Insecticidal activity of Paraherquamides, including paraherquamide H and paraherquamide I, two new alkaloids isolated from Penicillium cluniae
- PMID: 16608209
- DOI: 10.1021/jf0530998
Insecticidal activity of Paraherquamides, including paraherquamide H and paraherquamide I, two new alkaloids isolated from Penicillium cluniae
Abstract
Paraherquamide H (1) and paraherquamide I (2), two new compounds of the paraherquamide (PHQ) family, together with the already known paraherquamide A (3), paraherquamide B (4), paraherquamide E (5), VM55596 (N-oxide paraherquamide) (6), paraherquamide VM55597 (7), and five known diketopiperazines (8-12) have been isolated from the culture broth of Penicillium cluniae Quintanilla. The structure of 1 and 2, on the basis of NMR and MS analysis, was established. It is worth noticing that, in both cases, an unusual oxidative substitution in C-16 was found, which had only previously been detected in PHQ 7. Isolated compounds were tested for insecticidal activity against the hemipteran Oncopeltus fasciatus Dallas. Mortality data have allowed preliminary structure activity relationships to be proposed. The most potent product was 5 with a LD(50) of 0.089 microg/nymph.
Similar articles
-
Insecticidal activity of penitrems, including penitrem G, a new member of the family isolated from Penicillium crustosum.J Agric Food Chem. 2003 Apr 9;51(8):2156-60. doi: 10.1021/jf020983e. J Agric Food Chem. 2003. PMID: 12670149
-
Further novel metabolites of the paraherquamide family.J Antibiot (Tokyo). 1993 Sep;46(9):1355-63. doi: 10.7164/antibiotics.46.1355. J Antibiot (Tokyo). 1993. PMID: 8226314
-
Sclerotiamide: a new member of the paraherquamide class with potent antiinsectan activity from the sclerotia of Aspergillus sclerotiorum.J Nat Prod. 1996 Nov;59(11):1093-5. doi: 10.1021/np960607m. J Nat Prod. 1996. PMID: 8946752
-
Marcfortine and paraherquamide class of anthelmintics: discovery of PNU-141962.Curr Top Med Chem. 2002 Jul;2(7):779-93. doi: 10.2174/1568026023393705. Curr Top Med Chem. 2002. PMID: 12052190 Review.
-
Total synthesis and biosynthesis of the paraherquamides: an intriguing story of the biological Diels-Alder construction.Chem Pharm Bull (Tokyo). 2002 Jun;50(6):711-40. doi: 10.1248/cpb.50.711. Chem Pharm Bull (Tokyo). 2002. PMID: 12045324 Review.
Cited by
-
Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids.J Nat Prod. 2012 Apr 27;75(4):812-33. doi: 10.1021/np200954v. Epub 2012 Apr 15. J Nat Prod. 2012. PMID: 22502590 Free PMC article. Review.
-
Enzyme evolution in fungal indole alkaloid biosynthesis.FEBS J. 2020 Apr;287(7):1381-1402. doi: 10.1111/febs.15270. FEBS J. 2020. PMID: 32118354 Free PMC article. Review.
-
Anti-Insect Properties of Penicillium Secondary Metabolites.Microorganisms. 2023 May 16;11(5):1302. doi: 10.3390/microorganisms11051302. Microorganisms. 2023. PMID: 37317276 Free PMC article. Review.
-
Mining for a new class of fungal natural products: the evolution, diversity, and distribution of isocyanide synthase biosynthetic gene clusters.Nucleic Acids Res. 2023 Aug 11;51(14):7220-7235. doi: 10.1093/nar/gkad573. Nucleic Acids Res. 2023. PMID: 37427794 Free PMC article.
-
Studies Towards Paraherquamides E & F and Related C-labeled Putative Biosynthetic Intermediates: Stereocontrolled Synthesis of the α-Alkyl-β-Methylproline Ring System.Tetrahedron. 2008 Jul 21;64(30):7106-7111. doi: 10.1016/j.tet.2008.05.068. Tetrahedron. 2008. PMID: 20336192 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials