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A unified approach to systematic isosteric substitution for acidic groups and application to NMDA antagonists related to 2-amino-7-phosphonoheptanoate. [electronic resource] by
- Chenard, B L
- Lipinski, C A
- Dominy, B W
- Mena, E E
- Ronau, R T
- Butterfield, G C
- Marinovic, L C
- Pagnozzi, M
- Butler, T W
- Tsang, T
Producer: 19900406
In:
Journal of medicinal chemistry vol. 33
Availability: No items available.
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10.
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Characterization of the binding site for a novel class of noncompetitive alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor antagonists. [electronic resource] by
- Menniti, F S
- Chenard, B L
- Collins, M B
- Ducat, M F
- Elliott, M L
- Ewing, F E
- Huang, J I
- Kelly, K A
- Lazzaro, J T
- Pagnozzi, M J
- Weeks, J L
- Welch, W M
- White, W F
Producer: 20010118
In:
Molecular pharmacology vol. 58
Availability: No items available.
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11.
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(3R,4S)-3-[4-(4-fluorophenyl)-4-hydroxypiperidin-1-yl]chroman-4,7-diol: a conformationally restricted analogue of the NR2B subtype-selective NMDA antagonist (1S,2S)-1-(4-hydroxyphenyl)-2-(4-hydroxy-4-phenylpiperidino)- 1-propanol. [electronic resource] by
- Butler, T W
- Blake, J F
- Bordner, J
- Butler, P
- Chenard, B L
- Collins, M A
- DeCosta, D
- Ducat, M J
- Eisenhard, M E
- Menniti, F S
- Pagnozzi, M J
- Sands, S B
- Segelstein, B E
- Volberg, W
- White, W F
- Zhao, D
Producer: 19980504
In:
Journal of medicinal chemistry vol. 41
Availability: No items available.
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12.
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Atropisomeric quinazolin-4-one derivatives are potent noncompetitive alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists. [electronic resource] by
- Welch, W M
- Ewing, F E
- Huang, J
- Menniti, F S
- Pagnozzi, M J
- Kelly, K
- Seymour, P A
- Guanowsky, V
- Guhan, S
- Guinn, M R
- Critchett, D
- Lazzaro, J
- Ganong, A H
- DeVries, K M
- Staigers, T L
- Chenard, B L
Producer: 20010510
In:
Bioorganic & medicinal chemistry letters vol. 11
Availability: No items available.
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