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Results: 1-25 | 26-32
Results: 1-25/32
HETEROATOM-SUBSTITUTION AS A STRATEGY FOR INCREASING THE POTENCY OF COMPETITIVE NMDA ANTAGONISTS
Authors: ORNSTEIN PL ARNOLD MB LUNN WHW HEINZ LJ LEANDER JD LODGE D SCHOEPP DD
Citation: Pl. Ornstein et al., HETEROATOM-SUBSTITUTION AS A STRATEGY FOR INCREASING THE POTENCY OF COMPETITIVE NMDA ANTAGONISTS, Bioorganic & medicinal chemistry letters, 8(4), 1998, pp. 389-394
THE RACEMIC FORM OF LY300164, AN ORALLY EFFECTIVE AMPA RECEPTOR ANTAGONIST, SUPPRESSES PENTYLENETETRAZOL-INDUCED KINDLING IN MICE
Authors: WARBINTON D LEANDER JD
Citation: D. Warbinton et Jd. Leander, THE RACEMIC FORM OF LY300164, AN ORALLY EFFECTIVE AMPA RECEPTOR ANTAGONIST, SUPPRESSES PENTYLENETETRAZOL-INDUCED KINDLING IN MICE, Neurology, 50(4), 1998, pp. 3027-3027
EFFECTS OF THE RACEMIC FORM OF LY300164, AN ORALLY EFFECTIVE AMPA RECEPTOR ANTAGONIST, IN A MOUSE MODEL OF CLONIC STATUS EPILEPTICUS
Authors: LEANDER JD
Citation: Jd. Leander, EFFECTS OF THE RACEMIC FORM OF LY300164, AN ORALLY EFFECTIVE AMPA RECEPTOR ANTAGONIST, IN A MOUSE MODEL OF CLONIC STATUS EPILEPTICUS, Neurology, 50(4), 1998, pp. 3028-3028
SELECTIVE SEROTONIN REUPTAKE INHIBITORS POTENTIATE 8-OH-DPAT-INDUCED STIMULUS-CONTROL IN THE PIGEON
Authors: WOLFF MC LEANDER JD
Citation: Mc. Wolff et Jd. Leander, SELECTIVE SEROTONIN REUPTAKE INHIBITORS POTENTIATE 8-OH-DPAT-INDUCED STIMULUS-CONTROL IN THE PIGEON, European journal of pharmacology, 345(1), 1998, pp. 35-39
INCREASED FOOD-CONSUMPTION BY CLOZAPINE, BUT NOT BY OLANZAPINE, IN SATIATED RATS
Authors: BENVENGA MJ LEANDER JD
Citation: Mj. Benvenga et Jd. Leander, INCREASED FOOD-CONSUMPTION BY CLOZAPINE, BUT NOT BY OLANZAPINE, IN SATIATED RATS, Drug development research, 41(1), 1997, pp. 48-50
PHARMACOLOGICAL PROFILE OF LY301317, A POTENT AND SELECTIVE 5-HT1A AGONIST
Authors: WOLFF MC BENVENGA MJ CALLIGARO DO FULLER RW GIDDA JS HEMRICKLUECKE S LUCOT JB NELSON DL OVERSHINER CD LEANDER JD
Citation: Mc. Wolff et al., PHARMACOLOGICAL PROFILE OF LY301317, A POTENT AND SELECTIVE 5-HT1A AGONIST, Drug development research, 40(1), 1997, pp. 17-34
BEHAVIORAL PHARMACOLOGY OF OLANZAPINE - A NOVEL ANTIPSYCHOTIC DRUG
Authors: MOORE NA LEANDER JD BENVENGA MJ GLEASON SD SHANNON H
Citation: Na. Moore et al., BEHAVIORAL PHARMACOLOGY OF OLANZAPINE - A NOVEL ANTIPSYCHOTIC DRUG, The Journal of clinical psychiatry, 58, 1997, pp. 37-44
EFFECTS OF A 5-HT1A RECEPTOR AGONIST ON ACUTE AND DELAYED CYCLOPHOSPHAMIDE-INDUCED VOMITING
Authors: WOLFF MC LEANDER JD
Citation: Mc. Wolff et Jd. Leander, EFFECTS OF A 5-HT1A RECEPTOR AGONIST ON ACUTE AND DELAYED CYCLOPHOSPHAMIDE-INDUCED VOMITING, European journal of pharmacology, 340(2-3), 1997, pp. 217-220
DIFFERENTIATION OF 5-HT1A RECEPTOR LIGANDS BY DRUG DISCRIMINATION
Authors: WOLFF MC LEANDER JD
Citation: Mc. Wolff et Jd. Leander, DIFFERENTIATION OF 5-HT1A RECEPTOR LIGANDS BY DRUG DISCRIMINATION, European journal of pharmacology, 333(2-3), 1997, pp. 113-122
ANTICONFLICT EFFECTS OF 5HT(1A) AGONISTS IN PIGEONS ARE DEPENDENT ON THE LEVEL OF RESPONSE SUPPRESSION
Authors: BENVENGA MJ LEANDER JD
