Beauty - Cosmetic Science, Cultural Issues and Creative Developments 2021
DOI: 10.5772/intechopen.91145
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Chalcones in Dermatology

Abstract: The human skin is pivotal for protecting the body from various stresses and diseases, regulating several physiological aspects, and sensing any signal changes around the environment. To work and function optimally, the skin should be protected and cared regularly by using some treatments. Chalcone, as a privileged structure, exhibits wide and unique bioactivities related to several skin disorders such as in preventing and treating pigmentation disorders (melasma and vitiligo), cutaneous leishmaniasis, rashes (… Show more

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Cited by 4 publications
(5 citation statements)
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“…The shift of the C-6 protons of the mannopyranose rest to higher chemical shifts, specifically δ 4.85 (appearing as a multiplet, denoted as H-6a) and δ 4.81 (appearing as a multiplet, denoted as H-6b), compared to their initial values (~4.00 ppm in compound 6), indicated the attachment of the cinnamoyl group at the less hindered and more reactive position, namely, position 6. The remainder of the FTIR and 1 H-NMR spectra consistently matched the structure assigned to methyl 6-O-cinnamoyl-α-D-mannopyranoside (2) [22].…”
Section: Characterizationsupporting
confidence: 53%
See 1 more Smart Citation
“…The shift of the C-6 protons of the mannopyranose rest to higher chemical shifts, specifically δ 4.85 (appearing as a multiplet, denoted as H-6a) and δ 4.81 (appearing as a multiplet, denoted as H-6b), compared to their initial values (~4.00 ppm in compound 6), indicated the attachment of the cinnamoyl group at the less hindered and more reactive position, namely, position 6. The remainder of the FTIR and 1 H-NMR spectra consistently matched the structure assigned to methyl 6-O-cinnamoyl-α-D-mannopyranoside (2) [22].…”
Section: Characterizationsupporting
confidence: 53%
“…13 C NMR (100 MHz, CDCl 3 ): δ C 165 22. (C 6 H 5 CH=CHCO-), 144.20, 143.26 (×3), 138.49 (×3), 128.25 (×3), 128.24 (×3), 125.45 (×3), 20.69, 20.66 {3 × p-CH 3 C 6 H 4 SO 2 -}, 150.71 (C 6 H 5 CH=CHCO-), 132.63, 132.41, 129.56 (×2), 129.11 (×2) (C 6 H 5 CH=CHCO-), 122.32 (C 6 H 5 CH=CHCO-), 97.25 (C-1), 72.11 (C-2), 71.32 (C-4), 70.71 (C-3), 69.49 (C-5), 63.13 (C-6), 55.46 (1-OCH 3 ), 14.20, 14.11, 14.04 {3 × p-CH 3 C 6 H 4 SO 2-}.…”
mentioning
confidence: 99%
“…Therefore, the selectivity of the HDS process is suboptimal, and it can damage aromatic hydrocarbon compounds in crude oil during the HDS of DBT. 16,17 In general, the ODS process is used to convert refractory thiophenic compounds, such as DBT, into sulfone and sulfoxide species. This is achieved using various oxidants, including H 2 O 2 , 18 molecular oxygen, 19 formic acid, 20 and ozone, 21 at atmospheric pressure and low temperatures (50−70 °C).…”
Section: Approaches For Desulfurizationmentioning
confidence: 99%
“…High [9,14,15 In recent times, the traditional technologies of HM remediation (Figure 1B) include physical methods (physical adsorption [24], leaching [25], and electrokinetic remediation [26]), chemical methods (flocculation precipitation [27], electrolysis [28], ion exchange adsorption [29] and chemical precipitation [30]), and biological methods (phytoremediation [31], microbial adsorption [32], microbial fuel cell [33] and biomineralization [34]). Among the proposed methods, biological or microbiological methods have the advantages of relative sustainability, environmental benignity, and low cost [35][36][37].…”
Section: Introductionmentioning
confidence: 99%