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- Publications
- Influence
Heme Oxygenase-2 (HO-2) as a therapeutic target: Activators and inhibitors.
- Sebastiano Intagliata, L. Salerno, +7 authors G. Romeo
- Chemistry, Medicine
- European journal of medicinal chemistry
- 1 December 2019
Heme oxygenase (HO) enzymes are involved in heme catabolism and several physiological functions. Among the different HO isoforms, HO-2 stands out for its neuroprotective properties and modulatory… Expand
Novel Structural Insight into Inhibitors of Heme Oxygenase-1 (HO-1) by New Imidazole-Based Compounds: Biochemical and In Vitro Anticancer Activity Evaluation
- K. Greish, L. Salerno, +10 authors V. Pittalà
- Chemistry, Medicine
- Molecules
- 1 May 2018
In this paper, the design, synthesis, and molecular modeling of a new azole-based HO-1 inhibitors was reported, using compound 1 as a lead compound, in which an imidazole moiety is linked to a… Expand
Structure-activity relationships and molecular modeling studies of novel arylpiperazinylalkyl 2-benzoxazolones and 2-benzothiazolones as 5-HT(7) and 5-HT(1A) receptor ligands.
- L. Salerno, V. Pittalà, +7 authors G. Romeo
- Chemistry, Medicine
- European journal of medicinal chemistry
- 6 October 2014
A novel series of arylpiperazinylalkyl 2-benzoxazolones and 2-benzothiazolones 18-38 was designed, synthesized and tested to evaluate their affinity for the 5-HT7 and 5-HT1A receptors. Compounds with… Expand
Strategies to Improve Resveratrol Systemic and Topical Bioavailability: An Update
- Sebastiano Intagliata, M. Modica, L. Santagati, L. Montenegro
- Medicine
- Antioxidants
- 25 July 2019
In recent years, a great deal of attention has been paid to natural compounds due to their many biological effects. Polyphenols are a class of plant derivatives that have been widely investigated for… Expand
Protective Effects of Caffeic Acid Phenethyl Ester (CAPE) and Novel Cape Analogue as Inducers of Heme Oxygenase-1 in Streptozotocin-Induced Type 1 Diabetic Rats
- V. Sorrenti, M. Raffaele, +5 authors C. Di Giacomo
- Chemistry, Medicine
- International journal of molecular sciences
- 1 May 2019
Type 1 diabetes mellitus (T1D) is a chronic autoimmune disease resulting in the destruction of insulin producing β-cells of the pancreas, with consequent insulin deficiency and excessive glucose… Expand
Structure-Activity Relationships and Therapeutic Potentials of 5-HT7 Receptor Ligands: An Update.
- M. Modica, E. Lacivita, +4 authors M. Leopoldo
- Chemistry, Medicine
- Journal of medicinal chemistry
- 16 May 2018
Serotonin 5-HT7 receptor (5-HT7R) has been the subject of intense research efforts because of its presence in brain areas such as the hippocampus, hypothalamus, and cortex. Preclinical data link the… Expand
Targeting heme Oxygenase-1 with hybrid compounds to overcome Imatinib resistance in chronic myeloid leukemia cell lines.
- V. Sorrenti, V. Pittalà, +13 authors L. Salerno
- Chemistry, Medicine
- European journal of medicinal chemistry
- 5 October 2018
Heme oxygenase-1 (HO-1) is a cytoprotective enzyme and a survival-enhancing factor in a number of cancers. Chronic myeloid leukemia (CML) is a blood cancer caused by pathological kinase activity of… Expand
Solid Lipid Nanoparticles Loading Idebenone Ester with Pyroglutamic Acid: In Vitro Antioxidant Activity and In Vivo Topical Efficacy
- L. Montenegro, A. Panico, L. Santagati, E. A. Siciliano, Sebastiano Intagliata, M. Modica
- Chemistry, Medicine
- Nanomaterials
- 29 December 2018
Idebenone (IDE), a strong antioxidant widely investigated for the treatment of neurodegenerative diseases and skin disorders, shows low oral and topical bioavailability due to its unfavorable… Expand
Synthesis, in vitro and in silico studies of HO-1 inducers and lung antifibrotic agents.
- V. Pittalà, L. Vanella, +10 authors Valeria Sorrenti
- Chemistry, Medicine
- Future medicinal chemistry
- 30 August 2019
Aim: Dimethyl fumarate (DMF) analogs were synthesized to obtain inducers of HO-1 and antifibrotic agents. Methods: HO-1 expression levels were measured on lung fibroblasts (MRC5). NMR and docking… Expand
Synthesis and binding properties of new long-chain 4-substituted piperazine derivatives as 5-HT₁A and 5-HT₇ receptor ligands.
- M. Modica, Sebastiano Intagliata, +5 authors G. Romeo
- Chemistry, Medicine
- Bioorganic & medicinal chemistry letters
- 1 April 2015
New long-chain 4-substituted piperazines linked to a thienopyrimidine or a quinazoline system were synthesized and tested for their binding properties on human cloned 5-HT1A and 5-HT7 serotonin… Expand
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