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Results: 1-11 |
Results: 11
DEVELOPMENT AND VALIDATION OF A RADIOIMMUNOASSAY FOR PD 152247 (PNQX)EQUIVALENT CONCENTRATIONS IN RAT-BRAIN MICRODIALYSATE FLUID
Authors: BARKSDALE CM NORDBLOM GD DUDECK RC WELTY DF JORDAN S BIGGE CF YI CS
Citation: Cm. Barksdale et al., DEVELOPMENT AND VALIDATION OF A RADIOIMMUNOASSAY FOR PD 152247 (PNQX)EQUIVALENT CONCENTRATIONS IN RAT-BRAIN MICRODIALYSATE FLUID, Journal of clinical ligand assay, 21(3), 1998, pp. 324-330
MECHANISMS OF NEURONAL CELL INJURY DEATH AND TARGETS FOR DRUG INTERVENTION/
Authors: BOXER PA BIGGE CF
Citation: Pa. Boxer et Cf. Bigge, MECHANISMS OF NEURONAL CELL INJURY DEATH AND TARGETS FOR DRUG INTERVENTION/, Drug discovery today, 2(6), 1997, pp. 219-228
AMPA RECEPTOR AGONISTS, ANTAGONISTS AND MODULATORS - THEIR POTENTIAL FOR CLINICAL UTILITY
Authors: BIGGE CF NIKAM SS
Citation: Cf. Bigge et Ss. Nikam, AMPA RECEPTOR AGONISTS, ANTAGONISTS AND MODULATORS - THEIR POTENTIAL FOR CLINICAL UTILITY, Expert opinion on therapeutic patents, 7(10), 1997, pp. 1099-1114
SYNTHESIS OF N-DESMETHYL PNQX - ELABORATION INTO AN IMMUNOGENIC CONJUGATE AND A RADIOIODINATED LIGAND - RADIOIMMUNOASSAY FOR THE AMPA NMDA ANTAGONIST, PNQX/
Authors: BIGGE CF YI CS NORDBLOM GD
Citation: Cf. Bigge et al., SYNTHESIS OF N-DESMETHYL PNQX - ELABORATION INTO AN IMMUNOGENIC CONJUGATE AND A RADIOIODINATED LIGAND - RADIOIMMUNOASSAY FOR THE AMPA NMDA ANTAGONIST, PNQX/, Bioorganic & medicinal chemistry letters, 7(15), 1997, pp. 1979-1984
SYNTHESIS OF -METHYL-6-NITROPYRIDO[3,4-F]-QUINOXALINE-2,3-DIONE AND RELATED QUINOXALINEDIONES - CHARACTERIZATION OF LPHA-AMINO-3-HYDROXY-5-METHYL-4-ISOXAZOLEPROPIONIC ACID (AND N-METHYL-D-ASPARTATE) RECEPTOR AND ANTICONVULSANT ACTIVITY
Authors: BIGGE CF MALONE TC BOXER PA NELSON CB ORTWINE DF SCHELKUN RM RETZ DM LESCOSKY LJ BOROSKY SA VARTANIAN MG SCHWARZ RD CAMPBELL GW ROBICHAUD LJ WATJEN F
Citation: Cf. Bigge et al., SYNTHESIS OF -METHYL-6-NITROPYRIDO[3,4-F]-QUINOXALINE-2,3-DIONE AND RELATED QUINOXALINEDIONES - CHARACTERIZATION OF LPHA-AMINO-3-HYDROXY-5-METHYL-4-ISOXAZOLEPROPIONIC ACID (AND N-METHYL-D-ASPARTATE) RECEPTOR AND ANTICONVULSANT ACTIVITY, Journal of medicinal chemistry, 38(19), 1995, pp. 3720-3740
POTENT, ORALLY-ACTIVE, COMPETITIVE N-METHYL-D-ASPARTATE (NMDA) RECEPTOR ANTAGONISTS ARE SUBSTRATES FOR A NEUTRAL AMINO-ACID-UPTAKE SYSTEM IN CHINESE-HAMSTER OVARY CELLS
Authors: LI JH BIGGE CF WILLIAMSON RM BOROSKY SA VARTANIAN MG ORTWINE DF
