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Arylcyclopropanecarboxyl guanidines as novel, potent, and selective inhibitors of the sodium hydrogen exchanger isoform-1.
J Med Chem. 2001 Sep 27;44(20):3302-10. doi: 10.1021/jm010100v.
J Med Chem. 2001.
PMID: 11563929
Design, structure-activity relationships, X-ray crystal structure, and energetic contributions of a critical P1 pharmacophore: 3-chloroindole-7-yl-based factor Xa inhibitors.
Shi Y, Sitkoff D, Zhang J, Klei HE, Kish K, Liu EC, Hartl KS, Seiler SM, Chang M, Huang C, Youssef S, Steinbacher TE, Schumacher WA, Grazier N, Pudzianowski A, Apedo A, Discenza L, Yanchunas J, Stein PD, Atwal KS.
Shi Y, et al. Among authors: grazier n.
J Med Chem. 2008 Dec 11;51(23):7541-51. doi: 10.1021/jm800855x.
J Med Chem. 2008.
PMID: 18998662
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One-pot synthesis and conformational features of n,n'-disubstituted ketene aminals.
Shi Y, Zhang J, Grazier N, Stein PD, Atwal KS, Traeger SC, Callahan SP, Malley MF, Galella MA, Gougoutas JZ.
Shi Y, et al. Among authors: grazier n.
J Org Chem. 2004 Jan 9;69(1):188-91. doi: 10.1021/jo0352528.
J Org Chem. 2004.
PMID: 14703396
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