Date:   1/10/2007 1:22:59 AM ( 17 y ago)
Hits:   3,189
URL:   https://www.curezone.org/forums/fm.asp?i=807681

In reference to:


http://www.medscape.com/medline/abstract/7117297




Here's the abstract:

"
Stereochemical characterization of interactions of chiral 1,4-benzodiazepine-2-ones with liver microsomes.

Eur J Drug Metab Pharmacokinet. 1982; 7(2):137-46 (ISSN: 0398-7639)

Rendic S; Kajfez F

Microsomal P-450 cytochrome are stereoselective toward 7-Chloro-1,3-dihydro-3(S)-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one. (S)-1, and 7-chloro-1,3-dihydro-3(S)-isopropyl-5-phenyl-2H-1,4-benzodiazepin-2-one, (S)-2. (S)-enantiomers bind to a substrate binding site which accomodates the stable M-conformation (Ks =0.01 to 0.018 mmol/l). (R)-enantiomers, however, undergo a ligand type of interaction (Ks = 0.036 to 0.12 mmol/l). Prochiral desmethyldiazepam behaves similarly to the (S)-enantiomers of the above compounds. The ligand binding site does not differentiate between M- and P-conformers.
"

As the technically inclined can see, this abstract would seem to imply or to suggest [I use these words very cautiously] at the very least the possibility of interactions arising from certain drugs and certain benzodiazepine derivatives [That 'methyl' expression seems quite interesting, doesn't it]. Of course that's only my opinion once more, not a fact.
 

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