Page 94 - 《精细化工》2023年第9期
P. 94
·1942· 精细化工 FINE CHEMICALS 第 40 卷
[7] NASCIMENTO L, SANTOS E, AGUIAR A. Organic sunscreens. (E)-1-(benzo[d][1,3]dioxol-5-yl)-3-(2-chloro-6-fluorophenyl)prop-
Research, innovation and the organic synthesis importance[J]. 2-en-1-one[J]. Chemical Data Collections, 2021, 38: 100821.
Revista Virtual de Química, 2014, 6(2): 190-223. [29] OSTI S N, SOUZA S L, PALUDETTO S, et al. Structure and
[8] LIONETTI N, RIGANO L. The new sunscreens among formulation interaction roles in the release profile of chalcone-loaded
strategy, stability issues, changing norms, safety and efficacy liposomes[J]. Biophysical Chemistry, 2023, 292: 106930.
evaluations[J]. Cosmetics, 2017, 4: 15. [30] KUMAR S M, SHUBHAM J, SANDIP P, et al. Base-catalyzed
[9] MONTI D, BRINI I, TAMPUCCI S, et al. Skin permeation and traceless silylation and deoxygenative cyclization of chalcones to
distribution of two sunscreens: A comparison between reconstituted cyclopropanes[J]. The Journal of Organic Chemistry, 2022, 87:
human skin and hairless rat skin[J]. Skin Pharmacol Physiol, 2008, 6695-6709.
21(6): 318-325. [31] CHUKHLANTSEVA A N, DMITRIEV M V, MAIOROVA O A,
[10] KLIMOVÁ Z, HOJEROVÁ J, BERANKOVA M. Skin absorption et al. Synthesis and optical properties of new chalcones containing
and human exposure estimation of three widely discussed UV filters 4-[bis(2-hydroxyethyl)amino]phenyl fragment[J]. Mendeleev
in sunscreens-in vitro study mimicking real-life consumer habits[J]. Communications, 2022, 32(2): 274-277.
Food & Chemical Toxicology, 2015, 83: 237-250. [32] SANTOS A C, MARTO J, CHÁ-CHÁ R, et al. Nanotechnology-
[11] CAMERON G J, MICHAEL S R, HEATHER A E B. Systemic based sunscreens-A review[J]. Materials Today Chemistry, 2022, 23:
absorption of sunscreen after topical application[J]. Lancet, 1997, 100709.
350(9081): 863-864. [33] SHAATH N A. The encyclopedia of ultraviolet filter[J]. Journal of
[12] MEIER D, HERNÁNDEZ M V, VAN GEELEN L, et al. The Applied Cosmetology, 2008, 26(2): 94-96.
plant-derived chalcone xanthoangelol targets the membrane of [34] ZAINURI D A, RAZAK I A, ARSHAD S. Crystal structures, DFT
gram-positive bacteria[J]. Bioorganic & Medicinal Chemistry, 2019, studies and UV-visible absorption spectra of two anthracenyl chalcone
27(23): 1-30. derivatives[J]. Acta Crystallographica Section E: Crystallographic
[13] CAO Y Y, XU W X, HUANG Y Y, et al. A chalcone derivative from Communications, 2018, 74(10): 1491-1496.
glycyrrhiza inflata, as a multifunctional agent for the treatment of [35] XIAO Q F (肖乾芬), DAI X L (戴玄吏), WANG X D (王晓栋),
alzheimer's disease[J]. Natural Product Research, 2020, 34(5): 736-739. et al. Quantitative structure-genotoxicity of substituted benzene on
[14] EDEN W T, ALIGHIRI D, WIJAYATI N, et al. Synthesis of chalcone human cells[J]. China Environmental Sciences (中国环境科学),
derivative from clove leaf waste as a natural antioxidant[J]. 2005, 25(1): 18-22.
Pharmaceutical Chemistry Journal, 2021, 55(3): 269-274. [36] KHADIKAR P, MATHER K, SINGH S, et al. Study on quantitative
[15] RIZWAN A, MANISH R, SHAMA Y, et al. Facile synthesis of structure-toxicity relationships for benzene derivatives acting by
chalcone derivatives as antibacterial agents: Synthesis, DNA binding, narcosis[J]. Bioorganic and Medicinal Chemistry, 2002, 10(6):
molecular docking, DFT and antioxidant studies[J]. Journal of 1761-1766.
Molecular Structure, 2020, 1208(C): 127905. [37] ZENGER K, DUTTA S, WOLFF H, et al. In vitro structure-toxicity
[16] MELLADO M, MADRID A, MARTÍNEZ Ú, et al. Hansch's analysis relationship of chalcones in human hepatic stellate cells[J].
application to chalcone synthesis by Claisen-Schmidt reaction based in Toxicology, 2015, 336: 26-33.
DFT methodology[J]. Chemical Papers, 2017, 72(3): 703-709. [38] SINGH G, SINGH J, MANGAT S, et al. Synthetic approach towards
[17] OUYANG Y, LI J J, CHEN X Y, et al. Chalcone derivatives: Role in âclickâ modified chalcone based organotriethoxysilanes; UV-Vis
anticancer therapy[J]. Biomolecules, 2021, 11(6): 894. study[J]. RSC Advances, 2014, 4(105): 60853-60865.
