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We believe that the actual anion- cation directionality can best be dis- cerned from pharmacological data used with a detailed quantitative model which includes accurate study of agonist conformation: Thus, we can say that with relatively minor modifi- cation the same active conformations deduced with DIPA for the A-face hold also for the B-face approach.

Schulman, Disch and Venanzi reply – [PDF Document]

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E, Jr, and Murray-Rust, P.


ComAlloy acquired by Schulman – [PDF Document]

Add this book to a list You can add this book to any one of your lists. This face is neither B t nor! However the strongest evidence sup- porting our hypothesis is the fact that on the basis of a substrate-receptor inter- action via a B-type face, we established a structural criterion for the differen- tiation between the nicotinic and muscarinic mode of action.

Home Documents Schulman, Disch and Venanzi ascendenre.

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A key agonist is trans- 2-acetoxycyclopropylammonium cation ACTM.

Assuming sacendente, their model is based upon so-called ‘activity triangles” deduced from crystal- Iographic data on cholinergic agonists. El ascendente Martin Schulman. Comparison with ACTM suggests that: Add a alert Enter prices below and click ‘Add’.

This leads to a P’O distance of ca. You can add this book to any one of your lists. The de- termination of which face is actually used must await further study.

Nonetheless, the suggestion made by Gieren and Kokkinidis is an interesting one. Please include your email address if you’d like a reply. For instance, the conformation proposed by Schulman et al.

ComAlloy acquired by Schulman

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Schulman, Disch and Venanzi reply

This highly-potent el, [3-sttb- stituted ACh derivative counters the idea t that n-substitution necessarily de- creases muscarinic activity.

So-called ‘activity triangles ‘ formed by a monoatomic anion occupying a B-type face – as a model for the anionic binding site of the receptor – the quaternary nitrogen and a negative, partially charged atom of the agonist which corresponds to a second binding site, exhibit characteristic geometries which are associated with the nicotinic or muscarinic activity mode.

Soc,3 Schuiman, J. Rosenficld and Murray-Rust have reported 2 that in crystalline oxy- anion salts schulmna cholinergic agonists the oxygen positions are nearly evenly dis- tributed over the trimethylammonio- methyl surface.

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