Year |
Citation |
Score |
2017 |
Tumey LN, Li F, Rago B, Han X, Loganzo F, Musto S, Graziani EI, Puthenveetil S, Casavant J, Marquette K, Clark T, Bikker J, Bennett EM, Barletta F, Piche-Nicholas N, et al. Site Selection: a Case Study in the Identification of Optimal Cysteine Engineered Antibody Drug Conjugates. The Aaps Journal. PMID 28439809 DOI: 10.1208/S12248-017-0083-7 |
0.31 |
|
2012 |
Gopalsamy A, Bennett EM, Shi M, Zhang WG, Bard J, Yu K. Identification of pyrimidine derivatives as hSMG-1 inhibitors. Bioorganic & Medicinal Chemistry Letters. 22: 6636-41. PMID 23021994 DOI: 10.1016/J.Bmcl.2012.08.107 |
0.301 |
|
2009 |
Zask A, Kaplan J, Verheijen JC, Richard DJ, Curran K, Brooijmans N, Bennett EM, Toral-Barza L, Hollander I, Ayral-Kaloustian S, Yu K. Morpholine derivatives greatly enhance the selectivity of mammalian target of rapamycin (mTOR) inhibitors. Journal of Medicinal Chemistry. 52: 7942-5. PMID 19916508 DOI: 10.1021/Jm901415X |
0.311 |
|
2009 |
Petrelli R, Sham YY, Chen L, Felczak K, Bennett E, Wilson D, Aldrich C, Yu JS, Cappellacci L, Franchetti P, Grifantini M, Mazzola F, Di Stefano M, Magni G, Pankiewicz KW. Selective inhibition of nicotinamide adenine dinucleotide kinases by dinucleoside disulfide mimics of nicotinamide adenine dinucleotide analogues. Bioorganic & Medicinal Chemistry. 17: 5656-64. PMID 19596199 DOI: 10.1016/J.Bmc.2009.06.013 |
0.394 |
|
2009 |
Zask A, Kaplan J, Curran K, Verheijen JC, Richard DJ, Brooijmans N, Bennett E, Lucas J, Toral‐Barza L, Hollander I, Gibbons JJ, Abraham RT, Ayral‐Kaloustian S, Mansour TS, Yu K. Abstract B145: Highly selective pyrazolopyrimidine mTOR inhibitors with profound in vivo antitumor activity Molecular Cancer Therapeutics. 8. DOI: 10.1158/1535-7163.Targ-09-B145 |
0.347 |
|
2008 |
Labello NP, Bennett EM, Ferguson DM, Aldrich CC. Quantitative three dimensional structure linear interaction energy model of 5'-O-[N-(salicyl)sulfamoyl]adenosine and the aryl acid adenylating enzyme MbtA. Journal of Medicinal Chemistry. 51: 7154-60. PMID 18959400 DOI: 10.1021/Jm800668U |
0.39 |
|
2008 |
Neres J, Labello NP, Somu RV, Boshoff HI, Wilson DJ, Vannada J, Chen L, Barry CE, Bennett EM, Aldrich CC. Inhibition of siderophore biosynthesis in Mycobacterium tuberculosis with nucleoside bisubstrate analogues: structure-activity relationships of the nucleobase domain of 5'-O-[N-(salicyl)sulfamoyl]adenosine. Journal of Medicinal Chemistry. 51: 5349-70. PMID 18690677 DOI: 10.1021/Jm800567V |
0.361 |
|
2008 |
Chen L, Petrelli R, Felczak K, Olesiak M, Bennett EM, Magni G, Pankiewicz KW. Novel cofactor-type inhibitors of NAD-dependent enzymes. NAD-based therapeutics Collection of Czechoslovak Chemical Communications. 10: 71-79. DOI: 10.1135/Css200810071 |
0.396 |
|
2007 |
Qiao C, Gupte A, Boshoff HI, Wilson DJ, Bennett EM, Somu RV, Barry CE, Aldrich CC. 5'-O-[(N-acyl)sulfamoyl]adenosines as antitubercular agents that inhibit MbtA: an adenylation enzyme required for siderophore biosynthesis of the mycobactins. Journal of Medicinal Chemistry. 50: 6080-94. PMID 17967002 DOI: 10.1021/Jm070905O |
0.428 |
|
2007 |
Chen L, Gao G, Felczak K, Bonnac L, Patterson SE, Wilson D, Bennett EM, Jayaram HN, Hedstrom L, Pankiewicz KW. Probing binding requirements of type I and type II isoforms of inosine monophosphate dehydrogenase with adenine-modified nicotinamide adenine dinucleotide analogues. Journal of Medicinal Chemistry. 50: 5743-51. PMID 17958343 DOI: 10.1021/Jm070568J |
0.309 |
|
2007 |
Bonnac L, Gao GY, Chen L, Felczak K, Bennett EM, Xu H, Kim T, Liu N, Oh H, Tonge PJ, Pankiewicz KW. Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against enoyl-ACP reductase (InhA) of Mycobacterium tuberculosis. Bioorganic & Medicinal Chemistry Letters. 17: 4588-91. PMID 17560106 DOI: 10.1016/J.Bmcl.2007.05.084 |
