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Results: 1-21 |
Results: 21

Authors: KRAMER K ELZ S PERTZ HH SCHUNACK W
Citation: K. Kramer et al., N-ALPHA-ALKYLATED DERIVATIVES OF 2-PHENYLHISTAMINES - SYNTHESIS AND IN-VITRO ACTIVITY OF POTENT HISTAMINE H-1-RECEPTOR AGONISTS, Bioorganic & medicinal chemistry letters, 8(18), 1998, pp. 2583-2588

Authors: ELZ S KRAMER K PERTZ H SCHUNACK W
Citation: S. Elz et al., METHYLHISTAPRODIFEN AND CONGENERS - HIGHLY POTENT AND SELECTIVE HISTAMINE H-1 RECEPTOR AGONISTS, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 113-113

Authors: STARK H ELZ S PERTZ H LIGNEAU X ARRANG JM SCHWARTZ JC SCHUNACK W
Citation: H. Stark et al., CIPROXIFAN, A SELECTIVE ANTAGONIST OF HIGH IN-VITRO AND IN-VIVO POTENCY AT HISTAMINE H-3-RECEPTORS, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 99-99

Authors: HEIM R PERTZ H WALTHER I ELZ S
Citation: R. Heim et al., CONGENERS OF 3-(2-BENZYLAMINOETHYL)-2,4-QUINAZOLINEDIONE - PARTIAL AGONISTS FOR RAT VASCULAR 5-HT2A RECEPTORS, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 810-810

Authors: KRAMER K ELZ S SCHUNACK W
Citation: K. Kramer et al., ANALOGS OF HISTAPRODIFEN - POTENT PARTIAL AGONISTS FOR HISTAMINE H-1 RECEPTORS, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 910-910

Authors: ELZ S KRAMER K PERTZ H SCHUNACK W
Citation: S. Elz et al., METHYLHISTAPRODIFEN AND CONGENERS - HIGHLY POTENT AND SELECTIVE HISTAMINE H-1 RECEPTOR AGONISTS, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 924-924

Authors: MALINOWSKA B GODLEWSKI G KRAMER K ELZ S SCHUNACK W SCHLICKER E
Citation: B. Malinowska et al., EFFECTS OF THE NOVEL HISTAMINE H-1-RECEPTOR AGONISTS HISTAPRODIFEN, METHYLHISTAPRODIFEN, AND DIMETHYLHISTAPRODIFEN ON CARDIOVASCULAR PARAMETERS IN THE PITHED RAT, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 930-930

Authors: HEIM R PERTZ H ELZ S
Citation: R. Heim et al., DERIVATIVES OF 3-(2-AMINOETHYL)-2,4-QUINAZOLINEDIONE - PARTIAL AGONISM ON VASCULAR 5-HT2A RECEPTORS, Naunyn-Schmiedeberg's archives of pharmacology, 357(4), 1998, pp. 106-106

Authors: TIMM J MARR I WERTHWEIN S ELZ S SCHUNACK W SCHLICKER E
Citation: J. Timm et al., H-2 RECEPTOR-MEDIATED FACILITATION AND H-3 RECEPTOR-MEDIATED INHIBITION OF NORADRENALINE RELEASE IN THE GUINEA-PIG BRAIN, Naunyn-Schmiedeberg's archives of pharmacology, 357(3), 1998, pp. 232-239

Authors: LIGNEAU X LIN JS VANNIMERCIER G JOUVET M MUIR JL GANELLIN CR STARK H ELZ S SCHUNACK W SCHWARTZ JC
Citation: X. Ligneau et al., NEUROCHEMICAL AND BEHAVIORAL-EFFECTS OF CIPROXIFAN, A POTENT HISTAMINE H-3-RECEPTOR ANTAGONIST, The Journal of pharmacology and experimental therapeutics, 287(2), 1998, pp. 658-666

Authors: ELZ S KELLER A BLASCHKE G PERTZ H
Citation: S. Elz et al., STEREOSELECTIVITY AND EFFECTS OF NOVEL 5-HT4 RECEPTOR ANTAGONISTS ANDPARTIAL AGONISTS - COMPARISON OF RAT ESOPHAGUS AND GUINEA-PIG ILEUM, Naunyn-Schmiedeberg's archives of pharmacology, 355(4), 1997, pp. 95-95

