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1. (Article ID: 8159)
Haroon MH, Premaratne SR, Choudhry MI, Dharmaratne HR
A new β-glucuronidase inhibiting butyrolactone from the marine endophytic fungus Aspergillus terreus
Natural Product Research 27(12) (2013)
1060-1066
An endophytic fungus Aspergillus terreus, var. boedijnii (Blochwitz) was isolated from red marine alga Laurencia ceylanica, J. Agardh, cultured in large scale and extracted with EtOAc. The above-mentioned extract yielded a new butyrolactone, 3-hydroxy-4-(4-hydroxyphenyl)-5-methoxycarbonyl-5-(4-hydroxy-3-formylbenzyl)-2,5-dihydro-2-furanone (1), along with the previously reported nine compounds, butyrolactone-1 (2), 6-hydroxymellin (3), (3R, 4R)-6,7-dimethoxy-4-hydroxymellin (4), (+)-territonin (5), (+)-territonin-A (6), (+)-asterrelenin (7), (+)-terrein (8), oleic acid (9) and glucopyranosyl-β-sitosterol (10), on column and preparative thin-layer chromatography. Compounds 1-8 were subjected to β-glucuronidase inhibitory activity test, and 1 showed a remarkable activity, while 2 and 7 showed moderate activity.
β-glucuronidase, Aspergillus terreus, Laurencia ceylanica, butyrolactone, 3-hydroxy-4-(4-hydroxyphenyl)-5-methoxycarbonyl-5-(4-hydroxy-3-formylbenzyl)-2, 5-dihydro-2-furanone
NCBI PubMed ID: 22913423Publication DOI: 10.1080/14786419.2012.708659Journal NLM ID: 101167924Publisher: Milton Park, UK : Taylor & Francis Health Sciences
Correspondence: Dharmaratne HR
olemiss.edu>
Institutions: Natural Products Programme, Institute of Fundamental Studies, Kandy, Sri Lanka, Faculty of Applied Sciences, South Eastern University of Sri Lanka, Oluvil, Sri Lanka, H.E.J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan, National Center for Natural Products Research, School of Pharmacy, University of Mississippi, University, MS, USA
Methods: IR, NMR, TLC, UV
The publication contains the following compound(s):
- Compound ID: 20490
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b-D-Glcp-(1-3)-Subst
Subst = β-sitosterol = SMILES O{3}[C@H](C1)CC[C@@]2(C)C1=CC[C@]3([H])[C@@]2([H])CC[C@@]4(C)[C@]3([H])CC[C@]4([C@@H](C)CC[C@@H](CC)C(C)C)[H] |
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Structure type: monomer
Trivial name: daucosterol, β-daucosterol, β-sitosterol, β-sitosterol-β-D-glucoside, androsine, saxifragifolin B, β-sitosterol 3-O-β-D-glucopyranoside
Compound class: saponin glycoside, glycoside, steroid glycoside, triterpenoid glycoside
Reference(s) to other database(s): GenDB:MK026953.1
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