R. González-Muñiz

发表

De novo designed library of linear helical peptides: an exploratory tool in the discovery of protein-protein interaction modulators.

M. Martín-Martínez, I. Gomez-Monterrey, M. Bonache, 2014, ACS combinatorial science.

Peptides in biology and biomedicine: Walking towards the future.

R. González-Muñiz, M. Jiménez, 2019, Archives of biochemistry and biophysics.

2-Alkyl-2-carboxy-azetidines as scaffolds for the induction of γ-turns

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2007 .

Stereoselective synthesis of amino acid-derived β-lactams. Experimental evidence for TADDOL as a memory of chirality enhancer

M. Martín-Martínez, M. Bonache, M. García-López, 2006 .

Modulating Protein–Protein Interactions by Cyclic and Macrocyclic Peptides. Prominent Strategies and Examples

M. Bonache, R. González-Muñiz, M. J. Pérez de Vega, 2021, Molecules.

Exploring the binding pocket for pyridopyrimidine ligands at the CCK1 receptor by molecular docking

M. Martín-Martínez, B. Maigret, R. González-Muñiz, 2008, Journal of molecular modeling.

Solid-phase synthesis of a library of amphipatic hydantoins. Discovery of new hits for TRPV1 blockade.

J. González-Ros, F. Albericio, A. Fernández-Carvajal, 2011, ACS combinatorial science.

Advances in the Development of Non-steroidal Mineralocorticoid-receptor Antagonists

M. Martín-Martínez, R. González-Muñiz, Y. Rodríguez, 2019 .

Advances in the Development of Non-steroidal Mineralocorticoid-receptor Antagonists

M. Martín-Martínez, R. González-Muñiz, Y. Rodríguez, 2019, Aldosterone-Mineralocorticoid Receptor - Cell Biology to Translational Medicine.

Modulating Mineralocorticoid Receptor with Non-steroidal Antagonists. New Opportunities for the Development of Potent and Selective Ligands without Off-Target Side Effects.

M. Martín-Martínez, Ming-Ming Zhou, R. González-Muñiz, 2017, Journal of medicinal chemistry.

Highly Functionalized 1,2–Diamino Compounds through Reductive Amination of Amino Acid-Derived β–Keto Esters

J. González-Ros, A. Fernández-Carvajal, A. Ferrer-Montiel, 2013, PloS one.

Analogues of the neuroprotective tripeptide Gly-Pro-Glu (GPE): synthesis and structure-activity relationships.

M. Martín-Martínez, Sergio A Alonso de Diego, M. García-López, 2005, Bioorganic & medicinal chemistry letters.

Recent progress in non-opioid analgesic peptides.

A. Ferrer-Montiel, R. González-Muñiz, M. J. Pérez de Vega, 2018, Archives of biochemistry and biophysics.

The Parkinson's disease‐associated GPR37 receptor‐mediated cytotoxicity is controlled by its intracellular cysteine‐rich domain

L. Pardo, F. Ciruela, I. Stagljar, 2013, Journal of neurochemistry.

A role for ring‐closing metathesis in medicinal chemistry: Mimicking secondary architectures in bioactive peptides

R. González-Muñiz, M. J. Pérez de Vega, M. I. García-Aranda, 2011, Medicinal research reviews.

2-Amino-3-oxohexahydroindolizino[8,7-b]indole-5-carboxylate derivatives as new scaffolds for mimicking β-turn secondary structures. Molecular dynamics and stereoselective synthesis

M. García-López, R. González-Muñiz, I. Alkorta, 1995 .

β–Lactam TRPM8 Antagonist RGM8-51 Displays Antinociceptive Activity in Different Animal Models

G. Fernández-Ballester, A. Fernández-Carvajal, A. Ferrer-Montiel, 2022, International journal of molecular sciences.

Characterization of Novel Synthetic Polyphenols: Validation of Antioxidant and Vasculoprotective Activities

R. González-Muñiz, B. Sabater-Muñoz, B. Vázquez-Lasa, 2020, Antioxidants.

Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reaction

M. García-López, R. González-Muñiz, M. P. D. Vega, 2014 .

Disrupting VEGF–VEGFR1 Interaction: De Novo Designed Linear Helical Peptides to Mimic the VEGF13-25 Fragment

M. Bonache, Beatriz Balsera, M. Reille‐Seroussi, 2017, Molecules.

Repurposing ciclopirox as a pharmacological chaperone in a model of congenital erythropoietic porphyria

P. Dubus, J. Castilla, J. Oyarzábal, 2018, Science Translational Medicine.

Ketomethylene and (cyanomethylene)amino pseudopeptide analogues of the C-terminal hexapeptide of neurotensin.

