How Remdesivir does its damage, and the Ivermectin issue.
Update 5/12/2022: Info about Dr. Mercola’s article about ivermectin and its anti-cancer properties is at the end of this post.
Update 6/25/2022: Chinese study supporting the use of IVERMECTIN
Update 7/20/2022: Link to one of the best human doctors who is stressing the incredible importance of ivermectin and the possible healing of the GENE THERAPY in form of covdi ‘injections’: https://www.brighteon.com/c5384cbe-5965-45f8-8c8a-904af84dd68a
Dr. Group - Candida, Parasites and Natural Healing - Part 1
Update 12/15/2022: A great article by Dr. Yeadon, titled “Most Covid-19 Deaths were a direct result of the administration of Midazolam or Remdesivir – By Dr Mike Yeadon“ available at https://expose-news.com/2021/10/11/dr-mike-yeadon-midazolam-remdesivir-do-not-comply/
The begin of every modern drug starts with finding out to what it can bind in the human body, so it can inhibit that pathway, mainly via one protein, or nucleic acids, related supposedly to a certain disease. The list of all known crystallized proteins (~190,000 by now), very frequently bound to the chemicals, can be found in a NIH database known as RCSB PDB. This is the A and O of everything around chemical synthetic design of pharmaceutical drugs.
An example of the Gilead Sciences entry at https://www.rcsb.org/structure/7L1F is the one which describes remdesivir bound to the SARS-CoV-2 virus RNA-dependent RNA polymerase (RdRp), in order to stop its action, quote:
“remdesivir-stalled RNA-dependent RNA polymerase complex, revealing full incorporation of 3 copies of remdesivir monophosphate (RMP) and a partially incorporated fourth RMP in the active site. The structure reveals that RMP blocks RNA translocation after incorporation of 3 bases following RMP, resulting in delayed chain termination, which can guide the rational design of improved antiviral drugs.” Remdesivir, a monophosphate nucleoside analogue prodrug (ProTide), chemically mimics nucleotide (image from wiki):
but before it can bind to that SARS-CoV-2^3 replication machinery it needs HUMAN PROTEINS in order to get converted to that final ‘rescuing wonder’, here the pathway:
So not only it uses human body parts, three different proteins (each which participates in countless other biological functions, thus affecting them all) and water, in order to get converted to something supposedly useful, while affecting this way countless HUMAN functions, it can possibly bind to anything what would accept that 100% SYNTHETIC nucleotide portion of the molecule via that chemical mimicry^7, plus it actually steals 2 phosphates and leaves synthetics containing crap in the human body for every injected molecule! Thanks to Thomas from Alpha Omega Energy (Weaponized News Channel on substack) that ‘crap’ is nothing less than benzene (highly carcinogenic) and cyanide derivative of one of the most essential molecule in our bodies, ATP… And that is just one part, since as every aromatic molecule, it will absorb/emit UV radiations, interfering with human bioluminescence. Last but not least, will it ever leave the human body via complete degradation??? The deadly AZT (azidothymidine) was another nucleoside mimicking drug of completely devastating consequences. The book from Mr. Kennedy “The real Anthony Fauci” describes the ‘studies’ done on it, just unprecedented. Both Remdesivir and AZT being capable of intercalating natural genetic material (RNA or DNA), via the pi-pi bond stacking (attraction of parallel planar electron distributions), will end up killing.
ATP is the alpha and omega of human energy, and now even that got hacked, and now even in CHILDREN!!!! More info on that topic at https://altered-states.net/barry/newsletter576/
It is hard to find any resources about the frequency spectrum of Remdesivir, but it is known for ATP for example, that it activates Ca +2-permeable channels to increase release probability at interneuron synapse ( https://www.jneurosci.org/content/jneuro/23/19/7426.full.pdf). Like ATP, Remdesivir will have its own bioluminescence interferring with that one from natural ATP’s in the entire body. The works of Prof. Fritz-Albert Popp were all about bioluminescence, biophotons detection, distribution and behavior in the human body and organic world. He was able to detect the difference between the genetically modified food and natural organic counterpart. A synthetic drug is always a substance FOREIGN to the human body (everything foreign will also affect immune system), and preferred in particular when it is patented. We’ve been told SARS-CoV-2 is a virus with the available genome at: https://www.ncbi.nlm.nih.gov/nuccore/NC_045512.2 with that RNA-dependent RNA polymerase (RdRp) which will stop multiplying the virus when Remdesivir is added, BUT apparently THAT IS NOT what is happening! Before that can happen, your body will get literally poisoned by a chemical mimicry machinery of the petroleum industry: https://www.organic-chemistry.org/totalsynthesis/totsyn07/remdesivir-mackman.shtm
