About: The antityrosinase and antioxidant activities of flavonoids dominated by the number and location of phenolic hydroxyl groups

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scholarly article by Ai-Ren Zuo et al published 2018 in Chinese Medicine

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) im Januar 2018 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована у 2018 (uk) article scientifique publié en 2018 (fr) scholarly article by Ai-Ren Zuo et al published 2018 in Chinese Medicine (en)
publication date	wds:Q58586897-1FC92E88-B98A-45CB-835C-69A1067E2427
publication date	2018-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58586897-3561FA3D-C40C-4AFB-87E5-C34504C0C011
language of work or name	English
exact match	wds:Q58586897-0C5C058F-5238-46F2-A069-1A13CEDE8A7C
exact match	https://scigraph.springernature.com/pub.10.1186/s13020-018-0206-9
cites work	wds:Q58586897-007B18D0-8BD0-4269-B78B-FB24301D7726 wds:Q58586897-04950A22-7CA5-4D6E-8BF9-E80B335C91E3 wds:Q58586897-1E702FC2-009A-4DF0-8BF2-C02A8F60A25F wds:Q58586897-24EC92DF-67AB-4DE8-B7A6-4F56A3CEF589 wds:Q58586897-3EB2B9C9-4436-41FD-AD63-B17097191C6F wds:Q58586897-406A3494-4EA5-45BB-9885-1F92C080F160 wds:Q58586897-453722D3-D7F4-442A-B7A2-744BD6642AE1 wds:Q58586897-45C89B17-49A8-4855-B214-57DAA2B6EDB2 wds:Q58586897-4A7C3887-3B7E-4227-932A-C6A4431FCD91 wds:Q58586897-4C896399-0136-4CEC-AFB2-782CDFCDF236 wds:Q58586897-50B41DEF-E309-42D3-A05E-63AC5033C1CC wds:Q58586897-58405790-75DC-417A-BFB8-32549E088FD8 wds:Q58586897-5AF03935-8C33-408B-BD40-DB193C7DC182 wds:Q58586897-5DA4E738-9638-482D-AAC4-2DAA3A2999FF wds:Q58586897-656EFC7D-3597-4320-8718-B7198A34F835 wds:Q58586897-6B8BDC8E-40C4-45F9-96EC-4B3BF7D11714 wds:Q58586897-7DF8B8C8-FD94-4AF2-B834-5296602151D0 wds:Q58586897-82C96F3D-162B-4C7A-80F6-A3F3BDB1F85C wds:Q58586897-9815B6E7-E7D0-4856-AB54-74711D43A4F7 wds:Q58586897-9BACD1DA-F5B9-4779-BCC4-741CD0B208EE wds:Q58586897-9D7F2836-D8F6-40FA-8CCA-6D8BA2EC0101 wds:Q58586897-9F6658F2-EE10-4FA9-B255-DE9D5F3CDF12 wds:Q58586897-AF936B69-D3E0-4712-BF20-CA6C6C96D990 wds:Q58586897-B524592F-34CB-4D95-B22A-947BD9EE8C2E wds:Q58586897-B569DBF0-5BF6-4D9A-AE98-6E0A5CAA9799 wds:Q58586897-B7326687-86B8-4226-B212-1E54EC62BF85 wds:Q58586897-C006CA6C-5643-4FF5-B8D8-A028ADC7490F wds:Q58586897-C336230F-0F7E-4FE3-A6FB-878333D18777 wds:Q58586897-CAA528C3-6EA2-413A-8971-45C1F5AE5796 wds:Q58586897-D231116C-FEB1-48E4-88A1-4F35A5EBE293 wds:Q58586897-DC126516-D9AC-4A8F-9168-D978D70F2990 wds:Q58586897-E1590940-5241-4044-BDB5-82B216498C00 wds:Q58586897-E4D20497-236D-45E8-9D26-D49FA69AE5DF wds:Q58586897-E92B8810-7122-4FB4-8E79-DAA98DECB328 wds:Q58586897-E9AE06C8-5011-4AAF-8FAA-D9AE38D8682F wds:Q58586897-EA1A7B16-BB5B-44B5-8448-8DC8F3443673
cites work	Structure-radical scavenging activity relationships of flavonoids Structure-radical scavenging activity relationships of phenolic compounds from traditional Chinese medicinal plants. Inhibition of tyrosinase by flavonoids, stilbenes and related 4-substituted resorcinols: structure-activity investigations New therapeutic aspects of flavones: the anticancer properties of Scutellaria and its main active constituents Wogonin, Baicalein and Baicalin Involvement of reactive oxygen species, but not mitochondrial permeability transition in the apoptotic induction of human SK-Hep-1 hepatoma cells by shikonin A new stilbene with tyrosinase inhibitory activity from Chlorophora excelsa Chalcones as potent tyrosinase inhibitors: the effect of hydroxyl positions and numbers The flavonoid phloretin suppresses stimulated expression of endothelial adhesion molecules and reduces activation of human platelets. Isolation and identification of flavonoids in licorice and a study of their inhibitory effects