Antioxidant
Enzyme Activator
Zwitterion
PH Homeostasis
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Alkali Citrate
https://en.m.wikipedia.org/wiki/Alkali_citrate
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Adding Honey to Cold Process Soap
https://www.soapqueen.com/bath-and-body-tutorials/cold-process-soap/coconut-milk-soap-volcano-2/
the soap volcano only seems to happen when sugar is introduced with the lye & oil, so im baffeled, then it gets really hot, then into a gel phase, then hardens into soap, thats very odd reactions.
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Saponification Definition and Reaction
https://www.thoughtco.com/definition-of-saponification-605959
Neutralized Wood ash with vinegar as the ultimate flower fert
https://www.icmag.com/threads/neutralized-wood-ash-with-vinegar-as-the-ultimate-flower-fert.374596/
https://www.houzz.com/discussions/3146705/wood-ash-add-vinegar
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Disproportionation
Electronegativity
Regioselectivity
Amphoterism
Substitution Reaction
Electrophile
Nucleophile
Carbocation
Carbanion
Free Radical
Atom Transfer
Polymerization
https://en.m.wikipedia.org/wiki/Disproportionation
https://en.m.wikipedia.org/wiki/Amphoterism
https://en.m.wikipedia.org/wiki/Electronegativity
https://en.m.wikipedia.org/wiki/Regioselectivity
https://en.m.wikipedia.org/wiki/Substitution_reaction
https://en.m.wikipedia.org/wiki/Nucleophilic_acyl_substitution
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Electronegativity:
Acid Gases
Electropositivity:
Alkali Metals
Elements in the upper right of the periodic table of elements (oxygen, sulfur, chlorine) have the greatest electronegativity, and those in the lower-left (rubidium, caesium, and francium) the greatest electropositivity.
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Hydrolysis
Heterolysis
Enzymatic Hydrolysis
Heterolytic Fission
Nucleophile
Bond Energy
Bond Cleavage
https://en.m.wikipedia.org/wiki/Hydrolysis
https://en.m.wikipedia.org/wiki/Heterolysis_(chemistry)
https://en.m.wikipedia.org/wiki/Enzymatic_hydrolysis
https://en.m.wikipedia.org/wiki/Living_free-radical_polymerization
https://en.m.wikipedia.org/wiki/Bond_energy
https://en.m.wikipedia.org/wiki/Bond_cleavage
https://en.m.wikipedia.org/wiki/Nucleophile
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Carbon is a clear gas, like air, white vinegar or diamond, while Charcoal may be mostly Carbon, its the woodash minerals that make it such a good absorbent.
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The main factors that affect heterolysis rates are mainly the solvent's polarity, electrophilic and ionizing power.
The polarizability, nucleophilicity and cohesion of the solvent has a much weaker effect on heterolysis.
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Acyl
Acetic
Acetylation
Acetyltransferase
Acyltransferase
Polyketide
Polyketone
Polyelectrolyte
Disproportionation
Amphoterism
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Electronegativity and Bond Polarity
Metal Salts
Ionic Bond
Polyatomic Monoatomic Polyketide Chelate
Acetic Acetate
Electronegativity
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Polymorphism
Nucleomorph
Nucleophile
Granuloma
https://en.m.wikipedia.org/wiki/Granuloma
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Protein
Amino Acids
Alpha-Amino
Functional Group
https://en.m.wikipedia.org/wiki/Amino_acid
https://en.m.wikipedia.org/wiki/Functional_group
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Amino acids are organic compounds that contain both amino and carboxylic acid functional groups.
Functional groups can also be charged in carboxylate salts, which turns the molecule into a polyatomic ion or a complex ion.
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Food Thickening Agent
Hydrolysis
Saccharification
Polysaccharide
Xanthan Gum
https://en.m.wikipedia.org/wiki/Hydrolysis
https://en.m.wikipedia.org/wiki/Saccharification
https://en.m.wikipedia.org/wiki/Polysaccharide
https://en.m.wikipedia.org/wiki/Xanthan_gum
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Hydrolysis: Sucrose broken down into Glucose and Fructose, is Saccharification.
Thermolysis: Saccharification can also occur during Caramelization.
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take the vinegar minerals, (including the very top most part of the soot, not the very bottom larger particles), and start making gravity by using sugar, then slowly let it caramelize, then before its done, add a bit of water to keep from thickening into hard candy.
the caramelization without oil would become sticky like candy, with oil more like a gravy.
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decided a little sea salt might be important, being that the NOW minerals has no sodium.
