Prenyl Pterocarpans from Algerian <i>Bituminaria bituminosa</i> and Their Effects on Neuroblastoma
Hakim Benhabrou,
Fatma Bitam,
Luigia Cristino,
Alessandro Nicois,
Marianna Carbone,
Dibi Ammar,
Margherita Gavagnin,
Maria Letizia Ciavatta
Affiliations
Hakim Benhabrou
Université de Batna 1, Faculté des Sciences de la Matière, Département de Chimie, Laboratoire de Chimie et Chimie de l’Environnement (LCCE), Batna 05000, Algeria
Fatma Bitam
Université de Batna 2, Faculté de Médecine, Département de Pharmacie, Batna 05000, Algeria
Luigia Cristino
Consiglio Nazionale delle Ricerche, Istituto di Chimica Biomolecolare, Via Campi Flegrei 34, 80078 Pozzuoli, Italy
Alessandro Nicois
Consiglio Nazionale delle Ricerche, Istituto di Chimica Biomolecolare, Via Campi Flegrei 34, 80078 Pozzuoli, Italy
Marianna Carbone
Consiglio Nazionale delle Ricerche, Istituto di Chimica Biomolecolare, Via Campi Flegrei 34, 80078 Pozzuoli, Italy
Dibi Ammar
Université de Batna 1, Faculté des Sciences de la Matière, Département de Chimie, Laboratoire de Chimie et Chimie de l’Environnement (LCCE), Batna 05000, Algeria
Margherita Gavagnin
Consiglio Nazionale delle Ricerche, Istituto di Chimica Biomolecolare, Via Campi Flegrei 34, 80078 Pozzuoli, Italy
Maria Letizia Ciavatta
Consiglio Nazionale delle Ricerche, Istituto di Chimica Biomolecolare, Via Campi Flegrei 34, 80078 Pozzuoli, Italy
The pterocarpan fraction from aerial parts of Bituminaria bituminosa was investigated for both chemical characterization and biological evaluation. Chemical studies were in accordance with the literature data on Bituminaria genus resulting in the identification of typical 4,8-prenyl pterocarpans. Three new members, bituminarins A–C (1–3), were isolated along with main bitucarpin A (4), erybraedin C (5) and erybraedin D (6) already reported from this plant. Further, biological studies evidenced antiproliferative properties of the most abundant pterocarpans 4 and 5 on neuroblastoma SH-SY5Y cell line, in agreement with previously described antiproliferative activity of these compounds against cancer cell lines other than neuroblastoma. The structure and the stereochemistry of the new molecules was determined by extensive spectroscopic analysis and chemical derivatization methods. The biological investigation was carried out by using an assay platform based on a live-cell imaging system revealing an apoptotic cell death induction.