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Results: 1-19 |
Results: 19
AN UNUSUAL BY-PRODUCT FROM A NONSYNCHRONOUS REACTION BETWEEN ETHYL 1,2,4-TRIAZINE-3-CARBOXYLATE AND AN ENAMINE
Authors: MACOR JE KUIPERS W LACHICOTTE RJ
Citation: Je. Macor et al., AN UNUSUAL BY-PRODUCT FROM A NONSYNCHRONOUS REACTION BETWEEN ETHYL 1,2,4-TRIAZINE-3-CARBOXYLATE AND AN ENAMINE, Chemical communications, (9), 1998, pp. 983-984
CHALLENGES AND OPPORTUNITIES FOR DEVELOPING MUSCARINIC RECEPTOR SUBTYPE-BASED THERAPEUTIC AGENTS - INTRODUCTION
Authors: BLOSSER JC MACOR JE MESSER MS
Citation: Jc. Blosser et al., CHALLENGES AND OPPORTUNITIES FOR DEVELOPING MUSCARINIC RECEPTOR SUBTYPE-BASED THERAPEUTIC AGENTS - INTRODUCTION, Drug development research, 40(2), 1997, pp. 101-103
SYNTHESIS AND REACTIVITY OF PYRROLO[3,2-E]INDOLE - REMOVAL OF A N-BOMGROUP FROM AN UNACTIVATED INDOLE
Authors: MACOR JE FORMAN JT POST RJ RYAN K
Citation: Je. Macor et al., SYNTHESIS AND REACTIVITY OF PYRROLO[3,2-E]INDOLE - REMOVAL OF A N-BOMGROUP FROM AN UNACTIVATED INDOLE, Tetrahedron letters, 38(10), 1997, pp. 1673-1676
A DIRECT SYNTHESIS OF 3-(PYRROLIDIN-3-YL)INDOLES FOR USE AS CONFORMATIONALLY RESTRICTED ANALOGS OF TRYPTAMINES
Authors: MACOR JE BLANK DH RYAN K POST RJ
Citation: Je. Macor et al., A DIRECT SYNTHESIS OF 3-(PYRROLIDIN-3-YL)INDOLES FOR USE AS CONFORMATIONALLY RESTRICTED ANALOGS OF TRYPTAMINES, Synthesis, (4), 1997, pp. 443
CP-135,807, A SELECTIVE 5-HT1D AGONIST - EFFECTS IN DRUG DISCRIMINATION AND PUNISHMENT PROCEDURES IN THE PIGEON
Authors: MANSBACH RS ROVETTI CC MACOR JE
Citation: Rs. Mansbach et al., CP-135,807, A SELECTIVE 5-HT1D AGONIST - EFFECTS IN DRUG DISCRIMINATION AND PUNISHMENT PROCEDURES IN THE PIGEON, Psychopharmacology, 128(3), 1996, pp. 313-319
AN IMPROVED SYNTHESIS OF THE UNIQUE ANTIMIGRAINE AGENT CP-122,288 - ABROMINE ATOM PASSENGER IN AN INTRAMOLECULAR HECK REACTION
Authors: MACOR JE OGILVIE RJ WYTHES MJ
Citation: Je. Macor et al., AN IMPROVED SYNTHESIS OF THE UNIQUE ANTIMIGRAINE AGENT CP-122,288 - ABROMINE ATOM PASSENGER IN AN INTRAMOLECULAR HECK REACTION, Tetrahedron letters, 37(25), 1996, pp. 4289-4292
5-CARBOXAMIDOTRYPTAMINE, CP-122,288, AND DIHYDROERGOTAMINE BUT NOT SUMATRIPTAN, CP-93,129, AND SEROTONIN-5-O-CARBOXYMETHYLGLYCYL-TYROSINAMIDE BLOCK DURAL PLASMA-PROTEIN EXTRAVASATION IN KNOCKOUT MICE THAT LACK5-HYDROXYTRYPTAMINE(1B) RECEPTORS (VOL 49, PG 761, 1996)
Authors: YU XJ WAEBER C CASTANON N SCEARCE K HEN R MACOR JE CHAUVEAU J MOSKOWITZ MA
