Six new polyoxygenated steroids (1-6) along with clathriol (7) were isolated from the Korean marine sponge Clathria gombawuiensis. Based upon the results of combined spectroscopic analyses, the structures of gombasterols A-F (1-6) were elucidated to be those of highly oxygenated steroids possessing a 3β,4α,6α,7β-tetrahydroxy or equivalent (7β-sodium O-sulfonato for 3) substitution pattern and a C-15 keto group as common structural motifs. The relative and absolute configurations of these steroids, including the rare 14β configuration of 1-4, were determined by a combination of NOESY, J-based analyses, the 2-methoxy-2-(trifluoromethyl)phenylacetic acid (MTPA) method, and X-ray crystallographic analysis. The absolute configuration of 7 was also assigned by these methods. These compounds moderately enhanced 2-deoxy-2-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]-d-glucose (2-NBDG) uptake in differentiated 3T3-L1 adipocytes and phosphorylation of AMP-activated protein kinase (AMPK) and acetyl-CoA carboxylase (ACC) in differentiated mouse C2C12 skeletal myoblasts.
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http://dx.doi.org/10.1021/acs.jnatprod.7b00651 | DOI Listing |
Molecules
July 2023
Department of Chemistry, Higher Teacher Training College, University of Yaounde I, Yaounde P.O. Box 47, Cameroon.
Four polyoxygenated stigmastanes (-) alongside known analogues (-) and flavonoids (-) were isolated from a dichloromethane/methanol (1:1, /) extract of the whole plant of Sch. Bip. ex Walp.
View Article and Find Full Text PDFMar Drugs
March 2022
Doctoral Degree Program in Marine Biotechnology, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.
A polyoxygenated and halogenated labdane, spongianol (); a polyoxygenated steroid, 3β,5α,9α-trihydroxy-24-ethylcholest-7-en-6-one (); a rare seven-membered lactone B ring, (22,24)-ergosta-7,22-dien-3β,5α-diol-6,5-olide (); and an α,β-unsaturated fatty acid, ()-3-methyl-9-oxodec-2-enoic acid () as well as five known compounds, 10-hydroxykahukuene B (), pacifenol (), dysidamide (), 7,7,7-trichloro-3-hydroxy-2,2,6-trimethyl-4-(4,4,4-trichloro-3-methyl-1-oxobu-tylamino)-heptanoic acid methyl ester (), and the primary metabolite 2'-deoxynucleoside thymidine (), have been isolated from the Red Sea sponge sp. The stereoisomer of was discovered in , and metabolites and , isolated previously from red algae, were characterized unprecedentedly in the sponge. Compounds and have not been found before in the genus .
View Article and Find Full Text PDFPhytochemistry
February 2022
Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, 3 Taicheng Road, Yangling, 712100, Shaanxi, China. Electronic address:
Ganorbifates C-I, seven undescribed biosynthetically related polyoxygenated 3,4-seco-27-norlanostanoid congeners, were isolated from the edible mushroom, Ganoderma orbiforme. Ganorbifate C features a unique cyclobutene ring constructed at C19/C11, and both D and E incorporate an unusual cyclopropane ring formed by C-19/C-9 linkage. Their structures, including the absolute configurations, were determined by spectroscopic methods and ECD calculations.
View Article and Find Full Text PDFJ Nat Prod
December 2021
School of Environment and Science, Griffith University (Gold Coast Campus), Parklands Drive, Southport, QLD 4222, Australia.
During a recent biodiscovery study to identify new α-synuclein (α-syn) aggregation inhibitors, we screened 29 Australian marine sponge and ascidian extracts in an MS binding assay. This resulted in an extract from the ascidian showing activity toward α-syn. The bioassay and MS guided isolation process led to the identification of one new polyoxygenated sterol sulfate, sycosterol A ().
View Article and Find Full Text PDFPhytochemistry
April 2021
Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, 3 Taicheng Road, Yangling, 712100, Shaanxi, China. Electronic address:
Chaga mushroom, Inonotus obliquus, was used as food and nutrient food and traditional herbs in Russia, China and Japan, with anti-inflammatory and anticancer activities. Chemical investigations of the fruiting bodies of Chaga were carried to uncover the bioactive metabolites. As a result, seven undescribed lanostane-type triterpenoids, namely inonotusols H-N, were isolated, and all lanostanoids remarkably inhibited NO production in lipopolysaccharide-stimulated BV-2 microglial cells.
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