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Results: 1-17 |
Results: 17
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
[H-3]LY341495, A HIGHLY POTENT, SELECTIVE AND NOVEL RADIOLIGAND FOR LABELING GROUP-II METABOTROPIC GLUTAMATE RECEPTORS
Authors: ORNSTEIN PL ARNOLD MB BLEISCH TJ WRIGHT RA WHEELER WJ SCHOEPP DD
Citation: Pl. Ornstein et al., [H-3]LY341495, A HIGHLY POTENT, SELECTIVE AND NOVEL RADIOLIGAND FOR LABELING GROUP-II METABOTROPIC GLUTAMATE RECEPTORS, Bioorganic & medicinal chemistry letters, 8(14), 1998, pp. 1919-1922
A COMPREHENSIVE INVESTIGATION OF VARIATIONS IN MELTING RANGES AND NMRDATA OF 2,4-DINITROPHENYLHYDRAZINE DERIVATIVES
Authors: TAYYARI SF SPEAKMAN JL ARNOLD MB CAI W BEHFOROUZ M
Citation: Sf. Tayyari et al., A COMPREHENSIVE INVESTIGATION OF VARIATIONS IN MELTING RANGES AND NMRDATA OF 2,4-DINITROPHENYLHYDRAZINE DERIVATIVES, Journal of the Chemical Society. Perkin transactions. II (Print), (10), 1998, pp. 2195-2200
2-SUBSTITUTED MINO-2-((1SR,2SR)-2-CARBOXYCYCLOPROP-1-YL)GLYCINES AS POTENT AND SELECTIVE ANTAGONISTS OF GROUP-II METABOTROPIC GLUTAMATE RECEPTORS - 1 - EFFECTS OF ALKYL, ARYLALKYL, AND DIARYLALKYL SUBSTITUTION
Authors: ORNSTEIN PL BLEISCH TJ ARNOLD MB WRIGHT RA JOHNSON BG SCHOEPP DD
Citation: Pl. Ornstein et al., 2-SUBSTITUTED MINO-2-((1SR,2SR)-2-CARBOXYCYCLOPROP-1-YL)GLYCINES AS POTENT AND SELECTIVE ANTAGONISTS OF GROUP-II METABOTROPIC GLUTAMATE RECEPTORS - 1 - EFFECTS OF ALKYL, ARYLALKYL, AND DIARYLALKYL SUBSTITUTION, Journal of medicinal chemistry, 41(3), 1998, pp. 346-357
2-SUBSTITUTED MINO-2-((1SR,2SR)-2-CARBOXYCYCLOPROP-1-YL)GLYCINES AS POTENT AND SELECTIVE ANTAGONISTS OF GROUP-II METABOTROPIC GLUTAMATE RECEPTORS - 2 - EFFECTS OF AROMATIC-SUBSTITUTION, PHARMACOLOGICAL CHARACTERIZATION, AND BIOAVAILABILITY
Authors: ORNSTEIN PL BLEISCH TJ ARNOLD MB KENNEDY JH WRIGHT RA JOHNSON BG TIZZANO JP HELTON DR KALLMAN MJ SCHOEPP DD HERIN M
Citation: Pl. Ornstein et al., 2-SUBSTITUTED MINO-2-((1SR,2SR)-2-CARBOXYCYCLOPROP-1-YL)GLYCINES AS POTENT AND SELECTIVE ANTAGONISTS OF GROUP-II METABOTROPIC GLUTAMATE RECEPTORS - 2 - EFFECTS OF AROMATIC-SUBSTITUTION, PHARMACOLOGICAL CHARACTERIZATION, AND BIOAVAILABILITY, Journal of medicinal chemistry, 41(3), 1998, pp. 358-378
SYNTHESIS AND EVALUATION OF A SERIES OF NOVEL 2-[(4-CHLOROPHENOXY)METHYL]BENZIMIDAZOLES AS SELECTIVE NEUROPEPTIDE-Y Y1 RECEPTOR ANTAGONISTS
Authors: ZARRINMAYEH H NUNES AM ORNSTEIN PL ZIMMERMAN DM ARNOLD MB SCHOBER DA GACKENHEIMER SL BRUNS RF HIPSKIND PA BRITTON TC CANTRELL BE GEHLERT DR
Citation: H. Zarrinmayeh et al., SYNTHESIS AND EVALUATION OF A SERIES OF NOVEL 2-[(4-CHLOROPHENOXY)METHYL]BENZIMIDAZOLES AS SELECTIVE NEUROPEPTIDE-Y Y1 RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 41(15), 1998, pp. 2709-2719
SORPTION AND DESORPTION RATES OF CARBON-TETRACHLORIDE AND 1,2-DICHLOROBENZENE TO 3 ORGANOBENTONITES AND A NATURAL PEAT SOIL
Authors: DEITSCH JJ SMITH JA ARNOLD MB BOLUS J
Citation: Jj. Deitsch et al., SORPTION AND DESORPTION RATES OF CARBON-TETRACHLORIDE AND 1,2-DICHLOROBENZENE TO 3 ORGANOBENTONITES AND A NATURAL PEAT SOIL, Environmental science & technology, 32(20), 1998, pp. 3169-3177
