2844-24-8Relevant academic research and scientific papers
THERAPEUTIC AGENTS FOR SKIN DISEASES AND CONDITIONS
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Page/Page column 36; 48-49; 54, (2015/06/18)
The present invention relates to method(s) of treating a subject afflicted with a skin disease or condition, the method comprising administering to the subject or patient in need a composition comprising a therapeutically effective amount of a substituted cis or trans- stilbene or a stilbene hybrid. A method of treating or reducing the likelihood of a skin disease or condition in a patient is an additional embodiment of the present invention. Preferred pharmaceutical compositions of the invention include nanoemulsions comprising a therapeutically effective amount of a substituted cis or trans-stilbene or stilbene hybrid and at least one antibiotic.
Substituted CIS- and trans-stilbenes as therapeutic agents
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Page/Page column 22, (2010/11/28)
The present invention relates to method(s) of treating a subject afflicted with cancer or a precancerous condition, an inflammatory disease or condition, and/or stroke or other ischemic disease or condition, the method comprising administering to the subject or patient in need a composition comprising a therapeutically effective amount of a substituted cis or trans-stilbene.
Substituted trans-stilbenes, including analogues of the natural product resveratrol, inhibit the human tumor necrosis factor alpha-induced activation of transcription factor nuclear factor kappaB
Heynekamp, Justin J.,Weber, Waylon M.,Hunsaker, Lucy A.,Gonzales, Amanda M.,Orlando, Robert A.,Deck, Lorraine M.,Vander Jagt, David L.
, p. 7182 - 7189 (2007/10/03)
The transcription factor nuclear factor kappaB (NF-κB), which regulates expression of numerous antiinflammatory genes as well as genes that promote development of the prosurvival, antiapoptotic state is up-regulated in many cancer cells. The natural product resveratrol, a polyphenolic trans-stilbene, has numerous biological activities and is a known inhibitor of activation of NF-κB, which may account for some of its biological activities. Resveratrol exhibits activity against a wide variety of cancer cells and has demonstrated activity as a cancer chemopreventive against all stages, i.e., initiation, promotion, and progression. The biological activities of resveratrol are often ascribed to its antioxidant activity. Both antioxidant activity and biological activities of analogues of resveratrol depend upon the number and location of the hydroxy groups. In the present study, phenolic analogues of resveratrol and a series of substituted trans-stilbenes without hydroxy groups were compared with resveratrol for their abilities to inhibit the human tumor necrosis factor alpha-induced (TNF-α) activation of NF-κB, using the Panomics NF-κB stable reporter cell line 293/NF-κB-luc. A series of 75 compounds was screened to identify substituted trans-stilbenes that were more active than resveratrol. Dose-response studies of the most active compounds were carried out to obtain IC50 values. Numerous compounds were identified that were more active than resveratrol, including compounds that were devoid of hydroxy groups and were 100-fold more potent than resveratrol. The substituted trans-stilbenes that were potent inhibitors of the activation of NFκB generally did not exhibit antioxidant activity. The results from screening were confirmed using BV-2 microglial cells where resveratrol and analogues were shown to inhibit LPS-induced COX-2 expression.
Electronic Structure and Free-Energy Relationships for Some 4'-Substituted 4-Dimethylamino trans-Stilbenes by U.V. Photoelectron Spectroscopy
Cauletti, C.,Furlani, C.,Palma, A.,Piancastelli, M. N.,Schleinitz, K. D.,Gloyna, D.
, p. 829 - 836 (2007/10/02)
A series of 4'-substituted 4-dimethylamino trans-stilbenes 1-5 was investigated by UPS, in connection with conjugated donor-acceptor substituted double bond photochemistry.The measured and assigned spectra indicate a high sensitivity, depending on the changed electronic structure by 4'-substituents of compounds 1-5.Correlation of ionization energies in LFE-relationship with Hammett's ?p-values and other ground state data was proved, demonstrating UPS a powerful tool for substituent effect studies in conjugated double bond systems.
