Made from a plant that produces a complete composition of cannabinoids, terpenoids, flavonoids and bleeds. The inflorescence of the plant passes through a common and followed by decarboxylation. Full spectrum oil contains the richest and fullest possible composition of the hemp plant.

This oil is made from natural CBD which is distilled from the cannabis plant.
This means that this oil does not contain terpenes and other cannabinoids, is odourless and tasteless and completely THC-free.

See: CBD Oil

The Endo-cannabinoid system in the human body consists of ligands: anandamide and 2-AG, their coltans, the enzymes that break them down, and the carrier proteins that transport them into the cell. It is a central internal system that affects a very wide range of biological and chemical processes in the body and is a decisive factor in the health and integrity of the functioning of the systems in the body. The endocannabinoid system in the body maintains the balance of homeostasis substances through the entire body. It is this balance that allows the body to work in the most healthy way.
The endo-cannabinoid system in the human body serves as a menstruary, and its main function is to bring the body and mind into balance— homeostasis.
The mechanism of action of endocannabinoids is rare in nature, becoming the mechanism of action of the other neuro messengers and is called an “inverse signal” – RETROGRADE SIGNALING.
Cannabinoids affect the human body as a result of linking to endocannabinoid receptors (internal) across the memb rays of different cells. Two endocannabinoid receptors are known: CB1 (central) found in the brain and nervous system at high concentrations and CB2 (peripheral) found mainly in the periphery and immune cells.
Our bodies contain endocannabinoids, fatty acids, naturally produced molecular compounds, the most commonly known of which are: anandamide (affluent ethanol archidonyl AEA) and ARACHIDONIL GLYCEROL) 2-AG).
Endocannabinoids bind and activate the two cannabinoid receptors in our bodies. Despite the obvious differences in their chemical structure, both endo and some exo-(phyto)-cannabinoids bind to the same receptors in our bodies:
THC is associated with high affinity for CB1 and CB2 receptors, while CBD is not linked to them at all and its mechanisms of action differ and are not related to these receptors. The pharmacological activity of CBD is very interesting, since it does not work directly on CB1 and CB2 receptors, but it can block the activity of certain compounds that activate these receptors, such as THC.
FATY ACID AMIDE HYDROLASE – FAAH breaks down anandamide and 2AG, thus ending their operation with synapse quickly. Cannabidiol inhibits this enzyme (FAAH) and thus increases the pain-soothing and soothing activity of endocannabinoids through the endocannabinoid receptors.

Neurotransmitter is a molecule that passes between a neuron and any target cell through the synapse. The target cell can be another nerve cell, a muscle cell or a cell in the lout that cones insematants. Key brain systems that underpin cognition, emotion and motivation are shaped by the primary systems of neuroconductors. Therefore, it is difficult to speculate on the neural origins of human behaviour without understanding their role.
The neurotransmitters are synthesised and stored in a synaptic bladder, which is located at the axon end of a nerve cell. A nerve impulse transmitted through the axon of the presynaptic neuron causes the release of the neurotransmitter into the synaptic interval. In this way, the electrical signal is translated into a chemical signal. The molecules of the neuroscircle communicate to the receptors located on the surface of the post-Synapse target cell. This link activates ion ducts, which generate synaptic electrical potential in the target cell. The neuroconductors are the chemical messengers of the brain. They allow the transmission of messages between neurons in the nervous system through the process of synaptic transfer. The neurovixin could have an inhibitory or stimulating effect on the target cell.
The effect of neuroconductors focuses solely on the post-synaptic target cell because their concentration is the highest. The gaping process causes the dilution of the excreted neuro-condescenation. This process intensifies as the distance from the synapse increases, so that the concentration of the neuroscientary condit outside the synapse aspires to zero. In this way, the neuroscir pull secreted into a particular synapse will not be able to affect neighbouring synapses. In order for the activation of the target cell, the amount of neuroscientist that is released from the presynaptic cell must be sufficient to bring the electrical voltage of the receptor cell to its threshold value. The threshold value of each cell is affected by its rest voltage. If the voltage is lower than the threshold value, the target cell will not be activated.
Transferring a neural signal in this form is called Anterograde signalling

