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Results: 1-10 |
Results: 10
Conformationally restricted PACAP27 analogues incorporating type II/II ' IBTM beta-turn mimetics. Synthesis, NMR structure determination, and bindingaffinity
Authors: Gonzalez-Muniz, R Martin-Martinez, M Granata, C de Oliveira, E Santiveri, CM Gonzalez, C Frechilla, D Herranz, R Garcia-Lopez, MT Del Rio, J Jimenez, MA Andreu, D
Citation: R. Gonzalez-muniz et al., Conformationally restricted PACAP27 analogues incorporating type II/II ' IBTM beta-turn mimetics. Synthesis, NMR structure determination, and bindingaffinity, BIO MED CH, 9(12), 2001, pp. 3173-3183
Entry to new conformationally constrained amino acids. First synthesis of 3-unsubstituted 4-alkyl-4-carboxy-2-azetidinone derivatives via an intramolecular N-alpha-C-alpha-cyclization strategy
Authors: Gerona-Navarro, G Bonache, MA Herranz, R Garcia-Lopez, MT Gonzalez-Muniz, R
Citation: G. Gerona-navarro et al., Entry to new conformationally constrained amino acids. First synthesis of 3-unsubstituted 4-alkyl-4-carboxy-2-azetidinone derivatives via an intramolecular N-alpha-C-alpha-cyclization strategy, J ORG CHEM, 66(10), 2001, pp. 3538-3547
5-(tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c] pyrimidine-based potentand selective CCK1 receptor antagonists: Structure-activity relationship studies on the central 1,3-dioxoperhydropyrido[1,2-c]pyrimidine scaffold
Authors: Bartolome-Nebreda, JM Garcia-Lopez, MT Gonzalez-Muniz, R Cenarruzabeitia, E Latorre, M Del Rio, J Herranz, R
Citation: Jm. Bartolome-nebreda et al., 5-(tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c] pyrimidine-based potentand selective CCK1 receptor antagonists: Structure-activity relationship studies on the central 1,3-dioxoperhydropyrido[1,2-c]pyrimidine scaffold, J MED CHEM, 44(24), 2001, pp. 4196-4206
5-(tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c]pyrimidine-based potent and selective CCK1 receptor antagonists: Structure-activity relationship studies on the substituent at N2-position
Authors: Bartolome-Nebreda, JM Patino-Molina, R Martin-Martinez, M Gomez-Monterrey, I Garcia-Lopez, MT Gonzalez-Muniz, R Cenarruzabeitia, E Latorre, M Del Rio, J Herranz, R
Citation: Jm. Bartolome-nebreda et al., 5-(tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c]pyrimidine-based potent and selective CCK1 receptor antagonists: Structure-activity relationship studies on the substituent at N2-position, J MED CHEM, 44(13), 2001, pp. 2219-2228
New conformationally constrained tryptophans by N-alpha-C-alpha-cyclization to an azetidin-2-one core
Authors: Gerona-Navarro, G Bonache, MA Herranz, R Garcia-Lopez, MT Gonzalez-Muniz, R
Citation: G. Gerona-navarro et al., New conformationally constrained tryptophans by N-alpha-C-alpha-cyclization to an azetidin-2-one core, SYNLETT, (9), 2000, pp. 1249-1252
beta-turned dipeptoids as potent and selective CCK1 receptor antagonists
Authors: Martin-Martinez, M De la Figuera, N Latorre, M Herranz, R Garcia-Lopez, MT Cenarruzabeitia, E Del Rio, J Gonzalez-Muniz, R
Citation: M. Martin-martinez et al., beta-turned dipeptoids as potent and selective CCK1 receptor antagonists, J MED CHEM, 43(20), 2000, pp. 3770-3777
Highly constrained dipeptoid analogues containing a type II ' beta-turn mimic as novel and selective CCK-A receptor ligands
Authors: de la Figuera, N Martin-Martinez, M Herranz, R Garcia-Lopez, MT Latorre, M Cenarruzabeitia, E del Rio, J Gonzalez-Muniz, R
Citation: N. De La Figuera et al., Highly constrained dipeptoid analogues containing a type II ' beta-turn mimic as novel and selective CCK-A receptor ligands, BIOORG MED, 9(1), 1999, pp. 43-48
New scaffolds for peptidomimetics. Synthetic approaches towards 2,4-dioxooctahydropyrimido[1 ',6 ': 1,2]pyrido[3,4-b]-indole-6-carboxylic acid derivatives
Authors: De la Figuera, N Garcia-Lopez, MT Herranz, R Gonzalez-Muniz, R
Citation: N. De La Figuera et al., New scaffolds for peptidomimetics. Synthetic approaches towards 2,4-dioxooctahydropyrimido[1 ',6 ': 1,2]pyrido[3,4-b]-indole-6-carboxylic acid derivatives, HETEROCYCLE, 51(2), 1999, pp. 265-280
Stereoselective reductive amination of beta-keto esters derived from dipeptides. Stereochemical and mechanistic studies on the formation of 5-carboxymethyl-2-oxopiperazine derivatives
Authors: Patino-Molina, R Herranz, R Garcia-Lopez, T Gonzalez-Muniz, R
Citation: R. Patino-molina et al., Stereoselective reductive amination of beta-keto esters derived from dipeptides. Stereochemical and mechanistic studies on the formation of 5-carboxymethyl-2-oxopiperazine derivatives, TETRAHEDRON, 55(52), 1999, pp. 15001-15010
5-(Tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c]pyrimidine-based potent and selective CCK1 receptor antagonists: Structural modifications at the tryptophan domain
Authors: Bartolome-Nebreda, JM Gomez-Monterrey, I Garcia-Lopez, MT Gonzalez-Muniz, R Martin-Martinez, M Ballaz, S Cenarruzabeitia, E LaTorre, M Del Rio, J Herranz, R
Citation: Jm. Bartolome-nebreda et al., 5-(Tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c]pyrimidine-based potent and selective CCK1 receptor antagonists: Structural modifications at the tryptophan domain, J MED CHEM, 42(22), 1999, pp. 4659-4668
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