Authors: SCHLICKER E PERTZ H BITSCHNAU H PURAND K KATHMANN M ELZ S SCHUNACK W
Citation: E. Schlicker et al., EFFECTS OF IODOPROXYFAN, A POTENT AND SELECTIVE HISTAMINE H-3 RECEPTOR ANTAGONIST, ON ALPHA(2) AND 5-HT3 RECEPTORS, Inflammation research, 44(7), 1995, pp. 296-300

Authors: ELZ S HEIL WL
Citation: S. Elz et Wl. Heil, SYNTHESIS, BIOLOGICAL IN-VITRO EVALUATION AND STEREOSELECTIVITY OF ONDANSETRON ANALOGS - NOVEL 5-HT2A RECEPTOR ANTAGONISTS, Bioorganic & medicinal chemistry letters, 5(7), 1995, pp. 667-672

Authors: ELZ S KELLER A
Citation: S. Elz et A. Keller, PREPARATION AND IN-VITRO PHARMACOLOGY OF 5-HT4 RECEPTOR LIGANDS - PARTIAL AGONISM AND ANTAGONISM OF METOCLOPRAMIDE ANALOGOUS BENZOIC ESTERS, Archiv der pharmazie, 328(7-8), 1995, pp. 585-594

Authors: PERTZ H ELZ S
Citation: H. Pertz et S. Elz, IN-VITRO PHARMACOLOGY OF SARPOGRELATE AND THE ENANTIOMERS OF ITS MAJOR METABOLITE - 5-HT2A RECEPTOR SPECIFICITY, STEREOSELECTIVITY AND MODULATION OF RITANSERIN-INDUCED DEPRESSION OF 5-HT CONTRACTIONS IN RAT TAIL ARTERY, Journal of Pharmacy and Pharmacology, 47(4), 1995, pp. 310-316

Authors: LESCHKE C ELZ S GARBARG M SCHUNACK W
Citation: C. Leschke et al., SYNTHESIS AND HISTAMINE H-1 RECEPTOR AGONIST ACTIVITY OF A SERIES OF 2-PHENYLHISTAMINES, 2-HETEROARYLHISTAMINES, AND ANALOGS, Journal of medicinal chemistry, 38(8), 1995, pp. 1287-1294

Authors: MONTI JM JANTOS H LESCHKE C ELZ S SCHUNACK W
Citation: Jm. Monti et al., THE SELECTIVE HISTAMINE H-1-RECEPTOR AGONIST 2-(3-TRIFLUOROMETHYLPHENYL)HISTAMINE INCREASES WAKING IN THE RAT, European neuropsychopharmacology, 4(4), 1994, pp. 459-462

Authors: LOWE W ELZ S REISER H SCHOTT S
Citation: W. Lowe et al., 7-FLUORO-4-CHROMONE-3-SULFUR COMPOUNDS, Archiv der pharmazie, 327(4), 1994, pp. 267-269

Authors: RADWANSKY A ELZ S LEHMANN J
Citation: A. Radwansky et al., LACTONES .25. SYNTHESIS AND 5-HT2-RECEPTOR AFFINITY OF SOME FLUOROPHENYLATED ALPHA-AMINOMETHYLLACTONES, Archiv der pharmazie, 326(4), 1993, pp. 243-244

Authors: ELZ S ZIMMERMANN H REHSE K
Citation: S. Elz et al., SELECTIVITY OF STERICALLY FIXED TRYPTAMINE AND 5-METHOXYTRYPTAMINE DERIVATIVES FOR SEROTONIN RECEPTOR SUBTYPES .2. STRUCTURE-ACTIVITY-RELATIONSHIPS AND IN-VITRO PHARMACOLOGY OF N-ALKYL- AND -DIALKYL-3-INDOLYLBICYCLO-[2.2.1]-HEPTANE-2-AMINES, Archiv der pharmazie, 326(11), 1993, pp. 893-899

Authors: MALINOWSKA B LESCHKE C ELZ S SCHUNACK W SCHLICKER E
Citation: B. Malinowska et al., EFFECTS OF THE NOVEL H1 AGONISTS 2-(3-TRIFLUOROMETHYLPHENYL)-AND 2-(3-BROMOPHENYL)HISTAMINE AND OF 2-(2-THIAZOLYL)ETHYLAMINE ON CARDIOVASCULAR PARAMETERS IN THE PITHED RAT, Agents and actions, 38, 1993, pp. 257-259
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