AAAAAA

   
Results: 1-25 | 26-28
Results: 1-25/28
Purine nucleoside phosphorylase inhibitor BCX-1777 (immucillin-H) - a novel potent and orally active immunosuppressive agent
Authors: Bantia, S Miller, PJ Parker, CD Ananth, SL Horn, LL Kilpatrick, JM Morris, PE Hutchison, TL Montgomery, JA Sandhu, JS
Citation: S. Bantia et al., Purine nucleoside phosphorylase inhibitor BCX-1777 (immucillin-H) - a novel potent and orally active immunosuppressive agent, INT IMMUNO, 1(6), 2001, pp. 1199-1210
Synthesis and biological activity of 4 '-C-hydroxymethyl-2 '-fluoro-D-arabinofuranosylpurine nucleosides
Authors: Shortnacy-Fowler, AT Tiwari, KN Montgomery, JA Secrist, JA
Citation: At. Shortnacy-fowler et al., Synthesis and biological activity of 4 '-C-hydroxymethyl-2 '-fluoro-D-arabinofuranosylpurine nucleosides, NUCLEOS NUC, 20(8), 2001, pp. 1583-1598
Synthesis and antiproliferative activity of some 4 '-C-hydroxymethy-alpha-and -beta-D-arabino-pentofuranosyl pyrimidine nucleosides
Authors: Griffon, JF Montgomery, JA Secrist, JA
Citation: Jf. Griffon et al., Synthesis and antiproliferative activity of some 4 '-C-hydroxymethy-alpha-and -beta-D-arabino-pentofuranosyl pyrimidine nucleosides, NUCLEOS NUC, 20(4-7), 2001, pp. 649-652
Synthesis and biological activity of 4 '-thio-L-xylofuranosyl nucleosides
Authors: Tiwari, KN Messini, L Montgomery, JA Secrist, JA
Citation: Kn. Tiwari et al., Synthesis and biological activity of 4 '-thio-L-xylofuranosyl nucleosides, NUCLEOS NUC, 20(4-7), 2001, pp. 743-746
Synthesis and biological activity of 4 '-C-hydroxymethyl-2 '-fluoro-D-arabinofuranosylpurine nucleosides
Authors: Shortnacy-Fowler, AT Tiwari, KN Montgomery, JA Secrist, JA
Citation: At. Shortnacy-fowler et al., Synthesis and biological activity of 4 '-C-hydroxymethyl-2 '-fluoro-D-arabinofuranosylpurine nucleosides, NUCLEOS NUC, 20(4-7), 2001, pp. 747-750
Comparison of the anti-influenza virus activity of RWJ-270201 with those of oseltamivir and zanamivir
Authors: Bantia, S Parker, CD Ananth, SL Horn, LL Andries, K Chand, P Kotian, PL Dehghani, A El-Kattan, Y Lin, T Hutchison, TL Montgomery, JA Kellog, DL Babu, YS
Citation: S. Bantia et al., Comparison of the anti-influenza virus activity of RWJ-270201 with those of oseltamivir and zanamivir, ANTIM AG CH, 45(4), 2001, pp. 1162-1167
Systematic structure-based design and stereoselective synthesis of novel multisubstituted cyclopentane derivatives with potent antiinfluenza activity
Authors: Chand, P Kotian, PL Dehghani, A El-Kattan, Y Lin, TH Hutchison, TL Babu, YS Bantia, S Elliott, AJ Montgomery, JA
Citation: P. Chand et al., Systematic structure-based design and stereoselective synthesis of novel multisubstituted cyclopentane derivatives with potent antiinfluenza activity, J MED CHEM, 44(25), 2001, pp. 4379-4392
Convenient syntheses of 6-methylpurine and related nucleosides
Authors: Hassan, AEA Abou-Elkair, RAI Montgomery, JA Secrist, JA
Citation: Aea. Hassan et al., Convenient syntheses of 6-methylpurine and related nucleosides, NUCLEOS NUC, 19(7), 2000, pp. 1123-1134
A convenient synthesis of 2 '-deoxy-2-fluoroadenosine; a potential prodrugfor suicide gene therapy
Authors: Hassan, AEA Shortnacy-Fowler, AT Montgomery, JA Secrist, JA
