By feeding tryptophan to the marine-derived fungus sp. HNMF114 from the bivalve mollusk , 3 new quinazoline-containing indole alkaloids, named aspertoryadins H-J (-), along with 16 known ones (-), were obtained. The structures of the new compounds were elucidated by the analysis of spectroscopic data combined with quantum chemical calculations of nuclear magnetic resonance (NMR) chemical shifts and electron capture detector (ECD) spectra. Structurally, compound represents the first example of this type of compound, bearing an amide group at C-3. Compounds and showed potent α-glucosidase inhibitory activity with IC values of 7.18 and 5.29 μM, and compounds and showed a clear activation effect on the ryanodine receptor from (sfRyR), which reduced the [Ca] by 37.1 and 36.2%, respectively.
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http://dx.doi.org/10.3389/fmicb.2021.680879 | DOI Listing |
Front Microbiol
June 2021
College of Life Science, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of Ministry of Education, Hebei University, Baoding, China.
By feeding tryptophan to the marine-derived fungus sp. HNMF114 from the bivalve mollusk , 3 new quinazoline-containing indole alkaloids, named aspertoryadins H-J (-), along with 16 known ones (-), were obtained. The structures of the new compounds were elucidated by the analysis of spectroscopic data combined with quantum chemical calculations of nuclear magnetic resonance (NMR) chemical shifts and electron capture detector (ECD) spectra.
View Article and Find Full Text PDFJ Nat Prod
December 2019
Hainan Key Laboratory for Research and Development of Natural Product from Li Folk Medicine , Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agriculture Sciences , Haikou 571101 , People's Republic of China.
Seven new quinazoline-containing indole alkaloids (-) named aspertoryadins A-G, along with nine known ones (-), were isolated from the marine-derived fungus sp. HNMF114 from the bivalve mollusk . The structures of the new compounds were elucidated from spectroscopic data, X-ray diffraction analysis, ECD spectra analysis, and ECD calculations.
View Article and Find Full Text PDFJ Am Chem Soc
March 2011
Department of Chemical and Biomolecular Engineering, University of California Los Angeles, Los Angeles, California 90095, USA.
Tremorgenic mycotoxins are a group of indole alkaloids which include the quinazoline-containing tryptoquivaline (2) that are capable of eliciting intermittent or sustained tremors in vertebrate animals. The biosynthesis of this group of bioactive compounds, which are characterized by an acetylated quinazoline ring connected to a 6-5-5 imidazoindolone ring system via a 5-membered spirolactone, has remained uncharacterized. Here, we report the identification of a gene cluster (tqa) from P.
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