on tyrosinase Flavonoids as mushroom tyrosinase inhibitors: a fluorescence quenching study. Baicalein, an active component of Scutellaria baicalensis, protects against lipopolysaccharide-induced acute lung injury in rats Baicalein, an alpha-glucosidase inhibitor from Scutellaria baicalensis Rosmarinic acid, a photo-protective agent against UV and other ionizing radiations Characterization of a novel tyrosinase inhibitor, (2RS,4R)-2-(2,4-dihydroxyphenyl)thiazolidine-4-carboxylic acid (MHY384). Chalcones as potent tyrosinase inhibitors: the importance of a 2,4-substituted resorcinol moiety Rosmarinic acid extract for antioxidant, antiallergic, and α-glucosidase inhibitory activities, isolated by supramolecular technique and solvent extraction from Perilla leaves Enhancement of cisplatin induced apoptosis by suberoylanilide hydroxamic acid in human oral squamous cell carcinoma cell lines DNA strand breakage and oxygen tension: effects of beta-carotene, alpha-tocopherol and ascorbic acid Gnetol as a Potent Tyrosinase Inhibitor from GenusGnetum Skin whitening agents: medicinal chemistry perspective of tyrosinase inhibitors. Tyrosinase-mediated formation of a reactive quinone from the depigmenting agents, 4-tert-butylphenol and 4-tert-butylcatechol Endomorphins, endogenous opioid peptides, provide antioxidant defense in the brain against free radical-induced damage Chemical compositions, chromatographic fingerprints and antioxidant activities of Citri Exocarpium Rubrum (Juhong) Antioxidant activity and free radical-scavenging capacity of Gynura divaricata leaf extracts at different temperatures Molecular docking and QSAR analyses of aromatic heterocycle thiosemicarbazone analogues for finding novel tyrosinase inhibitors. Molecular modeling study of CP-690550 derivatives as JAK3 kinase inhibitors through combined 3D-QSAR, molecular docking, and dynamics simulation techniques. Inhibitory effects of resveratrol derivatives from dipterocarpaceae plants on tyrosinase activity Reevaluating the role of 1,10-phenanthroline in oxidative reactions involving ferrous ions and DNA damage Dehydrozingerone, chalcone, and isoeugenol analogues as in vitro anticancer agents Antioxidant properties of demethyldiisoeugenol Synthesis and antityrosinase mechanism of benzaldehyde thiosemicarbazones: novel tyrosinase inhibitors A novel ring-expanded product with enhanced tyrosinase inhibitory activity from classical Fe-catalyzed oxidation of rosmarinic acid, a potent antioxidative Lamiaceae polyphenol Chemical exploration of 4-(4-fluorobenzyl)piperidine fragment for the development of new tyrosinase inhibitors. Phytochemicals and potential health effects of Sambucus williamsii Hance (Jiegumu) Chemical constituents from a Gynostemma laxum and their antioxidant and neuroprotective activities. Hepatoprotective effects and antioxidant, antityrosinase activities of phloretin and phloretin isonicotinyl hydrazone
author name string	wds:Q58586897-01407403-54E1-459A-AD76-BD6D09B032C4 wds:Q58586897-135E10A4-EF65-4669-A98A-5513DC90657D wds:Q58586897-2054EA2F-E482-4371-859C-7EA8570DF305 wds:Q58586897-6385523A-3519-49B5-B3E2-C65C9E189BB0 wds:Q58586897-726F0F54-2BFD-455D-903A-2B2780B02FBC wds:Q58586897-878C1DD4-34A0-4942-935A-9203ACF0512B wds:Q58586897-E9A0AE26-2213-4B06-A7F4-C4713C97AC0F
author name string	Xiong-Ying Yu Shu-Wen Cao Yan-Ying Yu Huan-Huan Dong Ai-Ren Zuo Li-Xiang Zheng Qing-Long Shu
rdfs:label	The antityrosinase and antioxidant activities of flavonoids dominated by the number and location of phenolic hydroxyl groups (en) The antityrosinase and antioxidant activities of flavonoids dominated by the number and location of phenolic hydroxyl groups (nl)

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