About: Antioxidative effects of phenylethanoids from Cistanche deserticola

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scientific article published on 01 December 1996

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1996 (uk) im Dezember 1996 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 1996 (ast) scientific article published on 01 December 1996 (en)
publication date	wds:Q71976537-73A2B786-8A15-4605-B59D-1BE696F92DCB
publication date	1996-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q71976537-0F8542F9-2AB4-4B04-8542-ADEF58AA1E94 wds:Q71976537-1148B6B6-FA0C-4E58-AE66-89D43511496A wds:Q71976537-1381DCFC-0C82-4AFB-BFD0-6DF1A47C29CF wds:Q71976537-13BEE545-8DF8-4C85-A06F-A106DD33A4CD wds:Q71976537-22483634-B208-4AAD-B84A-DEA354806099 wds:Q71976537-285EEB51-E5D6-4105-85FA-F76C4C61FA43 wds:Q71976537-29D98EBF-8326-4940-A7E3-B075EC3D593C wds:Q71976537-2F1E560D-B977-4E0E-8D86-2F2EAF0D9C76 wds:Q71976537-3290BEEA-60FA-49EF-8D75-27FE0D549070 wds:Q71976537-619A3294-9717-4F06-BEC4-FC6CD031261C wds:Q71976537-6FFC7842-78CA-4AE6-A9AC-8233E7DD4B43 wds:Q71976537-70C094B7-EB38-47F2-8EFE-D69EE3ED1993 wds:Q71976537-73DA425A-EFBC-405E-B925-3F4AFAEA7720 wds:Q71976537-830F7FA6-063D-488B-AA54-899D374FEAE5 wds:Q71976537-99B846B1-2274-4736-AE0F-9F10708C4201 wds:Q71976537-A080F60B-0D0E-4713-8900-AA826827526F wds:Q71976537-AF6FC683-0D95-4645-8700-899E063A47D5 wds:Q71976537-B7ECC04A-73A4-48BE-9BDD-B1B274936C84 wds:Q71976537-C44C8F40-0249-40E3-AB63-49A7E5B02F6D wds:Q71976537-CD40C6DB-76FD-4CAF-A50C-663C59000BD7 wds:Q71976537-DBC7144C-F97A-4DA1-A480-7BD9CEFBA33B wds:Q71976537-EA0856A4-ED30-4C62-8148-98448AF3EFE5 wds:Q71976537-EC22E242-2161-447C-B638-F7372F32A041 wds:Q71976537-F4BA8C62-1740-49F2-9122-9B8E5CE8B9DA wds:Q71976537-F8F65898-E2EE-4FE8-985F-9ED6BB359DFF
cites work	Chelating and free radical scavenging mechanisms of inhibitory action of rutin and quercetin in lipid peroxidation Flavonoids are scavengers of superoxide anions. Bcl-2 functions in an antioxidant pathway to prevent apoptosis The pecking order of free radicals and antioxidants: lipid peroxidation, alpha-tocopherol, and ascorbate Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction Antineoplastic agents, 107. Isolation of acteoside and isoacteoside from Castilleja linariaefolia Mechanism of antihepatotoxic activity of glycyrrhizin. I: Effect on free radical generation and lipid peroxidation Most free-radical injury is iron-related: it is promoted by iron, hemin, holoferritin and vitamin C, and inhibited by desferoxamine and apoferritin The requirement for ferric in the initiation of lipid peroxidation by chelated ferrous iron Studies on constituents with cytotoxic and cytostatic activity of two Turkish medicinal plants Phlomis armeniaca and Scutellaria salviifolia [Pharmacological studies on Cistanchis Herba. I. Effects of the constituents of Cistanchis Herba on sex and learning behavior in chronic stressed mice (1)] Nine phenethyl alcohol glycosides from Stachys sieboldii 2'-O-acetylpoliumoside: a new phenylpropanoid glycoside from Orobanche ramosa Acteoside, a component of Stachys sieboldii MIQ, may