1. Academic Validation
  2. Phenanthrenoids from Juncus acutus L., new natural lipopolysaccharide-inducible nitric oxide synthase inhibitors

Phenanthrenoids from Juncus acutus L., new natural lipopolysaccharide-inducible nitric oxide synthase inhibitors

  • Chem Pharm Bull (Tokyo). 2007 Aug;55(8):1264-6. doi: 10.1248/cpb.55.1264.
Fathi Abdelmohsen Abdelhalim Behery 1 Zain Elabdin Metwally Naeem Galal Taha Maatooq Mohamed Mahmoud Abdelfattah Amer Zhi-Hong Wen Jyh-Horng Sheu Atallah Fouad Ahmed
Affiliations

Affiliation

  • 1 Department of Pharmacognosy, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.
Abstract

The novel natural product juncutol (1), 1,4,7-trimethyl-8,9-dihydro-4H-cyclopenta[def]phenanthrene-2,6-diol, along with the three related metabolites juncusol (2), dehydrojuncusol (3), and 6-hydroxymethyl-1-methyl-5-vinyl-9,10-dihydrophenanthrene-2-ol (4), were isolated from the rhizomes of Juncus acutus L. (Juncaceae) growing in Egypt. The structural identity of 1 was determined on the basis of spectroscopic analyses, including 2D NMR spectroscopy. The inhibitory effect of these Natural Products on the expression of inducible nitric oxide synthase (iNOS) in lipopolysaccharide-stimulated RAW264.7 macrophage cells was determined for the first time. The unprecedented symmetrical compound juncutol (1) was found to be the most potent inhibitor against the induction of the proinflammatory iNOS protein.

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