What is very strange about that SARS-CoV-2 replication machine, the RdRp enzyme, is that it has huge amount of homologies/similarities with the viral Spike protein, injected into billions of arms! BLAST search shows that for the 83% amino acid sequence coverage between those two, there are 48% identities, meaning almost as if the Spike itself had some kind of replicative properties or at least homolog to some RdRp features? That homology between the RdRp and Spike must have some purpose. Anyone interested in seeing these overlaps, please leave a comment below, can send you the data. There was a study published in March 2021, with computer graphics simulations showing that both RdRp and Spike might bind to IVERMECTIN, its title was: “"Exploring the binding efficacy of ivermectin against the key proteins of SARS-CoV-2 pathogenesis: an in silico approach” available at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7996102/pdf/fvl-2020-0342.pdf . Their simulation of the binding scheme to RdRp is taken out of the publication:
Since the 2015 Nobel Prize winning drug IVERMECTIN^5, the unique inhibitor of nuclear import^6 (meaning indirectly inhibiting a process of mixing species, which is always about transferring genetic material whether via viral infection or genetic treatments, like the covid injections), has been used for so long with extremely safe profile:
AND it can presumably bind BOTH, the RfRP replication machinery AND THE SPIKE, that question was for long time, why not to use it, when it can get rid of both enemies at once!?? It must be THE GENETICALLY MODIFYING INJECTION, Fauci and Co. just DID NOT WANT to spoil their plan of having the INJECTED SPIKE or possibly even its synthetic genome not bound to ivermectin (he does not care about the natural Spike which will get destroyed by innate immune system and end up with a better immunity profile than from the genetically modified synthetic version), but rather he wants to have that mRNA for the Spike in HUMAN bodies, later on in cells over the entire body, including the stem cells(!), to multiply the lethal damage done already while using remdesivir. A clear confirmation of this fact was published by the chinese, not long time ago in Nature article titled: “Structural biology of SARS-CoV-2: open the door for novel therapies” in which the essential Table 2 contains all SARS-CoV-2 components and the drugs targeting them and for the Spike (S protein) the number 1 drug is: IVERMECTIN. Here a paste from the printout at https://www.nature.com/articles/s41392-022-00884-5/tables/2:
Table 2 Overview of targets and potential drugs of SARS-CoV-2
Drug targets Approved/potential COVID-19 drugs
S Ivermectin,36 Arbidol,38 Lipopeptide EK1 and EK1C4,41 SSA09E2,368 Griffithsin,369 Nidazolamide and Tizolazolide,370 Heparin,371 Withaferin A,372 Tetracycline,373 Monoclonal antibodies targeted to S protein
E Hexamethylene amiloride (HMA) and Amantadine (AMT),98 Hm-methyleneamelory,374
Nsp1 Glycyrrhizic acid, Lobaric acid, Garcinolic acid and Tirilazad139
Nsp2 Nigellidine,146
Nsp3 VIR251,173 GRL-0617,151 YM155,175 Ribavirin,375 GRL-0667 and Mycophenolic acid376
Nsp4 Eribulin and Suvorexant184
Please note, the publication which investigated IVERMECTIN usage against the S protein, genetic code of which is being injected into billions of clueless victims, came out BEFORE introduction of these GENE THERAPIES:
36. Caly, L. et al. “The FDA-approved drug ivermectin inhibits the replication of SARS-CoV-2 in vitro”. Antivir. Res 178, 104787 (2020).
S. ̃Omura in his 2008 article “Ivermectin: 25 years and still going strong” (International Journal of Antimicrobial Agents 31 (2008) 91–9) shows in the Fig 1. how ivermectin blocks neurotransmission, interfering with neuromuscular synapses. It acts on glutamate-gated chloride channels, which are common in nematodes, insects and ticks, thereby paralysing pharyngeal and somatic muscles of those. But isn’t that the very same mechanism involved in the delivery of synthetic genetic material accross the cellular membrane in the universal gene therapy forced upon the entire humanity?
If anyone can give some other kind interpretation hint to that part, that would be nice.
The abstract of the above mentioned article^6 concluded:”The antiviral action and ADMET profile of ivermectin was on par with the currently used anticorona drugs such as hydroxychloroquine and remdesivir. Conclusion: Our study enlightens the candidature of ivermectin as an effective drug for treating COVID-19.”
