by EnergyUnlimited » Fri 23 Mar 2007, 08:27:28
$this->bbcode_second_pass_quote('Raphael', '[')b]SPG please read the following...
$this->bbcode_second_pass_quote('EnergyUnlimited', ' ')
I like to read this open discussion, to find out some silly ideas of this kind and I sometimes dispute those and watch reaction.
Kind of entertainment.
Yea that's right, 'limited energy' will check in occassionally, I suspect it is during FOX or CNN TV commercial breaks.
Interesting thing about Chirality...it suggests a preference for either right or left...and it is the reason AZT killed so many so early in the AIDS game...AZT can be broken down into a 'good and bad' mirror images...we should be very careful when experimenting with
graven images.
Please note: Did the fucking 'expert' Dr. SPG Egostein ever mention CHIRALITY in his posts on this thread folks?
Would you still trust him / her expert self-serving (serving the ego) opinions...?
Stop listening to the loud vexatious 'smarter than thou' remarks emanating from the deluded Masters like SPG, who ... if you learn to listen to your heart, the ewe will find the mindless bleats become heartfelt beats.
THEY killed many people intentionally with 'bad medicine'.
THEY knew about Chirality since the time of Pasteur.
THEY knew what they were doing ... it was intentional to kill gays, hemophilliacs and IV drug users...with an incorrect chiral compound.
Hell that's what I would do ... if I were THEY.
Did ewe also know that in
primates and sheep 
, brain lateralization has been found...specifically right brain hemisphere dominance used for face processsing...
Take a look in the mirror limited energy ... what do EWE see?
SPG?
namaste
Raphael

In general chirality has nothing to do with HIV causing or not causing AIDS, albeit hypothetical mirror image of HIV would certainly
cause any disease, as it would not be processed by cell "molecular machinery".
Building blocs of living organisms or viruses are D-carbohydrates and L-aminocids.
D- aminoacids are also making rare occurence in the nature but L-carbohydrates do not.
AZT is based on azido- D-desoxyribose and this is natural configuration of carbohydrate chain. Commercial product is a single enantiomer (chiral form).
Opposite enantiomer (based on L-desoxyribose) would be most likely devoid of specific pharmacological activity (DNA chain terminator) and only display some random effects.
In any case the opposite enantiomer (other chiral form) of AZT is not contaminating commercial product.
I am not aware of attempts to synthetise and test it anyway. It cannot be made by approach used to manufacture commercial AZT.
In respect of chirality in general.
It is well known, that only one of 4 fundamental forces in physics (according to standard model) shows some chirality (eg it breaks so called CP symmetry).
and it is also responsible for radioactive beta decay.
There is only one example of particle (neutral kaon), which is known to decay in "chiral" fashion.