THREE FORMULATIONS. THREE DISTINCT PROFILES.
FIND YOUR FORMULATION
Different cannabinoid ratios. Different terpene profiles.
Each formulated with intention.
HEMP + RESPONSIBLE USE INFORMATION
HEMP-DERIVED • ADULT USE 21+ • KEEP OUT OF REACH OF CHILDREN
RESPONSIBLE USE
Our hemp-derived products contain no more than 0.3% Δ9-THC by dry weight in accordance with the federal hemp definition currently in effect. Intended for adult use only (21+). Keep out of reach of children. Products containing Δ9-THC may cause impairment. Do not drive or operate machinery after use. Consult your healthcare provider before use, particularly if pregnant, nursing, taking prescription medications, or managing a medical condition.
IMPORTANT INFORMATION
These statements have not been evaluated by the Food and Drug Administration. These products are not intended to diagnose, treat, cure, or prevent any disease. Information provided by Dr. Murse/CannabisDNP is for educational purposes only and is not a substitute for individualized medical advice from a licensed healthcare professional.
What's Inside
EVERY INGREDIENT EARNS ITS PLACE.
Dr. Murse formulations combine intentionally selected hemp-derived cannabinoids and naturally occurring terpenes. Each is considered through the weight of available evidence, pharmacology, formulation goals, and an ongoing review of the science.
NOT EVERY INTERESTING MOLECULE BELONGS IN EVERY FORMULATION.
Cannabinoids
A chemistry note: CBGA—not CBG—is the biosynthetic precursor from which major cannabinoid acids including THCA and CBDA are formed. CBG is produced when CBGA decarboxylates.
CBD
Cannabidiol
A non-intoxicating phytocannabinoid with complex pharmacology extending well beyond CB1 and CB2. CBD interacts with multiple signaling systems, including serotonin and transient receptor potential (TRP) channels, while also influencing endocannabinoid signaling. Its effects are dose-, route-, and formulation-dependent, and the clinical evidence varies considerably by outcome.
Δ9-THC
Delta-9-Tetrahydrocannabinol
The primary intoxicating phytocannabinoid in cannabis. Δ9-THC acts primarily as a partial agonist at CB1 and CB2 cannabinoid receptors, with CB1 activity contributing substantially to its psychoactive effects. Response varies with dose, route, tolerance, individual physiology, and formulation.
CBG
Cannabigerol
A non-intoxicating phytocannabinoid with a distinct and still-emerging pharmacologic profile. Reported targets include α2-adrenergic, 5-HT1A, cannabinoid, and TRP receptors and channels. Much of this mechanistic evidence remains preclinical, and considerably more human research is needed.
β-CARYOPHYLLENE
Peppery • Woody • Spicy
TARGETS: CB2 • PPARα/γ
β-Caryophyllene is unusual among common cannabis terpenes because it is a well-characterized selective CB2 receptor agonist without CB1-mediated intoxication. Preclinical research links CB2 and related signaling to inflammatory and nociceptive pathways, making β-caryophyllene particularly interesting in research involving inflammation and discomfort. PubMed
Linalool
Floral • Lavender • Soft
TARGETS/PATHWAYS: GABAergic • Glutamatergic • Adenosine signaling
Linalool is widely studied for effects involving neuronal excitability and inhibitory signaling. Preclinical research has reported anxiolytic-, sedative-, and antinociceptive-like effects, while human evidence involving linalool-containing preparations also makes it an interesting compound in relaxation and stress-response research. The exact mechanisms remain more complex than a single receptor explanation.
β-MYRCENE
Earthy • Herbal • Musky
TARGETS/PATHWAYS: TRPV1 • α2-Adrenergic • inflammatory signaling
β-Myrcene is one of the more abundant terpenes found in many cannabis chemovars. Preclinical studies have investigated analgesic-, anti-inflammatory-, and sedative-like effects, with reported activity involving TRPV1, α2-adrenergic signaling, and inflammatory pathways. Human evidence remains limited, so claims that “myrcene makes you sleepy” go beyond what the clinical literature can presently establish.
