Israeli laboratory: Some existing drugs could stop COVID almost 100%



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A team of Israeli scientists from the Hebrew University of Jerusalem say they have identified from a library of pre-existing drug compounds several drugs that could potentially help treat, if not “cure”, people who develop COVID-19.

Professor Shy Arkin, a biochemist at the Alexander Silberman Institute of Life Science, told the Jerusalem Post that in laboratory tests in which cells infected with SARS-CoV-2 and placed with the drugs, “after two days, nothing happened – which means almost 100% of the cells were living despite being infected with the virus.

In contrast, without the compounds, about 50% of the cells died after coming into contact with the virus.

Arkin and his team have selected a library of more than 2,800 compounds approved for use, identifying 18 drugs that they believe may be effective. In unpublished work, the researchers were able to show that several of these compounds “showed remarkable potency against the whole virus in in vitro experiments”.

Two of these are Darapladib, used for the treatment of atherosclerosis, and Flumatinib, used for the treatment of certain blood cancers. Although he was hesitant to share the names of any of the drugs and said he could not recommend them until they had undergone appropriate clinical trials.

The team focused on reusing the drugs to potentially speed up future regulatory steps. Since the drugs are already in use for other indications, their toxicity and side effects, for example, are already known and approved.

The drugs work by inhibiting two targets in the virus: the protein or E channel (envelope) and channel 3a.

Protein E is the most conserved of all viral proteins. For example, while the peak proteins of SARS-CoV-2 and SARS-CoV-1 (the 2003 virus) are only about 75% identical, their E proteins are about 95% identical. This means the drugs would likely remain effective even when the virus mutates, Arkin told the Post.

The Pfizer and Moderna vaccines target the spike protein.

In previous studies, E and 3a proteins have been shown to be essential for viral infectivity. His team were among the first to study protein E from the first SARS coronavirus in 2004.

As part of research carried out by Arkin’s team for more than two decades, they identified that protein E is an ion channel, a type of protein family expressed by virtually all living cells which, due to its structure, has “served as a target for one-time pharmaceutical interventions,” the report says – including for cystic fibrosis, epilepsy, arrhythmia, neurodegenerative diseases, hypertension, angina pectoris and more.

Arkin said it is important that a “large arsenal” of drugs exist to fight SARS-CoV-2.

“We should never be in a situation where in our arsenal we only have one gun,” he said. “If we only have one and rely on him alone, and there comes a point where he fails, we will be in a very precarious situation.”

Now, Arkin believes his team is ready for in vitro and in vivo studies, and is looking for a pharmaceutical partner to help carry out those trials.

Citing Gilead’s success in securing Food and Drug Administration approval for the drug Remdesivir in record time at the start of the pandemic, he said he was “optimistic” that at least some of these compounds could be approved for. use against COVID “very quickly with the right partner.”



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