(Terpene) or – terpenoids, are a group of organic compounds composed of repetitive units of isoprene (C5H8). When it comes to pure isoprene units associated with each other, the substance terpene is called; When there are slight changes in the isoprene units (the addition of oxygen atoms, for example) it is called the substance Terpenoid or Isoprenoid. Large terpenes may contain dozens of isopran units. All terpenes are synthesize, using induced metabolic pathways, macastil CoA. The acetyl units gradually join together, gradually forming a terpene. Sometimes the isoprene chains close to the ring, making it difficult to identify the compound as a terpene at first glance. The different terpenes are divided into groups according to the number of isoprene units that make them up.
Terpenes are mainly produced by plants and constitute secondary metabolites. Many lubricants, fragrance, protection and colour, as well as essential oils, are terpenes. High-concentration terpenes can be extracted from the resin of trees, especially conifers (see turpentine). Rubber is a polytrapene containing dozens of isoprene units. Carotenoids are a group of dyes (pigments) composed of eight isoprene units that provide yellow, orange and red colours for fruits, flowers, flowers, and other structures in the plant. Many terpenes are an ingredient in alkaloids, the largest group of secondary metabolites in plants.
Plant flavour and smell molecules found in any “normal” flower also help strengthen the effects of the cannabis plant in their synergical action with cannabinoids to create its many effects and its many benefits. Often the terpenoids have a strong scent that evaporates quickly.

Decarboxylation is a heating process performed to make the cannabinoids found in the plant. Cannabinoid acids are psychoactively active. In this process, the COOH cooxyl group is removed from the rest of the molecule. A COH group that was
attached to the A ring, thus breaking down the same acids into active cannabinoids.

Flavonoids or bioflavonoids (Latin for flavus, yellow), formerly known as “vitamin P”, are a group of compounds synthesize by plants and found in fruits and vegetables. Flavonoids are secondary metabolites, which means that they are not immediately essential to the life of the plant cell. At the same time, they have several functions: pigments of plants that produce a red or blue yellow colour help attract pollinatory animals.
Attracting symbiotic bacteria called rhizobium and rejecting parasites.
Laboratory conditions showed antibacterial ability and rejection of fungi in plants.
The flavonoids were discovered during the 1930s by the Hungarian biochemist Albert Saint-Geirgi, who called them vitamin P.

Cannabinol is a psychoactive compound found in minimal amounts in the cannabis plant and for the most part in cannabis that is stored under unsuitable conditions.
Unlike the rest of the cannabinoids CBN is not created directly from cannabigerol (cannabigerol- CBG) or cannabigerolic acid (CBGA) but as a sub-product of tetrahydrocannabinolic acid.
CBN is the active substance that is exhausted in the process of de-carboxylation from the substance of origin CBNA.
CBN functions as a partial agonist for the endocannabinoid system CB1 receptors but has been associated with a higher affinity for CB2 receptors.
Relative to THC, cannabinol has a much lower affinity for receptors in the endocannabinoid system.

The mechanism of action of cannabinoids is rare in nature, becoming the mechanism of action of the other neuro messengers and is called the “inverse signal” RETROGRADE SIGNALING.
Endo-cannabinoid is produced in the post-synaptic nerve cell while the appropriate receptor is found in the presynaptic nerve cell.
In nerve cells that release the soothing neurotransmitter GAMA AMINO BUTIRIC ACID – GABA cannabinoids will prevent (suppress) further release of the soothing neurotransmitter and thus the overall effect will be stimulating.
In nerve cells that release the stimulant neurotransmitter GLUTAMATE – Glu the cannabinoid will suppress
and prevent the release of the stimulant nerve messenger – thus the overall effect will be soothing. It is this balance that allows the body to work in the most healthy way.

Gamma-Aminobutyric Acid (GABA) is a non-protein amino acid that exists in all animal realms: prokriots, single-celled aocriots, and all multicellular aocriots, including plants. GABA is a derivative of the amino acid glutamate. In animals GABA is the most common inhibiting neuro-conductor in the central nervous system and brain. Accordingly, most inhibiting synapses in the brain use GABA. GABA-sensitive neurons are concentrated mainly in brain regions such as the oceut lost, the thalamus, and the hypothalamus.
The drug pycrotoxin, which blocks GABA receptors, causes convulsions because muscle movement cannot be properly criticized without the inhibiting effect of GABA. Many anti-anxiety medications inhibit the breakdown of GABA and thus increase its activity. In vertebrate owners, GABA acts as a neurotransmitter in inhibitory synapses in the brain. GABA binds to receptor on the mems of presynaptic and post-synaptic nerve cells. The connection of the molecule to the receptor leads to the opening of selective ion canals – potassium canals or chlorine ducts. The exit of positively charged potassium ions from the cell, or the introduction of negatively charged chlorine ions into the cell, increases the electrical potential difference between the cell’s interior and the excellular solution, a condition known as hyperplorization.
As a result, the membrane tension of the cell’s interior moves away from the threshold value needed to induce a nerve impulse. This is how GABA is used as an inhibitory neurotransmitter.
GABA is derived from the amino acid glutamate using the enzyme L-glutamic acid decarboxylase and with the help of a phosphoric form of vitamin B6 used as a co-factor. It should be noted that glutamate acts as a major stimulating neurotransmitter in the central nervous system: About 80% of the synapses in the brain use glutamate as a neurotransmitter. That is, the most common inhibitor neuro-reflyst is a derivative of the most common stimulative neuroscirous.
Following its inhibiting effect on neural activity, the GABA neurodetric agent plays a major role in some forms of psychopathology. For example, low levels of GABA can lead to neuronal hypertension, which is manifested in a feeling of anxiety.
In nerve cells that release the soothing neurotransmitter Gamma-Aminobutyric Acid (GABA) cannabinoids will prevent (suppress) further release of the soothing neurotransmitter and thus the overall effect will be stimulating.

