Over the years, we have been perfecting the blend that helped digestive issues, heartburn, etc. We started with Re-Member, which originally was for Alzheimer’s and ADD, etc., to calm and focus the mind and it turned out to also be great to help the other heater/fire chakra, the belly.
We have since come up with the blend that has done nothing less than perform miracles on digestive issues, including, the story of someone that had a mass show up on their pancreas in X Ray, and using this new formula, dissolved it…yes, it is gone.
Of course, other things were done by the individual, eating healthy, etc to assist in creating this healing circuit, but the blend definitely went a long way to help. So why?
What is that Blend? HAPPY BELLY ©
The other day, I happened upon a youtube that talked about using ‘Turpentine’ to heal the liver.
What she recommended was the turpentine you have to special order and what is
the major chemical constituent? Terpenes.
So, I thought about that. There are many terpenes of various types (see following info) that make up essential oils.
Over the past 25 years, teaching about Frankincense, I often hear people say: ‘That smells like turpentine!’….well yes, it does have terpenes.
And many other healing chemical constituents, but we are focusing on just one aspect today.
First off, look at that word, ter-pene, or ter-pine.
What other essential oil has lots of terpenes? Pine, major constituent, L-Pinene.
Of course, that comes from pine oil and both produce sap that are used.
So, we have the Pine Cone….which is a fractal.
It is also at the door of Vatican Court. Yes, a great big old pine cone. Why?
A fractal is self-replicating.
In mathematics a fractal is an abstract object used to describe and simulate naturally occurring objects. Artificially created fractals commonly exhibit similar patterns at increasingly small scales. It is also known as expanding symmetry or evolving symmetry. If the replication is exactly the same at every scale, it is called a self-similar pattern. An example of this is the Menger sponge. Fractals can also be nearly the same at different levels. This latter pattern is illustrated in small magnifications of the Mandelbrot set] Fractals also include the idea of a detailed pattern that repeats itself
Now to this, let us add the ‘PINE-AL’ GLAND. Remember, EL or AL, is Gd of the Old Testament and is either the root or suffix to many words, like EL-e-ment or AL-Chem-y. El Shaddai, or Ang-EL. EL-ect, etc.
The pineal gland is a small, pinecone shaped gland of the endocrine system. A structure of the diencephalon of the brain, the pineal gland produces the hormone melatonin. Melatonin influences sexual development and sleep-wake cycles. The pineal gland is composed of cells called pinealocytes and cells of the nervous system called glial cells. The pineal gland connects the endocrine system with the nervous system in that it converts nerve signals from the sympathetic system of
The peripheral nervous system into hormone signals.
Over time, calcium deposits build-up in the pineal and its accumulation can lead to calcification in the elderly.
Terpenes (/ˈtɜːrpiːn/) are a large and diverse class of organic compounds, produced by a variety of plants, particularly conifers, and by some insects such as termites or swallowtail butterflies, which emit terpenes from their osmeteria. They often have a strong odor and may protect the plants that produce them by deterring herbivores and by attracting predators and parasites of herbivores. The difference between terpenes and terpenoids is that terpenes are hydrocarbons, whereas terpenoids contain additional functional groups.
They are the major components of resin, and of turpentine produced from resin. The name "terpene" is derived from the word "turpentine". In addition to their roles as end-products in many organisms, terpenes are major biosynthetic building blocks within nearly every living creature. Steroids, for example, are derivatives of the triterpene squalene.
When terpenes are modified chemically, such as by oxidation or rearrangement of the carbon skeleton, the resulting compounds are generally referred to as terpenoids. Some authors will use the term terpene to include all terpenoids. Terpenoids are also known as isoprenoids.
Terpenes and terpenoids are the primary constituents of the essential oils of many types of medicinal plants and flowers. Essential oils are used widely as fragrances in perfumery, and in medicine and alternative medicines such as aromatherapy. Synthetic variations and derivatives of natural terpenes and terpenoids also greatly expand the variety of aromas used in perfumery and flavors used in food additives. Vitamin A is a terpenoid.
Higher amounts of terpenes are released by trees in warmer weather, acting as a natural form of cloud seeding. The clouds reflect sunlight, allowing the forest to regulate its temperature. The aroma and flavor of hops comes, in part, from sesquiterpenes (mainly alpha-humulene and beta-caryophyllene), which affect beer quality. Terpenes are also major constituents of Cannabis sativa plants, which contain at least 120 identified compounds.
