplant
No verified dispensaries on file — find it on Leafly.
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What would Dragons Blood Hashplant × ? 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 Dragons Blood Hashplant indica or sativa?
Dragons Blood Hashplant is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in Dragons Blood Hashplant?
Myrcene is shown as the dominant terpene at approximately ~60%. Pinene follows as the secondary terpene.
Is Dragons Blood Hashplant good for daytime use?
Dragons Blood Hashplant 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.