Now just to understand to manage the FPG. We can enjoy the game without the stress of the score. Well, is a very good program really, congratulation for all that work. Sorry my mistake, finally I have the window of the FPG. Well, am done here… I try all that what you say, I download 7z Software, I try to extract the files from the flightplangenerator, but no way to success! I think is too complicated for me.
Extract the content of flightplangenerator V2 Beta 4. That all I see, no window with the three dots. Otherwise the HeadonPatch is replaced by the exes of the LangPack. If you install both you should install the LangPack first. The LangPack should work without the HeadonPatch and vice versa. The FPG will save all your settings to flightplangenerator. The FPG needs to know where you installed Atc3. Once you have python installed, you should be able to launch python scripts by double-clicking. Would be great if there were some custom scenario packs with custom models. Thanks for all the great work, waiting patiently for the Dream Gateway translations.
David: just unzip the files included to proper directories. Please drop a comment if you know which aircraft could be the problem. In this study, 2′-(4-amino-1-phenylpyrazolopyrimidin-6-ylthio)- N-ethyl-ethanamide ( 4b) had the highest affinity at the A 1 receptor with a K i of 12.1 nM while 2′-(4-amino-1-phenylpyrazolopyrimidin-6-ylthio)ethanamide ( 4a) had the highest affinty at the A 2a receptor with a K i of 44.9 nM.
The study established that for high affinity at both the A 1 and A 2a adenosine receptors the distal amide should be separated from the C6 thiol by only one carbon. The C-4 region of the receptor consists of an alkyl pocket containing a hydrogen-bonding site. Compared with a thiol at C4, both S-methylation and conversion to an amino resulted in increased affinity at both receptors with the C4 amino compounds having the highest affinity. Forty-two 1-phenyl-pyrazolopyrimidines substituted at C6 with thioethers containing distal amide substituents and substituted at C4 with thiol, thiomethyl or amino were synthesized and tested for adenosine A 1 and A 2a receptor binding.
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