Puerarin (Q4392082)

PubChem

canonical SMILES

C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O

2 references

C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O

0 references

found in taxon

Pueraria calycina

1 reference

Large scale purification of puerarin from Puerariae Lobatae Radix through resins adsorption and acid hydrolysis.

Pueraria edulis

1 reference

Large scale purification of puerarin from Puerariae Lobatae Radix through resins adsorption and acid hydrolysis.

Pueraria montana var. lobata

11 references

Large scale purification of puerarin from Puerariae Lobatae Radix through resins adsorption and acid hydrolysis.

Dual High-Resolution α-Glucosidase and Radical Scavenging Profiling Combined with HPLC-HRMS-SPE-NMR for Identification of Minor and Major Constituents Directly from the Crude Extract of Pueraria lobata

Puerarin inhibits acid-sensing ion channels and protects against neuron death induced by acidosis

Identification of isoflavones in the roots of Pueraria lobata.

Isoflavone glucosides exist as their 6''-O-malonyl esters in Pueraria lobata and its cell suspension cultures.

Studies on the constituents of Pueraria lobata. III. Isoflavonoids and related compounds in the roots and the voluble stems.

In vitro isoflavonoid production in callus from different organs of Pueraria lobata (Wild.) Ohwi.

Constituents of the roots of Pueraria lobata inhibit formation of advanced glycation end products (AGEs)

Separation and purification of isoflavones from Pueraria lobata by high-speed counter-current chromatography

Isolation and high performance liquid chromatography (HPLC) of isoflavonoids from the Pueraria root

Effects of isoflavones extracted from kudzu, Pueraria lobata (Willd.) Ohwi, on glyoxalase I activity and the growth of cultured cells.

Pueraria montana var. montana

1 reference

Large scale purification of puerarin from Puerariae Lobatae Radix through resins adsorption and acid hydrolysis.

Fabaceae

3 references

Puerarin suppresses AGEs-induced inflammation in mouse mesangial cells: a possible pathway through the induction of heme oxygenase-1 expression

Anti-arrhythmic Action of Bretylium

Isolation and high performance liquid chromatography (HPLC) of isoflavonoids from the Pueraria root

Sorbus cuspidata

1 reference

Neurocytoprotective effects of the bioactive constituents of Pueraria thomsonii in 6-hydroxydopamine (6-OHDA)-treated nerve growth factor (NGF)-differentiated PC12 cells

Clematis hexapetala

1 reference

Chemical Constituents From The Roots And Rhizomes Of Clematis Hexapetala Pall.

Ziziphus jujuba

1 reference

Flavonoids from Ziziphus jujuba Mill var. spinosa

Bupleurum chinense

1 reference

Flavonoids from aerial part of Bupleurum chinense DC.

Pueraria tuberosa

1 reference

Analysis of isoflavones in Puerariae radix by high-performance liquid chromatography with amperometric detection

Griffitharia vestita

1 reference

Neurocytoprotective effects of the bioactive constituents of Pueraria thomsonii in 6-hydroxydopamine (6-OHDA)-treated nerve growth factor (NGF)-differentiated PC12 cells

Toxicopueraria peduncularis

1 reference

Large scale purification of puerarin from Puerariae Lobatae Radix through resins adsorption and acid hydrolysis.

Neustanthus phaseoloides

1 reference

Large scale purification of puerarin from Puerariae Lobatae Radix through resins adsorption and acid hydrolysis.

Pueraria

4 references

Molecular mechanism of suppression of MDR1 by puerarin from Pueraria lobata via NF-kappaB pathway and cAMP-responsive element transcriptional activity-dependent up-regulation of AMP-activated protein kinase in breast cancer MCF-7/adr cells

Puerariae radix isoflavones and their metabolites inhibit growth and induce apoptosis in breast cancer cells.

Determination of puerarin and daidzein in Puerariae radix and its medicinal preparations by micellar electrokinetic capillary chromatography with electrochemical detection

Induction of apoptosis by puerarin in colon cancer HT-29 cells

Cephalotaxus harringtonii var. harringtonii

1 reference

Inhibitors of osteoclast differentiation from Cephalotaxus koreana

Scutellaria baicalensis

1 reference

Flavonoids identified from Korean Scutellaria baicalensis induce apoptosis by ROS generation and caspase activation on human fibrosarcoma cells

Trifolium pratense

1 reference

LC-ESI-MS study of the flavonoid glycoside malonates of red clover (Trifolium pratense)

subject has role

vasodilator agent

1 reference

Medical Subject Headings

MeSH descriptor ID

C033607

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

15 March 2018

Identifiers

InChI

0 references

1 reference

ChEBI release 2020-09-01

CAS Registry Number

3681-99-0

1 reference

https://commonchemistry.cas.org/detail?cas_rn=3681-99-0

10 April 2021

ChemSpider ID

4445119

1 reference

English Wikipedia

PubChem CID

5281807

1 reference

ChEBI ID

8633

mapping relation type

exact match

2 references

ChEBI release 2019-10-02

International Chemical Identifier

InChI

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

ChEMBL ID

CHEMBL486386

1 reference

2 references

inferred from InChIKey

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

NMRShiftDB structure ID

20218081

1 reference

DSSTox substance ID

DTXSID30958020

1 reference

DSSTOX compound identifier

DTXCID001385940

0 references

EC number

609-296-1

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.130.674

ECHA Substance Infocard ID

27 December 2018

title

8-b-D-Glucopyranosyl-7-hydroxy-3-(4-hydroxy-phenyl)-4H-1-benzopyran-4-one (English)

quotation

CAS no.: 3681-99-0 (English)

100.130.674

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.130.674

27 December 2018

title

8-b-D-Glucopyranosyl-7-hydroxy-3-(4-hydroxy-phenyl)-4H-1-benzopyran-4-one (English)

quotation

CAS no.: 3681-99-0 (English)

0 references

1 reference

https://ja.wikipedia.org/w/index.php?title=プエラリン&oldid=67727629

Japanese Wikipedia

Wikimedia import URL

MeSH descriptor ID

C033607

1 reference

Medical Subject Headings

14 March 2018

1 reference

Human Metabolome Database ID

HMDB0240265

2 references

based on heuristic

inferred from InChIKey

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

0 references

0 references

1 reference

15 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

Freebase ID

/m/07kg_j5

0 references

Microsoft Academic ID

0 references

1 reference

26 January 2022

UMLS CUI

C0072591

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023