1nhx: Difference between revisions

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==Overview==
==Overview==
The analysis of the X-ray structures of two xanthine inhibitors bound to, PEPCK and a comparison to the X-ray structure of GTP bound to PEPCK are, reported. The SAR at N-1, N-7 and developing SAR at C-8 are consistent, with information gained from the X-ray structures of compounds 1 and 2, bound to PEPCK. Representative N-3 modifications of compound 2 that led to, the discovery of 3-cyclopropylmethyl and its carboxy analogue as optimal, N-3 groups are presented.
The analysis of the X-ray structures of two xanthine inhibitors bound to PEPCK and a comparison to the X-ray structure of GTP bound to PEPCK are reported. The SAR at N-1, N-7 and developing SAR at C-8 are consistent with information gained from the X-ray structures of compounds 1 and 2 bound to PEPCK. Representative N-3 modifications of compound 2 that led to the discovery of 3-cyclopropylmethyl and its carboxy analogue as optimal N-3 groups are presented.


==Disease==
==Disease==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Dunten, P.]]
[[Category: Dunten, P.]]
[[Category: Foley, L.H.]]
[[Category: Foley, L H.]]
[[Category: Gubler, M.L.]]
[[Category: Gubler, M L.]]
[[Category: Ramsey, G.]]
[[Category: Ramsey, G.]]
[[Category: Wang, P.]]
[[Category: Wang, P.]]
[[Category: Wertheimer, S.J.]]
[[Category: Wertheimer, S J.]]
[[Category: EDO]]
[[Category: EDO]]
[[Category: FTB]]
[[Category: FTB]]
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[[Category: xanthine]]
[[Category: xanthine]]


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