congrats knowing my luck ill end up with aboy
time to start naming! if you havent already
ive also herd from moms it hurt, i dont think its a one size fits all thing
Random Jibber Jabber Thread
- Thread starter Trolling
- Start date
time to start naming! if you havent already
tyler.durden
Well-Known Member
My second wife's breast pump crapped out on us one night, and my wife's titties were SORE and needed milking. Being the good, adventurous husband that I was, I offered to suck her dry. I went for a little over 5 minutes on them and I was FULL, couldn't take another gulp. It was warm and surprisingly sweet, like whole milk mixed with cantaloupe juice. She was still sore, but said I helped. I held my erect penis and said, 'your turn!' She chuckled and left the room. It wasn't a bad experience, but I'm not looking forward to ever doing it again...
Last edited:
Elwood Diggler
Well-Known Member
im not a lactation expert but i'll give it a whirl
mr sunshine
Well-Known Member
There are bars or a bar somewhere that serve tittyi milk straight out the tap. I seen it on hbo, so it's true
april
Pickle Queen
Bodybuilders also drink it..
tyler.durden
Well-Known Member
^^ Good to hear, 'cause I lift, bro...
Hookabelly
Well-Known Member
Sorry to say she was a total bitch. LOL. Not helpful and only succeed in focusing on the negative.
Indagrow
Well-Known Member
Those dudes are little babies anyways
Been there too.
It has a taste I remembered. : )
tyler.durden
Well-Known Member
Yummy! I'd eat your cookies...Cookies !
qwizoking
Well-Known Member
tell me why when i actually use my degrees and try to help.. no likes.
is it just too long to read? ive posted things that arent on the internet period. like my cdlsa, similar to acid. never studied or even theorized.
but i talk like an ignorant mafucker like i also am...lots of likes.
its frustrating
take a couple posts like this, or my posts on how curing actually works making @SimonD disappear
ive done this many times
no likes
and lol at the fermentation theory someone spread
i mean this stuff is gold
cb1 receptors respond to the c-9 position of the cyclohexane ring, the phenolic hydroxyl and carbon/non polar side chains at c3...
check structure of win 55,not the dame class, not a terpenoid like thc. but look
napthalene ring - cyclohexane ring, carbonyl group -phenolic hydroxyl, and morpholinoethyl group..quite potent
thc binds through
2 oxygens a phenolic hydroxyl at position 1 and an oxygen pyran ring opposite,interacting through hydrogen bonding th cb leaving a lysine residue..the opening of the pyran ring not being significant...
as far as potency and activation..
acyclic ring was found to be better than a heterocyclic ring, with a cyclohexane ring being optimal. In addition, the size and the position of the substituent on the cyclic ring is important to maintenance of CB1 affinity...position of double bonds within the cyclohexane ring effect activity. For example, moving the double bond of 9-THC to position 8 (as in 8-THC) decreases CB1affinity. about 30%
methyl (less likely to hydrogen bond) ethyl etc generally kills short side chains kill activity, 4-6 is best, branched chain increases activity.. increasing ring size to say heptane increases activity of both, conversion to a pyran cuts cb2 .adding oxy, hydroxy ketones increase cb2 .a sulfur substitution anywhere ruins it.
oxy in the phenyl ring increases cb1 can't substitute the phenol or alter placement as I was mentioning about delta 8, serious alterations ruin it
, degree of saturation as well as the position of the double bond in the cyclohexane ring effects cb.
or how thc is produced...
so inside the trichomes
Geranyl pyrophosphate and a precursor to olivetolic acid react, a c12 (for pentyl) c10(for propyl)polyketide,then through cyclization yielding olivetolic acid..then catalyzed by an enzyme to produce cannabigerolic acid along with alkylation.. The production of Thc (and propyl)thcv cbd cbdv and cbc cbcv are controlled by 3 different enzymes Thca synthase being the enzyme converting cbga to thca through an oxidative cyclization of the geranyl group on cbga(of course this is all a bit, well really simplified for y'all) geranyl diphosphate + olivetolate =cannabigerolate + diphosphate.. cannabigerolate + O(2) = Delta(9)-tetrahydrocannabinolate + H(2)O(2)
and how you could help out these processes increasing production
is it just too long to read? ive posted things that arent on the internet period. like my cdlsa, similar to acid. never studied or even theorized.
but i talk like an ignorant mafucker like i also am...lots of likes.
its frustrating
take a couple posts like this, or my posts on how curing actually works making @SimonD disappear
ive done this many times
no likes
and lol at the fermentation theory someone spread
i mean this stuff is gold
cb1 receptors respond to the c-9 position of the cyclohexane ring, the phenolic hydroxyl and carbon/non polar side chains at c3...
check structure of win 55,not the dame class, not a terpenoid like thc. but look
napthalene ring - cyclohexane ring, carbonyl group -phenolic hydroxyl, and morpholinoethyl group..quite potent
thc binds through
2 oxygens a phenolic hydroxyl at position 1 and an oxygen pyran ring opposite,interacting through hydrogen bonding th cb leaving a lysine residue..the opening of the pyran ring not being significant...
as far as potency and activation..
acyclic ring was found to be better than a heterocyclic ring, with a cyclohexane ring being optimal. In addition, the size and the position of the substituent on the cyclic ring is important to maintenance of CB1 affinity...position of double bonds within the cyclohexane ring effect activity. For example, moving the double bond of 9-THC to position 8 (as in 8-THC) decreases CB1affinity. about 30%
methyl (less likely to hydrogen bond) ethyl etc generally kills short side chains kill activity, 4-6 is best, branched chain increases activity.. increasing ring size to say heptane increases activity of both, conversion to a pyran cuts cb2 .adding oxy, hydroxy ketones increase cb2 .a sulfur substitution anywhere ruins it.
oxy in the phenyl ring increases cb1 can't substitute the phenol or alter placement as I was mentioning about delta 8, serious alterations ruin it
, degree of saturation as well as the position of the double bond in the cyclohexane ring effects cb.
or how thc is produced...
so inside the trichomes
Geranyl pyrophosphate and a precursor to olivetolic acid react, a c12 (for pentyl) c10(for propyl)polyketide,then through cyclization yielding olivetolic acid..then catalyzed by an enzyme to produce cannabigerolic acid along with alkylation.. The production of Thc (and propyl)thcv cbd cbdv and cbc cbcv are controlled by 3 different enzymes Thca synthase being the enzyme converting cbga to thca through an oxidative cyclization of the geranyl group on cbga(of course this is all a bit, well really simplified for y'all) geranyl diphosphate + olivetolate =cannabigerolate + diphosphate.. cannabigerolate + O(2) = Delta(9)-tetrahydrocannabinolate + H(2)O(2)
and how you could help out these processes increasing production
Gary Goodson
Well-Known Member
BarnBuster
Virtually Unknown Member
qwiz, you gotta dumb it down for most of us
Flaming Pie
Well-Known Member
Most people don't have the patience to read/talk textbook chemistry.
Singlemalt
Well-Known Member
I don't mind, its nostalgia for me; keep posting chem/biochem/physiology
I'm learning so many things for example I don't know but I've been told that organic chocolate has less fat and fewer calories than the non-organicAhh, what might have been. I dated a vegan many years ago, I dumped her cuz she wouldn't swallow because it was anti-vegan. Had I only known this I coulda convinced her
over unity for the win.
cannabineer
Ursus marijanus
And none of those pesky CHEMICALS!!I'm learning so many things for example I don't know but I've been told that organic chocolate has less fat and fewer calories than the non-organic
Oh and wanna go way over unity? Life energy bitchez!