P. Suzdak, I. Gomez-Monterrey, M. García-López, 1995, Journal of medicinal chemistry.

Prolonged antinociceptive activity of pseudodipeptide analogues of Lys-Trp(Nps) and Trp(Nps)-Lys

I. Gomez-Monterrey, M. García-López, R. González-Muñiz, 1992, Peptides.

Pseudopeptide CCK-4 analogues incorporating the Ψ[CH(CN)NH] peptide bond surrogate

M. García-López, R. González-Muñiz, M. Suárez-Gea, 1997 .

5-(Tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c]pyrimidine-based potent and selective CCK(1) receptor antagonists: structural modifications at the tryptophan domain.

M. Martín-Martínez, J. Bartolomé-Nebreda, I. Gomez-Monterrey, 1999, Journal of medicinal chemistry.

Synthesis and anti-HCMV activity of 1-acyl-beta-lactams and 1-acylazetidines derived from phenylalanine.

E. De Clercq, M. García-López, R. González-Muñiz, 2004, Bioorganic & medicinal chemistry letters.

Synthesis and SAR studies on azetidine-containing dipeptides as HCMV inhibitors

M. García-López, R. González-Muñiz, J. Balzarini, 2010, Bioorganic & Medicinal Chemistry.

From 1-acyl-beta-lactam human cytomegalovirus protease inhibitors to 1-benzyloxycarbonylazetidines with improved antiviral activity. A straightforward approach to convert covalent to noncovalent inhibitors.

E. De Clercq, M. García-López, R. González-Muñiz, 2005, Journal of medicinal chemistry.

Solid phase synthesis of a fully active analogue of cholecystokinin using the acid-stable Boc-Phe (p-CH2) SO3H as a substitute for Boc-Tyr(SO3H) in CCK8.

B. Roques, D. Ficheux, R. González-Muñiz, 2009, International journal of peptide and protein research.

Ketomethylene and methyleneamino pseudopeptide analogues of insect allatostatins inhibit juvenile hormone and vitellogenin production in the cockroach Blattella germanica.

M. García-López, R. González-Muñiz, D. Andreu, 1997, Insect biochemistry and molecular biology.

New transient receptor potential TRPV1, TRPM8 and TRPA1 channel antagonists from a single linear β,γ-diamino ester scaffold

A. Fernández-Carvajal, A. Ferrer-Montiel, R. González-Muñiz, 2016 .

Mutations of TRPM8 channels: Unraveling the molecular basis of activation by cold and ligands

M. Martín-Martínez, R. González-Muñiz, Alejandro Plaza-Cayón, 2022, Medicinal research reviews.

Pharmacological evaluation of IQM‐95,333, a highly selective CCKA receptor antagonist with anxiolytic‐like activity in animal models

M. Martín-Martínez, I. Gomez-Monterrey, M. García-López, 1997, British journal of pharmacology.

A role for ring‐closing metathesis in medicinal chemistry: Mimicking secondary architectures in bioactive peptides

R. González-Muñiz, M. J. Pérez de Vega, M. I. García-Aranda, 2011, Medicinal research reviews.

Simple access to novel azetidine-containing conformationally restricted amino acids by chemoselective reduction of β-lactams

M. Bonache, M. García-López, R. González-Muñiz, 2004 .

Divergent, stereoselective access to heterocyclic α,α-quaternary- and β(2,3,3)-amino acid derivatives from a N-Pmp-protected Orn-derived β-lactam.

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2015, Organic & biomolecular chemistry.

Combination of molecular modeling, site-directed mutagenesis, and SAR studies to delineate the binding site of pyridopyrimidine antagonists on the human CCK1 receptor.

