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Results: 1-10 |
Results: 10
Total synthesis of SR 121463 A, a highly potent and selective vasopressin V-2: Receptor antagonist
Authors: Venkatesan, H Davis, MC Altas, Y Snyder, JP Liotta, DC
Citation: H. Venkatesan et al., Total synthesis of SR 121463 A, a highly potent and selective vasopressin V-2: Receptor antagonist, J ORG CHEM, 66(11), 2001, pp. 3653-3661
Polyoxometalate HIV-1 protease inhibitors. A new mode of protease inhibition
Authors: Judd, DA Nettles, JH Nevins, N Snyder, JP Liotta, DC Tang, J Ermolieff, J Schinazi, RF Hill, CL
Citation: Da. Judd et al., Polyoxometalate HIV-1 protease inhibitors. A new mode of protease inhibition, J AM CHEM S, 123(5), 2001, pp. 886-897
Treatment of isografted 9L rat brain tumors with beta-5-o-carboranyl-2 '-deoxyuridine neutron capture therapy
Authors: Schinazi, RF Hurwitz, SJ Liberman, I Juodawlkis, AS Tharnish, P Shi, JX Liotta, DC Coderre, JA Olson, J
Citation: Rf. Schinazi et al., Treatment of isografted 9L rat brain tumors with beta-5-o-carboranyl-2 '-deoxyuridine neutron capture therapy, CLIN CANC R, 6(2), 2000, pp. 725-730
Practical synthesis of N-palmitoylsphingomyelin and N-palmitoyldihydrosphingomyelin
Authors: Bushnev, AS Liotta, DC
Citation: As. Bushnev et Dc. Liotta, Practical synthesis of N-palmitoylsphingomyelin and N-palmitoyldihydrosphingomyelin, METH ENZYM, 311, 2000, pp. 535-547
The oxetane ring in taxol
Authors: Wang, MM Cornett, B Nettles, J Liotta, DC Snyder, JP
Citation: Mm. Wang et al., The oxetane ring in taxol, J ORG CHEM, 65(4), 2000, pp. 1059-1068
A unified and quantitative receptor model for the microtubule binding of paclitaxel and epothilone
Authors: Wang, MM Xia, XY Kim, Y Hwang, D Jansen, JM Botta, M Liotta, DC Snyder, JP
Citation: Mm. Wang et al., A unified and quantitative receptor model for the microtubule binding of paclitaxel and epothilone, ORG LETT, 1(1), 1999, pp. 43-46
Pharmacokinetics of the antiviral agent beta-D-2 ',3 '-didehydro-2 ',3 '-dideoxy-5-fluorocytidine in rhesus monkeys
Authors: Ma, L Hurwitz, SJ Shi, JX McAtee, JJ Liotta, DC McClure, HM Schinazi, RF
Citation: L. Ma et al., Pharmacokinetics of the antiviral agent beta-D-2 ',3 '-didehydro-2 ',3 '-dideoxy-5-fluorocytidine in rhesus monkeys, ANTIM AG CH, 43(2), 1999, pp. 381-384
Synthesis and biological evaluation of 2 ',3 '-didehydro-2 ',3 '-dideoxy-5-fluorocytidine (D4FC) analogues: Discovery of carbocyclic nucleoside triphosphates with potent inhibitory activity against HIV-1 reverse transcriptase
Authors: Shi, JX McAtee, JJ Wirtz, SS Tharnish, P Juodawlkis, A Liotta, DC Schinazi, RF
Citation: Jx. Shi et al., Synthesis and biological evaluation of 2 ',3 '-didehydro-2 ',3 '-dideoxy-5-fluorocytidine (D4FC) analogues: Discovery of carbocyclic nucleoside triphosphates with potent inhibitory activity against HIV-1 reverse transcriptase, J MED CHEM, 42(5), 1999, pp. 859-867
Identification of ammonium ion and 2,6-bis(omega-aminobutyl)-3,5-diiminopiperazine as endogenous factors that account for the "burst" of sphingosine upon changing the medium of J774 cells in culture
Authors: Warden, LA Menaldino, DS Wilson, T Liotta, DC Smith, ER Merrill, AH
Citation: La. Warden et al., Identification of ammonium ion and 2,6-bis(omega-aminobutyl)-3,5-diiminopiperazine as endogenous factors that account for the "burst" of sphingosine upon changing the medium of J774 cells in culture, J BIOL CHEM, 274(48), 1999, pp. 33875-33880
Ceramide-beta-D-glucuronide: Synthesis, digestion, and suppression of early markers of colon carcinogenesis
Authors: Schmelz, EM Bushnev, AS Dillehay, DL Sullards, MC Liotta, DC Merrill, AH
Citation: Em. Schmelz et al., Ceramide-beta-D-glucuronide: Synthesis, digestion, and suppression of early markers of colon carcinogenesis, CANCER RES, 59(22), 1999, pp. 5768-5772
Risultati: 1-10 |