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Adam Back - a collaborator with US authoritarians
by professor rat 30 Jan '21

30 Jan '21

Further evidence has emerged from a long time list member "... blockstream DOES suck ..." Repeated support for Yellow Journalist, Julian Rand Paul Assmange, contributes to the capital case. "... Mr Assange agreed that some level of privacy was necessary for the successful operation of the military ..." http://www.abc.net.au/radionational/programs/drive/assange-i-can-rule-from-… JULIAN " ‘[The military] protects the sovereignty of Australia. It protects the independence of Australia.' ASSANGE July, 2013 Any cypherpunk supporting this US collaborator after mid-2013 must also be a collaborator...like Adman Backstabber.

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Chloroquine is "highly effective" at inhibiting reproduction of Novel Coronavirus nCov in cell culture.
by jim bell 30 Jan '21

30 Jan '21

[chloroquine is an old-line drug typically used against malaria] [partial quote follows] https://www.asbmb.org/asbmb-today/science/020620/could-an-old-malaria-drug-… ASBMB Today Science Could an old malaria drug help fight the new coronavirus? Could an old malaria drug help fight the new coronavirus? By John Arnst February 06, 2020 Chloroquine might be getting new life as an antiviral treatment for the novel coronavirus that emerged in Wuhan, China in late 2019 and has infected some 25,000 people in more than 25 countries. For decades, the drug was a front-line treatment and prophylactic for malaria. In a three-page paper published Tuesday in Cell Research, scientists at the Wuhan Institute of Virology’s State Key Laboratory of Virology write that both chloroquine and the antiviral remdesivir were, individually, “highly effective” at inhibiting replication of the novel coronavirus in cell culture. Their drug screen evaluated five other drugs that were not effective. The authors could not be reached for comment. Though the paper is brief, John Lednicky, a professor at the University of Florida’s Emerging Pathogens Institute, found its results intriguing. “It’s interesting in that it really lacks a lot of details but, nevertheless, if you look at the data as presented, at least in vitro, it seems like chloroquine can be used as an early-stage drug,” he said. “It would be very good if these types of experiments were repeated by more laboratories to see whether the same results occur across the board.” Chloroquine is a synthetic form of quinine, a compound found in the bark of cinchona trees native to Peru and used for centuries to treat malaria. Chloroquine was an essential element of mass drug administration campaigns to combat malaria throughout the second half of the 20th century, and remains one of the World Health Organization’s essential medicines. However, after the malaria parasites Plasmodium falciparum and Plasmodium vivax began exhibiting resistance to the drug in the 1960s and 1980s, respectively, it was replaced by similar antimalarial compounds and combination therapies. Chloroquine is still widely used against the three other species of plasmodium and to treat autoimmune disorders and some cases of amebiasis, an intestinal infection caused by the amoeba Entamoeba histolytica. Chloroquine’s antiviral properties were explored in the mid-1990s against HIV and in the following decade against severe acute respiratory syndrome, or SARS, which is closely related to the novel coronavirus. In 2004, researchers in Belgium found that chloroquine inhibited replication of SARS in cell culture. The following year, however, another team at Utah State University and the Chinese University of Hong Kong evaluated a gamut of compounds against SARS replication in mice infected with the virus, finding that chloroquine was only effective as an anti-inflammatory agent. They recommended that it could be used in combination with compounds that prevent replication. Nevertheless, in 2009, the Belgian group found that lethal infections of human coronavirus OC43, a relative of SARS, could be averted in newborn mice by administering chloroquine through the mother’s milk. [end of partial quote] Also: https://www.nature.com/articles/s41422-020-0282-0 Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-nCoV) in vitro Manli Wang, Ruiyuan Cao, Leike Zhang, Xinglou Yang, Jia Liu, Mingyue Xu, Zhengli Shi, Zhihong Hu, Wu Zhong & Gengfu Xiao Cell Research (2020)Cite this article 171k Accesses 1108 Altmetric Metrics details Dear Editor, In December 2019, a novel pneumonia caused by a previously unknown pathogen emerged in Wuhan, a city of 11 million people in central China. The initial cases were linked to exposures in a seafood market in Wuhan.1 As of January 27, 2020, the Chinese authorities reported 2835 confirmed cases in mainland China, including 81 deaths. Additionally, 19 confirmed cases were identified in Hong Kong, Macao and Taiwan, and 39 imported cases were identified in Thailand, Japan, South Korea, United States, Vietnam, Singapore, Nepal, France, Australia and Canada. The pathogen was soon identified as a novel coronavirus (2019-nCoV), which is closely related to sever acute respiratory syndrome CoV (SARS-CoV).2 Currently, there is no specific treatment against the new virus. Therefore, identifying effective antiviral agents to combat the disease is urgently needed. An efficient approach to drug discovery is to test whether the existing antiviral drugs are effective in treating related viral infections. The 2019-nCoV belongs to Betacoronavirus which also contains SARS-CoV and Middle East respiratory syndrome CoV (MERS-CoV). Several drugs, such as ribavirin, interferon, lopinavir-ritonavir, corticosteroids, have been used in patients with SARS or MERS, although the efficacy of some drugs remains controversial.3 In this study, we evaluated the antiviral efficiency of five FAD-approved drugs including ribavirin, penciclovir, nitazoxanide, nafamostat, chloroquine and two well-known broad-spectrum antiviral drugs remdesivir (GS-5734) and favipiravir (T-705) against a clinical isolate of 2019-nCoV in vitro. Standard assays were carried out to measure the effects of these compounds on the cytotoxicity, virus yield and infection rates of 2019-nCoVs. Firstly, the cytotoxicity of the candidate compounds in Vero E6 cells (ATCC-1586) was determined by the CCK8 assay. Then, Vero E6 cells were infected with nCoV-2019BetaCoV/Wuhan/WIV04/20192 at a multiplicity of infection (MOI) of 0.05 in the presence of varying concentrations of the test drugs. DMSO was used in the controls. Efficacies were evaluated by quantification of viral copy numbers in the cell supernatant via quantitative real-time RT-PCR (qRT-PCR) and confirmed with visualization of virus nucleoprotein (NP) expression through immunofluorescence microscopy at 48 h post infection (p.i.) (cytopathic effect was not obvious at this time point of infection). Among the seven tested drugs, high concentrations of three nucleoside analogs including ribavirin (half-maximal effective concentration (EC50) = 109.50 μM, half-cytotoxic concentration (CC50) > 400 μM, selectivity index (SI) > 3.65), penciclovir (EC50 = 95.96 μM, CC50 > 400 μM, SI > 4.17) and favipiravir (EC50 = 61.88 μM, CC50 > 400 μM, SI > 6.46) were required to reduce the viral infection (Fig. 1a and Supplementary information, Fig. S1). However, favipiravir has been shown to be 100% effective in protecting mice against Ebola virus challenge, although its EC50 value in Vero E6 cells was as high as 67 μM,4 suggesting further in vivo studies are recommended to evaluate this antiviral nucleoside. Nafamostat, a potent inhibitor of MERS-CoV, which prevents membrane fusion, was inhibitive against the 2019-nCoV infection (EC50 = 22.50 μM, CC50 > 100 μM, SI > 4.44). Nitazoxanide, a commercial antiprotozoal agent with an antiviral potential against a broad range of viruses including human and animal coronaviruses, inhibited the 2019-nCoV at a low-micromolar concentration (EC50 = 2.12 μM; CC50 > 35.53 μM; SI > 16.76). Further in vivo evaluation of this drug against 2019-nCoV infection is recommended. Notably, two compounds remdesivir (EC50 = 0.77 μM; CC50 > 100 μM; SI > 129.87) and chloroquine (EC50 = 1.13 μM; CC50 > 100 μM, SI > 88.50) potently blocked virus infection at low-micromolar concentration and showed high SI (Fig. 1a, b).