M. Martín-Martínez, B. Maigret, M. García-López, 2005, Journal of medicinal chemistry.

Synthesis of 8-amino-3-oxoindolizidine-1-carboxylic acid derivatives as conformationally restricted templates for use in design of peptide mimetics

M. García-López, R. González-Muñiz, R. Herranz, 1995 .

Pharmacological Study of IQM-97,423, a Potent and Selective CCK1 Receptor Antagonist with Protective Effect in Experimental Acute Pancreatitis

J. Bartolomé-Nebreda, M. García-López, R. González-Muñiz, 2004, Pharmacology.

Identification, functional gastrointestinal stability and molecular docking studies of lentil peptides with dual antioxidant and angiotensin I converting enzyme inhibitory activities.

M. Martín-Martínez, R. González-Muñiz, E. Peñas, 2017, Food chemistry.

Quaternary α,α-2-oxoazepane α-amino acids: synthesis from ornithine-derived β-lactams and incorporation into model dipeptides.

M. Martín-Martínez, M. Bonache, M. García-López, 2011, The Journal of organic chemistry.

Synthesis and stereochemical structure-activity relationships of 1,3-dioxoperhydropyrido[1,2-c]pyrimidine derivatives: potent and selective cholecystokinin-A receptor antagonists.

M. Martín-Martínez, J. Bartolomé-Nebreda, I. Gomez-Monterrey, 1997, Journal of medicinal chemistry.

Old Molecules for New Receptors: Trp(Nps) Dipeptide Derivatives as Vanilloid TRPV1 Channel Blockers

M. Bonache, A. Ferrer-Montiel, M. García-López, 2006, ChemMedChem.

Synthesis of highly functionalized γ-lactam derivatives for use as conformational constraints in peptides

M. Martín-Martínez, M. García-López, R. González-Muñiz, 1996 .

β-Lactams derived from phenylalanine and homologues : effects of the distance between the aromatic rings and the α-stereogenic reactive center on the memory of chirality

M. Bonache, M. García-López, R. González-Muñiz, 2006 .

Memory of chirality in the stereoselective synthesis of β-lactams: importance of the starting amino acid derivative

M. Martín-Martínez, M. Bonache, M. García-López, 2003 .

From theoretical calculations to the enantioselective synthesis of a 1,3,4-trisubstituted Gly-derived 2-azetidinone

M. García-López, R. González-Muñiz, I. Alkorta, 2008 .

Modulation of protein-protein interactions by stabilizing/mimicking protein secondary structure elements.

Mercedes Martín-Martínez, M. Martín-Martínez, M. J. P. de Vega, 2007, Current topics in medicinal chemistry.

β-Lactams Through Single Bond Ring Closing: Methods, Transformations and Bioactivity

R. González-Muñiz, Inmaculada Martín‐Torres, Inmaculada Martín-Torres, 2017 .

Studies on the synthesis of β-keto esters derived from dipeptides: search for a low-epimerizing method

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2000, Letters in Peptide Science.

Chiral 1,3,6-trisubstituted 2,4-dioxohexahydropyrimidines: a convenient stereoselective synthesis from aspartic acid derivatives

M. García-López, R. González-Muñiz, M. P. D. Vega, 2007 .

Simple, Highly Enantioselective Access to Quaternary 1,3,4,4-Tetrasubstituted β-Lactams from Amino Acids : A Solid-Phase Approach

M. García-López, R. González-Muñiz, Paula Pérez-Faginas, 2008 .

Easy access to orthogonally protected α-alkyl aspartic acid and α-alkyl asparagine derivatives by controlled opening of β-lactams

M. García-López, R. González-Muñiz, G. Gerona-Navarro, 2003 .

Synthesis of Highly Functionalized γ-Lactam Derivatives for Use as Conformational Constraints in Peptides.

M. Martín-Martínez, M. García-López, R. González-Muñiz, 1996 .

Exploring solid-phase approaches for the preparation of new β-lactams from amino acids

F. Albericio, M. García-López, R. González-Muñiz, 2004, Molecular Diversity.

Azetidine-derived amino acids versus proline derivatives. alternative trends in reverse turn induction.

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2008, The Journal of organic chemistry.

Exceptional Stereoselectivity in the Synthesis of 1,3,4-Trisubstituted 4-Carboxy β-Lactam Derivatives from Amino Acids

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2007 .

General approach for the stereocontrolled construction of the beta-lactam ring in amino acid-derived 4-alkyl-4-carboxy-2-azetidinones.

M. García-López, R. González-Muñiz, G. Gerona-Navarro, 2002, The Journal of organic chemistry.

Amino Acid-derived 4-Alkyl-4-carboxy-2-azetidinones. New Insights into b-Lactam Ring Formation and N-Deprotection

M. Bonache, M. García-López, R. González-Muñiz, 2002 .

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.