Citation: Xj. Yu et al., 5-CARBOXAMIDOTRYPTAMINE, CP-122,288, AND DIHYDROERGOTAMINE BUT NOT SUMATRIPTAN, CP-93,129, AND SEROTONIN-5-O-CARBOXYMETHYLGLYCYL-TYROSINAMIDE BLOCK DURAL PLASMA-PROTEIN EXTRAVASATION IN KNOCKOUT MICE THAT LACK5-HYDROXYTRYPTAMINE(1B) RECEPTORS (VOL 49, PG 761, 1996), Molecular pharmacology, 50(4), 1996, pp. 1055-1055
5-CARBOXAMIDO-TRYPTAMINE, CP-122,288 AND DIHYDROERGOTAMINE BUT NOT SUMATRIPTAN, CP-93,129, AND SEROTONIN-5-O-CARBOXYMETHYL-GLYCYL-TYROSINAMIDE BLOCK DURAL PLASMA-PROTEIN EXTRAVASATION IN KNOCKOUT MICE THAT LACK 5-HYDROXYTRYPTAMINE(1B) RECEPTORS
Authors: YU XJ WAEBER C CASTANON N SCEARCE K HEN R MACOR JE CHAVEAU J MOSKOWITZ MA
Citation: Xj. Yu et al., 5-CARBOXAMIDO-TRYPTAMINE, CP-122,288 AND DIHYDROERGOTAMINE BUT NOT SUMATRIPTAN, CP-93,129, AND SEROTONIN-5-O-CARBOXYMETHYL-GLYCYL-TYROSINAMIDE BLOCK DURAL PLASMA-PROTEIN EXTRAVASATION IN KNOCKOUT MICE THAT LACK 5-HYDROXYTRYPTAMINE(1B) RECEPTORS, Molecular pharmacology, 49(5), 1996, pp. 761-765
SYNTHESIS AND USE OF 5-VINYL-1,2,4-OXADIAZOLES AS MICHAEL ACCEPTORS -A RAPID SYNTHESIS OF THE POTENT MUSCARINIC AGONIST L-670,548
Authors: MACOR JE ORDWAY T SMITH RL VERHOEST PR MACK RA
Citation: Je. Macor et al., SYNTHESIS AND USE OF 5-VINYL-1,2,4-OXADIAZOLES AS MICHAEL ACCEPTORS -A RAPID SYNTHESIS OF THE POTENT MUSCARINIC AGONIST L-670,548, Journal of organic chemistry, 61(10), 1996, pp. 3228-3229
O-1-[3-(N-METHYLPYRROLIDIN-2R-YLMETHYL)INDOL-5-YL] BENZIMIDAZOLE (CP-161,242) - A POTENT, CENTRALLY ACTIVE 5-HT1D RECEPTOR AGONIST AND BENZODIAZEPINE PARTIAL AGONIST
Authors: MACOR JE BLANK DH DESAI K FOX CB KOE BK LEBEL LA POST RJ SCHMIDT AW SCHULZ DW SEYMOUR PA
Citation: Je. Macor et al., O-1-[3-(N-METHYLPYRROLIDIN-2R-YLMETHYL)INDOL-5-YL] BENZIMIDAZOLE (CP-161,242) - A POTENT, CENTRALLY ACTIVE 5-HT1D RECEPTOR AGONIST AND BENZODIAZEPINE PARTIAL AGONIST, Bioorganic & medicinal chemistry letters, 5(20), 1995, pp. 2391-2396
THE DISCOVERY OF A NOVEL AND POTENT BENZODIAZEPINE RECEPTOR PHARMACOPHORE
Authors: MACOR JE BLAKE JF DESAI K POST RJ SCHMIDT AW
Citation: Je. Macor et al., THE DISCOVERY OF A NOVEL AND POTENT BENZODIAZEPINE RECEPTOR PHARMACOPHORE, Bioorganic & medicinal chemistry letters, 5(20), 1995, pp. 2397-2402
AN UNUSUAL BY-PRODUCT IN A CONCISE SYNTHESIS OF A ROTATIONALLY RESTRICTED PHENOLIC ANALOG OF SEROTONIN
Authors: MACOR JE
Citation: Je. Macor, AN UNUSUAL BY-PRODUCT IN A CONCISE SYNTHESIS OF A ROTATIONALLY RESTRICTED PHENOLIC ANALOG OF SEROTONIN, Tetrahedron letters, 36(39), 1995, pp. 7019-7022
THE IN-VIVO PHARMACOLOGICAL PROFILE OF A 5-HT1 RECEPTOR AGONIST, CP-122,288, A SELECTIVE INHIBITOR OF NEUROGENIC INFLAMMATION
Authors: GUPTA P BROWN D BUTLER P ELLIS P GRAYSON KL LAND GC MACOR JE ROBSON SF WYTHES MJ SHEPPERSON NB