Citation: Aea. Hassan et al., A convenient synthesis of 2 '-deoxy-2-fluoroadenosine; a potential prodrugfor suicide gene therapy, NUCLEOS NUC, 19(3), 2000, pp. 559-565
Synthesis of 4 '-thio-beta-D-arabinofuranosylcytosine (4 '-thio-ara-C) andcomparison of its anticancer activity with that of ara-C
Authors: Tiwari, KN Shortnacy-Fowler, AT Cappellacci, L Parker, WB Waud, WR Montgomery, JA Secrist, JA
Citation: Kn. Tiwari et al., Synthesis of 4 '-thio-beta-D-arabinofuranosylcytosine (4 '-thio-ara-C) andcomparison of its anticancer activity with that of ara-C, NUCLEOS NUC, 19(1-2), 2000, pp. 329-340
Synthesis and biological activity of a novel class of purine nucleoside phosphorylase inhibitors
Authors: Morris, PE Elliott, AJ Walton, SP Williams, CH Montgomery, JA
Citation: Pe. Morris et al., Synthesis and biological activity of a novel class of purine nucleoside phosphorylase inhibitors, NUCLEOS NUC, 19(1-2), 2000, pp. 379-404
Preclinical, antitumor activity of 2-chloro-9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine (Cl-F-ara-A)
Authors: Waud, WR Schmid, SM Montgomery, JA Secrist, JA
Citation: Wr. Waud et al., Preclinical, antitumor activity of 2-chloro-9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine (Cl-F-ara-A), NUCLEOS NUC, 19(1-2), 2000, pp. 447-460
Synthesis and structure activity relationships of 5-substituted-4 '-thio-beta-D-arabinofuranosylcytosines
Authors: Tiwari, KN Shortnacy-Fowler, AT Cappellacci, L Waud, WR Parker, WB Montgomery, JA Secrist, JA
Citation: Kn. Tiwari et al., Synthesis and structure activity relationships of 5-substituted-4 '-thio-beta-D-arabinofuranosylcytosines, NUCLEOS NUC, 19(10-12), 2000, pp. 2005-2017
BCX-1812 (RWJ-270201): Discovery of a novel, highly potent, orally active,and selective influenza neuraminidase inhibitor through structure-based drug design
Authors: Babu, YS Chand, P Bantia, S Kotian, P Dehghani, A El-Kattan, Y Lin, TH Hutchison, TL Elliott, AJ Parker, CD Ananth, SL Horn, LL Laver, GW Montgomery, JA
Citation: Ys. Babu et al., BCX-1812 (RWJ-270201): Discovery of a novel, highly potent, orally active,and selective influenza neuraminidase inhibitor through structure-based drug design, J MED CHEM, 43(19), 2000, pp. 3482-3486
A complete basis set model chemistry. VII. Use of the minimum population localization method
Authors: Montgomery, JA Frisch, MJ Ochterski, JW Petersson, GA
Citation: Ja. Montgomery et al., A complete basis set model chemistry. VII. Use of the minimum population localization method, J CHEM PHYS, 112(15), 2000, pp. 6532-6542
Hydrophobic benzoic acids as inhibitors of influenza neuraminidase
Authors: Atigadda, VR Brouillette, WJ Duarte, F Babu, YS Bantia, S Chand, P Chu, NM Montgomery, JA Walsh, DA Sudbeck, E Finley, J Air, GM Luo, M Laver, GW
Citation: Vr. Atigadda et al., Hydrophobic benzoic acids as inhibitors of influenza neuraminidase, BIO MED CH, 7(11), 1999, pp. 2487-2497
Striatal metabolism of hexanal, a lipid peroxidation product, in the rat
Authors: Jaar, V Ste-Marie, L Montgomery, JA
Citation: V. Jaar et al., Striatal metabolism of hexanal, a lipid peroxidation product, in the rat, METAB BRAIN, 14(2), 1999, pp. 71-82
