Results: 1-7 |
Results: 7
DISTRIBUTION OF TACRINE AND METABOLITES IN RAT-BRAIN AND PLASMA AFTERSINGLE-AND MULTIPLE-DOSE REGIMENS - EVIDENCE FOR ACCUMULATION OF TACRINE IN BRAIN-TISSUE
Authors: MCNALLY WP POOL WF SINZ MW DEHART P ORTWINE DF HUANG CC CHANG T WOOLF TF
Citation: Wp. Mcnally et al., DISTRIBUTION OF TACRINE AND METABOLITES IN RAT-BRAIN AND PLASMA AFTERSINGLE-AND MULTIPLE-DOSE REGIMENS - EVIDENCE FOR ACCUMULATION OF TACRINE IN BRAIN-TISSUE, Drug metabolism and disposition, 24(6), 1996, pp. 628-633
NOVEL SERIES OF ACHIRAL, LOW-MOLECULAR-WEIGHT, AND POTENT HIV-1 PROTEASE INHIBITORS
Authors: PRASAD JVNV PARA KS LUNNEY EA ORTWINE DF DUNBAR JB FERGUSON D TUMMINO PJ HUPE D TAIT BD DOMAGALA JM HUMBLET C BHAT TN LIU BS GUERIN DMA BALDWIN ET ERICKSON JW SAWYER TK
Citation: Jvnv. Prasad et al., NOVEL SERIES OF ACHIRAL, LOW-MOLECULAR-WEIGHT, AND POTENT HIV-1 PROTEASE INHIBITORS, Journal of the American Chemical Society, 116(15), 1994, pp. 6989-6990
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
SUBSTITUTED 2-BENZOTHIAZOLAMINE AS SODIUM FLUX INHIBITORS - QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS AND ANTICONVULSANT ACTIVITY
Authors: HAYS SJ RICE MJ ORTWINE DF JOHNSON G SCHWARZ RD BOYD DK COPELAND LF VARTANIAN MG BOXER PA
Citation: Sj. Hays et al., SUBSTITUTED 2-BENZOTHIAZOLAMINE AS SODIUM FLUX INHIBITORS - QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS AND ANTICONVULSANT ACTIVITY, Journal of pharmaceutical sciences, 83(10), 1994, pp. 1425-1432
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
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
X-RAY STRUCTURE OF A HYDROXAMATE INHIBITOR COMPLEX OF STROMELYSIN CATALYTIC DOMAIN AND ITS COMPARISON WITH MEMBERS OF THE ZINC METALLOPROTEINASE SUPERFAMILY
Authors: DHANARAJ V YE QZ JOHNSON LL HUPE DJ ORTWINE DF DUBAR JB RUBIN JR PAVLOVSKY A HUMBLET C BLUNDELL TL
Citation: V. Dhanaraj et al., X-RAY STRUCTURE OF A HYDROXAMATE INHIBITOR COMPLEX OF STROMELYSIN CATALYTIC DOMAIN AND ITS COMPARISON WITH MEMBERS OF THE ZINC METALLOPROTEINASE SUPERFAMILY, Structure, 4(4), 1996, pp. 375-386
Risultati: 1-7 |