about
Recent advances in biosynthesis of bioactive compounds in traditional Chinese medicinal plantsModulation of glucose transporter protein by dietary flavonoids in type 2 diabetes mellitusNatural product biosynthesis in Medicago species.Antagonism of human formyl peptide receptor 1 (FPR1) by chromones and related isoflavones.Structural basis for non-genuine phenolic acceptor substrate specificity of Streptomyces roseochromogenes prenyltransferase CloQ from the ABBA/PT-barrel superfamily2-Oxoglutarate-dependent dioxygenases in the biosynthesis of simple coumarins.The genus Machaerium (Fabaceae): taxonomy, phytochemistry, traditional uses and biological activities.Glucosylation of isoflavonoids in engineered Escherichia coliDe novo transcriptome sequencing in Pueraria lobata to identify putative genes involved in isoflavones biosynthesis.Dietary Isoflavones as Modulators of Drug Metabolizing Enzymes and Transporters: Effect on Prescription Medicines.A patent review of the therapeutic potential of isoflavones (2012-2016).Identification and Characterization of Daurichromenic Acid Synthase Active in Anti-HIV Biosynthesis.Deciphering composition and connectivity of a natural product with the assistance of MS and 2D NMR.Current understanding of the pathways of flavonoid biosynthesis in model and crop plants.Metabolite fingerprinting, pathway analyses, and bioactivity correlations for plant species belonging to the Cornaceae, Fabaceae, and Rosaceae families.Photo-induced Carboiodination: A Simple Way to Synthesize Functionalized Dihydrobenzofurans and Indolines.Historical textile dyeing with Genista tinctoria L.: a comprehensive study by UPLC-MS/MS analysis
P2860
Q26769057-0D6F930E-C336-443D-B942-6B9C3D604A1FQ28081094-87F7289A-BE67-4B89-99A4-46C7700D4662Q34401171-B54F4B54-13FE-4B91-A66C-38DD879CCC0CQ35039823-0B76C0FE-6558-4B0B-B0F6-75665016425EQ36327019-7474D14B-8E0F-42E9-A2D4-4BCBD099590CQ38269018-D63A9D2E-61DC-4928-B731-AF67C354B689Q38324144-7A7816C7-1281-48E4-913E-6C5A587044CBQ38440831-ADDAFFA9-7978-4957-8C85-D533C9581C0AQ38468517-AE71F6E5-1B8C-435B-95D4-6D3E5FB75722Q38631590-DA7D1C71-5C3D-40EE-9DD9-50D77490B066Q38674207-B3B1CA28-223F-4A0F-B823-FF70E53AC2ABQ38692413-30CCA35A-D1E5-47FC-B20B-B488BB4257F9Q46266982-4D388013-76ED-4C4E-AF0D-0600CFD56E93Q46304962-93495E04-67F0-4D78-842E-C9C25C282181Q46527220-510812C9-AD4B-4CB7-BCB1-A9FCDDEE4B07Q50221113-2D60A83C-B7A8-4AF6-9184-BCB1A81B5100Q58166052-A5CE0D98-A9A9-4060-BE1E-706EBC936B5F
P2860
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Isoflavonoids of the leguminosae.
@en
Isoflavonoids of the leguminosae.
@nl
type
label
Isoflavonoids of the leguminosae.
@en
Isoflavonoids of the leguminosae.
@nl
prefLabel
Isoflavonoids of the leguminosae.
@en
Isoflavonoids of the leguminosae.
@nl
P2860
P356
P1476
Isoflavonoids of the leguminosae.
@en
P2093
Nigel C Veitch
P2860
P304
P356
10.1039/C3NP70024K
P577
2013-07-01T00:00:00Z