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STRUCTURAL REQUIREMENTS FOR THE DEVELOPMENT OF POTENT N-METHYL-D-ASPARTIC ACID (NMDA) RECEPTOR ANTAGONISTS
被引:49
作者
:
BIGGE, CF
论文数:
0
引用数:
0
h-index:
0
BIGGE, CF
机构
:
来源
:
BIOCHEMICAL PHARMACOLOGY
|
1993年
/ 45卷
/ 08期
关键词
:
D O I
:
10.1016/0006-2952(93)90294-7
中图分类号
:
R9 [药学];
学科分类号
:
1007 ;
摘要
:
引用
收藏
页码:1547 / 1561
页数:15
相关论文
共 84 条
[1]
SYNTHESIS AND NMDA ANTAGONISTIC PROPERTIES OF THE ENANTIOMERS OF 4-(3-PHOSPHONOPROPYL)PIPERAZINE-2-CARBOXYLIC ACID (CPP) AND OF THE UNSATURATED ANALOG (E)-4-(3-PHOSPHONOPROP-2-ENYL)PIPERAZINE-2-CARBOXYLIC ACID (CPP-ENE)
AEBISCHER, B
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
AEBISCHER, B
FREY, P
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
FREY, P
HAERTER, HP
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
HAERTER, HP
HERRLING, PL
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
HERRLING, PL
MUELLER, W
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
MUELLER, W
OLVERMAN, HJ
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
OLVERMAN, HJ
WATKINS, JC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
WATKINS, JC
[J].
HELVETICA CHIMICA ACTA,
1989,
72
(05)
: 1043
-
1051
[2]
N-METHYL-D-ASPARTATE ANTAGONISTS - READY FOR CLINICAL-TRIAL IN BRAIN ISCHEMIA
ALBERS, GW
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
ALBERS, GW
GOLDBERG, MP
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
GOLDBERG, MP
CHOI, DW
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
CHOI, DW
[J].
ANNALS OF NEUROLOGY,
1989,
25
(04)
: 398
-
403
[3]
KINETIC-ANALYSIS OF ANTAGONIST ACTION AT N-METHYL-D-ASPARTIC ACID RECEPTORS - 2 BINDING-SITES EACH FOR GLUTAMATE AND GLYCINE
BENVENISTE, M
论文数:
0
引用数:
0
h-index:
0
机构:
Unit of Neurophysiology and Biophysics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland
BENVENISTE, M
MAYER, ML
论文数:
0
引用数:
0
h-index:
0
机构:
Unit of Neurophysiology and Biophysics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland
MAYER, ML
[J].
BIOPHYSICAL JOURNAL,
1991,
59
(03)
: 560
-
573
[4]
EXPLORATION OF N-PHOSPHONOALKYL-SPACED, N-PHOSPHONOALKENYL-SPACED, AND N-(PHOSPHONOALKYL)PHENYL-SPACED ALPHA-AMINO-ACIDS AS COMPETITIVE N-METHYL-D-ASPARTIC ACID ANTAGONISTS
BIGGE, CF
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
BIGGE, CF
JOHNSON, G
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
JOHNSON, G
ORTWINE, DF
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
ORTWINE, DF
DRUMMOND, JT
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
DRUMMOND, JT
RETZ, DM
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
RETZ, DM
BRAHCE, LJ
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
BRAHCE, LJ
COUGHENOUR, LL
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
COUGHENOUR, LL
MARCOUX, FW
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
MARCOUX, FW
PROBERT, AW
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
PROBERT, AW
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1992,
35
(08)
: 1371
-
1384
[5]
BIGGE CF, 1992, MULTIPLE SIGMA PCP R, P1
[6]
CARTER CJ, 1990, J PHARMACOL EXP THER, V253, P475
[7]
PROTEIN-KINASE-C REDUCES MG2+ BLOCK OF NMDA-RECEPTOR CHANNELS AS A MECHANISM OF MODULATION
CHEN, L
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV TEXAS, MED BRANCH, INST MARINE BIOMED, GALVESTON, TX 77550 USA
CHEN, L
HUANG, LYM
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV TEXAS, MED BRANCH, INST MARINE BIOMED, GALVESTON, TX 77550 USA
HUANG, LYM
[J].