Cortisol
Ergosterol
Adrenal Gland
Endocrine Gland
Inflammation
Glucocorticoid Receptor
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Polyketide
Oligosaccharide
https://en.m.wikipedia.org/wiki/Oligosaccharide
Galactooligosaccharides (GOS), which also occur naturally, consist of short chains of galactose molecules. Human milk is an example of this and contains oligosaccharides, known as human milk oligosaccharides (HMOs), which are derived from lactose.
HMOs can also protect infants by acting as decoy receptors against viral infection. HMOs accomplish this by mimicking viral receptors which draws the virus particles away from host cells. Experimentation has been done to determine how glycan-binding occurs between HMOs and many viruses such as influenza, rotavirus, human immunodeficiency virus (HIV), and respiratory syncytial virus (RSV). The strategy HMOs employ could be used to create new antiviral drugs.
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A nonenzymatic method for cleaving polysaccharides to yield oligosaccharides for structural analysis
https://www.nature.com/articles/s41467-020-17778-1
Reconstitution of the lipid-linked oligosaccharide pathway for assembly of high-mannose N-glycans
https://www.nature.com/articles/s41467-019-09752-3
Oligosaccharide
https://www.healthline.com/nutrition/oligosaccharides#what-they-are
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Alkaline Hydrolysis
https://homeliftup.com/pesticides-alkaline-acidic/
Alkaline hydrolysis degrades pesticides by rendering them non-toxic. This happens through the dissociation of pesticide molecules which leads to the release of electrically charged atoms.
Sodium Acetate
https://en.m.wikipedia.org/wiki/Sodium_acetate
Sodium acetate is used in the textile industry to neutralize sulfuric acid waste streams and also as a photoresist while using aniline dyes.
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https://en.m.wikipedia.org/wiki/Cyclodextrin
https://en.m.wikipedia.org/wiki/AOH1996
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Ringer's Solution
Tyrode's Solution
https://en.m.wikipedia.org/wiki/Ringer%27s_solution
https://en.m.wikipedia.org/wiki/Ringer%27s_lactate_solution
https://en.m.wikipedia.org/wiki/Tyrode%27s_solution
https://en.m.wikipedia.org/wiki/Lactic_acid
In solution, it can ionize by loss of a proton to produce the lactate ion. Compared to acetic acid, its pKa is 1 unit less, meaning lactic acid is ten times more acidic than acetic acid. This higher acidity is the consequence of the intramolecular hydrogen bonding between the α-hydroxyl and the carboxylate group.
Ringer's acetate may be a better alternative with the lactate replaced by acetate. In Scandinavia Ringer's acetate is typically used.
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Acetate-buffered crystalloid fluids
https://www.sciencedirect.com/science/article/abs/pii/S0883944116300661
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Synthesis of benzimidazole by mortar–pestle grinding method
https://en.m.wikipedia.org/wiki/Benzimidazole
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Acetic
Acetate
Adenosine
Citrate
Glucocorticoid
Oxalate
Acetyl-CoA (ACSS2)
Bicarbonate Precursor
Haemodynamics
Hyperoxaluria
Hyperuricemia
Haemodialysis
Colloid
Crystalloid
Monosodium Urate
Acetate Revisited: A Key Biomolecule at the Nexus of Metabolism, Epigenetics and Oncogenesis—Part 1: Acetyl-CoA, Acetogenesis and Acyl-CoA Short-Chain Synthetases
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689297/
Acetate Revisited: A Key Biomolecule at the Nexus of Metabolism, Epigenetics, and Oncogenesis – Part 2: Acetate and ACSS2 in Health and Disease
https://www.frontiersin.org/articles/10.3389/fphys.2020.580171/full
The Role of Acetate in the Antagonization of Oxalate: A Potential Causative Molecule for Heart Disease and Cancer Death
https://journals.sagepub.com/doi/full/10.1177/1934578X20913697
Acetyl-CoA synthetase 2 promotes acetate utilization and maintains cancer cell growth under metabolic stress
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297291/
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https://en.m.wikipedia.org/wiki/Ester
https://en.m.wikipedia.org/wiki/Lipid_metabolism
https://en.m.wikipedia.org/wiki/Beta_oxidation
https://en.m.wikipedia.org/wiki/Alkaline_hydrolysis
https://en.m.wikipedia.org/wiki/Acid_hydrolysis
https://en.m.wikipedia.org/wiki/Metabolic_acidosis
https://en.m.wikipedia.org/wiki/Common-ion_effect
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Alkaline Hydrolysis
Hydron
Hydroxide
Hydroxide Ion
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Sodium Acetate as a Replacement for Sodium Bicarbonate in Medical Toxicology: a Review
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771004/
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Berberine
Iminium
Tyrosine
Adenosine
Radical SAM
Metal Acetylacetonates
Metallacycle
Metallacyclopentanes
https://en.m.wikipedia.org/wiki/Berberine
https://en.m.wikipedia.org/wiki/Iminium
https://en.m.wikipedia.org/wiki/Tyrosine
https://en.m.wikipedia.org/wiki/Adenosine
https://en.m.wikipedia.org/wiki/Radical_SAM
https://en.m.wikipedia.org/wiki/Metal_acetylacetonates
https://en.m.wikipedia.org/wiki/Metallacycle
https://en.m.wikipedia.org/wiki/Metallacyclopentanes
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Lactate Acid
https://en.m.wikipedia.org/wiki/Lactic_acid
Lactate Acid is one of the main components of lactated Ringer's solution and Hartmann's solution.
These intravenous fluids consist of sodium and potassium cations along with lactate and chloride anions in solution with distilled water, generally in concentrations isotonic with human blood. It is most commonly used for fluid resuscitation after blood loss due to trauma, surgery, or burns.
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Zwitterion
Isoelectric Point
Electrophoresis
Zeta Potential
Polyelectrolytes
Electrokinetic Phenomena
https://en.m.wikipedia.org/wiki/Zwitterion
https://en.m.wikipedia.org/wiki/Isoelectric_point
https://en.m.wikipedia.org/wiki/Zeta_potential
https://en.m.wikipedia.org/wiki/Polyelectrolyte
https://en.m.wikipedia.org/wiki/Electrokinetic_phenomena
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all disease & parasitic toxic are fundamental a shift from PH homeostasis, creating inflammation, and misfolded proteins, making amyloid plaque a result of this process over time.
the reversing of the root case must be from neutralizing ions, smaller then the source of disease.
Fenbendazole is doing this in the form of Polyketide.
"Polyketides, metabolites built primarily from combinations of acetate units."
Acetate is electrolytes salts (base) & vinegar acetic (acid).
monoatomic minerals & carbon acids like simple sugars, into Antioxidant, Polyketide, Acetate, Zwitterion, Polyelectrolyte ect..
bind to parasites & free radical mycotoxins as a charged ion antioxidant agent.
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Trigonelline
https://en.m.wikipedia.org/wiki/Trigonelline
https://www.sciencedirect.com/topics/medicine-and-dentistry/trigonelline
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Acetic acid dressings: Finding the Holy Grail for infected wound management
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868106/
An Update on the Biologic Effects of Fenbendazole
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413524/
Myelosuppression
Bone Marrow Suppression
https://en.m.wikipedia.org/wiki/Bone_marrow_suppression
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Polyketide
Heterocycle
Electrolyte Ions
Niacin (Nitrogen)
Vinegar (Carbon)
Minerals (Electrolyte)
https://en.m.wikipedia.org/wiki/Picolinic_acid
https://en.m.wikipedia.org/wiki/Hammick_reaction
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Icosahedral virus structures and the protein data bank
https://www.sciencedirect.com/science/article/pii/S002192582100332X
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Stem Cell
Lipid Metabolism
Lipogenesis
Haematopoiesis
Fatty Acid
Beta-Oxidation
Hematopoietic Stem Cells
Intestinal Stem Cells
Cancer Stem Cells
Neural Progenitor Cells
https://en.m.wikipedia.org/wiki/Haematopoiesis
https://en.m.wikipedia.org/wiki/Lipogenesis
https://en.m.wikipedia.org/wiki/Acetyl-CoA
Lipid Mediated Regulation of Adult Stem Cell Behavior
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058546/
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Xenoestrogen
Dioxin
Cytochrome P450
Monooxygenase
Beta Oxidation
Acetyl-CoA
https://en.m.wikipedia.org/wiki/Xenoestrogen
https://en.m.wikipedia.org/wiki/Dioxins_and_dioxin-like_compounds
https://en.m.wikipedia.org/wiki/Cytochrome_P450
https://en.m.wikipedia.org/wiki/Monooxygenase
https://en.m.wikipedia.org/wiki/Dioxane_(compounds)
https://en.m.wikipedia.org/wiki/1,2-Dioxane
https://en.m.wikipedia.org/wiki/Gamma-Hydroxybutyraldehyde
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Metabolism of Dioxins
Enzyme systems for biodegradation of polychlorinated Dioxins
The angular dioxygenase, cytochrome P450, lignin peroxidase, and dehalogenase are known as dioxin-metabolizing enzymes. All of these enzymes have metal ions in their active centers, and the enzyme systems except for peroxidase.
https://en.m.wikipedia.org/wiki/Dehalogenase
https://en.m.wikipedia.org/wiki/Reductive_dehalogenases
https://en.m.wikipedia.org/wiki/Halorespiration
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Chloroethylene Oxide
The science behind dioxins, vinyl chloride, and proven remediations
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the normal protocol for Fenbendazole is for a few months, so i just combined the old folk remedy antiparasitic Caster & Pine Terpinene, chemistry even looks like Suramin.