So, you see how complex this becomes? This is just one aspect of over 20 oils, which the Happy Belly, mixed to perfection provides. For all stomach ailments, esophageal, Crohn's, Acid Reflux, heartburn, etc.
There is so much more to add to this, but we will save that for another day, when we go deeper into what chemical constituents are and give further explanations.
Terpene, chemical compound, Alternative Title: terpenoid
camphene, limonene , mycene, phellandrene, pinene
alpha terpenene, azulene, beta bisabolene, beta carpphyll, farmasene, germacene, sabinene, abietic acid , lycopene, Isoprene
Terpenes are derived biosynthetically from units of isoprene, which has the molecular formula C5H8. The basic molecular formula of terpenes are multiples of that, (C5H8)n where n is the number of linked isoprene units. This is called the biogenetic isoprene rule or the C5 rule. In 1953, the Croatian chemist Leopold Ružička discovered that the isoprene units may be linked together "head to tail" to form linear chains or they may be arranged to form rings. One can consider the isoprene unit as one of nature's common building blocks.
Isoprene itself does not undergo the building process, but rather activated forms, isopentenyl pyrophosphate (IPP or also isopentenyl diphosphate) and dimethylallyl pyrophosphate (DMAPP or also dimethylallyl diphosphate), are the components in the biosynthetic pathway. IPP is formed from acetyl-CoA via the intermediacy of mevalonic acid in the HMG-CoA reductase pathway. An alternative, totally unrelated biosynthesis pathway of IPP is known in some bacterial groups and the plastids of plants, the so-called MEP(2-Methyl-D-erythritol-4-phosphate)-pathway, which is initiated from C5-sugars. In both pathways, IPP is isomerized to DMAPP by the enzyme isopentenyl pyrophosphate isomerase.
As chains of isoprene units are built up, the resulting terpenes are classified sequentially by size as hemiterpenes, monoterpenes, sesquiterpenes, diterpenes, sesterterpenes, triterpenes, and tetraterpenes. Essentially, they are all synthesized by terpene synthase.
Second- or third-instar caterpillars of Papilio glaucus emit terpenes from their osmeterium.
Terpenes may be classified by the number of isoprene units in the molecule; a prefix in the name indicates the number of terpene units needed to assemble the molecule.
Hemiterpenes consist of a single isoprene unit. Isoprene itself is considered the only hemiterpene, but oxygen-containing derivatives such as prenol and isovaleric acid are hemiterpenoids.
Monoterpenes consist of two isoprene units and have the molecular formula C10H16. Examples of monoterpenes and monoterpenoids include geraniol, terpineol (present in lilacs), limonene (present in citrus fruits), myrcene (present in hops), linalool (present in lavender) or pinene (present in pine trees). Iridoids derive from monoterpenes.
Sesquiterpenes consist of three isoprene units and have the molecular formula C15H24. Examples of sesquiterpenes and sesquiterpenoids include humulene, farnesenes, farnesol. (The sesqui- prefix means one and a half.)
Diterpenes are composed of four isoprene units and have the molecular formula C20H32. They derive from geranylgeranyl pyrophosphate. Examples of diterpenes and diterpenoids are cafestol, kahweol, cembrene and taxadiene (precursor of taxol). Diterpenes also form the basis for biologically important compounds such as retinol, retinal, and phytol.
Sesterterpenes, terpenes having 25 carbons and five isoprene units, are rare relative to the other sizes. (The sester- prefix means half to three, i.e. two and a half.) An example of a sesterterpenoid is geranylfarnesol.
Triterpenes consist of six isoprene units and have the molecular formula C30H48. The linear triterpene squalene, the major constituent of shark liver oil, is derived from the reductive coupling of two molecules of farnesyl pyrophosphate. Squalene is then processed biosynthetically to generate either lanosterol or cycloartenol, the structural precursors to all the steroids.
Sesquarterpenes are composed of seven isoprene units and have the molecular formula C35H56. Sesquarterpenes are typically microbial in their origin. Examples of sesquarterpenoids are ferrugicadiol and tetraprenylcurcumene.
Tetraterpenes contain eight isoprene units and have the molecular formula C40H64. Biologically important tetraterpenoids include the acyclic lycopene, the monocyclic gamma-carotene, and the bicyclic alpha- and beta-carotenes.
Polyterpenes consist of long chains of many isoprene units. Natural rubber consists of polyisoprene in which the double bonds are cis. Some plants produce a polyisoprene with trans double bonds, known as gutta-percha.