M. Bonache, M. García-López, R. González-Muñiz, 2001, The Journal of organic chemistry.

Optically active 1,3,4,4-tetrasubstituted β-lactams: synthesis and evaluation as tumor cell growth inhibitors.

M. García-López, R. González-Muñiz, C. Cuevas, 2011, European journal of medicinal chemistry.

Further evidence for 2-alkyl-2-carboxyazetidines as gamma-turn inducers.

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2009, The Journal of organic chemistry.

Pharmacology of TRP Channels

G. Fernández-Ballester, A. Fernández-Carvajal, A. Ferrer-Montiel, 2015 .

TRPV1 modulators: structure-activity relationships using a rational combinatorial approach.

F. Albericio, A. Ferrer-Montiel, M. García-López, 2011, Bioorganic & medicinal chemistry letters.

Monitor – New TRPV1-targeting agents for pain management

R. González-Muñiz, 2005 .

Bicyclic lactams as templates for peptidomimetics. Studies on stereoselective synthetic routes to 6-oxoperhydropyrrolo[1,2-a]pyrazines

M. Martín-Martínez, M. García-López, R. González-Muñiz, 1996 .

Diimine Reduction of C=C Double Bonds: Scope and Limitations of the Application to Solid‐Phase Peptide Synthesis

M. García-López, R. González-Muñiz, M. P. D. Vega, 2009 .

Experimental and theoretical studies on the rearrangement of 2-oxoazepane α,α-amino acids into 2'-oxopiperidine β(2,3,3) -amino acids: an example of intramolecular catalysis.

M. Martín-Martínez, J. Elguero, M. Bonache, 2015, Chemistry.

5-(Tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c]pyrimidine-based potent and selective CCK(1) receptor antagonists: structure-activity relationship studies on the central 1,3-dioxoperhydropyrido[1,2-c]pyrimidine scaffold.

J. Bartolomé-Nebreda, M. García-López, R. González-Muñiz, 2001, Journal of medicinal chemistry.

3,6-dioxoperhydropyrrolo[1,2-a]pyrazines. A new approach to conformationally restricted tripeptides

M. Martín-Martínez, M. García-López, R. González-Muñiz, 1992 .

Synthesis and Inhibitory Activities against Aminopeptidase B and Enkephalin‐Degrading Enzymes of Ketomethylene Dipeptide Analogues of Arphamenines

M. L. de Ceballos, I. Gomez-Monterrey, R. González-Muñiz, 1992, Archiv der Pharmazie.

2-Alkyl-2-carboxyazetidines as γ-turn inducers: incorporation into neurotrophin fragments

M. Martín-Martínez, M. Bonache, M. García-López, 2010, Amino Acids.

Azepane quaternary amino acids as effective inducers of 3(10) helix conformations.

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2012, The Journal of organic chemistry.

Branched peptides and conformationally constrained analogues from cyanomethyleneamino pseudopeptides

M. García-López, R. González-Muñiz, M. Suárez-Gea, 1996 .

Chalcones as positive allosteric modulators of α7 nicotinic acetylcholine receptors: a new target for a privileged structure.

F. Sala, L. M. Valor, L. Svobodová, 2014, European journal of medicinal chemistry.

Regio- and enantioselectivity of the Candida antarctica lipase catalyzed amidations of Cbz-l- and Cbz-d-glutamic acid diesters

R. González-Muñiz, S. Conde, C. Chamorro, 1995 .

Conformationally restricted PACAP27 analogues incorporating type II/II' IBTM beta-turn mimetics. Synthesis, NMR structure determination, and binding affinity.

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2001, Bioorganic & medicinal chemistry.

Stereochemical and mechanistic studies on the formation of the 3-oxoindolizidine skeleton from ornithine derivatives

M. Martín-Martínez, M. García-López, R. González-Muñiz, 1995 .

Stereoselective reductive amination of β-keto esters derived from dipeptides. Stereochemical and mechanistic studies on the formation of 5-carboxymethyl-2-oxopiperazine derivatives

M. García-López, R. González-Muñiz, R. Herranz, 1999 .

One-pot stereospecific synthesis of 8a-hydroxy- and 8a-alkoxy-2,2,8-trisubstituted-3-oxoindolizidines. Mechanistic studies on the elaboration of the 8a-substituted indolizidine ring

M. García-López, R. González-Muñiz, M. Domínguez, 1993 .

Synthesis of 2-substituted 8-amino-3-oxoindolizidine-2-carboxylic acid derivatives as peptide conformation mimetics

M. García-López, R. González-Muñiz, M. Domínguez, 1992 .

A facile synthesis of 8-amino-3-oxoindolizidine derivatives as conformationally restricted ornithyl pseudodipeptides

I. Gomez-Monterrey, M. García-López, R. González-Muñiz, 1991 .

Highly constrained dipeptoid analogues containing a type II' beta-turn mimic as novel and selective CCK-A receptor ligands.

M. Martín-Martínez, M. García-López, R. González-Muñiz, 1999, Bioorganic & medicinal chemistry letters.

Boc-Trp-Orn(Z)-Asp-NH2 and derivatives: a new family of CCK antagonists.

B. Roques, R. González-Muñiz, F. Bergeron, 1990, Journal of medicinal chemistry.

Stereospecific synthesis of (2R,3S)-3-amino-2-piperidineacetic acid derivatives for use as conformational constraint in peptides

I. Gomez-Monterrey, R. González-Muñiz, R. Herranz, 1993 .

Natural Polyhydroxy Flavonoids, Curcuminoids, and Synthetic Curcumin Analogs as α7 nAChRs Positive Allosteric Modulators

F. Sala, R. González-Muñiz, S. Sala, 2021, International journal of molecular sciences.

Disulfide and amide-bridged cyclic peptide analogues of the VEGF₈₁₋₉₁ fragment: synthesis, conformational analysis and biological evaluation.

M. Martín-Martínez, M. Vidal, M. García-López, 2011, Bioorganic & medicinal chemistry.

On the modulation of TRPM channels: Current perspectives and anticancer therapeutic implications

A. Bertamino, I. Gomez-Monterrey, R. González-Muñiz, 2023, Frontiers in Oncology.

Larger helical populations in peptides derived from the dimerization helix of the capsid protein of HIV-1 results in peptide binding toward regions other than the "hotspot" interface.

M. G. Mateu, J. Neira, R. González-Muñiz, 2011, Biomacromolecules.

Factor J, an inhibitor of the classical and alternative complement pathway, does not inhibit esterolysis by factor D.

M. López-Trascasa, R. González-Muñiz, M. Jiménez-Clavero, 1996, Biochimica et biophysica acta.

Running title : Lentil peptides with dual antioxidant / ACE inhibitory activities

M. Martín-Martínez, M. Bonache, R. González-Muñiz, 2016 .

Clicked bis-PEG-peptide conjugates for studying calmodulin-Kv7.2 channel binding.

M. Bonache, R. González-Muñiz, A. Villarroel, 2014, Organic & biomolecular chemistry.

Transient Receptor Potential Melastatin 8 Channel (TRPM8) Modulation: Cool Entryway for Treating Pain and Cancer.

Antonio Ferrer-Montiel, I. Gomez-Monterrey, A. Ferrer-Montiel, 2016, Journal of medicinal chemistry.

TRPM8 Channels: Advances in Structural Studies and Pharmacological Modulation

M. Martín-Martínez, I. Gomez-Monterrey, R. González-Muñiz, 2021, International journal of molecular sciences.

Investigational drugs in early phase clinical trials targeting thermotransient receptor potential (thermoTRP) channels

G. Fernández-Ballester, A. Fernández-Carvajal, A. Ferrer-Montiel, 2020, Expert opinion on investigational drugs.

Recent Progress in TRPM8 Modulation: An Update

I. Gomez-Monterrey, M. Bonache, R. González-Muñiz, 2019, International journal of molecular sciences.

Advances in modulating thermosensory TRP channels

J. González-Ros, G. Fernández-Ballester, A. Fernández-Carvajal, 2012, Expert opinion on therapeutic patents.

Studies on N-deprotection of ψ(CH2NH) pseudodipeptide methyl esters. Cyclization to 2-ketopiperazines

I. Gomez-Monterrey, M. García-López, R. González-Muñiz, 1991 .

Helical peptides from VEGF and Vammin hotspots for modulating the VEGF-VEGFR interaction.

