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Methods and Protocols|November 21, 2023
Protocol for Facile Synthesis of Fmoc-N-Me-AA-OH Using 2-CTC Resin as Temporary and Reusable Protecting GroupTanya Román, Gerardo Acosta, Constanza Cárdenas, et al.
ACS Medicinal Chemistry Letters|August 18, 2022
Novel CA(1-7)M(2-9) Analogs: Synthesis, Characterization, and Antibacterial EvaluationTalia Chetty, Jessica T Mhlongo, Ayman Y Waddad, et al.
Journal of Combinatorial Chemistry|January 11, 2005
Multicomponent reactions with dihydroazines: efficient synthesis of a diverse set of pyrido-fused tetrahydroquinolinesInés Carranco, José Luis Díaz, Oscar Jiménez, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|April 21, 2006
Design of a minimized cyclic tetrapeptide that neutralizes bacterial endotoxinsPuig Mora, Carlos Mas-Moruno, Silvia Tamborero, et al.
ACS Combinatorial Science|February 15, 2018
Solid-Phase Synthesis of Pyrrole Derivatives through a Multicomponent Reaction Involving Lys-Containing PeptidesYahya E Jad, Santosh K Gudimella, Thavendran Govender, et al.
Nature Communications|May 22, 2015
New peptide architectures through C-H activation stapling between tryptophan-phenylalanine/tyrosine residuesLorena Mendive-Tapia, Sara Preciado, Jesús García, et al.
Journal of Medicinal Chemistry|May 26, 2006
Synthesis and structure-activity relationship study of potent cytotoxic analogues of the marine alkaloid Lamellarin DDaniel Pla, Antonio Marchal, Christian A Olsen, et al.
Biopolymers|July 29, 2009
Design and facile solid-phase synthesis of peptide-based LPS-inhibitors containing PEG-like functionalitiesCarlos Mas-Moruno, Laura Cascales, Puig Mora, et al.
Nanomedicine (London, England)|October 25, 2014
Gold nanoparticles for photothermally controlled drug releaseAriel R Guerrero, Natalia Hassan, Carlos A Escobar, et al.
ACS Omega|March 24, 2020
Synthesis of Stable Cholesteryl-Polyethylene Glycol-Peptide Conjugates with Non-Disperse Polyethylene Glycol LengthsEdgar Cristóbal-Lecina, Daniel Pulido, Pau Martin-Malpartida, et al.
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