‘Active Principles’ Of Potentized Drugs Are ‘Molecular Imprints’ Of ‘Functional Groups’
PATHOGENIC MOLECULES produce diseases by binding their active FUNCTIONAL GROUPS to the specific biological molecules in the organism due to their molecular affinity, and producing molecular errors.
During drug proving, poisoning and crude molecular actions, DRUG MOLECULES produce bio-molecular errors and symptoms in the healthy organism by binding their FUNCTIONAL GROUPS to the biological molecules.
When disease symptoms and drug symptoms appear SIMILAR, that means functional groups of pathogenic molecules and drug molecules were similar, so that they could bind to similar bio-molecular targets and produce similar molecular errors in the organism.
HYDROSOMES or ‘molecular imprints’ of ‘functional groups’ of drug molecules contained in the potentized drugs can act as ‘artificial binding sites or LIGAND TRAPS towards the SIMILAR pathogenic molecules, due to their COMPLEMENTARY conformation.
It is now obvious that when using SIMILIMUM as therapeutic agents, we are actually using MOLECULAR IMPRINTS of ‘functional groups’ of drug molecules to bind to the ‘functional groups’ of pathogenic molecules and deactivate the.
This observation leads us to some very important conclusions: What we actually need is the MOLECULAR IMPRINTS of biologically active FUNCTIONAL GROUPS. If we can prepare molecular imprints of all biologically active functional groups, and make them available as homeopathic remedies, we will not need all these thousands of different drug substances. We will require only a very limited number of drugs, which could be universally applied as per homeopathic indications.
We will have to prepare MOLECULAR IMPRINTS of only following classes of FUNCTIONAL GROUPS to make our wonderful therapeutic arsenal:
Functional Groups consisting of Hydrocarbons: Alkyl ( Ethane), Alkenyl ( Ethylene) , Alkynyl (Acetylene), Phenyl (Cumene), Benzyl (Benzyl bromide).
Functional Groups containing Halogens: Halo ( Chloroethane), fluoro (Fluoromethane), chloro (Chloromethane), bromo (Bromomethane), iodo (Iodomethane).
Functional Groups containing oxygen: Hydroxyl (Methanol), Carbonyl (Butanone), Aldehyde (Acetaldehyde), Haloformyl (Acetyl chloride), Carbonate ester (Triphosgene), Carboxylate (Sodium acetate), Carboxyl (Acetic acid), Ester (Ethyl butyrate), Methoxy, Hydroperoxy (Methyl ethyl ketone peroxide), Peroxy (Di-tert-butyl peroxide), Ether (Diethyl ether), Hemiacetal, Hemiketal, Acetal, Ketal , Orthoester, Orthocarbonate ester.
Functional Groups containing nitrogen: Carboxamide (Acetamide), Primary amine (Methylamine), Secondary amine (Dimethylamine), Tertiary amine (Trimethylamine), 4° ammonium ion (Choline), Primary ketimine, Secondary ketimine, Primary aldimine, Secondary aldimine, Imide (Succinimide), Azide (Phenyl azide), Azo (Methyl orange), Cyanate (Methyl cyanate), Isocyanate (Methyl isocyanate), Nitrate (Amyl nitrate), Nitrile (Benzonitrile), Isonitrile (Methyl isocyanide), Nitrosooxy (Isoamyl nitrite), Nitro (Nitromethane), Nitroso (Nitrosobenzene), Pyridyl (Nicotine).
Functional Groups containing sulphur: Sulfhydryl (Ethanethiol), Sulfide (Dimethyl sulfide), Disulfide (Dimethyl disulfide), Sulfinyl (Dimethyl sulfoxide), Sulfonyl (Dimethyl sulfone ), Sulfino (2-Aminoethanesulfinic acid), Sulfo (Benzenesulfonic acid), Thiocyanate (Phenyl thiocyanate), Isothiocyanate (Allyl isothiocyanate), Carbonothioyl (Diphenylmethanethione), Carbonothioyl.
Groups containing phosphorus: Phosphino (Methylpropylphosphane), Phosphono (Benzylphosphonic acid), Phosphate (Glyceraldehyde 3-phosphate), Phosphodiester (O‑[(2‑Guanidinoethoxy)hydroxyphosphoryl]‑l‑serine).
Groups containing boron: Borono, Boronate, Borino, Borinate.
THIS IS ONLY A PRELIMINARY THOUGHT IN THIS DIRECTION.
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