Acacetin: Inhibiting Spike, Protecting the Endothelium and Taming the Macrophage

Acacetin Actions

The article:  https://wmcresearch.substack.com/p/friday-hope-acacetin-inhibiting-spike

(Tom: The article is heavy on medical data and light on the sources and use of those sources so I asked Grok.com:
What are the highest natural sources of acacetin?

Grok replied:
The highest natural sources of acacetin (a flavone also known as linarigenin or 5,7-dihydroxy-4′-methoxyflavone) are the flowers and flower heads of specific herbs and plants, where it occurs primarily in glycoside forms.

Exact quantitative data (e.g., mg/g or mg/100g) is limited in public literature, but the richest sources—based on traditional use, phytochemical isolation, and research—are ranked below by concentration/ubiquity for dietary consumption:

Top Sources (Highest Concentration)
– Chamomile flowers (Matricaria chamomilla or Chamomela nobile): Dried flower heads are repeatedly cited as among the highest dietary sources of acacetin. Brewed as tea or used as an infusion; this is one of the most accessible and concentrated ways to consume it naturally.
– Chrysanthemum (Dendranthema morifolium / Chrysanthemum indicum): Dried blossoms are rich in acacetin (often studied in extracts); a staple in East Asian herbal teas with high levels reported.
– Damiana (Turnera diffusa): Leaves are heavily researched for high acacetin content; traditionally brewed as a tea or used in extracts.

Other Notable Sources (Good but Lower or More Modest Amounts)
– Black locust flowers (Robinia pseudoacacia): Historically the original isolation source (used by early chemists); flower clusters are aromatic and edible, though not commonly brewed as tea.
– Artichoke (Cynara scolymus): Edible buds and specialized leaf extracts contain measurable levels.
– Fresh herbs/spices (lower concentration): Rosemary, thyme, oregano, and parsley leaves (Petroselinum crispum) contain detectable amounts.
– Citrus peels (modest): Especially bitter orange zest; not a primary source.

Acacetin is lipophilic (fat-soluble) and often occurs as glycosides, so gentle simmering or steeping in hot water (avoiding prolonged boiling) maximizes extraction. Pairing with healthy fats (e.g., in ghee or with meals) can improve absorption.

These plants are widely available as teas, supplements, or fresh ingredients—chamomile and chrysanthemum teas are particularly easy starting points. Always check for quality (organic, tested) and consult a healthcare provider before using any herbals, especially if you have conditions or take medications. The substack article highlights acacetin’s potential benefits, but natural dietary intake via these sources provides a gentle, traditional approach.)

Florida Sues Pfizer Over Safety of COVID-19 Vaccine

James Uthemeier

Florida Attorney General James Uthmeier has filed a major lawsuit against pharmaceutical titan Pfizer and its chief executive officer, Albert Bourla, alleging the company deceptively marketed its COVID-19 mRNA vaccine while concealing severe health risks from the public.

The legal action accuses Pfizer of running an aggressive marketing campaign that Uthmeier says was backed by roughly $10 billion in advertising and generated over $80 billion in revenue while withholding crucial information on adverse reactions.

“Pfizer told Florida families that mass vaccination with their mRNA COVID vaccine was necessary to stop the spread, and that there were no material safety risks,” Uthmeier said, accusing Bourla of claiming that unvaccinated people put loved ones in jeopardy while dismissing critics.

The suit contends Pfizer misled consumers regarding the shot’s safety profile, specifically pointing to documented cases of myocarditis in teenagers and young adults, cardiovascular complications, strokes, and alleged risks to pregnant women.

“What they didn’t say that they knew about [was] myocarditis in teenagers and young adults,” Uthmeier stated. “They had reason to know the shot posed risks to pregnant women and unborn babies in the first trimester.”

The filing highlights recent revelations from U.S. Senators Rand Paul and Ron Johnson, who exposed communications involving federal health officials—including Dr. Anthony Fauci—acknowledging that the second dose theoretically carried risks of early-term miscarriages. Despite internal awareness, federal agencies like the CDC and the Surgeon General continued telling the public the vaccine was entirely safe for expectant mothers.