Glutamic acid is one of the 20 most common amino acids in nature.
Glutamic acid is not an “essential amino acid”, since the cells of the human body are able to produce this acid themselves from another amino acid. In addition to the structural role of glutamic acid as an ingredient in the protein, the acid also acts as a neurotransmitter in the brain and as a starting material for the formation of GABA, another neurotransmitter.
The glutamic acid is similar in composition to aspartic acid, another amino acid, but in its shire there are two groups of methylene (CH2) and not one. The resin of glutamic acid is therefore composed of two methylene groups and a carboxyl group (COOH). Glutamic and aspartic acids are the only amino acids with acidic residuals. The carboxyl group tends to lose its hydrogen atom, hence its acidity. When this occurs, it becomes a carbonoxyte (-COO) lyon, and then the compound is called glutamate. This happens in neutral pH. Glutamate’s electrical charge is -1, due to the negative carbaxylt ion. The density of the material is 1.46 grams per gram per gram, soluble in water – 7.5 grams per liter. The amino acid glutamine is a derivative of the glutamic acid. Its remnant consists of a wealthy group (CONH) instead of a carboxil group. It is formed when the glutamic acid reacts with ammonia. Due to the proximity between the two acids, there is a long symbol indicating glutamine or glutamic acid – as well as a short symbol – E.

In nerve cells that release the stimulant neurotransmitter GLUTAMATE (Glu) cannabeidol (CBD) will suppress and prevent the release of the stimulant neurotransmitter and thus the overall effect will be soothing.
In 1992, Professor Raphael Meshulam and his group isolated a new component of the brain, which he called Anandamide. The anandamide, which is a derivative of oily acid, differs in structure from the plant cannabinoid, and has the same activity profile as THC. Meshulam’s group isolated another endo-cannabinoid from the spleen 2-arachidonoyl glycerol 2AG.
The Breaks down anandamide and AG-2, thus ending their operation with a synapse quickly. Cannabidiol inhibits this enzyme (FAAH) and thus increases their pain-soothing activity of the cannabinoids, through the endocannabinoid receptors. and the 2AG are the two main endo-cannabinoids identified so far. This study not only helped establish the way cannabinoids work, but also promoted the understanding of cognition, appetite, memory and emotions. The work of many groups shows the involvement of the endocannabinoid in such processes. The importance of plant cannabinoids and endo-cannabinoids in many physiological processes and pathological conditions such as neuroprotection, sleep, vascular dilation, cancer, inflammation, breastfeeding, bone building and insulin-dependent diabetes.

A neurotransmitter formed in the synthesis of archival acid and ethanolamine. The origin of the name Anandamide is a connection between the word “ananda” in Sanskrit means “inner happiness”, a well-to-do extension that is the chemical residus in the molecule found. Anandamide (ANA), also known as N-arachidonoylethanolamine (AEA), is a fatty acid neurotransmitter. Discovered in 1992 at the Hebrew University of Jerusalem.
Anandamide is important for fetal development in pregnancy and is apparently related to feelings of happiness and joy. It is an endogenous cannabinoid and although it is relatively different from them in its chemical structure, it is similar in its lipopyllic properties to Phyto-cannabinoids found in cannabis, such as CBD and THC. To date, a number of neurotransmitter receptors have been found for anandamide in particular and cannabinoids in general, known among them CB1 CB2 and GRP55.
Unlike many neurotransmitters, the anandamide (like the rest of the cannabinoids) moves at the synaptic interval precisely from the post-synaptic nerve to the presynaptic nerve.
A diet of foods containing archidonic acid and other essential fatty acids and especially omega-3 affects the production of anandamide and other endocannbinoids in the brain.

Breaks down anandamide and AG-2, thus ending their operation with a synapse quickly. Cannabidiol inhibits this enzyme (FAAH) and thus increases their pain-soothing activity of the cannabinoids, through the endocannabinoid receptors.