be a promising antinephritic agent (2): Effect of acteoside on leukocyte accumulation in the glomeruli of nephritic rats Oxygen radicals — Biochemical basis for their efficacy Effects of interaction of tannins with co-existing substances. VII. Inhibitory effects of tannins and related polyphenols on xanthine oxidase Inhibition of the autoxidation of linoleic acid by phenylpropanoid glycosides from Pedicularis in micelles Inhibition of iron toxicity in rat hepatocyte culture by natural phenolic compounds Generation of hydroxyl radical from linoleic acid hydroperoxide in the presence of epinephrine and iron Iron redox reactions and lipid peroxidation. Protection of rat myocardial phospholipid against peroxidative injury through superoxide-(xanthine oxidase)-dependent, iron-promoted Fenton chemistry by the male contraceptive gossypol Phenylpropanoid esters from Lamium album flowers Aging--causes and defenses [Studies on Stachys sieboldii MIQ. II. Anti-anoxia action and the active constituents] Free radicals from 1-palmitoyl-2-arachidonoylphosphatidylcholine liposomes in Fe2+/ascorbic acid solution
access restriction status	wds:Q71976537-DB72FB44-EF75-4AAA-B625-7E1C58BA8576
access restriction status	open access
author name string	wds:Q71976537-6798DED4-2D97-4815-AC65-4A0377F144E2 wds:Q71976537-CF83BD3E-B1C4-4361-8B1B-B051E84D6E27 wds:Q71976537-E2C76A28-A764-4705-BB81-F1C669FF48C7 wds:Q71976537-EE039204-82D2-4E04-B869-DC247EC9DCD7
author name string	S Kadota T Tani T Namba Q Xiong
rdfs:label	Antioxidative effects of phenylethanoids from Cistanche deserticola (en) Antioxidative effects of phenylethanoids from Cistanche deserticola (nl)
skos:prefLabel	Antioxidative effects of phenylethanoids from Cistanche deserticola (en) Antioxidative effects of phenylethanoids from Cistanche deserticola (nl)
name	Antioxidative effects of phenylethanoids from Cistanche deserticola (en) Antioxidative effects of phenylethanoids from Cistanche deserticola (nl)
title	wds:Q71976537-A7A856EE-1EC4-4A8F-A7D9-F6B4A0F4480F
title	Antioxidative effects of phenylethanoids from Cistanche deserticola (en)
page(s)	wds:Q71976537-D5F3B062-4855-4886-93D6-C6D833CE3426
page(s)	1580-1585
instance of	wds:Q71976537-C9A5AFCE-7B76-46F2-AE46-8A3C29D0B322
instance of	scholarly article
main subject	wds:Q71976537-0941F95B-0A67-43A9-B804-0795DCDEE40F wds:Q71976537-1427E914-A95B-4935-AC79-79933BBD8F9D wds:Q71976537-24736D71-2A2D-4125-ABEE-9D5B72B3C7E3 wds:Q71976537-38562750-3ACF-4123-A504-3DA0109E72C3 wds:Q71976537-3CBABCF9-A769-4EAB-ACBB-E5A838DFC1DB wds:Q71976537-7A279B92-0C0A-412B-8D7B-7E3542D25561 wds:Q71976537-8A32A44D-36FB-4409-9782-DA9C11FE38F1 wds:Q71976537-A4F7A3F0-810C-4017-82EA-B5AB61003202 wds:Q71976537-C6B3FA65-5135-406C-B031-3AF5A342DBBD wds:Q71976537-DF42C834-DD08-473A-AB32-8B0F612115D3 wds:Q71976537-EEE49E59-C5A6-41FD-ADB5-C17BE67DE27D wds:Q71976537-FA69AD6E-EB84-456D-B893-B439C7BE87B6
main subject	Cistanche deserticola echinacoside verbascoside isoacteoside Cistanoside F 2-Acetylacteoside Rha(a1-3)[coumaroyl(3-OH)(-4)]b-Glc Syringalide A 3'-rhamnoside

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