ACTIVES Tetra - carboxy - methyl - naringenin - chalcone , a new active to treat rosacea
نویسنده
چکیده
Tetra-carboxy-methyl-naringenin-chalcone (TCM-NC) is a new cosmetic active derived from naringenin, a flavanone naturally occurring in the peel of citrus fruit and tomato skin. The naringenin isomer naringenin-chalcone has been reported to have potent anti-allergic properties. For this reason the effect of TCM-NC was studied in an in vitro assay mimicking the inflammation pathway of rosacea skin and skin redness. In rosacea skin, an overexpression and release of cathelicidin by surface keratinocytes leads to an inflammatory reaction in neighboring keratinocytes. If not treated, a chronic inflammation can develop inducing increased local blood flow and angiogenesis. In this paper, the inhibitory effect of the new TCM-NC on the cathelicidin-induced inflammatory reaction in human epidermal keratinocytes is reported. In a clinical study performed on volunteers with rosacea skin, TCM-NC clearly diminishes capillary blood flow and thereby the appearance of facial redness.
منابع مشابه
Identification of amino acid residues important in the cyclization reactions of chalcone and stilbene synthases.
Chalcone synthase (CHS) and stilbene synthase (STS) catalyse condensation reactions of p-coumaroyl-CoA and three C(2) units from malonyl-CoA up to a common tetraketide intermediate but then catalyse different cyclization reactions to produce naringenin chalcone and resveratrol respectively. On the basis of sequence alignment with other condensing enzymes including 3-ketoacyl-(acyl carrier prote...
متن کاملEvidence for catalytic cysteine-histidine dyad in chalcone synthase.
Chalcone and stilbene synthases (CHS and STS) catalyze condensation reactions of p-coumaroyl-CoA and three C(2)-units from malonyl-CoA, but catalyze different cyclization reactions to produce naringenin chalcone and resveratrol, respectively. Condensing activities of wild-type CHS and STS as well as STS-C60S mutant were inhibited by iodoacetamide (Idm) and diethyl pyrophosphate (DPC). DPC also ...
متن کاملCross-reaction of chalcone synthase and stilbene synthase overexpressed in Escherichia coli.
Chalcone synthase (CHS) and stilbene synthase (STS) are related plant polyketide synthases belonging to the CHS superfamily. CHS and STS catalyze common condensation reactions of p-coumaroyl-CoA and three C(2)-units from malonyl-CoA but different cyclization reactions to produce naringenin chalcone and resveratrol, respectively. Using purified Pueraria lobata CHS and Arachis hypogaea STS overex...
متن کاملEnzymatic Properties and Mutational Studies of Chalcone Synthase from Physcomitrella patens
PpCHS is a member of the type III polyketide synthase family and catalyses the synthesis of the flavonoid precursor naringenin chalcone from p-coumaroyl-CoA. Recent research reports the production of pyrone derivatives using either hexanoyl-CoA or butyryl-CoA as starter molecule. The Cys-His-Asn catalytic triad found in other plant chalcone synthase predicted polypeptides is conserved in PpCHS....
متن کاملSynthesis and antihepatotoxic activity of some new chalcones containing 1, 4 - dioxane ring system.
Silybum marianum is a medicinal plant used widely for treating liver diseases. The silymarin, a mixture of three flavolignan isomers namely silybin (1), silydianin (2), and silychristin (3) is an active constituent of the plant. However, silybin containing 1, 4-dioxane ring is the most potent antihepatotoxic agent. In contrast, other isomers do not possess 1, 4-dioxane ring, and thus do not exh...
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تاریخ انتشار 2013