Synthesis and biological activity of 5-azacytosine nucleosides derived from 4-thio-2-deoxy-L-threo-pentofuranose and 4-thio-2-deoxy-D-erythro-pentofuranose
Authors: Cappellacci, L Tiwari, KN Montgomery, JA Secrist, JA
Citation: L. Cappellacci et al., Synthesis and biological activity of 5-azacytosine nucleosides derived from 4-thio-2-deoxy-L-threo-pentofuranose and 4-thio-2-deoxy-D-erythro-pentofuranose, NUCLEOS NUC, 18(4-5), 1999, pp. 613-614
Synthesis and biological activity of 4 '-thio-2 '-deoxy purine nucleosides
Authors: Messini, L Tiwari, KN Montgomery, JA Secrist, JA
Citation: L. Messini et al., Synthesis and biological activity of 4 '-thio-2 '-deoxy purine nucleosides, NUCLEOS NUC, 18(4-5), 1999, pp. 683-685
Gene therapy of cancer: Activation of nucleoside prodrugs with E-coli purine nucleoside phosphorylase
Authors: Secrist, JA Parker, WB Allan, PW Bennett, LL Waud, WR Truss, JW Fowler, AT Montgomery, JA Ealick, SE Wells, AH Gillespie, GY Gadi, VK Sorscher, EJ
Citation: Ja. Secrist et al., Gene therapy of cancer: Activation of nucleoside prodrugs with E-coli purine nucleoside phosphorylase, NUCLEOS NUC, 18(4-5), 1999, pp. 745-757
Certain 3,9-dideazapurines as inhibitors of purine nucleoside phosphorylase
Authors: Rose, JD Secrist, JA Montgomery, JA
Citation: Jd. Rose et al., Certain 3,9-dideazapurines as inhibitors of purine nucleoside phosphorylase, NUCLEOS NUC, 18(11-12), 1999, pp. 2443-2461
Quantifying tillage translocation and deposition rates due to moldboard plowing in the Palouse region of the Pacific Northwest, USA
Authors: Montgomery, JA McCool, DK Busacca, AJ Frazier, BE
Citation: Ja. Montgomery et al., Quantifying tillage translocation and deposition rates due to moldboard plowing in the Palouse region of the Pacific Northwest, USA, SOIL TILL R, 51(3-4), 1999, pp. 175-187
Comparison of the mechanism of cytotoxicity of 2-chloro-9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine, 2-chloro-9-(2-deoxy-2-fluoro-beta-D-ribofuranosyl)adenine and 2-chloro-9-(2-deoxy-2,2-difluoro-beta-D-ribofuranosyl)adenine in CEM Cells
Authors: Parker, WB Shaddix, SC Rose, LM Shewach, DS Hertel, LW Secrist, JA Montgomery, JA Bennett, LL
Citation: Wb. Parker et al., Comparison of the mechanism of cytotoxicity of 2-chloro-9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine, 2-chloro-9-(2-deoxy-2-fluoro-beta-D-ribofuranosyl)adenine and 2-chloro-9-(2-deoxy-2,2-difluoro-beta-D-ribofuranosyl)adenine in CEM Cells, MOLEC PHARM, 55(3), 1999, pp. 515-520
Potent inhibition of influenza sialidase by a benzoic acid containing a 2-pyrrolidinone substituent
Authors: Atigadda, VR Brouillette, WJ Duarte, F Ali, SM Babu, YS Bantia, S Chand, P Chu, N Montgomery, JA Walsh, DA Sudbeck, EA Finley, J Luo, M Air, GM Laver, GW
Citation: Vr. Atigadda et al., Potent inhibition of influenza sialidase by a benzoic acid containing a 2-pyrrolidinone substituent, J MED CHEM, 42(13), 1999, pp. 2332-2343
New syntheses of 7-substituted-2-aminothieno- and furo[3,2-d]pyrimidines
Authors: Morris, PE Elliott, AJ Montgomery, JA
Citation: Pe. Morris et al., New syntheses of 7-substituted-2-aminothieno- and furo[3,2-d]pyrimidines, J HETERO CH, 36(2), 1999, pp. 423-427
Risultati: 1-25 | 26-28