0.328 |
|
2007 |
Qiao C, Wilson DJ, Bennett EM, Aldrich CC. A mechanism-based aryl carrier protein/thiolation domain affinity probe. Journal of the American Chemical Society. 129: 6350-1. PMID 17469819 DOI: 10.1021/Ja069201E |
0.318 |
|
2007 |
Chen L, Gao G, Bonnac L, Wilson DJ, Bennett EM, Jayaram HN, Pankiewicz KW. Methylenebis(sulfonamide) linked nicotinamide adenine dinucleotide analogue as an inosine monophosphate dehydrogenase inhibitor. Bioorganic & Medicinal Chemistry Letters. 17: 3152-5. PMID 17395461 DOI: 10.1016/J.Bmcl.2007.03.035 |
0.345 |
|
2007 |
Bonnac L, Chen L, Pathak R, Gao G, Ming Q, Bennett E, Felczak K, Kullberg M, Patterson SE, Mazzola F, Magni G, Pankiewicz KW. Probing binding requirements of NAD kinase with modified substrate (NAD) analogues. Bioorganic & Medicinal Chemistry Letters. 17: 1512-5. PMID 17258457 DOI: 10.1016/J.Bmcl.2007.01.012 |
0.373 |
|
2006 |
Somu RV, Wilson DJ, Bennett EM, Boshoff HI, Celia L, Beck BJ, Barry CE, Aldrich CC. Antitubercular nucleosides that inhibit siderophore biosynthesis: SAR of the glycosyl domain. Journal of Medicinal Chemistry. 49: 7623-35. PMID 17181146 DOI: 10.1021/Jm061068D |
0.41 |
|
2006 |
Vannada J, Bennett EM, Wilson DJ, Boshoff HI, Barry CE, Aldrich CC. Design, synthesis, and biological evaluation of beta-ketosulfonamide adenylation inhibitors as potential antitubercular agents. Organic Letters. 8: 4707-10. PMID 17020283 DOI: 10.1021/Ol0617289 |
0.366 |
|
2006 |
Somu RV, Boshoff H, Qiao C, Bennett EM, Barry CE, Aldrich CC. Rationally designed nucleoside antibiotics that inhibit siderophore biosynthesis of Mycobacterium tuberculosis. Journal of Medicinal Chemistry. 49: 31-4. PMID 16392788 DOI: 10.1021/Jm051060O |
0.353 |
|
2004 |
Anand R, Hoskins AA, Bennett EM, Sintchak MD, Stubbe J, Ealick SE. A model for the Bacillus subtilis formylglycinamide ribonucleotide amidotransferase multiprotein complex. Biochemistry. 43: 10343-52. PMID 15301532 DOI: 10.1021/Bi0491292 |
0.663 |
|
2004 |
Bauer JA, Bennett EM, Begley TP, Ealick SE. Three-dimensional structure of YaaE from Bacillus subtilis, a glutaminase implicated in pyridoxal-5'-phosphate biosynthesis. The Journal of Biological Chemistry. 279: 2704-11. PMID 14585832 DOI: 10.1074/Jbc.M310311200 |
0.647 |
|
2003 |
Bennett EM, Anand R, Allan PW, Hassan AE, Hong JS, Levasseur DN, McPherson DT, Parker WB, Secrist JA, Sorscher EJ, Townes TM, Waud WR, Ealick SE. Designer gene therapy using an Escherichia coli purine nucleoside phosphorylase/prodrug system. Chemistry & Biology. 10: 1173-81. PMID 14700625 DOI: 10.1016/J.Chembiol.2003.11.008 |
0.642 |
|
2003 |
Bennett EM, Li C, Allan PW, Parker WB, Ealick SE. Structural basis for substrate specificity of Escherichia coli purine nucleoside phosphorylase. The Journal of Biological Chemistry. 278: 47110-8. PMID 12937174 DOI: 10.1074/Jbc.M304622200 |
0.653 |
|
2003 |
Tolbert WD, Zhang Y, Cottet SE, Bennett EM, Ekstrom JL, Pegg AE, Ealick SE. Mechanism of human S-adenosylmethionine decarboxylase proenzyme processing as revealed by the structure of the S68A mutant. Biochemistry. 42: 2386-95. PMID 12600205 DOI: 10.1021/Bi0268854 |
0.56 |
|
2002 |
Bennett EM, Ekstrom JL, Pegg AE, Ealick SE. Monomeric S-adenosylmethionine decarboxylase from plants provides an alternative to putrescine stimulation. Biochemistry. 41: 14509-17. PMID 12463749 DOI: 10.1021/Bi026710U |
0.602 |
|
2002 |
Cheng G, Bennett EM, Begley TP, Ealick SE. Crystal structure of 4-amino-5-hydroxymethyl-2-methylpyrimidine phosphate kinase from Salmonella typhimurium at 2.3 A resolution. Structure (London, England : 1993). 10: 225-35. PMID 11839308 DOI: 10.1016/S0969-2126(02)00708-6 |
0.553 |
|
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