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6,7,8-trimethoxycoumarin

 
National Institutes of Health

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Coumarins

Papers overview

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2019
2019
Anti-inflammatory activity of coumarins isolated from Tagetes lucida Cav.
The anti-inflammatory activity of hexane (TlH) and acetone (TlAc) extracts from the aerial parts of Tagetes lucida were evaluated… Expand
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2015
2015
Gastroprotective Efficacy and Safety Evaluation of Scoparone Derivatives on Experimentally Induced Gastric Lesions in Rodents
This study investigated the gastroprotective efficacy of synthesized scoparone derivatives on experimentally induced gastritis… Expand
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2013
2013
Total Synthesis of Six 3,4-Unsubstituted Coumarins
In this article we describe a new methodology for the total synthesis of 3,4-unsubstituted coumarins from commercially available… Expand
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Highly Cited
2009
Highly Cited
2009
In silico target fishing for rationalized ligand discovery exemplified on constituents of Ruta graveolens.
The identification of targets whose interaction is likely to result in the successful treatment of a disease is of growing… Expand
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2004
2004
Methyltransferase activity in Allanthm altissima cell suspension cultures
Enzymes for the methylation of 1hydroxycanthin-6-one and a series of coumarins have been isolated from Ailanthus altissima cell… Expand
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Highly Cited
1999
Highly Cited
1999
Antiviral flavonoid from Pterocaulon sphacelatum, an Australian Aboriginal medicine.
The antipicornaviral activity of an ethanolic extract of the green aerial parts of the Australian plant Pterocaulon sphacelatum… Expand
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1996
1996
Constituents from the stem wood of Euphorbia quinquecostata with phorbol dibutyrate receptor-binding inhibitory activity.
Bioassay-guided fractionation of an EtOAc extract of the stem wood of Euphorbia quinquecostata using a phorbol dibutyrate… Expand
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1994
1994
Antibiotic activity and absolute configuation of 8S-heptadeca-2(Z),9(Z)-diene-4,6-diyne-1,8-diol from Bupleurum salicifolium.
A polyacetylene has been isolated from Bupleurum salicifolium. Its structure and absolute configuration were determined to be 8S… Expand
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