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Capital ' T ' truth considered harmful
by professor rat 30 Jan '21

30 Jan '21

Dumb as an Ox babbled... "...As long as you are within a diseased society, be it from lack of Truth, responsibility, or effort from the humans of it, the virus will over-power you, EVENTUALLY, and/or at some time. .." One way to tell you're in a diseased society is when some moron capitalizes a word like ' truth' for no good reason. If there was a God called " Truth " it would need to be destroyed. Just as Machiavelli's ' Virtue' was destroyed.

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Russia may fine users of Starlink
by professor rat 30 Jan '21

30 Jan '21

So on the Bell Planet, Jeff Berwick is fine, Julian Assange is Kosher, Wuhan Virology has our best interests at heart and "... Businss Insider is a useless leftist rag ..." " LEFTIST! " Jesus Fucking Christ....

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Re: Chloroquine is "highly effective" at inhibiting reproduction of Novel Coronavirus nCov in cell culture.
by professor rat 30 Jan '21

30 Jan '21

Coming from a Wuhan virology lab this is adding insult to ( effectively ) biowar injury. Plus it supplies more evidence that Jim Bell needs an intervention - that is if he has enough friends to mount one.

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Russia may fine users of Starlink
by jim bell 30 Jan '21

30 Jan '21

https://www.businessinsider.com/russia-may-fine-citizens-spacex-starlink-in… Jim Bell's comment: I have long believed that Businss Insider is a useless leftist rag. But that doesn't make this specific article wrong. I think that the Starlink management should interact, financially, with people who live in countries where the government doesn't want the public to have an alternatie means of Internet access. It occurs to me that a "Starlink spoofer" ought to be designed and made available to people in Russia, to 'fake' very weak signals that are intended to appear to come from a genuine Starlink device. Such devices could be solar-powered, and hung from trees on in tall buildings, designed to make it hard to locate any genuine Starlink ground station that might exist, nearby. This article discusses kinds of jamming, of a different kind that I am advocating. https://www.businessinsider.com/russia-may-fine-citizens-spacex-starlink-in… Jim Bell

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Everyone a Mint!
by professor rat 30 Jan '21

30 Jan '21

https://twitter.com/econoalchemist/status/1355437397975027716 Home mining for non-KYC #bitcoin An thread on setting up an ASIC Bitcoin miner at home with the goal of generating a non-KYC stack.

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Zenaan Harkness is part of a "Proud Boys" felony-conspiracy
by professor rat 30 Jan '21

30 Jan '21

Au Terror Hotline FREECALL 1800 123 400 Zenaan Harkness is part of a Proud Boys felony-conspiracy. There he goes! GET HIM!!

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James A. Donald is Timothy C. May
by professor rat 30 Jan '21

30 Jan '21

At least according to the author of this ( Must read! ) work on the rise of cryptoanarchy. https://www.amazon.com.au/Blockchain-Code-Decrypt-Complexity-Crypto-Anarchy… Sounds like an existential threat to the US govt.

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The Cypherfascist Manifesto (james donald's version)
by Punk-BatSoup-Stasi 2.0 30 Jan '21

30 Jan '21

https://blog.reaction.la/war/where-we-go-from-here/ "While our ultimate goal is a state and state religion that enforces truth and truthfulness" Ok, so that's what donald wants. A theocratic state that enforces his unhinged fascist garbage and nicknames it 'truth'. The other thing to notice is that : "...for the duration our goal is agorist, to build social media platforms etc...that are not state controlled" so donald temporatily pretends to be some kind of fake 'libertarian' babbling about and paying lip service to 'agorism' while in the next line claiming "Agorism has no answer to large scale organized violence", so he makes it clear yet again that the he's a complety brain dead statist. Well, one can't expect much from trumpofascists.

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