NATURE,
1992,
356
(6369)
: 521
-
523
[8]
EVALUATION OF A COMPETITIVE NMDA ANTAGONIST (D-CPPENE) IN FELINE FOCAL CEREBRAL-ISCHEMIA
CHEN, M
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
CHEN, M
BULLOCK, R
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
BULLOCK, R
GRAHAM, DI
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
GRAHAM, DI
FREY, P
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
FREY, P
LOWE, D
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
LOWE, D
MCCULLOCH, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
MCCULLOCH, J
[J].
ANNALS OF NEUROLOGY,
1991,
30
(01)
: 62
-
70
[9]
SEPARATION OF ALPHA-1 ADRENERGIC AND N-METHYL-D-ASPARTATE ANTAGONIST ACTIVITY IN A SERIES OF IFENPRODIL COMPOUNDS
CHENARD, BL
论文数:
0
引用数:
0
h-index:
0
机构:
Central Research Division, Pfizer Inc., Groton
CHENARD, BL
SHALABY, IA
论文数:
0
引用数:
0
h-index:
0
机构:
Central Research Division, Pfizer Inc., Groton
SHALABY, IA
KOE, BK
论文数:
0
引用数:
0
h-index:
0
机构:
Central Research Division, Pfizer Inc., Groton
KOE, BK
RONAU, RT
论文数:
0
引用数:
0
h-index:
0
机构:
Central Research Division, Pfizer Inc., Groton
RONAU, RT
BUTLER, TW
论文数:
0
引用数:
0
h-index:
0
机构:
Central Research Division, Pfizer Inc., Groton
BUTLER, TW
PROCHNIAK, MA
论文数:
0
引用数:
0
h-index:
0
机构:
Central Research Division, Pfizer Inc., Groton
PROCHNIAK, MA
SCHMIDT, AW
论文数:
0
引用数:
0
h-index:
0
机构:
Central Research Division, Pfizer Inc., Groton
SCHMIDT, AW
FOX, CB
论文数:
0
引用数:
0
h-index:
0
机构:
Central Research Division, Pfizer Inc., Groton
FOX, CB
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1991,
34
(10)
: 3085
-
3090
[10]
EXCITATORY AMINO-ACID RECEPTORS AND SYNAPTIC PLASTICITY
COLLINGRIDGE, GL
论文数:
0
引用数:
0
h-index:
0
机构:
MAX PLANCK INST BRAIN RES,NEUROPHYSIOL,W-6000 FRANKFURT 71,GERMANY
MAX PLANCK INST BRAIN RES,NEUROPHYSIOL,W-6000 FRANKFURT 71,GERMANY
COLLINGRIDGE, GL
SINGER, W
论文数:
0
引用数:
0
h-index:
0
机构:
MAX PLANCK INST BRAIN RES,NEUROPHYSIOL,W-6000 FRANKFURT 71,GERMANY
MAX PLANCK INST BRAIN RES,NEUROPHYSIOL,W-6000 FRANKFURT 71,GERMANY
SINGER, W
[J].
TRENDS IN PHARMACOLOGICAL SCIENCES,
1990,
11
(07)
: 290
-
296
←
1
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共 84 条
[1]
SYNTHESIS AND NMDA ANTAGONISTIC PROPERTIES OF THE ENANTIOMERS OF 4-(3-PHOSPHONOPROPYL)PIPERAZINE-2-CARBOXYLIC ACID (CPP) AND OF THE UNSATURATED ANALOG (E)-4-(3-PHOSPHONOPROP-2-ENYL)PIPERAZINE-2-CARBOXYLIC ACID (CPP-ENE)
AEBISCHER, B
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
AEBISCHER, B
FREY, P
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
FREY, P
HAERTER, HP
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
HAERTER, HP
HERRLING, PL
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
HERRLING, PL
MUELLER, W
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
MUELLER, W
OLVERMAN, HJ
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
OLVERMAN, HJ
WATKINS, JC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
WATKINS, JC
[J].
