Arylcyclopropanecarboxyl Guanidines as Novel, Potent, and Selective Inhibitors of the Sodium Hydrogen Exchanger Isoform-1-Reference-Cited by-同舟云学术

Arylcyclopropanecarboxyl Guanidines as Novel, Potent, and Selective Inhibitors of the Sodium Hydrogen Exchanger Isoform-1

Published:2001-08-30 Issue:20 Volume:44 Page:3302-3310
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Ahmad Saleem¹,Doweyko Lidia M.¹,Dugar Sundeep¹,Grazier Nyeemah¹,Ngu Khehyong¹,Wu Shung C.¹,Yost Kenneth J.¹,Chen Bang-Chi¹,Gougoutas Jack Z.¹,DiMarco John D.¹,Lan Shih-Jung¹,Gavin Brian J.¹,Chen Alice Y.¹,Dorso Charles R.¹,Serafino Randy¹,Kirby Mark¹,Atwal Karnail S.¹

Affiliation:

1. Bristol-Myers Squibb Pharmaceutical Research Institute, P.O. Box 4000, Princeton, New Jersey 08543

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm010100v

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4. Molecular cloning of putative members of the Na/H exchanger gene family. cDNA cloning, deduced amino acid sequence, and mRNA tissue expression of the rat Na/H exchanger NHE-1 and two structurally related proteins.

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