D-Limonene
Citrus • Bright • Fresh
TARGETS/PATHWAYS: Serotonergic • Adenosine • TRP signaling
D-Limonene is being studied across serotonergic, adenosine, TRP, and inflammatory signaling pathways. Preclinical findings include anxiolytic-, antidepressant-, and anti-inflammatory-like effects, while limited human research makes mood and stress-response outcomes particularly interesting areas for continued investigation. These findings do not establish limonene as a treatment for anxiety or depression.
α-Pinene
Pine • Fresh • Resinous
TARGETS/PATHWAYS: Cholinergic • inflammatory signaling
α-Pinene is being investigated for effects involving acetylcholine signaling, neuroinflammatory pathways, and cognition. Preclinical work has generated interest in memory, attention, and inflammatory outcomes, but direct human evidence remains limited. Its pharmacology is more nuanced than the common claim that α-pinene simply “improves focus.”
terpinolene
Fresh • Herbal • Lightly Floral
TARGETS/PATHWAYS: GABAergic • serotonergic • oxidative/inflammatory pathways
Terpinolene is one of the less extensively characterized terpenes in the Dr. Murse formulations. Preclinical research has explored sedative-, antioxidant-, and anti-inflammatory-like activity, but its receptor pharmacology and human clinical evidence are far less developed than those of compounds such as β-caryophyllene. That uncertainty is part of the science—not something to hide.
Recent reviews discuss possible GABAergic, serotonergic, olfactory, and other mechanisms, but the evidence is heterogeneous.
TERPENES
Terpenes are aromatic compounds with pharmacology of their own. Receptor and pathway research helps explain why they are scientifically interesting—but mechanistic and preclinical findings should not be mistaken for proven clinical outcomes.
Reported molecular targets and outcomes vary by experimental model, concentration, route of administration, and study design. Much of the terpene literature remains preclinical.
THE MOLECULE IS INTERESTING.
THE QUALITY OF THE EVIDENCE MATTERS MORE.
Dr. Murse formulations are informed by the totality of available evidence—not a single study, mechanism, marketing claim, or trendy ingredient.
THE DETAILS MATTER.
We prioritize safety, accuracy, and quality in every product we make — so you always know exactly what you're getting, and why. Here's how we hold ourselves to that standard, every step of the way.
Quality Plants
Our hemp is cultivated on USDA-compliant farms in Wisconsin and across the Midwest, operating under strict state hemp program guidelines for quality and sustainability. Every plant is grown without synthetic pesticides or herbicides — verified through rigorous third-party testing — so every taffy starts with clean, carefully sourced Cannabis Sativa L.
Made Clean
Every batch is crafted in an FDA-registered, GMP-compliant facility — the same rigorous standard used in food-grade manufacturing. Our supercritical CO₂ extraction process is a clean, solvent-free method recognized for preserving the purity, potency, and full-spectrum cannabinoid profile of each plant — with no residual solvents introduced at any stage.
Lab Tested
We partner with independent ISO/IEC 17025-accredited labs to test at multiple stages — from raw hemp through final taffy. Each batch is analyzed for cannabinoid potency, residual solvents, pesticides, heavy metals, and microbial contaminants, giving you verifiable confidence in what's in every piece.
Meet Dr. Murse
Jesse Cole Christianson, DNP, APRN, AGPCNP-BC
Jesse is a board-certified nurse practitioner with advanced training in cannabis science and pharmacology. Blending clinical knowledge with a genuine commitment to transparency, he crafts hemp-based edibles rooted in evidence-informed formulation — not hype. His mission is to give you a cleaner, more thoughtful way to explore what hemp can bring to your daily wellness routine.
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Molly K, WI
"I took a half of a calm blend taffy and felt great all day yesterday! Gave my husband a chew lastnight because of increased stress, and he felt very calm throughout the evening."
Minh N, Wi
"The candies are excellent!! I haven't taken more than half at a time, effects were perfect I thought."
James B, WI
"I've experienced a notable improvement in my sleep since using the Rest & Recovery taffy!"