Citation: Mj. Benvenga et Jd. Leander, ANTICONFLICT EFFECTS OF 5HT(1A) AGONISTS IN PIGEONS ARE DEPENDENT ON THE LEVEL OF RESPONSE SUPPRESSION, Behavioural pharmacology, 7(6), 1996, pp. 540-550
STRUCTURE-ACTIVITY STUDIES OF 6-(TETRAZOLYLALKYL)-SUBSTITUTED DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID AMPA RECEPTOR ANTAGONISTS .1. EFFECTSOF STEREOCHEMISTRY, CHAIN-LENGTH, AND CHAIN SUBSTITUTION
Authors: ORNSTEIN PL ARNOLD MB ALLEN NK BLEISCH T BORROMEO PS LUGAR CW LEANDER JD LODGE D SCHOEPP DD
Citation: Pl. Ornstein et al., STRUCTURE-ACTIVITY STUDIES OF 6-(TETRAZOLYLALKYL)-SUBSTITUTED DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID AMPA RECEPTOR ANTAGONISTS .1. EFFECTSOF STEREOCHEMISTRY, CHAIN-LENGTH, AND CHAIN SUBSTITUTION, Journal of medicinal chemistry, 39(11), 1996, pp. 2219-2231
STRUCTURE-ACTIVITY STUDIES OF 6-SUBSTITUTED DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID AMPA RECEPTOR ANTAGONISTS .2. EFFECTS OF DISTAL ACID BIOISOSTERIC SUBSTITUTION, ABSOLUTE STEREOCHEMICAL PREFERENCES, AND IN-VIVO ACTIVITY
Authors: ORNSTEIN PL ARNOLD MB ALLEN NK BLEISCH T BORROMEO PS LUGAR CW LEANDER JD LODGE D SCHOEPP DD
Citation: Pl. Ornstein et al., STRUCTURE-ACTIVITY STUDIES OF 6-SUBSTITUTED DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID AMPA RECEPTOR ANTAGONISTS .2. EFFECTS OF DISTAL ACID BIOISOSTERIC SUBSTITUTION, ABSOLUTE STEREOCHEMICAL PREFERENCES, AND IN-VIVO ACTIVITY, Journal of medicinal chemistry, 39(11), 1996, pp. 2232-2244
OLANZAPINE, AN ATYPICAL ANTIPSYCHOTIC, INCREASES RATES OF PUNISHED RESPONDING IN PIGEONS
Authors: BENVENGA MJ LEANDER JD
Citation: Mj. Benvenga et Jd. Leander, OLANZAPINE, AN ATYPICAL ANTIPSYCHOTIC, INCREASES RATES OF PUNISHED RESPONDING IN PIGEONS, Psychopharmacology, 119(2), 1995, pp. 133-138
EFFECTS OF COMPETITIVE EXCITATORY AMINO-ACID ANTAGONISTS ON PUNISHED RESPONDING IN PIGEONS
Authors: BENVENGA MJ LEANDER JD
Citation: Mj. Benvenga et Jd. Leander, EFFECTS OF COMPETITIVE EXCITATORY AMINO-ACID ANTAGONISTS ON PUNISHED RESPONDING IN PIGEONS, Behavioural pharmacology, 6(5-6), 1995, pp. 615-616
PHARMACOLOGICAL CHARACTERIZATION OF ENANTIOMERS OF 8-THIOMETHYL-2-(DI-N-PROPYLAMINO)TETRALIN, POTENT AND SELECTIVE 5-HT1A RECEPTOR AGONISTS
Authors: FOREMAN MM FULLER RW LEANDER JD NELSON DL CALLIGARO DO LUCAITES VL WONG DT ZHANG L BARRETT JE SCHAUS JM
Citation: Mm. Foreman et al., PHARMACOLOGICAL CHARACTERIZATION OF ENANTIOMERS OF 8-THIOMETHYL-2-(DI-N-PROPYLAMINO)TETRALIN, POTENT AND SELECTIVE 5-HT1A RECEPTOR AGONISTS, Drug development research, 34(1), 1995, pp. 66-85
COMPARISON OF THE ANTIEMETIC EFFECTS OF A 5-HT1A AGONIST, LY228729, AND 5-HT3 ANTAGONISTS IN THE PIGEON
Authors: WOLFF MC LEANDER JD
Citation: Mc. Wolff et Jd. Leander, COMPARISON OF THE ANTIEMETIC EFFECTS OF A 5-HT1A AGONIST, LY228729, AND 5-HT3 ANTAGONISTS IN THE PIGEON, Pharmacology, biochemistry and behavior, 52(3), 1995, pp. 571-575
IN-VITRO AND IN-VIVO ANTAGONISM OF AMPA RECEPTOR ACTIVATION BY ZOLE-5-YL)ETHYL]DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
Authors: SCHOEPP DD LODGE D BLEAKMAN D LEANDER JD TIZZANO JP WRIGHT RA PALMER AJ SALHOFF CR ORNSTEIN PL
Citation: Dd. Schoepp et al., IN-VITRO AND IN-VIVO ANTAGONISM OF AMPA RECEPTOR ACTIVATION BY ZOLE-5-YL)ETHYL]DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID, Neuropharmacology, 34(9), 1995, pp. 1159-1168
