- Puerarin
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Puerarin 7-Hydroxy-3-(4-hydroxyphenyl)-8-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-oneOther namesDaidzein-8-C-glucoside
7,4'-Dihydroxy-8-C-glucosylisoflavoneIdentifiers CAS number 3681-99-0 PubChem 5486172 ChemSpider 4445119 ChEMBL CHEMBL486386 Jmol-3D images Image 1 - O=C2c3c(O/C=C2/c1ccc(O)cc1)c(c(O)cc3)[C@@H]4O[C@@H]([C@@H](O)[C@H](O)[C@H]4O)CO
Properties Molecular formula C21H20O9 Molar mass 416.38 g mol−1 Exact mass 416.110732 (verify) (what is: / ?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)Infobox references Puerarin is one of several known isoflavones. Puerarin is found in a number of plants and herbs like the root of Pueraria (Radix puerariae)[1] notably of the kudzu plant.
Puerarin is the 8-C-glucoside of daidzein.
Puerarin is a 5-HT2C receptor and benzodiazepine site antagonist.[2]
Puerarin is being investigated as a self-microemulsifying drug delivery system.[citation needed]
List of plants that contain the chemical
Notes & references
- ^ Puerarin, an isoflavonoid derived from Radix puerariae, potentiates endothelium-independent relaxation via the cyclic AMP pathway in porcine coronary artery, Dennis K.Y. Yeunga, Susan W.S. Leung, a, , Yan Chun Xua, Paul M. Vanhouttea and Ricky Y.K. Mana, 2006
- ^ Overstreet DH, Kralic JE, Morrow AL, Ma ZZ, Zhang YW, Lee DY (2003). "NPI-031G (puerarin) reduces anxiogenic effects of alcohol withdrawal or benzodiazepine inverse or 5-HT2C agonists.". Pharmacology, biochemistry, and behavior 75 (3): 619–625. doi:10.1016/S0091-3057(03)00114-X. PMID 12895679.
- ^ Wang, Lingzhao et al.; Yang, BAO; Du, Xiuqiao (2009). "Investigation of supercritical fluid extraction of puerarin from Pueraria Lobata". Journal of Food Process Engineering (John Wiley & Sons) 32 (5): 682–691. doi:10.1111/j.1745-4530.2007.00238.x.
- ^ Chen, Gang et al.; Zhang, J; Ye, J (2001). "Determination of puerarin, daidzein and rutin in Pueraria lobata (Wild.) Ohwi by capillary electrophoresis with electrochemical detection". Journal of Chromatography A (Elsevier) 923 (1 - 2): 255–262. doi:10.1016/S0021-9673(01)00996-7. PMID 11510548.
- ^ Kintzios, Spiridon et al.; Makri, Olga; Pistola, Eleni; Matakiadis, Theodoros; Ping Shi, He; Economou, Athanassios (2004). "Scale-up production of puerarin from hairy roots of Pueraria phaseoloides in an airlift bioreactor". Biotechnology Letters (Springer) 26 (13): 1057–1059. doi:10.1023/B:BILE.0000032963.41208.e8. ISSN 0141-5492.
- ^ Shi, H. P; S. Kintzies (2003). "Genetic transformation of Pueraria phaseoloides with Agrobacterium rhizogenes and puerarin production in hairy roots". Plant Cell Reports (Springer) 21 (11): 1103–1107. doi:10.1007/s00299-003-0633-6. ISSN 0721-7714.
Isoflavones O-methylated isoflavones Biochanin A | Calycosin | Formononetin | Glycitein | Irigenin | 5-O-methylgenistein | Pratensein | Prunetin | Psi-tectorigenin | Retusin | TectorigeninGlycosides Prenylated isoflavones Bidwillol A | Derrubone | Luteone | WighteonePyranoisoflavones Alpinumisoflavone | Barbigerone | Di-O-methylalpinumisoflavone | 4'-methyl-alpinumisoflavoneMisc RotenoidsSynthetic This article about a natural phenol is a stub. You can help Wikipedia by expanding it.