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Results: 1-11 |
Results: 11
A new phase-switch method for application in organic synthesis programs employing immobilization through metal-chelated tagging
Authors: Ley, SV Massi, A Rodriguez, F Horwell, DC Lewthwaite, RA Pritchard, MC Reid, AM
Citation: Sv. Ley et al., A new phase-switch method for application in organic synthesis programs employing immobilization through metal-chelated tagging, ANGEW CHEM, 40(6), 2001, pp. 1053
Utilization of an intramolecular hydrogen bond to increase the CNS penetration of an NK1 receptor antagonist
Authors: Ashwood, VA Field, MJ Horwell, DC Julien-Larose, C Lewthwaite, RA McCleary, S Pritchard, MC Raphy, J Singh, L
Citation: Va. Ashwood et al., Utilization of an intramolecular hydrogen bond to increase the CNS penetration of an NK1 receptor antagonist, J MED CHEM, 44(14), 2001, pp. 2276-2285
Design and biological evaluation of non-peptide analogues of omega-conotoxin MVIIA
Authors: Menzler, S Bikker, JA Suman-Chauhan, N Horwell, DC
Citation: S. Menzler et al., Design and biological evaluation of non-peptide analogues of omega-conotoxin MVIIA, BIOORG MED, 10(4), 2000, pp. 345-347
The design and synthesis of the high efficacy, non-peptide CCK1 receptor agonist PD 170292
Authors: Bernad, N Burgaud, BGM Horwell, DC Lewthwaite, RA Martinez, J Pritchard, MC
Citation: N. Bernad et al., The design and synthesis of the high efficacy, non-peptide CCK1 receptor agonist PD 170292, BIOORG MED, 10(11), 2000, pp. 1245-1248
Dendroid peptide structural mimetics of omega-conotoxin MVIIA based on a 2(1H)-quinolinone core
Authors: Guo, ZX Cammidge, AN Horwell, DC
Citation: Zx. Guo et al., Dendroid peptide structural mimetics of omega-conotoxin MVIIA based on a 2(1H)-quinolinone core, TETRAHEDRON, 56(29), 2000, pp. 5169-5175
A convenient and versatile method for the synthesis of protected guanidines
Authors: Guo, ZX Cammidge, AN Horwell, DC
Citation: Zx. Guo et al., A convenient and versatile method for the synthesis of protected guanidines, SYN COMMUN, 30(16), 2000, pp. 2933-2943
An in vitro investigation into conformational aspects of gabapentin
Authors: Bryans, JS Horwell, DC Ratcliffe, GS Receveur, JM Rubin, JR
Citation: Js. Bryans et al., An in vitro investigation into conformational aspects of gabapentin, BIO MED CH, 7(5), 1999, pp. 715-721
Synthesis and biological evaluation of conformationally restricted Gabapentin analogues
Authors: Receveur, JM Bryans, JS Field, MJ Singh, L Horwell, DC
Citation: Jm. Receveur et al., Synthesis and biological evaluation of conformationally restricted Gabapentin analogues, BIOORG MED, 9(16), 1999, pp. 2329-2334
Generation of unnatural alpha,alpha-disubstituted amino acid derivatives from cyclic sulfamidates
Authors: Boulton, LT Stock, HT Raphy, J Horwell, DC
Citation: Lt. Boulton et al., Generation of unnatural alpha,alpha-disubstituted amino acid derivatives from cyclic sulfamidates, J CHEM S P1, (11), 1999, pp. 1421-1429
N- vs O-alkylation in 2(1H)-quinolinone derivatives
Authors: Guo, ZX Cammidge, AN McKillop, A Horwell, DC
Citation: Zx. Guo et al., N- vs O-alkylation in 2(1H)-quinolinone derivatives, TETRAHEDR L, 40(38), 1999, pp. 6999-7002
Design of non-peptide agonists and antagonists for neuropeptide receptors
Authors: Horwell, DC Pritchard, MC Raphy, J
Citation: Dc. Horwell et al., Design of non-peptide agonists and antagonists for neuropeptide receptors, ADV AMIN AC, 2, 1999, pp. 165-190
Risultati: 1-11 |