Fenbendazole
Suramin
this is essentially what made it double strength.
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Fenbendazole acts as a moderate microtubule destabilizing agent and causes cancer cell death by modulating multiple cellular pathways
https://www.nature.com/articles/s41598-018-30158-6
Bioprospecting of Nitrogenous Heterocyclic Scaffolds with Potential Action for Neglected Parasitosis: A Review
https://hal.science/hal-02908646/document
Electrolyte Chelate
https://www.healthline.com/health/chelated-zinc#types
Carboxytherapy
https://en.m.wikipedia.org/wiki/Carboxytherapy
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Nitrogenous Heterocyclic Polyketide Ion Zwitterion Scaffolds
smaller molecules then parasites, and acts like a biological detergent.
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Distribution and diversity of mycoplasma plasmids: lessons from cryptic genetic elements
https://bmcmicrobiol.biomedcentral.com/articles/10.1186/1471-2180-12-257
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Biosynthesis of oxygen and nitrogen-containing heterocycles in polyketides
https://www.beilstein-journals.org/bjoc/articles/12/148
Nature loves nitrogen heterocycles
https://www.sciencedirect.com/science/article/abs/pii/S004040391401939X?via%3Dihub
Heterocyclic nitrogenous pollutants in the environment and their treatment options
https://www.sciencedirect.com/science/article/abs/pii/S096085240700140X
The mutagenic potential of nitrogenous heterocyclic compounds increase with increasing number of rings, and hence quinoline is found to be more mutagenic than pyridine. Growth impairment increased with increase in the number of rings per compound and with increase in nitrogen content within the ring.
https://en.m.wikipedia.org/wiki/Heterocyclic_compound
Aziridine is produced industrially from aminoethanol by the Nippon Shokubai process, requires an oxide catalyst and high temperatures to effect the dehydration.
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CBG
Cannabigerol
https://en.m.wikipedia.org/wiki/Cannabigerol
https://en.m.wikipedia.org/wiki/Olivetol
https://en.m.wikipedia.org/wiki/Cannabigerolic_acid
https://en.m.wikipedia.org/wiki/Dihydroxybenzoic_acid
https://en.m.wikipedia.org/wiki/GC376
https://en.m.wikipedia.org/wiki/Protease_inhibitor_(pharmacology)
The Origin and Biomedical Relevance of Cannabigerol
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322760/
Choline and acetylcholine: what a difference an acetate makes!
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309389/
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https://en.m.wikipedia.org/wiki/Buckminsterfullerene#Synthesis
https://en.m.wikipedia.org/wiki/Fullerene_chemistry
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Synthesis of Heterocycles
Ammonium Acetate
Enamine
Quinoline
Fenbendazole
https://en.m.wikipedia.org/wiki/Ammonium_acetate
https://en.m.wikipedia.org/wiki/Enamine
https://en.m.wikipedia.org/wiki/Quinoline
https://en.m.wikipedia.org/wiki/Paal%E2%80%93Knorr_synthesis
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Indole-3-Acetic Acid
https://en.m.wikipedia.org/wiki/Indole-3-acetic_acid
Horseradish Peroxidase
https://en.m.wikipedia.org/wiki/Horseradish_peroxidase
Synthesis and Applications of Nitrogen-Containing Heterocycles as Antiviral Agents
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101374/
Hydrogen peroxide is a mediator of indole-3-acetic acid/horseradish peroxidase-induced apoptosis
https://www.sciencedirect.com/science/article/pii/S0014579306001438
Bioorthogonal Catalysis for Treatment of Solid Tumors Using Thermostable, Self-Assembling, Single Enzyme Nanoparticles and Natural Product Conversion with Indole-3-acetic Acid
https://pubs.acs.org/doi/10.1021/acsnano.1c11560
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Differentiation between enamines and tautomerizable imines in the oxidation reaction with TEMPO
https://www.nature.com/articles/s41467-018-07534-x/
The redox interplay between nitrite and nitric oxide: From the gut to the brain
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757698/
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Xenoestrogen
Xenohormone
https://en.m.wikipedia.org/wiki/Xenoestrogen
https://en.m.wikipedia.org/wiki/Xenohormone
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Mitochondrial metabolism and DNA methylation: a review of the interaction between two genomes
https://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/s13148-020-00976-5
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Apicomplexa
The Elusive Mitochondrial Genomes of Apicomplexa: Where Are We Now?
