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Results:
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Results: 20
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
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
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
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
Authors:
Tolbert, WD
Ekstrom, JL
Mathews, II
Secrist, JA
Kapoor, P
Pegg, AE
Ealick, SE
Citation: Wd. Tolbert et al., The structural basis for substrate specificity and inhibition of human S-adenosylmethionine decarboxylase (vol 40, pg 9484, 2001), BIOCHEM, 40(43), 2001, pp. 13124-13124
Authors:
Tolbert, WD
Ekstrom, JL
Mathews, II
Secrist, JA
Kapoor, P
Pegg, AE
Ealick, SE
Citation: Wd. Tolbert et al., The structural basis for substrate specificity and inhibition of human S-adenosylmethionine decarboxylase, BIOCHEM, 40(32), 2001, pp. 9484-9494
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
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
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
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
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
Authors:
Parker, WB
Shaddix, SC
Rose, LM
Waud, WR
Shewach, DS
Tiwari, KN
Secrist, JA
Citation: Wb. Parker et al., Metabolism of 4 '-thio-beta-D-arabinofuranosylcytosine in CEM cells, BIOCH PHARM, 60(12), 2000, pp. 1925-1932
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
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
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
Authors:
Elzagheid, MI
Oivanen, M
Walker, RT
Secrist, JA
Citation: Mi. Elzagheid et al., Kinetics for the acid-catalyzed hydrolysis of purine and cytosine 2 '-deoxy-4 '-thionucleosides, NUCLEOS NUC, 18(2), 1999, pp. 181-186
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
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
Authors:
Nandanan, E
Camaioni, E
Jang, SY
Kim, YC
Cristalli, G
Herdewijn, P
Secrist, JA
Tiwari, KN
Mohanram, A
Harden, TK
Boyer, JL
Jacobson, KA
Citation: E. Nandanan et al., Structure-activity relationships of bisphosphate nucleotide derivatives asP2Y(1) receptor antagonists and partial agonists, J MED CHEM, 42(9), 1999, pp. 1625-1638
Authors:
Shortnacy-Fowler, AT
Tiwari, KN
Montgomery, JA
Buckheit, RW
Secrist, JA
Seela, FA
Citation: At. Shortnacy-fowler et al., Synthesis and biological activity of 2 '-fluoro-D-arabinofuranosylpyrazolo[3,4-d]pyrimidine nucleosides, HELV CHIM A, 82(12), 1999, pp. 2240-2245
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