[18] AYANDA I Z, OGUNYEMI O O, CUAN K, et al. Synthesis, [39] SCHULTZ T, YARBROUGH J. Trends in structure-toxicity relationships
structure and in vitro anti-trypanosomal activity of non-toxic arylpyrrole- for carbonyl-containing alpha, beta-unsaturated compounds[J]. SAR
based chalcone derivatives[J]. Molecules, 2020, 25(7): 1668. and QSAR in Environmental Research, 2004, 15(2): 139-146.
[19] MICHELINI L, CASTRO M, CUSTODIO J, et al. A novel potential [40] OLEXANDR I, BAKHTIYOR R, LEONID G, et al. Structure-
anticancer chalcone: Synthesis, crystal structure and cytotoxic toxicity relationships of nitroaromatic compounds[J]. Molecular
assay[J]. Journal of Molecular Structure, 2018, 1168: 309-315. Diversity, 2006, 10(2): 233-245.
[20] RAGHAVENDER M, KUMAR A, SUNITHA V, et al. Synthesis and [41] LAI G Q (来国侨), XING S M (幸松民). Synthesis technology and
cytotoxicity of chalcone based 1, 2, 3-triazole derivatives[J]. Russian application of organosilicon products[M]. Beijing: Chemical Industry
Journal of General Chemistry, 2020, 90(4): 697-702. Press (化学工业出版社), 2009.
[21] ARINA N, MUSTOFA M, INDWIANI A, et al. Cytotoxic activity of [42] BALDWIN S. ChemInform Abstract: Synthetic aspects of 2+2
methoxy-4'amino chalcone derivatives against leukemia cell lines[J]. cycloadditions of α, β-unsaturated carbonyl compounds[J]. Chemischer
Molecular and Cellular Biomedical Sciences, 2019, 3(1): 34-43. Informationsdienst, 1981, 12(44): 123-225.
[22] FRIMAYANTI N, ISKANDAR B, PUTRI R D. Docking studies of [43] SCHUBERT W, SWEENEY W. The effect of ring strain on the
chalcone analogue compounds as inhibitors for breast cancer MCF7 ultraviolet spectra of α,β-unsaturated carbonyl compounds[J]. Journal
cell line[J]. Der Pharma Chemica, 2019, 11(2): 31-35. of the American Chemical Society, 1955, 77(8): 2297-2300.
[23] STANTLIFF T M, KRZYSIAK A J. Investigations of the mechanism [44] RANGASWAMI S, RAO V, SESHADRI T. Reactivity of the double
of action for lung cancer cell death by a 4'-trifluoromethoxy substituted bond in coumarins and related α, β-unsaturated carbonyl compounds[J].
chalcone derivative[J]. The FASEB Journal, 2019, 33(S1): 417-418. Proceedings-Mathematical Sciences, 1938, 7(5): 312-318.
[24] LUCIA W W, RESPATI T S, WONKOO L, et al. Synthesis and [45] HANSON K M, CUTULI M, RIVAS T, et al. Effects of solvent and
evaluation of chalcone derivatives as novel sunscreen agent[J]. micellar encapsulation on the photostability of avobenzone[J].
Molecules, 2021, 26: 2698. Photochemical & Photobiological Sciences, 2020, 19(3): 390-398.
[25] EGERTON P, PITTS E, REISER A. Photocycloaddition in solid [46] SIMONE D, ALESSANDRA A, LUCIA C, et al. Environmentally
poly(vinyl cinnamate). The photoreactive polymer matrix as an ensemble friendly sunscreens: Mechanochemical synthesis and characterization
of chromophore sites[J]. Macromolecules, 1981, 14(1): 95-100. of beta-CD inclusion complexes of avobenzone and octinoxate with
[26] FURUMI S, ICHIMURA K, SATA H, et al. Photochemical improved photostability[J]. ACS Sustainable Chemistry & Engineering,
manipulation of discotic liquid crystal alignment by a poly(vinyl 2020, 8(35): 13215-13225.
cinnamate) thin film[J]. Applied Physics Letters, 2000, 77(17): 2689. [47] ANKITA P, RAJASHREE S M, ARCHANA S P, et al. Microsponge
[27] ZHANG J (张洁), LONG Y (龙泳), XUAN W M (宣为民), et al. gel approach to increase the stability and efficacy of avobenzone as a
Preparation and photocrosslinking properties of polyacid-chalone sun-protective agent[J]. Journal of Pharmaceutical Innovation,
hybrid molecules[J]. Chinese Science Bulletin (科学通报), 2017, 2022,17(4): 1347-1359.
62(7): 685-692. [48] Cosmetics-Sun protection test methods-In vivo determination of
[28] HUSNA N, FATIHAH J, MOHD N, et al. Synthesis, structural sunscreen UVA protection: ISO 24443—2012[S]. Switzerland, 2012:
investigation and computational analysis on a new chalcone derivative: 2-10.