SCHEDULE-CONTROLLED BEHAVIORAL-EFFECTS OF THE SELECTIVE AMINO-3-(5-METHYL-3-HYDROXYISOXAZOL-4-YL)PROPANOIC ACID ANTAGONIST LY293558 IN PIGEONS
Authors: BENVENGA MJ ORNSTEIN PL LEANDER JD
Citation: Mj. Benvenga et al., SCHEDULE-CONTROLLED BEHAVIORAL-EFFECTS OF THE SELECTIVE AMINO-3-(5-METHYL-3-HYDROXYISOXAZOL-4-YL)PROPANOIC ACID ANTAGONIST LY293558 IN PIGEONS, The Journal of pharmacology and experimental therapeutics, 275(1), 1995, pp. 164-170
H-TETRAZOL-5-YL)DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID, A NOVEL, COMPETITIVE, SYSTEMICALLY ACTIVE NMDA AND AMPA RECEPTOR ANTAGONIST
Authors: ORNSTEIN PL ARNOLD MB ALLEN NK LEANDER JD TIZZANO JP LODGE D SCHOEPP DD
Citation: Pl. Ornstein et al., H-TETRAZOL-5-YL)DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID, A NOVEL, COMPETITIVE, SYSTEMICALLY ACTIVE NMDA AND AMPA RECEPTOR ANTAGONIST, Journal of medicinal chemistry, 38(25), 1995, pp. 4885-4890
ANTIEMETIC EFFECTS OF 5-HT1A AGONISTS IN THE PIGEON
Authors: WOLFF MC LEANDER JD
Citation: Mc. Wolff et Jd. Leander, ANTIEMETIC EFFECTS OF 5-HT1A AGONISTS IN THE PIGEON, Pharmacology, biochemistry and behavior, 49(2), 1994, pp. 385-391
ANTICONVULSANT PROPERTIES OF N-SUBSTITUTED ALPHA,ALPHA-DIAMINO ACID-DERIVATIVES
Authors: KOHN H SAWHNEY KN ROBERTSON DW LEANDER JD
Citation: H. Kohn et al., ANTICONVULSANT PROPERTIES OF N-SUBSTITUTED ALPHA,ALPHA-DIAMINO ACID-DERIVATIVES, Journal of pharmaceutical sciences, 83(5), 1994, pp. 689-691
DISCOVERY OF A POTENT, PERIPHERALLY SELECTIVE TRANS-3,4-DIMETHYL-4-(3-HYDROXYPHENYL)PIPERIDINE OPIOID ANTAGONIST FOR THE TREATMENT OF GASTROINTESTINAL MOTILITY DISORDERS
Authors: ZIMMERMAN DM GIDDA JS CANTRELL BE SCHOEPP DD JOHNSON BG LEANDER JD
Citation: Dm. Zimmerman et al., DISCOVERY OF A POTENT, PERIPHERALLY SELECTIVE TRANS-3,4-DIMETHYL-4-(3-HYDROXYPHENYL)PIPERIDINE OPIOID ANTAGONIST FOR THE TREATMENT OF GASTROINTESTINAL MOTILITY DISORDERS, Journal of medicinal chemistry, 37(15), 1994, pp. 2262-2265
LY246736 - A SELECTIVE ANTAGONIST FOR PERIPHERAL MU-OPIOID RECEPTORS
Authors: EVANS DC JACOBS J JOHNSON BG CANTRELL BE ROTHMAN RB SCHOEPP DD ZIMMERMAN DM LEANDER JD GIDDA JS
Citation: Dc. Evans et al., LY246736 - A SELECTIVE ANTAGONIST FOR PERIPHERAL MU-OPIOID RECEPTORS, Gastroenterology, 106(4), 1994, pp. 10000495-10000495
UNUSUAL STEREOCHEMICAL PREFERENCES OF DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID COMPETITIVE NMDA ANTAGONISTS
Authors: ORNSTEIN PL ARNOLD MB AUGENSTEIN NK DEETER JB LEANDER JD LODGE D CALLIGARO DO SCHOEPP DD
Citation: Pl. Ornstein et al., UNUSUAL STEREOCHEMICAL PREFERENCES OF DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID COMPETITIVE NMDA ANTAGONISTS, Bioorganic & medicinal chemistry letters, 3(10), 1993, pp. 2067-2072
PRECLINICAL STUDIES ON LY228729 - A POTENT AND SELECTIVE SEROTONIN(1A) AGONIST
Authors: FOREMAN MM FULLER RW LEANDER JD BENVENGA MJ WONG DT NELSON DL CALLIGARO DO SWANSON SP LUCOT JB FLAUGH ME
Citation: Mm. Foreman et al., PRECLINICAL STUDIES ON LY228729 - A POTENT AND SELECTIVE SEROTONIN(1A) AGONIST, The Journal of pharmacology and experimental therapeutics, 267(1), 1993, pp. 58-71
Risultati: 1-25 | 26-32