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As described in this work, compound 8 (a close structural isomer of compound 7) was observed by mass spectrometry to form PRPP-derived adducts in biochemical experiments. Compound 58 also forms an adduct with PRPP, as evidenced by mass spectrometry analysis of biochemical inhibition reaction mixtures, and we recently solved a crystal structure of phosphoribosylated- 58 in complex with Nampt. The details associated with the biochemical and crystallography experiments involving the PRPP-derived phosphoribosylated adduct of compound 58 will be reported in a separate disclosure: manuscript in preparation.
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As described in this work, compound 8 (a close structural isomer of compound 7) was observed by mass spectrometry to form PRPP-derived adducts in biochemical experiments. Compound 58 also forms an adduct with PRPP, as evidenced by mass spectrometry analysis of biochemical inhibition reaction mixtures, and we recently solved a crystal structure of phosphoribosylated- 58 in complex with Nampt. The details associated with the biochemical and crystallography experiments involving the PRPP-derived phosphoribosylated adduct of compound 58 will be reported in a separate disclosure: Oh, A.; Ho, Y.-C.; Zak, M.; Liu, Y.; Liu, Y.; Yuen, P.-w.; Zheng, X.; Dragovich, P. S.; Wang, W. manuscript in preparation.
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WO 2003029252.
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Walker, D. P.; Piotrowski, D. W.; Jacobsen, E. J.; Acker, B. A.; Wishka, D. G.; Reitz, S. C.; Groppi, V. E., Jr. Preparation of N-(azabicyclyl)arylamides for therapeutic use as nicotinic acetylcholine receptor agonists. WO 2003029252, 2003.
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(2003)
Preparation of N-(azabicyclyl)arylamides for Therapeutic Use As Nicotinic Acetylcholine Receptor Agonists
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Walker, D.P.1
Piotrowski, D.W.2
Jacobsen, E.J.3
Acker, B.A.4
Wishka, D.G.5
Reitz, S.C.6
Groppi Jr., V.E.7
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