HELVETICA CHIMICA ACTA,
1989,
72
(05)
: 1043
-
1051
[2]
N-METHYL-D-ASPARTATE ANTAGONISTS - READY FOR CLINICAL-TRIAL IN BRAIN ISCHEMIA
ALBERS, GW
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
ALBERS, GW
GOLDBERG, MP
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
GOLDBERG, MP
CHOI, DW
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
CHOI, DW
[J].
ANNALS OF NEUROLOGY,
1989,
25
(04)
: 398
-
403
[3]
KINETIC-ANALYSIS OF ANTAGONIST ACTION AT N-METHYL-D-ASPARTIC ACID RECEPTORS - 2 BINDING-SITES EACH FOR GLUTAMATE AND GLYCINE
BENVENISTE, M
论文数:
0
引用数:
0
h-index:
0
机构:
Unit of Neurophysiology and Biophysics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland
BENVENISTE, M
MAYER, ML
论文数:
0
引用数:
0
h-index:
0
机构:
Unit of Neurophysiology and Biophysics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland
MAYER, ML
[J].
BIOPHYSICAL JOURNAL,
1991,
59
(03)
: 560
-
573
[4]
EXPLORATION OF N-PHOSPHONOALKYL-SPACED, N-PHOSPHONOALKENYL-SPACED, AND N-(PHOSPHONOALKYL)PHENYL-SPACED ALPHA-AMINO-ACIDS AS COMPETITIVE N-METHYL-D-ASPARTIC ACID ANTAGONISTS
BIGGE, CF
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
BIGGE, CF
JOHNSON, G
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
JOHNSON, G
ORTWINE, DF
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
ORTWINE, DF
DRUMMOND, JT
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
DRUMMOND, JT
RETZ, DM
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
RETZ, DM
BRAHCE, LJ
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
BRAHCE, LJ
COUGHENOUR, LL
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
COUGHENOUR, LL
MARCOUX, FW
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
MARCOUX, FW
PROBERT, AW
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor
PROBERT, AW
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1992,
35
(08)
: 1371
-
1384
[5]
BIGGE CF, 1992, MULTIPLE SIGMA PCP R, P1
[6]
CARTER CJ, 1990, J PHARMACOL EXP THER, V253, P475
[7]
PROTEIN-KINASE-C REDUCES MG2+ BLOCK OF NMDA-RECEPTOR CHANNELS AS A MECHANISM OF MODULATION
CHEN, L
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV TEXAS, MED BRANCH, INST MARINE BIOMED, GALVESTON, TX 77550 USA
CHEN, L
HUANG, LYM
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV TEXAS, MED BRANCH, INST MARINE BIOMED, GALVESTON, TX 77550 USA
HUANG, LYM
[J].
NATURE,
1992,
356
(6369)
: 521
-
523
[8]
EVALUATION OF A COMPETITIVE NMDA ANTAGONIST (D-CPPENE) IN FELINE FOCAL CEREBRAL-ISCHEMIA
CHEN, M
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
CHEN, M
BULLOCK, R
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
BULLOCK, R
GRAHAM, DI
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
GRAHAM, DI
FREY, P
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
FREY, P
LOWE, D
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
LOWE, D
MCCULLOCH, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
UNIV GLASGOW,WELLCOME NEUROSCI GRP,GARSCUBE ESTATE,BEARSDEN RD,GLASGOW G61 1QH,SCOTLAND
MCCULLOCH, J
[J].
ANNALS OF NEUROLOGY,
1991,
30
(01)
: 62
-
70
[9]
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机构:
Central Research Division, Pfizer Inc., Groton
CHENARD, BL
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Central Research Division, Pfizer Inc., Groton
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Central Research Division, Pfizer Inc., Groton
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RONAU, RT
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机构:
Central Research Division, Pfizer Inc., Groton
BUTLER, TW
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机构:
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PROCHNIAK, MA
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0
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机构:
Central Research Division, Pfizer Inc., Groton
SCHMIDT, AW
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MAX PLANCK INST BRAIN RES,NEUROPHYSIOL,W-6000 FRANKFURT 71,GERMANY
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机构:
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