Citation: Jh. Li et al., POTENT, ORALLY-ACTIVE, COMPETITIVE N-METHYL-D-ASPARTATE (NMDA) RECEPTOR ANTAGONISTS ARE SUBSTRATES FOR A NEUTRAL AMINO-ACID-UPTAKE SYSTEM IN CHINESE-HAMSTER OVARY CELLS, Journal of medicinal chemistry, 38(11), 1995, pp. 1955-1965
NS-257 L-2-OXOBENZO[2,1-B-3,4-C']DIPYRROLE-5-SULFONAMIDE) IS A POTENT, SYSTEMICALLY ACTIVE AMPA RECEPTOR ANTAGONIST
Authors: WATJEN F BIGGE CF JENSEN LH BOXER PA LESCOSKY LJ NIELSEN EO MALONE TC CAMPBELL GW COUGHENOUR LL ROCK DM DREJER J MARCOUX FW
Citation: F. Watjen et al., NS-257 L-2-OXOBENZO[2,1-B-3,4-C']DIPYRROLE-5-SULFONAMIDE) IS A POTENT, SYSTEMICALLY ACTIVE AMPA RECEPTOR ANTAGONIST, Bioorganic & medicinal chemistry letters, 4(2), 1994, pp. 371-376
PHOTOISOMERIZATION MECHANISM OF THE RHODOPSIN CHROMOPHORE - PICOSECOND PHOTOLYSIS OF PIGMENT CONTAINING 11-CIS-LOCKED 8-MEMBERED RING RETINAL
Authors: MIZUKAMI T KANDORI H SHICHIDA Y CHEN AH DERGUINI F CALDWELL CG BIGGE CF NAKANISHI K YOSHIZAWA T
Citation: T. Mizukami et al., PHOTOISOMERIZATION MECHANISM OF THE RHODOPSIN CHROMOPHORE - PICOSECOND PHOTOLYSIS OF PIGMENT CONTAINING 11-CIS-LOCKED 8-MEMBERED RING RETINAL, Proceedings of the National Academy of Sciences of the United Statesof America, 90(9), 1993, pp. 4072-4076
SYNTHESIS OF RETINALS WITH 8-MEMBERED AND 9-MEMBERED RINGS IN THE SIDE-CHAIN - MODELS FOR RHODOPSIN PHOTOBLEACHING INTERMEDIATES
Authors: CALDWELL CG DERGUINI F BIGGE CF CHEN AH HU SH WANG J SASTRY L NAKANISHI K
Citation: Cg. Caldwell et al., SYNTHESIS OF RETINALS WITH 8-MEMBERED AND 9-MEMBERED RINGS IN THE SIDE-CHAIN - MODELS FOR RHODOPSIN PHOTOBLEACHING INTERMEDIATES, Journal of organic chemistry, 58(13), 1993, pp. 3533-3537
SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF 4A-PHENANTHRENAMINE DERIVATIVES ACTING AT THE PHENCYCLIDINE BINDING-SITE OF THE N-METHYL-D-ASPARTATE RECEPTOR COMPLEX
Authors: BIGGE CF MALONE TC HAYS SJ JOHNSON G NOVAK PM LESCOSKY LJ RETZ DM ORTWINE DF PROBERT AW COUGHENOUR LL BOXER PA ROBICHAUD LJ BRAHCE LJ SHILLIS JL
Citation: Cf. Bigge et al., SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF 4A-PHENANTHRENAMINE DERIVATIVES ACTING AT THE PHENCYCLIDINE BINDING-SITE OF THE N-METHYL-D-ASPARTATE RECEPTOR COMPLEX, Journal of medicinal chemistry, 36(14), 1993, pp. 1977-1995
STRUCTURAL REQUIREMENTS FOR THE DEVELOPMENT OF POTENT N-METHYL-D-ASPARTIC ACID (NMDA) RECEPTOR ANTAGONISTS
Authors: BIGGE CF
Citation: Cf. Bigge, STRUCTURAL REQUIREMENTS FOR THE DEVELOPMENT OF POTENT N-METHYL-D-ASPARTIC ACID (NMDA) RECEPTOR ANTAGONISTS, Biochemical pharmacology, 45(8), 1993, pp. 1547-1561
Risultati: 1-11 |