Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Puerarin

From Wikipedia, the free encyclopedia
Puerarin
Names
IUPAC name
8-(β-D-Glucopyranosyl)-4′,7-dihydroxyisoflavone
Systematic IUPAC name
7-Hydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-1-benzopyran-4-one
Other names
Daidzein-8-C-glucoside
7,4'-Dihydroxy-8-C-glucosylisoflavone
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard100.130.674Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C21H20O9/c22-7-14-17(26)18(27)19(28)21(30-14)15-13(24)6-5-11-16(25)12(8-29-20(11)15)9-1-3-10(23)4-2-9/h1-6,8,14,17-19,21-24,26-28H,7H2/t14-,17-,18+,19-,21+/m1/s1 checkY
    Key: HKEAFJYKMMKDOR-VPRICQMDSA-N checkY
  • C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O
  • 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
C21H20O9
Molar mass416.382 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

Puerarin, one of several knownisoflavones, is found in a number of plants and herbs, such as the root of thekudzu plant.[1]

Puerarin is the 8-C-glucoside ofdaidzein.[2]

List of plants that contain the chemical

[edit]

Notes and references

[edit]
  1. ^Dennis K.Y. Yeunga; Susan W.S. Leung; Yan Chun Xua; Paul M. Vanhouttea; Ricky Y.K. Mana (2006). "Puerarin, an isoflavonoid derived from Radix puerariae, potentiates endothelium-independent relaxation via the cyclic AMP pathway in porcine coronary artery".European Journal of Pharmacology.552 (1–3):105–11.doi:10.1016/j.ejphar.2006.08.078.PMID 17027964.
  2. ^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.S2CID 22252214.
  3. ^Wang, Lingzhao; Yang, BAO; Du, Xiuqiao; et al. (2009). "Investigation of supercritical fluid extraction of puerarin fromPueraria Lobata".Journal of Food Process Engineering.32 (5).John Wiley & Sons:682–691.doi:10.1111/j.1745-4530.2007.00238.x.
  4. ^Chen, Gang; Zhang, J; Ye, J; et al. (2001). "Determination of puerarin, daidzein and rutin inPueraria lobata (Wild.) Ohwi by capillary electrophoresis with electrochemical detection".Journal of Chromatography A.923 (1–2).Elsevier:255–262.doi:10.1016/S0021-9673(01)00996-7.PMID 11510548.
  5. ^Kintzios, Spiridon; Makri, Olga; Pistola, Eleni; Matakiadis, Theodoros; Ping Shi, He; Economou, Athanassios; et al. (2004). "Scale-up production of puerarin from hairy roots ofPueraria phaseoloides in an airlift bioreactor".Biotechnology Letters.26 (13).Springer:1057–1059.doi:10.1023/B:BILE.0000032963.41208.e8.ISSN 0141-5492.PMID 15218379.S2CID 23425268.
  6. ^Shi, H. P; S. Kintzies (2003). "Genetic transformation ofPueraria phaseoloides withAgrobacterium rhizogenes and puerarin production in hairy roots".Plant Cell Reports.21 (11).Springer:1103–1107.doi:10.1007/s00299-003-0633-6.ISSN 0721-7714.PMID 12836005.S2CID 21825544.
Isoflavones and theirglycosides
Isoflavones
O-methylated isoflavones
Glycosides
Prenylated isoflavones
Pyranoisoflavones
Derivatives
Synthetic
Receptor
(ligands)
P0 (adenine)
P1
(adenosine)
P2
(nucleotide)
P2X
(ATPTooltip Adenosine triphosphate)
P2Y
Transporter
(blockers)
CNTsTooltip Concentrative nucleoside transporters
ENTsTooltip Equilibrative nucleoside transporters
PMATTooltip Plasma membrane monoamine transporter
Enzyme
(inhibitors)
XOTooltip Xanthine oxidase
Others
Others


Stub icon

This article about anaromatic compound is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Puerarin&oldid=1269828247"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp