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Journal of Medicinal Chemistry|December 6, 2011
Synthesis and evaluation of 1,5-disubstituted tetrazoles as rigid analogues of combretastatin A-4 with potent antiproliferative and antitumor activityRomeo Romagnoli, Pier Giovanni Baraldi, Maria Kimatrai Salvador, et al.
ACS Medicinal Chemistry Letters|April 15, 2026
Potent Neuronal Nicotinamide Adenine Dinucleotide-Boosting Tetrahydroquinoxalines: Structure-Activity Relationships and Early Drug Metabolism and Pharmacokinetics EvaluationPetra Cuřínová, Melissa Jöe, Filip Cesar, et al.
European Journal of Medicinal Chemistry|October 27, 2011
One-pot synthesis and biological evaluation of 2-pyrrolidinyl-4-amino-5-(3',4',5'-trimethoxybenzoyl)thiazole: a unique, highly active antimicrotubule agentRomeo Romagnoli, Pier Giovanni Baraldi, Carlota Lopez Cara, et al.
Free Radical Biology & Medicine|April 24, 2013
S[+] Apomorphine is a CNS penetrating activator of the Nrf2-ARE pathway with activity in mouse and patient fibroblast models of amyotrophic lateral sclerosisRichard J Mead, Adrian Higginbottom, Scott P Allen, et al.
Bioorganic & Medicinal Chemistry|September 9, 2009
Design, synthesis and structure-activity relationship of 2-(3',4',5'-trimethoxybenzoyl)-benzo[b]furan derivatives as a novel class of inhibitors of tubulin polymerizationRomeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Journal of Medicinal Chemistry|December 4, 2013
Design, synthesis, and biological evaluation of 1-phenylpyrazolo[3,4-e]pyrrolo[3,4-g]indolizine-4,6(1H,5H)-diones as new glycogen synthase kinase-3β inhibitorsValeria La Pietra, Giuseppe La Regina, Antonio Coluccia, et al.
Biomaterials|February 22, 2021
Sulfonated cryogel scaffolds for focal delivery in ex-vivo brain tissue culturesDimitri Eigel, Romy Schuster, Max J Männel, et al.
Molecular Cancer Therapeutics|March 2, 2021
The Discovery of a Novel Antimetastatic Bcl3 InhibitorJitka Soukupová, Cinzia Bordoni, Daniel J Turnham, et al.
Journal of Medicinal Chemistry|March 14, 2009
Indolylarylsulfones bearing natural and unnatural amino acids. Discovery of potent inhibitors of HIV-1 non-nucleoside wild type and resistant mutant strains reverse transcriptase and coxsackie B4 virusFrancesco Piscitelli, Antonio Coluccia, Andrea Brancale, et al.
Antiviral Research|May 29, 2018
Structure-activity relationship study of itraconazole, a broad-range inhibitor of picornavirus replication that targets oxysterol-binding protein (OSBP)Lisa Bauer, Salvatore Ferla, Sarah A Head, et al.
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