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The majority of chemical suppliers sold research chemicals in bulk form as powder, not as pills, as selling in pill form would invalidate the claims that they were being sold for non-consumptive research. Active dosages vary widely from substance to substance, ranging from micrograms to hundreds of milligrams, but while it is critical for the end user to weigh doses with a precision scale, instead of guessing ("eyeballing"), many users did not do this and this led to many emergency room visits and several deaths, which were a prominent factor leading to the emergency scheduling of several substances and eventually Operation Web Tryp. Some compounds such as 2C-B and 5-Meo-DiPT did eventually increase in popularity to the point that they were sold in pill form to reach a wider market, and acquired popular street names ("Nexus" and "Foxy," respectively). Once a chemical reaches this kind of popularity, it is usually just a matter of time before it is added to the list of scheduled (., illegal) drugs.

But if you read the analysis of the Danish team, it’s obvious it’s garbage. For instance, they complain that once you subtract the best fit theoretical template, the remaining signal is correlated. Well, frankly, duh. The templates aren’t perfect matches – they’re theoretical templates constructed for possible signals, but they have finite resolution, so the actual signal is a little off the template. So, after subtracting the template, there’s a bit of signal left, which correlates with the bit of signal left in the other detector. Ditto when the noise is the sea of low power gravitational waves we can’t isolate from one another – that should have the same lag time and be correlated.

The in vitro cell line model was predictive for non-small cell lung cancer under the disease-oriented approach, for breast and ovarian cancers under the compound-oriented approach, and for all four tumor types together. The mouse allograft model was not predictive. The human xenograft model was not predictive for breast or colon cancers, but was predictive for non-small cell lung and ovarian cancers when panels of xenografts were used. Voskoglou et al . Clinical Cancer Research Vol. 9, 4227-4239.

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