Isosteric Analogues of Nicotinamide Adenine Dinucleotide Derived from Furanfurin, Thiophenfurin, and Selenophenfurin as Mammalian Inosine Monophosphate Dehydrogenase (Type I and II) Inhibitors-Reference-Cited by-同舟云学术

Isosteric Analogues of Nicotinamide Adenine Dinucleotide Derived from Furanfurin, Thiophenfurin, and Selenophenfurin as Mammalian Inosine Monophosphate Dehydrogenase (Type I and II) Inhibitors

Published:1998-04-21 Issue:10 Volume:41 Page:1702-1707
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Franchetti Palmarisa¹,Cappellacci Loredana¹,Perlini Paolo¹,Jayaram Hiremagalur N.¹,Butler Adrian¹,Schneider Bryan P.¹,Collart Frank R.¹,Huberman Eliezer¹,Grifantini Mario¹

Affiliation:

1. Dipartimento di Scienze Chimiche, Università di Camerino, Via S. Agostino, 1, 62032 Camerino, Italy, Laboratory for Experimental Oncology, Indiana University School of Medicine, Indianapolis, Indiana 46202, and Argonne National Laboratory, Argonne, Illinois 60439

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm970772e

Reference27 articles.

1. Conversion of 2-β-D-ribofuranosylselenazole-4-carboxamide to an analogue of nad with potent imp dehydrogenase-inhibitory properties

2. The conversion of 2-β-D-ribofuranosylthiazole-4-carboxamide to an analogue of NAD with potent IMP dehydrogenase-inhibitory properties

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