Norisoprenoids, such as the C13-norisoprenoids 3-oxo-α-ionol present in Muscat of Alexandria leaves and 7,8-dihydroionone derivatives, such as megastigmane-3,9-diol and 3-oxo-7,8-dihydro-α-ionol found in Shiraz leaves (both grapes in the species Vitis vinifera) or wine (responsible for some of the spice notes in Chardonnay), can be produced by fungal peroxidases or glycosidases.
Terpenes have properties as chemicals in food, cosmetics, pharmaceutical and biotechnology industries. Chemical synthesis of terpenes can be problematic because of their complex structure, and plants produce small amounts of terpenes, making it difficult, time-consuming and expensive to extract them directly from plants. The genomes of 17 plant species contain genes that encode terpenoid synthase enzymes imparting terpenes with their basic structure, and cytochrome P450s that modify this basic structure.
Research into terpenes has found that many of them possess qualities that make them useful active ingredients as part of natural agricultural pesticides. Terpenes are used by termites of the Nasutitermitinae family to ward off predatory insects, through the use of a specialized mechanism called a fontanellar gun.
Terpene, any of a class of hydrocarbons occurring widely in plants and animals and empirically regarded as built up from isoprene, a hydrocarbon consisting of five carbon atoms attached to eight hydrogen atoms (C5H8). The term is often extended to the terpenoids, which are oxygenated derivatives of these hydrocarbons.
Biological formation of the terpenes occurs by the combination of two molecules of acetic acid to give mevalonic acid (C6H12O4) and conversion of the latter to isopentenyl pyrophosphate, which contains the five-carbon isoprene skeleton. Further transformations of the isopentenyl compound yield the true terpenes and the terpenoids.
The true terpenes are usually grouped according to the number of isoprene (C5H8) units in the molecule: monoterpenes (C10H16) contain two such units; sesquiterpenes (C15H24), three; diterpenes (C20H32), four; triterpenes (C30H48), six; and tetraterpenes (C40H64), eight. Rubber and gutta-percha are polyterpenes in which 1,000–5,000 isoprene units are joined in a long chain. Monoterpenes, sesquiterpenes, and diterpenes are abundant in the essential oils of plants: turpentine contains several monoterpenes, and the rosin acids are diterpenes. Vitamin A is another important diterpene. The triterpene squalene, obtainable from shark-liver oil, may be converted to cholesterol and many other steroids. The carotenoid pigments are the best known tetraterpenes.
Terpenes are a large and diverse class of organic compounds, produced by a variety of plants, particularly conifers, though also by some insects such as termites or swallowtail butterflies, which emit terpenes from their osmeteria. They are often strong-smelling. They may protect the plants that produce them by deterring herbivores and by attracting predators and parasites of herbivores.
Essential oil, highly volatile substance isolated by a physical process from an odoriferous plant of a single botanical species. The oil bears the name of the plant from which it is derived; for example, rose oil or peppermint oil. Such oils were called essential because they were thought to represent the very essence of odour and flavour.
The first records of essential oils come from ancient India, Persia, and Egypt; and both Greece and Rome conducted extensive trade in odoriferous oils and ointments with the countries of the Orient. Most probably these products were extracts prepared by placing flowers, roots, and leaves in fatty oils. In most ancient cultures, odorous plants or their resinous products were used directly. Only with the coming of the golden age of Arab culture was a technique developed for the distillation of essential oils. The Arabs were the first to distill ethyl alcohol from fermented sugar, thus providing a new solvent for the extraction of essential oils in place of the fatty oils that had probably been used for several millennia.
The knowledge of distillation spread to Europe during the Middle Ages, and isolation of essential oils by distillation was described during the 11th to 13th centuries. These distilled products became a specialty of the European medieval pharmacies, and by about 1500 the following products had been introduced: oils of cedarwood, calamus, costus, rose, rosemary, spike, incense, turpentine, sage, cinnamon, benzoin, and myrrh. The alchemical theories of the Swiss physician and alchemist Paracelsus played a role in stimulating physicians and pharmacists to seek essential oils from aromatic leaves, woods, and roots.
In some oils one or only a few components predominate: thus oil of wintergreen contains about 98 percent of methyl salicylate; orange oil, about 90 percent of d-limonene; bois de rose, 90 percent of linalool; and cassia, up to 95 percent of cinnamaldehyde. In most oils there is a mixture of anywhere from a few dozen to several hundred individual compounds. Trace components are very important, since they give the oil a characteristic and natural odour.