M. Martín-Martínez, M. Reille‐Seroussi, N. Gagey-Eilstein, 2013, Organic & biomolecular chemistry.

Parallel solid-phase synthesis of a small library of linear and hydrocarbon-bridged analogues of VEGF(81-91): potential biological tools for studying the VEGF/VEGFR-1 interaction.

M. Martín-Martínez, M. Vidal, M. García-López, 2011, Bioorganic & medicinal chemistry.

1,3-diphenylpropan-1-ones as allosteric modulators of α7 nACh receptors with analgesic and antioxidant properties.

F. Sala, Beatriz Balsera, A. Fernández-Carvajal, 2016, Future medicinal chemistry.

1-(2',5'-Dihydroxyphenyl)-3-(2-fluoro-4-hydroxyphenyl)-1-propanone (RGM079): A positive allosteric modulator of α7 nicotinic receptors with analgesic and neuroprotective activity.

F. Sala, A. Fernández-Carvajal, A. Ferrer-Montiel, 2019, ACS chemical neuroscience.

Evolution in non-peptide α-helix mimetics on the road to effective protein-protein interaction modulators.

M. Martín-Martínez, R. González-Muñiz, Sergio Algar, 2020, European journal of medicinal chemistry.

Small Library of Triazolyl Polyphenols Correlating Antioxidant Activity and Stability with Number and Position of Hydroxyl Groups.

M. Bonache, R. González-Muñiz, B. Sabater-Muñoz, 2018, ACS combinatorial science.

DD04107-Derived neuronal exocytosis inhibitor peptides: Evidences for synaptotagmin-1 as a putative target.

M. Martín-Martínez, O. Abián, A. Velázquez‐Campoy, 2021, Bioorganic chemistry.

Disulfide Bonds versus Trp⋅⋅⋅Trp Pairs in Irregular β‐Hairpins: NMR Structure of Vammin Loop 3‐Derived Peptides as a Case Study

R. González-Muñiz, M. Jiménez, M. J. Pérez de Vega, 2009, Chembiochem : a European journal of chemical biology.

Phenylalanine-Derived β-Lactam TRPM8 Modulators. Configuration Effect on the Antagonist Activity

G. Fernández-Ballester, I. Gomez-Monterrey, M. Bonache, 2021, International journal of molecular sciences.

Highly functionalized β-lactams and 2-ketopiperazines as TRPM8 antagonists with antiallodynic activity

G. Fernández-Ballester, M. Bonache, A. Fernández-Carvajal, 2020, Scientific Reports.

Antinociceptive effects in rodents of the dipeptide Lys-Trp (Nps) and related compounds

M. García-López, R. González-Muñiz, J. Naranjo, 1986, Peptides.

Bioactive peptides from food protein degradation : Legume peptides

R. González-Muñiz, 2019 .

Synthesis of methyl 6-aralkl-2,5-diketopiperidine-3-carboxylates as synthons of conformationally constrained pseudopeptides

I. Gomez-Monterrey, M. García-López, R. González-Muñiz, 1991 .

Peptide Revolution: Genomics, Proteomics & Therapeutics

F. Albericio, A. Ferrer-Montiel, R. González-Muñiz, 2004 .

SARS‐CoV‐2 main protease inhibitors: What is moving in the field of peptides and peptidomimetics?

M. Bonache, R. González-Muñiz, Sergio Algar‐Lizana, 2022, Journal of peptide science : an official publication of the European Peptide Society.

The neuroprotective activity of GPE tripeptide analogues does not correlate with glutamate receptor binding affinity.

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2006, Bioorganic & medicinal chemistry letters.

Constrained C-terminal hexapeptide neurotensin analogues containing a 3-oxoindolizidine skeleton

P. Suzdak, M. García-López, R. González-Muñiz, 1995, Letters in Peptide Science.

2(S)-amino-3-oxo-11b(R)-hexahydroindolizino[8,7-b]indole-5(S)-carboxylate as a new type of β-turn dipeptide mimetic

M. García-López, R. González-Muñiz, I. Rozas, 1994 .

Conformationally constrained CCK4 analogues incorporating IBTM and BTD beta-turn mimetics.

Mercedes Martín-Martínez, M. Martín-Martínez, M. García-López, 2005, Journal of medicinal chemistry.

Amino acid and peptide prodrugs of diphenylpropanones positive allosteric modulators of α7 nicotinic receptors with analgesic activity.

