RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:Share price taken downHarveyTwoface wrote: I appreciate your very intelligent answer. Thanks for being a beacon in the board darkness.
Thanks Harvey ... just trying to understand our potential and the potential of the drug.
What did Dan say ... 20+ molecules and we are presently using 3 of them ... something like that.
I think one is for the NSAIDs - one for the the IBD drug - and one was potentially for the future replacement to our NSAIDs (likely for 340 trials at this time). Lots of others and maybe we're adding with the academic studies. There are potentially tuneables out there and we need to get to them first in this wild-west of drug development in gaseous mediators.
Something else I see w.r.t. H2S donors is the types of release mechanisms that exist.
First there's hydrolysis-triggering molecules but they have less control than others (assuming).
There are pH-controlled H2S release agents, Thiol-triggered, Enzime-triggered ... and the list goes on.
I just can't see what ATE actually has dibs on. Hoping that becomes more and more apparent with time - or with other digging that people do.
Cheers all - may the rest of 2021 be more fun than the first part of the year. : )