Florida prosecutors also charged that Pfizer aggressively promoted the shots as a way to interrupt virus transmission despite failing to conduct clinical trials proving the vaccine prevented transmission before rushing it to market.

“What they did was wrong. They assumed Florida families could not be trusted with the truth,” Uthmeier declared. “My office will hold them accountable.”

Pfizer, according to the lawsuit, urged people to get the shot to protect others, even though the company never tested whether the vaccine stopped the virus from spreading.

Finish reading: https://flvoicenews.com/florida-sues-pfizer-ceo-albert-bourla-over-covid-19-vaccine-safety-claims/

(Tom:
Conman: noun a swindler who exploits the confidence of his victim.

Swindler: noun a person who swindles you by means of deception or fraud. One who swindles, or defrauds grossly; one who makes a practice of defrauding others by imposition or deliberate artifice; a cheat.

Fraud: noun A deception practiced in order to induce another to give up possession of property or surrender a right. A deceiver; a cheat; a pretender; also, a fraudulent production; something intended to deceive.

Victim: noun One who is harmed or killed by another, especially by someone committing a criminal or unlawful act.

Mark: noun Slang A person who is the intended victim of a swindler; a dupe.

Dupe: noun A person who is easily deceived or is used to carry out the designs of another.

The Medical/Pharmaceutical monopoly operates to maximise profits. That does not work in your interests. It works in theirs. Cures are not anywhere near as profitable as permanently managing a condition with medication.)

COVID mRNA Vaccine Hides Up to 30% of Endotoxin Activity in FDA Test

Endotoxin Hidden

Studies show lipid particles can take up endotoxin and hide over 90% of it from testing, raising questions about whether mRNA vaccine lipids conceal manufacturing E. coli LPS endotoxin contamination.

Studies show lipid particles can take up endotoxin and hide over 90% of it from testing, raising questions about whether mRNA vaccine lipids conceal manufacturing E. coli LPS endotoxin contamination.

All FDA-approved and emergency-use-authorized mRNA vaccines use E. coli to produce so-called starting DNA or other manufacturing materials, creating a lipopolysaccharide (LPS) endotoxin contamination risk that manufacturers test for in the finished shots.

Endotoxin has been shown to drive cardiac injury and abnormal clotting in experimental studies, and other outcomes that overlap with myocarditis, blood clots, and other serious events reported after Pfizer’s COVID-19 mRNA vaccine, raising the question of whether endotoxin was adequately excluded as a contributor.

No publicly available information tells us specifically how much endotoxin is present in finished mRNA vaccine vials.

In a January 2022 memo, the FDA reported adding a known amount of endotoxin to three samples of Moderna’s finished COVID vaccine to check whether its test could detect it.

Its test only recovered 80%, 71%, and 70% of the added activity.

Meaning 20%, 29%, and 30% of the control signal went undetected while the added endotoxin was present in the samples.

The endotoxin was still there.

FDA knew how much it had added.

Yet something in the vaccine samples prevented the test from detecting up to 30% of its activity.

FDA nevertheless accepted all three results, raising questions:

If the test missed up to 30% of a control added after manufacture, what could it miss when endotoxin enters the vaccine’s lipid particles during manufacture?

Why did FDA call the measured loss only “slight inhibition”?

And why did the agency allow a complete finished-product release test to wait until after its Spikevax approval decision?

Why have regulators and manufacturers not told us exactly how much LPS endotoxin is present in finished mRNA vaccine vials?

Why do post-mRNA vaccination adverse events track endotoxin exposure symptoms?

Australian regulator TGA did test Pfizer’s mRNA COVID vaccine batches as “less than 5 EU/mL.”

But that means the assay couldn’t see endotoxin above a prespecified cutoff, and only after it was diluted.

It is not a count of how much total endotoxin is in each vial.

Moreover, studies examined below found that liposomes and other lipid preparations can hide over 90% of incorporated endotoxin from detection, raising the question of what happens in the lipid nanoparticles used in mRNA vaccines.

