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Phytochemical constituents of Salsola komarovii and their effects on NGF induction

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dc.contributor.authorCho, H.K.-
dc.contributor.authorSuh, W.S.-
dc.contributor.authorKim, K.H.-
dc.contributor.authorKim, S.Y.-
dc.contributor.authorLee, K.R.-
dc.date.available2020-02-28T18:45:31Z-
dc.date.created2020-02-12-
dc.date.issued2014-06-
dc.identifier.issn1226-3907-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/13042-
dc.description.abstractFive lignan glycosides, seven megastigmane glycosides, and seven phenolic compounds were isolated by repeated column chromatography from the MeOH extract of Salsola komarovii. Their structures were determined to be lariciresinol-9-O-β-D-glucopyranoside (1), alangilignoside C (2), conicaoside (3), (+)- lyoniresinol 9'-O-β-D-glucopyranoside (4), (8S,8'R,7'R)-9'-[(β-glucopyranosyl)oxy]lyoniresinol (5), blumenyl B β- D-glucopyranoside (6), blumenyl A β-D-glucopyranoside (7), staphylionoside D (8), icariside B2 (9), (6R,9S)-3- oxo-α-ionol β-D-glucopyranoside (10), 3-oxo-α-ionol 9-O-β-D-apiofuranosyl-(1→6)-β-D-glucopyranoside (11), blumenol B 9-O-β-D-apiofuranosyl-(1→6)-β-D-glucopyranoside (12), benzyl 6-O-β-D-apiofuranosyl-β-Dglucopyranoside (13), canthoside C (14), tachioside (15), isotachioside (16), biophenol 2 (17), 2-(3,4-dihydroxy)- phenyl-ethyl-β-D-glucopyranoside (18), and cuneataside C (19) by spectroscopic methods. All the isolated compounds 1 - 19 were reported from this source for the first time. Compounds 2, 3 and 6 upregulated NGF secretion to 118.8 ± 3.6%, 128.2 ± 9.3% and 111.1 ± 7.1% without significant cell toxicity. © 2014, Korean Society of Pharmacognosy. All Rights Reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherKorean Society of Pharmacognosy-
dc.relation.isPartOfNatural Product Sciences-
dc.titlePhytochemical constituents of Salsola komarovii and their effects on NGF induction-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.bibliographicCitationNatural Product Sciences, v.20, no.2, pp.95 - 101-
dc.identifier.kciidART001886309-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-84908505932-
dc.citation.endPage101-
dc.citation.startPage95-
dc.citation.titleNatural Product Sciences-
dc.citation.volume20-
dc.citation.number2-
dc.contributor.affiliatedAuthorKim, S.Y.-
dc.type.docTypeArticle-
dc.subject.keywordAuthorChemopodiaceae-
dc.subject.keywordAuthorLignan-
dc.subject.keywordAuthorNGF regulation-
dc.subject.keywordAuthorSalsola komarovii-
dc.subject.keywordPlus2 (3,4 dihydroxy) phenyl ethyl beta dextro glucopyranoside-
dc.subject.keywordPlus3 oxo alpha ionol 9 o beta dextro apiofuranosyl (1-6) beta dextro glucopyranoside-
dc.subject.keywordPlus3 oxo alpha ionol beta dextro glucopyranoside-
dc.subject.keywordPlus9&apos-
dc.subject.keywordPlus[(beta glucopyranosyl)oxy]lyoniresino-
dc.subject.keywordPlusalangilignoside C-
dc.subject.keywordPlusbenzyl 6 o beta dextro apiofuranosyl beta dextro glucopyranoside-
dc.subject.keywordPlusbiophenol 2-
dc.subject.keywordPlusblumenol B 9 o beta dextro apiofuranosyl (1-6) beta dextro glucopyranoside-
dc.subject.keywordPlusblumenyl A beta dextro glucopyranoside-
dc.subject.keywordPlusblumenyl B beta dextro glucopyranoside-
dc.subject.keywordPluscanthoside C-
dc.subject.keywordPlusconicaoside-
dc.subject.keywordPluscuneataside C-
dc.subject.keywordPlusglycoside-
dc.subject.keywordPlusicariside B2-
dc.subject.keywordPlusisotachioside-
dc.subject.keywordPluslariciresinol 9 o beta dextro glucopyranoside-
dc.subject.keywordPluslignan glycoside-
dc.subject.keywordPluslyoniresinol 9&apos-
dc.subject.keywordPluso beta dextro glucopyranoside-
dc.subject.keywordPlusmegastigmane glycoside-
dc.subject.keywordPlusmethanol-
dc.subject.keywordPlusnerve growth factor-
dc.subject.keywordPlusphenol derivative-
dc.subject.keywordPlusplant medicinal product-
dc.subject.keywordPlusstaphylionoside D-
dc.subject.keywordPlustachioside-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPlusanimal cell-
dc.subject.keywordPlusArticle-
dc.subject.keywordPluscarbon nuclear magnetic resonance-
dc.subject.keywordPlusdrug cytotoxicity-
dc.subject.keywordPlusdrug determination-
dc.subject.keywordPlusdrug isolation-
dc.subject.keywordPlusdrug structure-
dc.subject.keywordPlushigh performance liquid chromatography-
dc.subject.keywordPlusinfrared spectroscopy-
dc.subject.keywordPlusmass spectrometry-
dc.subject.keywordPlusnonhuman-
dc.subject.keywordPlusproton nuclear magnetic resonance-
dc.subject.keywordPlusrat-
dc.subject.keywordPlusSalsola-
dc.subject.keywordPlusSalsola komarovii-
dc.subject.keywordPlusstructure analysis-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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