And there is another issue there, in addition to double the damage control with remdesivir. That the final leftover Remdesivir ‘active nucleoside’ is part of the same family of chemicals, to which the 1-Methyl-pseudouridine belongs, the synthetic nucleoside in all the covid genetically modifying injections, is interesting, maybe related to future plans. To close this short note, just one long sentence from a publication titled “Selecting Fully-Modified XNA Aptamers Using Synthetic Genetics“ (Current Protocols in Chemical Biology e44), quote:
“This unit describes the application of “synthetic genetics,” i.e., the replication
of xeno nucleic acids (XNAs), artificial analogs of DNA and RNA bearing alternative backbone or sugar congeners, to the directed evolution of synthetic oligonucleotide ligands (XNA aptamers) specific for target proteins or nucleic acid motifs, using a cross-chemistry selective exponential enrichment (X-SELEX) approach.“
That XNA can be reverse transcribed, using a directly-binding primer or by addition of a poly(dA) tail (lot of the inverted poly(A)^1 pieces in Mod-E-RNA/Pfizer injections!!), to allow cDNA amplification or sequencing…
This is just a bad imagination, but what if many of the chemicals can be remotely driven, via wi-fi, to become something different^1,2?? Polyethylene glycol in nanoform is the part of the covid injection materials for some brands. Here an image from the first publication describing the changing of the polyethylene structure in microwave fields:
The Remdesivir, modified synthetic mRNA injections, all for Fauci’s paycheck, involving HUMAN poisoned and lost LIVES, those who paid him for doing this, and now even the LOST FUTURE, the CHILDREN, is just the biggest tragedy in the human history, which now might be at its end!
Update 5/11/2022: Dr. J. Mercola posted a wonderful article about Ivermectin today:https://articles.mercola.com/sites/articles/archive/2022/05/12/ivermectin-antitumor-effects.aspx
It describes its ANTI-CANCER properties, which would align perfectly well with its, once again feature of being: the unique inhibitor of nuclear import^6 !! Using it in a liposomal form, like many other supplemental nutrients (Vit C or Glutathione) is the best choice, due to the direct delivery over the cellular membrane, ironically the very same way all GENETICALLY MODIFYING covid injections do. Since Dr. Mercola’s articles can’t be displayed for longer than 4 days, I’ll post here his citation list in regard to anit-cancer ivermectin properties (hope he allows me to do so;) :
1. Eva Bäckström et al. “Trash to Treasure: Microwave-Assisted Conversion of Polyethylene to Functional Chemicals” Ind. Eng. Chem. Res. 2017, 56, 14814−14821. https://pubs.acs.org/doi/pdf/10.1021/acs.iecr.7b04091
2. M. Iannelli, H. Ritter”Microwave‐Assisted Direct Synthesis and Polymerization of Chiral Acrylamide” Macromolec. Chem. Phys. Volume206, Issue3 February 3, 2005 Pages 349-353.
3. The picture of the SARS-CoV-2 virus generated by somebuddy^4 anonymous, never possible to overwrite, can be found at wiki at: https://en.wikipedia.org/wiki/Severe_acute_respiratory_syndrome_coronavirus_2
it looks very much distorted:
Since SARS-CoV-2 Spike is ~30% IDENTICAL in the amino acid sequence with the patented SWINE FLU VACCINE, a following link might be of interest. That’s the TIP of a ‘viral oversimplification’ in no less than the most prestigious DOE lab at APS, from their 2010 main page at “https://www.aps.anl.gov/APS-Science-Highlight/2010/structure-swine-flu-virus“ an article from 2010
in an article titled ”The Structure of the "Swine Flu" Virus” with the only picture on this page like this:
Well, that’s NOT A VIRUS, that’s a protein complex.
4. somebuddy: redefintion of ‘somebody’, according to wildly accepted rules of the FDA/CDC/NIH new world language, in which innate immunity does not exist anymore and in which ‘genetic modification treatment’ got under its ‘shaddow’ of the old world language of a ‘vaccine’.
5. artemisin is a related compound derived from extremely healing plant Artemisia annua (artemisia extracts can be seen on some anti-covid protocols as a supplement, the species Artemisia absinthium also called wormwood, can be found in many anti-parasitic herbal extracts, and also in anti-cancer supplements..)
6. Kylie M. Wagstaff et al. “An AlphaScreen®-Based Assay for High-throughput Screening for Specific Inhibitors of nuclear Import” Journal of Biomolecular screening 16(2); 2011.
7. Please read inbetween the lines from https://pubchem.ncbi.nlm.nih.gov/compound/Remdesivir#section=Pharmacology-and-Biochemistry
“Due to much higher selectivity of mammalian DNA and RNA polymerases, including human mitochondrial RNA polymerase, for ATP over remdesivir triphosphate, remdesivir is not a significant inhibitor of these enzymes, which contributes to its overall tolerability and safety profile.”!!???
Well, that’s exactly the issue, Remdesivir is the inhibitor of those HUMAN essential ENZYMES.
this is incredibly sad... was reading firsthand accounts this morning of people whose loved ones were killed in hospital after this drug was administered... they had no idea until too late how dangerous it was.., and now the kiddie version???
(attribution to Paris Green on Substack) anagram for Veklury (the kiddie version of Remdesivir) = (Albert) Kluyver... ‘what is true for bacteria is also true for elephants’ or genetic code universality.
they are monsters.