FDA’s January 4, 2022 memo identifies the three finished Spikevax lots it tested for bacterial endotoxin; the recovery figures and redacted results appear on the following page.

FDA’s Spikevax results table shows only 80%, 71%, and 70% recovery of added endotoxin activity at 1:1,000 dilution. FDA and Moderna’s actual lot results, and the passing specification, are redacted, while every lot is marked “yes.” (Note: “Spike recovery” here has nothing to do with the vaccine’s purported spike protein. A spike is a known amount of endotoxin deliberately added to a sample to check how much the test can detect.)

https://jonfleetwood.substack.com/p/covid-mrna-vaccine-hides-up-to-30

COVID ‘mRNA’ Vaccines Never Directly Shown to Do What They’re Claimed to Do

Comirnaty Never Shown To Do What Claimed

Did they say ANYTHING that was true?

Researchers have not directly demonstrated the complete physical input-to-output chain claimed for these products, raising basic questions about what went in and what came out.

The claim is specific: material identified as “mRNA” is injected, and human cells allegedly produce a defined “spike” protein.

This article does not claim that nothing happens after vaccination, nor that the vial contains nothing dangerous.

Biological changes, immune responses, symptoms, adverse events, and death have been reported after vaccination.

And the contents of the vial raise many serious safety questions.

The narrower question is whether the specific molecular identities claimed for the injected material and the alleged translation product have been directly established.

I found no published experiment that demonstrates either of the following:

  • An intact physical molecule recovered from a finished vaccine vial, with a complete experimentally determined sequence matching the complete intended sequence.
  • An intact physical product recovered from a vaccinated human, with a complete experimentally determined amino-acid sequence matching the complete intended “spike” sequence.

Which raises questions:

  • Where is the complete physical sequence (not the “intended” one) of the material injected into people?
  • Why is Pfizer’s “100% maximum sequence coverage” treated as proof of a complete molecule when only 55.6% was said to be uniquely assigned and the remainder depended on repeated-position assumptions?
  • Where is the complete physical sequence of the product allegedly produced inside vaccinated people?
  • How can one reported mass-spectrometry signal (“LDPPEAEVQIDR”) establish the identity of an entire alleged “spike” protein?
  • Why is a mechanism being treated as directly demonstrated when neither the complete physical input nor the complete physical output has been directly identified?

Finish reading:  https://jonfleetwood.substack.com/p/covid-mrna-vaccines-never-directly

Do you know why doctors and nurses remained silent about all the clots, strokes, etc. after the COVID shot rollout?

Dr In Hospital Corridor

Answer: Because they didn’t want to lose their job. And I wish I was kidding about that.
Steve Kirsch

If you remain silent about what you observe, you get to keep your job. That’s how the medical system works. Do not challenge the “medical consensus.” It is a sacred cow.

Executive summary

After the COVID shots rolled out, critical care units of hospitals were seeing massive spikes in clots and strokes.

Why didn’t they speak up?

Because they didn’t want to lose their job (or their medical license).

I wish I was kidding about this, but I’m not.

I heard this directly from the nursing staff at a large hospital I was just at.

This is why people don’t trust doctors. It’s not the fault of “misinformation spreaders.” It’s because doctors aren’t allowed to tell us the truth.

Finish reading: https://open.substack.com/pub/stevekirsch/p/do-you-know-why-doctors-and-nurses

Dr. Charles Hoffe Testimony On Covid Shot Damages

Dr Charles Hoffe COVID Vaccine Testimony

“The COVID injections were more dangerous than COVID.”

“The increase in all cause mortality started after the vaccine rollout.”

“In the United Stated they had had approximately one million excess deaths since hte COVID vaccine rollout.”

“So this idea that the vaccines have saved millions of lives is absurd. The number of people dying is higher than ever.”

“Vaccine injury reporting in Canada appeared to have been censored.”

“The open VAERS in the United States records 39,000 people who died unexpectedly within 28 days of their COVID shot. And 72,000 who were permanently disabled within 28 days of their COVID shot.”

Click to view the video: https://www.facebook.com/share/v/1E4zbzXkQz/