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Results: 1-10 |
Results: 10
STEREOSELECTIVE CONVERSION OF 2',3'-DIDEOXYDIDEHYDRO CARBOCYCLIC NUCLEOSIDES INTO 2'-DEOXY CARBOCYCLIC NUCLEOSIDES
Authors: BARKLEY JV DHANDA A KNUTSEN LJS NIELSEN MB ROBERTS SM VARLEY DR
Citation: Jv. Barkley et al., STEREOSELECTIVE CONVERSION OF 2',3'-DIDEOXYDIDEHYDRO CARBOCYCLIC NUCLEOSIDES INTO 2'-DEOXY CARBOCYCLIC NUCLEOSIDES, Chemical communications, (10), 1998, pp. 1117-1118
THE SYNTHESIS OF NEW ADENOSINE A(3) SELECTIVE LIGANDS CONTAINING BIOISOSTERIC ISOXAZOLES
Authors: MOGENSEN JP ROBERTS SM BOWLER AN THOMSEN C KNUTSEN LJS
Citation: Jp. Mogensen et al., THE SYNTHESIS OF NEW ADENOSINE A(3) SELECTIVE LIGANDS CONTAINING BIOISOSTERIC ISOXAZOLES, Bioorganic & medicinal chemistry letters, 8(13), 1998, pp. 1767-1770
UNEXPECTED NEUROPROTECTION OBSERVED WITH THE ADENOSINE A(2A) RECEPTORAGONIST CGS-21680 (VOL 39, PG 108, 1996)
Authors: SHEARDOWN MJ KNUTSEN LJS
Citation: Mj. Sheardown et Ljs. Knutsen, UNEXPECTED NEUROPROTECTION OBSERVED WITH THE ADENOSINE A(2A) RECEPTORAGONIST CGS-21680 (VOL 39, PG 108, 1996), Drug development research, 40(1), 1997, pp. 99-99
C-14 LABELING OF A NOVEL ANTIISCHEMIC ADENOSINE A(1) AGONIST AT PURINE C-8
Authors: VALSBORG JS KNUTSEN LJS FOGED C
Citation: Js. Valsborg et al., C-14 LABELING OF A NOVEL ANTIISCHEMIC ADENOSINE A(1) AGONIST AT PURINE C-8, Journal of labelled compounds & radiopharmaceuticals, 38(5), 1996, pp. 497-507
UNEXPECTED NEUROPROTECTION OBSERVED WITH THE ADENOSINE A(2A) RECEPTORAGONIST CGS-21680
Authors: SHEARDOWN MJ KNUTSEN LJS
Citation: Mj. Sheardown et Ljs. Knutsen, UNEXPECTED NEUROPROTECTION OBSERVED WITH THE ADENOSINE A(2A) RECEPTORAGONIST CGS-21680, Drug development research, 39(1), 1996, pp. 108-114
PREPARATION AND DETERMINATION OF THE ABSOLUTE-CONFIGURATION OF OPTICALLY-ACTIVE 9-HYDROXY-7-OXABICYCLO[4.3.0]NON-4-EN-8-ONES
Authors: HIBBS DE HURSTHOUSE MB KNUTSEN LJS MALIK KMA OLIVO HF ROBERTS SM VARLEY DR XIONG H
Citation: De. Hibbs et al., PREPARATION AND DETERMINATION OF THE ABSOLUTE-CONFIGURATION OF OPTICALLY-ACTIVE 9-HYDROXY-7-OXABICYCLO[4.3.0]NON-4-EN-8-ONES, Acta chemica Scandinavica, 49(2), 1995, pp. 122-127
SYNTHESIS OF [8-C-14]-2,6-DICHLORO-9H-PURINE, A RADIOLABELED PRECURSOR FOR C-14 NUCLEOSIDES
Authors: VALSBORG JS KNUTSEN LJS LUNDT I FOGED C
Citation: Js. Valsborg et al., SYNTHESIS OF [8-C-14]-2,6-DICHLORO-9H-PURINE, A RADIOLABELED PRECURSOR FOR C-14 NUCLEOSIDES, Journal of labelled compounds & radiopharmaceuticals, 36(5), 1995, pp. 457-464
THE SYNTHESIS AND BIOCHEMICAL EVALUATION OF NEW A(1) SELECTIVE ADENOSINE RECEPTOR AGONISTS CONTAINING 6-HYDRAZINOPURINE MOIETIES
Authors: KNUTSEN LJS LAU J SHEARDOWN MJ THOMSEN C
Citation: Ljs. Knutsen et al., THE SYNTHESIS AND BIOCHEMICAL EVALUATION OF NEW A(1) SELECTIVE ADENOSINE RECEPTOR AGONISTS CONTAINING 6-HYDRAZINOPURINE MOIETIES, Bioorganic & medicinal chemistry letters, 3(12), 1993, pp. 2661-2666
THE SYNTHESIS OF NOVEL GABA UPTAKE INHIBITORS .1. ELUCIDATION OF THE STRUCTURE-ACTIVITY STUDIES LEADING TO THE CHOICE OF ETHYL-2-THIENYL)-3-BUTENYL]-3-PIPERIDINECARBOXYLIC ACID (TIAGABINE) AS AN ANTICONVULSANTDRUG CANDIDATE
Authors: ANDERSEN KE BRAESTRUP C GRONWALD FC JORGENSEN AS NIELSEN EB SONNEWALD U SORENSEN PO SUZDAK PD KNUTSEN LJS
Citation: Ke. Andersen et al., THE SYNTHESIS OF NOVEL GABA UPTAKE INHIBITORS .1. ELUCIDATION OF THE STRUCTURE-ACTIVITY STUDIES LEADING TO THE CHOICE OF ETHYL-2-THIENYL)-3-BUTENYL]-3-PIPERIDINECARBOXYLIC ACID (TIAGABINE) AS AN ANTICONVULSANTDRUG CANDIDATE, Journal of medicinal chemistry, 36(12), 1993, pp. 1716-1725
CONTRASTING EFFECTS OF ADENOSINE-A1 AND ADENOSINE-A2 RECEPTOR LIGANDSIN DIFFERENT CHEMOCONVULSIVE RODENT MODELS
Authors: KLITGAARD H KNUTSEN LJS THOMSEN C
Citation: H. Klitgaard et al., CONTRASTING EFFECTS OF ADENOSINE-A1 AND ADENOSINE-A2 RECEPTOR LIGANDSIN DIFFERENT CHEMOCONVULSIVE RODENT MODELS, European journal of pharmacology, 242(3), 1993, pp. 221-228
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