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RF-3192C and other polyketides from the marine endophytic Aspergillus niger ASSB4: structure assignment and bioactivity investigation.
Mahmoud, Manar M; Abdel-Razek, Ahmed S; Hamed, Abdelaaty; Soliman, Hesham S M; Ponomareva, Larissa V; Thorson, Jon S; Shaaban, Khaled A; Shaaban, Mohamed.
Afiliação
  • Mahmoud MM; Pharmacognosy Department, Faculty of Pharmacy, Helwan University, Helwan, Cairo 11795, Egypt.
  • Abdel-Razek AS; Organic and Bioorganic Chemistry, Faculty of Chemistry, Bielefeld University, D-33501 Bielefeld, Germany.
  • Hamed A; Organic and Bioorganic Chemistry, Faculty of Chemistry, Bielefeld University, D-33501 Bielefeld, Germany.
  • Soliman HSM; Microbial Chemistry Department, Genetic Engineering and Biotechnology Research Division, National Research Centre, El-Buhouth St. 33, Dokki-Giza 12622, Egypt.
  • Ponomareva LV; Organic and Bioorganic Chemistry, Faculty of Chemistry, Bielefeld University, D-33501 Bielefeld, Germany.
  • Thorson JS; Chemistry Department, Faculty of Science, Al-Azhar University, Nasr City-Cairo 11884, Egypt.
  • Shaaban KA; Pharmacognosy Department, Faculty of Pharmacy, Helwan University, Helwan, Cairo 11795, Egypt.
  • Shaaban M; Center for Pharmaceutical Research and Innovation, College of Pharmacy, University of Kentucky, Lexington, KY 40536, USA.
Med Chem Res ; 30(3): 647-654, 2021 Mar.
Article em En | MEDLINE | ID: mdl-38576441
ABSTRACT
Chemical investigation of the methanolic extract of endophytic Aspergillus niger SB4, isolated from the marine alga Laurencia obtuse, afforded the pentacyclic polyketide, RF-3192C (1), the dimeric coumarin orlandin (2), fonsecin B (3), TMC-256A1 (4), cyclo-(Leu-Ala) (5), and cerebroside A (6).The chemical structure of RF-3192C (1) is assigned herein for the first time using 1D/2D NMR and HRESI-MS. Additionally, the revision of the NMR assignments of orlandin (2) was reported herein as well. Investigation of the antimicrobial activities of isolated compounds revealed the high activity of RF-3192C (1) against Pseudomonas aeruginosa and Bacillus subtilis, and moderate activity against yeast. Moreover, an in vitro cytotoxic activity against liver (HEPG2), cervical (HELA), lung (A549), prostate (PC3), and breast (MCF7) cancer cell lines of the isolated compounds was evaluated. The isolation and taxonomical characterization of the producing fungus was reported as well.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article