Citation: P. Gupta et al., THE IN-VIVO PHARMACOLOGICAL PROFILE OF A 5-HT1 RECEPTOR AGONIST, CP-122,288, A SELECTIVE INHIBITOR OF NEUROGENIC INFLAMMATION, British Journal of Pharmacology, 116(5), 1995, pp. 2385-2390
THE IN-VIVO PHARMACOLOGICAL PROFILE OF CP-122,288, A SELECTIVE INHIBITOR OF NEUROGENIC INFLAMMATION
Authors: GUPTA P BUTLER P ELLIS P GRAYSON KL LAND GC MACOR JE ROBSON SF SHEPPERSON NB WYTHES MJ
Citation: P. Gupta et al., THE IN-VIVO PHARMACOLOGICAL PROFILE OF CP-122,288, A SELECTIVE INHIBITOR OF NEUROGENIC INFLAMMATION, British Journal of Pharmacology, 115, 1995, pp. 7-7
A SHORT SYNTHESIS OF A CONFORMATIONALLY RESTRICTED ANALOG OF THE NEUROTRANSMITTER SEROTONIN WITH REDUCED BASICITY
Authors: MACOR JE RYAN K
Citation: Je. Macor et K. Ryan, A SHORT SYNTHESIS OF A CONFORMATIONALLY RESTRICTED ANALOG OF THE NEUROTRANSMITTER SEROTONIN WITH REDUCED BASICITY, Heterocycles, 37(3), 1994, pp. 1447-1450
DOPAMINE UPTAKE INHIBITORY ACTIVITY OF NOVEL TRYPTAMINE 5-HT, RECEPTOR LIGANDS
Authors: LEBEL LA NOWAKOWSKI JT MACOR JE FOX CB KOE BK
Citation: La. Lebel et al., DOPAMINE UPTAKE INHIBITORY ACTIVITY OF NOVEL TRYPTAMINE 5-HT, RECEPTOR LIGANDS, Drug development research, 33(4), 1994, pp. 413-421
THE SYNTHESIS OF CONFORMATIONALLY ROTATIONALLY RESTRICTED ANALOGS OF THE NEUROTRANSMITTER SEROTONIN
Authors: MACOR JE BLANK DH POST RJ
Citation: Je. Macor et al., THE SYNTHESIS OF CONFORMATIONALLY ROTATIONALLY RESTRICTED ANALOGS OF THE NEUROTRANSMITTER SEROTONIN, Tetrahedron letters, 35(1), 1994, pp. 45-48
USE OF 2,5-DIMETHYLPYRROLE AS AN AMINO-PROTECTING GROUP IN AN EFFICIENT SYNTHESIS OF MINO-3-[(N-METHYL-PYRROLIDIN-2(R)-YL)METHYL]INDOLE
Authors: MACOR JE CHENARD BL POST RJ
Citation: Je. Macor et al., USE OF 2,5-DIMETHYLPYRROLE AS AN AMINO-PROTECTING GROUP IN AN EFFICIENT SYNTHESIS OF MINO-3-[(N-METHYL-PYRROLIDIN-2(R)-YL)METHYL]INDOLE, Journal of organic chemistry, 59(24), 1994, pp. 7496-7498
5-[(3-NITROPYRID-2-YL)AMINO]INDOLES - NOVEL SEROTONIN AGONISTS WITH SELECTIVITY FOR THE 5-HT1D RECEPTOR - VARIATION OF THE C3 SUBSTITUENT ON THE INDOLE TEMPLATE LEADS TO INCREASED 5-HT1D RECEPTOR SELECTIVITY
Authors: MACOR JE BLANK DH FOX CB LEBEL LA NEWMAN ME POST RJ RYAN K SCHMIDT AW SCHULZ DW KOE BK
Citation: Je. Macor et al., 5-[(3-NITROPYRID-2-YL)AMINO]INDOLES - NOVEL SEROTONIN AGONISTS WITH SELECTIVITY FOR THE 5-HT1D RECEPTOR - VARIATION OF THE C3 SUBSTITUENT ON THE INDOLE TEMPLATE LEADS TO INCREASED 5-HT1D RECEPTOR SELECTIVITY, Journal of medicinal chemistry, 37(16), 1994, pp. 2509-2512
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