Ana Montero

发表

Probing the bioactive conformation of an archetypal natural product HDAC inhibitor with conformationally homogeneous triazole-modified cyclic tetrapeptides.

M Reza Ghadiri, W Seth Horne, John M. Beierle, 2009, Angewandte Chemie.

A virocidal amphipathic α-helical peptide that inhibits hepatitis C virus infection in vitro

F. Chisari, M. Ghadiri, P. Gallay, 2008, Proceedings of the National Academy of Sciences.

Macrocyclic peptoid-Peptide hybrids as inhibitors of class I histone deacetylases.

M. Ghadiri, C. Olsen, L. Leman, 2012, ACS medicinal chemistry letters.

Self-assembling peptide nanotubes with antiviral activity against hepatitis C virus.

F. Chisari, M. Ghadiri, M. Law, 2011, Chemistry & biology.

Total synthesis and biological evaluation of (+)- and (-)-bisanthraquinone antibiotic BE-43472B and related compounds.

K. Nicolaou, Ana Montero, Y. H. Lim, 2009, Journal of the American Chemical Society.

Design, synthesis, biological evaluation, and structural characterization of potent histone deacetylase inhibitors based on cyclic alpha/beta-tetrapeptide architectures.

John M. Beierle, M. Ghadiri, C. Olsen, 2009, Journal of the American Chemical Society.

Design, synthesis, and biological evaluation of platensimycin analogues with varying degrees of molecular complexity.

A. Stepan, K. Nicolaou, Yefeng Tang, 2008, Journal of the American Chemical Society.

Total synthesis and antibacterial properties of carbaplatensimycin.

A. Stepan, K. Nicolaou, Yefeng Tang, 2007, Journal of the American Chemical Society.

Adamantaplatensimycin: a bioactive analogue of platensimycin.

K. Nicolaou, T. Lister, Ana Montero, 2007, Angewandte Chemie.

Synthesis and biological evaluation of 2',4'- and 3',4'-bridged nucleoside analogues.

D. Burton, K. Nicolaou, A. Hessell, 2011, Bioorganic & medicinal chemistry.

Pyrazolo[3,4-d]pyrimidines as sigma-1 receptor ligands for the treatment of pain. Part 1: 4-acylamino derivatives.

J. Díaz, J. Corbera, Ana Montero, 2017, MedChemComm.

The Overman rearrangement in carbohydrate chemistry: stereoselective synthesis of functionalized 3-amino-3,6-dihydro-2H-pyrans and incorporation in peptide derivatives☆

B. Herradón, E. Mann, Ana Montero, 2005 .

Studies on aromatic compounds: inhibition of calpain I by biphenyl derivatives and peptide-biphenyl hybrids.

J. M. Navas, B. Herradón, E. Mann, 2004, Bioorganic & medicinal chemistry letters.

Synthesis of a 24-membered cyclic peptide-biphenyl hybrid

F. Albericio, B. Herradón, Ana Montero, 2007 .

Solid-phase combinatorial synthesis of peptide-biphenyl hybrids as calpain inhibitors.

F. Albericio, B. Herradón, Ana Montero, 2004, Organic letters.

Peptide‐Biphenyl Hybrids as Calpain Inhibitors

B. Herradón, E. Mann, Ana Montero, 2004, Chemistry & biodiversity.

Synthesis and Crystal Structure of Peptide-2,2'-Biphenyl Hybrids

B. Herradón, M. Maestro, E. Mann, 2002 .

Preparation of Sugar Amino Acids by Claisen-Johnson Rearrangement: Synthesis and Incorporation into Enkephalin Analogues

B. Herradón, Ana Montero, Enrique Mann, 2004 .

Synthesis and applications of a chiral-oxygenated 3-chloro-3,6-dihydro-2H-pyran obtained under Overman rearrangement conditions

B. Herradón, E. Benito, Ana Montero, 2010 .

Crystallization-induced dynamic resolution and analysis of the non-covalent interactions in the crystal packing of peptide–biphenyl hybrids

B. Herradón, M. Maestro, Ana Montero, 2004 .

Synthesis and structure-activity relationship study of a new series of selective σ(1) receptor ligands for the treatment of pain: 4-aminotriazoles.

Rosalia Pascual, Carmen Almansa, Adriana Port, 2015, Journal of medicinal chemistry.

Tricyclic Triazoles as σ1 Receptor Antagonists for Treating Pain.

A. I. Oliva, J. Díaz, J. Vela, 2021, Journal of medicinal chemistry.

Pyrazolo[3,4-d]pyrimidines as sigma-1 receptor ligands for the treatment of pain. Part 2: Introduction of cyclic substituents in position 4.

J. Díaz, J. Corbera, Ana Montero, 2017, MedChemComm.

Asymmetric synthesis and biological properties of uncialamycin and 26-epi-uncialamycin.

K. Nicolaou, Ana Montero, Jason S. Chen, 2008, Angewandte Chemie.

EST64454: a Highly Soluble σ1 Receptor Antagonist Clinical Candidate for Pain Management.

J. Díaz, R. Maldonado, A. Torrens, 2020, Journal of medicinal chemistry.

Cyclic tetrapeptide HDAC inhibitors as potential therapeutics for spinal muscular atrophy: Screening with iPSC-derived neuronal cells.

M. Ghadiri, C. Olsen, J. Gottesfeld, 2017, Bioorganic & medicinal chemistry letters.

Guanidinium and aminoimidazolinium derivatives of N-(4-piperidyl)propanamides as potential ligands for mu opioid and I2-imidazoline receptors: synthesis and pharmacological screening.

Ana Montero, L. Callado, J. Meana, 2002, Bioorganic & medicinal chemistry.

Potential Agents for Treating Cystic Fibrosis: Cyclic Tetrapeptides that Restore Trafficking and Activity of ΔF508-CFTR.

Monica A. Chalfant, M. Ghadiri, W. Balch, 2011, ACS medicinal chemistry letters.

Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic α / β -Tetrapeptide Architectures

John M. Beierle, M. Ghadiri, C. Olsen, 2009 .

Guanidinium and Aminoimidazolinium Derivatives of N‐(4‐Piperidyl)propanamides as Potential Ligands for μ Opioid and I2‐Imidazoline Receptors: Synthesis and Pharmacological Screening.

Ana Montero, L. Callado, J. Meana, 2002 .

Synthesis and biological evaluation of 2',4'- and 3',4'-bridged nucleoside analogues.

D. Burton, K. Nicolaou, A. Hessell, 2011, Bioorganic & medicinal chemistry.