Deleted member 170540
Bluelight Crew
Recently I posted some pictures about GHB derivatives I thought of in the random molecule drawing thread...
Researching the subject more, I found an interesting article on the subject. The binding affinities of several GHB analogs were measured in the study and one compound (HOCPCA) had an affinity for the GHB receptor that was 39 times higher than that of GHB itself.
The full text of the article can be found at http://jpet.aspetjournals.org/content/315/1/346.full
GHB is known to bind to both GABA-B receptors and GHB receptors. I think that the euphoric effects are caused by binding to GHB receptors because the GABA-B agonist baclofen doesn't usually cause euphoria.
The question is: It's said that the sedating effects of GHB are caused mainly by binding to GABA-B receptors. Would a selective GHB receptor agonist be a stimulant instead of a sedative? GHB receptors are excitatory.
I don't think these compounds will become popular recreational drugs though, as they are lot harder to synth than GHB itself...
Researching the subject more, I found an interesting article on the subject. The binding affinities of several GHB analogs were measured in the study and one compound (HOCPCA) had an affinity for the GHB receptor that was 39 times higher than that of GHB itself.
The full text of the article can be found at http://jpet.aspetjournals.org/content/315/1/346.full
GHB is known to bind to both GABA-B receptors and GHB receptors. I think that the euphoric effects are caused by binding to GHB receptors because the GABA-B agonist baclofen doesn't usually cause euphoria.
The question is: It's said that the sedating effects of GHB are caused mainly by binding to GABA-B receptors. Would a selective GHB receptor agonist be a stimulant instead of a sedative? GHB receptors are excitatory.
I don't think these compounds will become popular recreational drugs though, as they are lot harder to synth than GHB itself...
