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Results: 1-10 |
Results: 10
THERAPEUTIC APPROACHES TO THE TREATMENT OF NEUROINFLAMMATORY DISEASES
Authors: HAYS SJ
Citation: Sj. Hays, THERAPEUTIC APPROACHES TO THE TREATMENT OF NEUROINFLAMMATORY DISEASES, Current pharmaceutical design, 4(4), 1998, pp. 335-348
2-AMINO-4H-3,1-BENZOXAZIN-4-ONES AS INHIBITORS OF C1R SERINE-PROTEASE
Authors: HAYS SJ CAPRATHE BW GILMORE JL AMIN N EMMERLING MR MICHAEL W NADIMPALLI R NATH R RASER KJ STAFFORD D WATSON D WANG K JAEN JC
Citation: Sj. Hays et al., 2-AMINO-4H-3,1-BENZOXAZIN-4-ONES AS INHIBITORS OF C1R SERINE-PROTEASE, Journal of medicinal chemistry, 41(7), 1998, pp. 1060-1067
ALZHEIMERS-DISEASE AND BETA-AMYLOID - PATENT ACTIVITY BETWEEN MAY 1995 AND JULY 1996
Authors: HAYS SJ
Citation: Sj. Hays, ALZHEIMERS-DISEASE AND BETA-AMYLOID - PATENT ACTIVITY BETWEEN MAY 1995 AND JULY 1996, Expert opinion on therapeutic patents, 6(10), 1996, pp. 1035-1046
SYNTHESIS AND EVALUATION OF 2-ARYL-4H-3,1-BENZOXAZIN-4-ONES AS C1R SERINE-PROTEASE INHIBITORS
Authors: GILMORE JL HAYS SJ CAPRATHE BW LEE C EMMERLING MR MICHAEL W JAEN JC
Citation: Jl. Gilmore et al., SYNTHESIS AND EVALUATION OF 2-ARYL-4H-3,1-BENZOXAZIN-4-ONES AS C1R SERINE-PROTEASE INHIBITORS, Bioorganic & medicinal chemistry letters, 6(6), 1996, pp. 679-682
AN ALPHA-MERCAPTOACRYLIC ACID-DERIVATIVE IS A SELECTIVE NONPEPTIDE CELL-PERMEABLE CALPAIN INHIBITOR AND IS NEUROPROTECTIVE
Authors: WANG KKW NATH R POSNER A RASER KJ BUROKERKILGORE M HAJIMOHAMMADREZA I PROBERT AW MARCOUX FW YE QH TAKANO E HATANAKA M MAKI M CANER H COLLINS JL FERGUS A LEE KS LUNNEY EA HAYS SJ YUEN PW
Citation: Kkw. Wang et al., AN ALPHA-MERCAPTOACRYLIC ACID-DERIVATIVE IS A SELECTIVE NONPEPTIDE CELL-PERMEABLE CALPAIN INHIBITOR AND IS NEUROPROTECTIVE, Proceedings of the National Academy of Sciences of the United Statesof America, 93(13), 1996, pp. 6687-6692
PREPARATION OF AN AUTOLYSIS-RESISTANT INTERLEUKIN-1-BETA CONVERTING-ENZYME MUTANT
Authors: DANG LC TALANIAN RV BANACH D HACKETT MC GILMORE JL HAYS SJ MANKOVICH JA BRADY KD
Citation: Lc. Dang et al., PREPARATION OF AN AUTOLYSIS-RESISTANT INTERLEUKIN-1-BETA CONVERTING-ENZYME MUTANT, Biochemistry, 35(47), 1996, pp. 14910-14916
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 PHENYLACETAMIDES AS SODIUM-CHANNEL BLOCKERS
Authors: ROUFOS I HAYS SJ DOOLEY DJ SCHWARZ RD CAMPBELL GW PROBERT AW
Citation: I. Roufos et al., SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF PHENYLACETAMIDES AS SODIUM-CHANNEL BLOCKERS, Journal of medicinal chemistry, 37(2), 1994, pp. 268-274
SPECIFIC BINDING OF THE NOVEL NA-SUBUNIT OF RAT-BRAIN NA+ CHANNELS( CHANNEL BLOCKER PD85,639 TO THE ALPHA)
Authors: THOMSEN W HAYS SJ HICKS JL SCHWARZ RD CATTERALL WA
Citation: W. Thomsen et al., SPECIFIC BINDING OF THE NOVEL NA-SUBUNIT OF RAT-BRAIN NA+ CHANNELS( CHANNEL BLOCKER PD85,639 TO THE ALPHA), Molecular pharmacology, 43(6), 1993, pp. 955-964
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
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