Results 161 to 170 of about 6,879 (216)

<i>Drosera rotundifolia</i> L. as <i>E. coli</i> biofilm inhibitor: Insights into the mechanism of action using proteomics/metabolomics and toxicity studies. [PDF]

open access: yesBiofilm
Gerschler S   +12 more
europepmc   +1 more source

The Use of Naphthoquinones and Furano-naphthoquinones as Antiinvasive Agents

open access: yesCurrent Medicinal Chemistry, 2019
Background: Cancer is a leading cause of mortality in the world and metastasis is to blame. A number of naphthoquinones (NQs) have shown ability to reduce cancer stemness and metastatic potential. Furano-naphthoquinones (FNQs), which is a class of NQ characterized by the incorporation of an additional furan ring, have demonstrated improved anti ...
Nga Yi, Tsang   +5 more
openaire   +3 more sources

Naphthoquinone metabolites of the fungi

Phytochemistry, 1998
Structures and physico-chemical properties of 100 naphthoquinone metabolites produced by filamentous fungi are reviewed. The conditions of pigment formation, biogenesis and the mechanism of biosynthesis of pigments by fungi are described. Sixty-three fungi cultures able to produce naphthoquinone are listed.
A G, Medentsev, V K, Akimenko
openaire   +2 more sources

Dihydroxyacetone Naphthoquinone Sunscreen

JAMA: The Journal of the American Medical Association, 1972
To the Editor.— During the past decade, we have successfully used a sunscreen containing dihydroxyacetone/ naphthoquinone (lawsone) for patients with all types of cutaneous photosensitivity. 1 An advantage of this sunscreen is its capacity to induce a broad "ultraviolet shield" (290 to 405 nm) in the uppermost layer of the skin.
R M, Fusaro, J A, Johnson
openaire   +2 more sources

Iodinated 1,4-naphthoquinones

Russian Chemical Bulletin, 2005
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
N. V. Ivashkina   +4 more
openaire   +1 more source

Potent antitumor activity of synthetic 1,2-Naphthoquinones and 1,4-Naphthoquinones

Bioorganic & Medicinal Chemistry, 2003
Rhinacanthone (1) and two 1,2-pyranonaphthoquinones (2,3) were synthesized and found to show very potent cytotoxicity against three cancer cell lines (KB, HeLa and HepG(2)) with IC(50) values of 0.92-9.63 microM, whereas the corresponding hydroxylated derivative 4 had reduced cytotoxicity (IC(50) values of 7.61-24.13 microM).
Ngampong, Kongkathip   +8 more
openaire   +2 more sources

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