NAVELBINE (NVB) PLUS MITOMYCIN (MMC) OR MITOXANTRONE (MTZ) AS SALVAGEREGIMEN IN METASTATIC BREAST-CANCER (MBC) - A RANDOMIZED TRIAL
Authors: LOZANO M ARRIETA J POLERA J URANGA G BONICATTO S FERRO A MARTINEZ J ARNOLD MB ROSEMBROCK C BLOCK J
Citation: M. Lozano et al., NAVELBINE (NVB) PLUS MITOMYCIN (MMC) OR MITOXANTRONE (MTZ) AS SALVAGEREGIMEN IN METASTATIC BREAST-CANCER (MBC) - A RANDOMIZED TRIAL, European journal of cancer, 33, 1997, pp. 684-684
HIGHLY EFFICIENT AND PRACTICAL SYNTHESES OF LAVENDAMYCIN METHYL-ESTERAND RELATED NOVEL QUINOLINDIONES
Authors: BEHFOROUZ M HADDAD J CAI W ARNOLD MB MOHAMMADI F SOUSA AC HORN MA
Citation: M. Behforouz et al., HIGHLY EFFICIENT AND PRACTICAL SYNTHESES OF LAVENDAMYCIN METHYL-ESTERAND RELATED NOVEL QUINOLINDIONES, Journal of organic chemistry, 61(19), 1996, pp. 6552-6555
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
NAVELBINE (NVB) PLUS MITOMYCIN (MMC) OR MITOXANTRONE (MTZ) - A RANDOMIZED TRIAL IN ANTHRACYCLINE BREAST-CANCER RESISTANT (ABCR) PATIENTS - PRELIMINARY-REPORT
Authors: BONICATO S POLERA J MARTINEZ J ARNOLD MB ARRIETA J ARBOIT L FERRO A MARANTZ A LITOSKA S TRIGUBOFF E URANGA G FEIN L MURO H TRIGO M REALE M
Citation: S. Bonicato et al., NAVELBINE (NVB) PLUS MITOMYCIN (MMC) OR MITOXANTRONE (MTZ) - A RANDOMIZED TRIAL IN ANTHRACYCLINE BREAST-CANCER RESISTANT (ABCR) PATIENTS - PRELIMINARY-REPORT, European journal of cancer, 31A, 1995, pp. 358-358
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
CORRELATION OF COGNITIVE TEST-SCORES AND ADEQUACY OF TREATMENT IN ADOLESCENTS WITH CONGENITAL HYPOTHYROIDISM
Authors: ARNOLD MB BIGOS ST BRINK S BROWN J BROWN R BROWN T CAREY D CRAWFORD JD CRIGLER JF FAIX J FREDERICK D GENEL M GRUPPUSO P HADDOW JE HERMOS RJ LANDT K LARSEN PR LEE M LEVITZKY L MACCRACKEN J MAN E MARTHA P MITCHELL ML NAJJAR S ORSIN JM PACCIA J PAGE L RATZAN S REITER E RUBIN K SADEGHINEJAD A SENIOR B WAISBREN SE WORKMANDANIELS K KLEIN RZ
Citation: Mb. Arnold et al., CORRELATION OF COGNITIVE TEST-SCORES AND ADEQUACY OF TREATMENT IN ADOLESCENTS WITH CONGENITAL HYPOTHYROIDISM, The Journal of pediatrics, 124(3), 1994, pp. 383-387
STEREOSELECTIVE SYNTHESIS OF 6-SUBSTITUTED DECAHYDROISOQUINOLINE-3-CARBOXYLATES - INTERMEDIATES FOR THE PREPARATION OF CONFORMATIONALLY CONSTRAINED ACIDIC AMINO-ACIDS
Authors: ORNSTEIN PL AUGENSTEIN NK ARNOLD MB
Citation: Pl. Ornstein et al., STEREOSELECTIVE SYNTHESIS OF 6-SUBSTITUTED DECAHYDROISOQUINOLINE-3-CARBOXYLATES - INTERMEDIATES FOR THE PREPARATION OF CONFORMATIONALLY CONSTRAINED ACIDIC AMINO-ACIDS, Journal of organic chemistry, 59(25), 1994, pp. 7862-7869
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
AZOL-5-YL)ETHYL]DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID - A STRUCTURALLY NOVEL, SYSTEMICALLY ACTIVE, COMPETITIVE AMPA RECEPTOR ANTAGONIST
Authors: ORNSTEIN PL ARNOLD MB AUGENSTEIN NK LODGE D LEANDER JD SCHOEPP DD
Citation: Pl. Ornstein et al., AZOL-5-YL)ETHYL]DECAHYDROISOQUINOLINE-3-CARBOXYLIC ACID - A STRUCTURALLY NOVEL, SYSTEMICALLY ACTIVE, COMPETITIVE AMPA RECEPTOR ANTAGONIST, Journal of medicinal chemistry, 36(14), 1993, pp. 2046-2048
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