Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Ayanin"'
Publikováno v:
Vitae, Vol 28, Iss 2 (2021)
Background: Ayanin (3,7,4’-Tri-O-methylquercetin) and 3,7-Di-O-methylquercetin (DMQ) are the main active metabolites isolated by bioguided fractionation from Croton schiedeanus, species known popularly in Colombia as “almizclillo”, which has be
Externí odkaz:
https://doaj.org/article/751f1f2968f544c591200579958bce15
Akademický článek
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Publikováno v:
Vitae, Volume: 28, Issue: 2, Article number: e3, Published: 08 MAR 2022
Vitae, Vol 28, Iss 2 (2021)
Vitae, Vol 28, Iss 2 (2021)
Background: Ayanin (3,7,4'-Tri-O-methylquercetin) and 3,7-Di-O-methylquercetin (DMQ) are the main active metabolites isolated by bioguided fractionation from Croton schiedeanus, species known popularly in Colombia as “almizclillo”, which has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9c8d79f373d181b1e155ef07415311a
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-40042021000200003&lng=en&tlng=en
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-40042021000200003&lng=en&tlng=en
Publikováno v:
Fitoterapia. 156:105088
The first natural product isolation studies of Nothofagus gunnii (Hook.f.) Oerst and Nothofagus cunninghamii (Hook.f.) Oerst have been undertaken. A previously unreported stilbene derivative, pinosylvin monoacetate, was isolated from the leaves of N.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66e4a1faa0b435ff78d498bee5bcbcdb
https://doi.org/10.1016/j.fitote.2021.105088
https://doi.org/10.1016/j.fitote.2021.105088
Akademický článek
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Publikováno v:
Applied Biological Chemistry. 62
To investigate the effects of extraction solvents and drying methods on Plectranthus hadiensis var. tomentosus quality, eight compounds were isolated and the content of active compounds with their antioxidant activities were compared. Compounds 1 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::987dd1678ef5de90da9b464cb392b93d
https://doi.org/10.1186/s13765-019-0464-y
https://doi.org/10.1186/s13765-019-0464-y
Akademický článek
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Autor:
Roberto Rodríguez, Sang Hoon Joo, Young Hee Choi, Sangho Choi, Young-Won Chin, Joongku Lee, Dong-Chan Oh, Minsun Chang, Yihua Pei, Jongmin Ahn, Seong-Hwan Kim, Hee-Sung Chae, Yun Seon Song, Jinwoong Kim, Young-Mi Kim
Publikováno v:
Molecules, Vol 23, Iss 2, p 302 (2018)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules; Volume 23; Issue 2; Pages: 302
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules; Volume 23; Issue 2; Pages: 302
Bioactivity-guided fractionation for the stems of leaves of Larrea nitida Cav., using interleukin-6 (IL-6) inhibitory assay in human mast cells (HMC-1), led to the isolation of three new compounds with an unprecedented skeleton in nature (1–3) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dd5326a5ddeefe04d5a677904993dde
http://www.mdpi.com/1420-3049/23/2/302
http://www.mdpi.com/1420-3049/23/2/302
Autor:
Yusuke Asai, Javzan Batkhuu, Erdenechimeg Selenge, Kento Suganuma, Toshihiro Murata, Fumihiko Yoshizaki
Publikováno v:
Phytochemistry Letters. 6:552-555
Two new chromone acyl glucosides, 5-hydroxy-7-O-(6-O-p-cis-coumaroyl-β- D -glucopyranosyl)-chromone (1) and 5-hydroxy-7-O-(6-O-p-trans-coumaroyl-β- D -glucopyranosyl)-chromone (2), and a new flavonoid glucoside, ayanin 3′-O-β- D -glucopyranoside
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0029eebbe03d1aa2cef26fac786889b1
https://doi.org/10.1016/j.phytol.2013.07.004
https://doi.org/10.1016/j.phytol.2013.07.004
Autor:
Xue-yan Hao, Zhenhua Wang, Guangxiang Luan, Zhenzhen Yuan, Gang Li, Yourui Suo, Honglun Wang, Ji Li
Publikováno v:
Chemistrybiodiversity. 14(6)
Potentilla parvifolia Fisch. (Rosaceae) is a traditional medicinal plant in P. R. China. In this study, seven flavonoids, ayanin (1), tricin (2), quercetin (3), tiliroside (4), miquelianin (5), isoquercitrin (6), and astragalin (7), were separated an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3cceefb92dcac926b40bea0016d66c7
https://pubmed.ncbi.nlm.nih.gov/28294523
https://pubmed.ncbi.nlm.nih.gov/28294523