L. Naesens, F. Sala, Beatriz Balsera, 2018, European journal of medicinal chemistry.

New Gly-Pro-Glu (GPE) analogues: expedite solid-phase synthesis and biological activity.

M. García-López, R. González-Muñiz, C. Cativiela, 2006, Bioorganic & medicinal chemistry letters.

Cyclic amino acid linkers stabilizing key loops of brain derived neurotrophic factor.

David Andreu, Mercedes Martín-Martínez, M. Martín-Martínez, 2012, Bioorganic & medicinal chemistry letters.

Novel 1,4-Dihydropyridine Derivatives as Mineralocorticoid Receptor Antagonists

M. Martín-Martínez, R. González-Muñiz, R. Pellicciari, 2023, International journal of molecular sciences.

PACAP27 Analogues Incorporating Type II/II’ β-Turn Mimetics

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2001 .

Synthesis and biological properties of beta-turned Abeta(31-35) constrained analogues.

M. García-López, R. González-Muñiz, D. Andreu, 2008, Bioorganic & medicinal chemistry letters.

Disulfide Bonds versus Trp⋅⋅⋅Trp Pairs in Irregular β‐Hairpins: NMR Structure of Vammin Loop 3‐Derived Peptides as a Case Study

R. González-Muñiz, M. Jiménez, M. J. Pérez de Vega, 2009, Chembiochem : a European journal of chemical biology.

Advances in modulating thermosensory TRP channels

J. González-Ros, G. Fernández-Ballester, A. Fernández-Carvajal, 2012, Expert opinion on therapeutic patents.

Analgesic dipeptide derivatives. 4. Linear and cyclic analogues of the analgesic compounds arginyl-2-[(o-nitrophenyl)sulfenyl]tryptophan and lysyl-2-[(o-nitrophenyl)sulfenyl]tryptophan.

M. García-López, R. González-Muñiz, J. del Río, 1988, Journal of medicinal chemistry.

Analgesic dipeptide derivatives. 3. Synthesis and structure-activity relationships of o-nitrophenyl-modified analogues of the analgesic compound H-Lys-Trp(NPS)-OMe.

M. García-López, R. González-Muñiz, J. Naranjo, 1987, Journal of medicinal chemistry.

Trp-Trp pairs as β-hairpin stabilisers: hydrogen-bonded versus non-hydrogen-bonded sites.

R. González-Muñiz, M. J. Pérez de Vega, C. Santiveri, 2011, Organic & biomolecular chemistry.

Optically active 1,3,4,4-tetrasubstituted β-lactams: synthesis and evaluation as tumor cell growth inhibitors.

M. García-López, R. González-Muñiz, C. Cuevas, 2011, European journal of medicinal chemistry.

De novo designed library of linear helical peptides: an exploratory tool in the discovery of protein-protein interaction modulators.

M. Martín-Martínez, I. Gomez-Monterrey, M. Bonache, 2014, ACS combinatorial science.

Strategies for design of non peptide CCK1R agonist/antagonist ligands.

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2007, Current Topics in Medicinal Chemistry.

β-Turn Induction by a Diastereopure Azepane-Derived Quaternary Amino Acid

M. Martín-Martínez, R. González-Muñiz, Ignacio Romero‐Muñiz, 2023, The Journal of organic chemistry.

Synthesis, high-throughput screening and pharmacological characterization of β–lactam derivatives as TRPM8 antagonists

G. Fernández-Ballester, M. Bonache, Beatriz Balsera, 2017, Scientific Reports.

Effects of the incorporation of IBTM beta-turn mimetics into the dipeptoid CCK(1) receptor agonist PD 170292.

M. Martín-Martínez, M. García-López, R. González-Muñiz, 2002, Bioorganic & medicinal chemistry letters.

General Approach for the Stereocontrolled Construction of the β-Lactam Ring in Amino Acid-Derived 4-Alkyl-4-carboxy-2-azetidinones.

M. García-López, R. González-Muñiz, G. Gerona-Navarro, 2002 .

Entry to New Conformationally Constrained Amino Acids. First Synthesis of 3‐Unsubstituted 4‐Alkyl‐4‐carboxy‐2‐azetidinone Derivatives via an Intramolecular Nα‐Cα‐Cyclization Strategy.

M. Bonache, M. García-López, R. González-Muñiz, 2001 .