sameAs
Antagonizing effects and mechanisms of afzelin against UVB-induced cell damage.Melanocyte-protective effect of afzelin is mediated by the Nrf2-ARE signalling pathway via GSK-3β inactivation.Afzelin positively regulates melanogenesis through the p38 MAPK pathway.Afzelin ameliorates D-galactosamine and lipopolysaccharide-induced fulminant hepatic failure by modulating mitochondrial quality control and dynamics.Simultaneous determination of myricetrin, quercitrin and afzelin in leaves of Cercis chinensis by a fast and effective method of ionic liquid microextraction coupled with HPLC.Antibacterial effects of afzelin isolated from Cornus macrophylla on Pseudomonas aeruginosa, a leading cause of illness in immunocompromised individuals.Plant nutraceuticals (Quercetrin and Afzelin) capped silver nanoparticles exert potent antibiofilm effect against food borne pathogen Salmonella enterica serovar typhimurium and curtail planktonic growth in zebrafish infection model.Discovery of UDP-Glycosyltransferases and BAHD-Acyltransferases Involved in the Biosynthesis of the Antidiabetic Plant Metabolite Montbretin AAnti-complementary constituents of Houttuynia cordata and their targets in complement activation cascadeAfzelin suppresses proinflammatory responses in particulate matter-exposed human keratinocytesSimultaneous Enrichment and Separation of Four Flavonoids from Zanthoxylum bungeanum Leaves by Ultrasound-Assisted Extraction and Macroporous Resins with Evaluation of Antioxidant ActivitiesHigh level production of flavonoid rhamnosides by metagenome-derived Glycosyltransferase C in Escherichia coli utilizing dextrins of starch as a single carbon sourceDynamic changes of secondary metabolites and tyrosinase activity of Malus pumila flowersSpectrum-effect relationship of antioxidant and tyrosinase activity with Malus pumila flowers by UPLC-MS/MS and component knock-out methodEvaluation of the chemical composition and antioxidant activity of extracts and fractions of Ocotea notata (Ness) Mez (Lauraceae)A novel acylated quercetin glycoside and compounds of inhibitory effects on α-glucosidase from Panax ginseng flower buds
P921
Q34692579-456D2702-ED98-4722-8298-32E19AAEAD88Q39089266-5FF2AE54-5743-4A98-B663-01F3980CDCAAQ42696177-83208C03-A316-4C7D-803C-C761A00BDCDCQ51319161-C9D9A70B-6395-4DB4-B15B-BBCEBD96B214Q52677793-3D173AA8-5E1A-4315-91C9-C9C0EC64B65AQ53595600-C1851743-A0D8-4156-851D-4B0C5AB085DEQ54223909-2E174C77-80D7-46E2-9A34-7A593883DEEFQ60421804-0297E1FF-0E0F-47AE-B58D-6D995A539EFDQ60421804-16E913D6-29BD-4C4F-BFC6-3F31E130C070Q87095190-82EB39AF-3742-41FC-B058-3B10FC1577E5Q90266612-A2951CE3-5803-493C-940A-AD6BF836CBFEQ90771281-76B6E4DF-E6BE-4D09-A50B-C8CE95544E63Q92023389-E9BAF26F-AAF2-4E6B-9029-1A6CA5C0D189Q92438006-AAB39178-D051-4C6B-9666-A6AEA93514C9Q92544493-80F54E6F-7433-4C7D-8FBC-5651E583CCFCQ92544493-CDBAB6FE-BD1C-47B4-B910-7B5402FD2881Q93124194-5135E89A-0E35-45FD-87E0-A86935DDB676Q93205564-6D6ECDAA-A25D-4779-A899-587041F72590
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
Afzelin
@sh
Afzelin
@sr
Afzéline
@fr
afzelin
@en
afzelina
@pl
type
label
Afzelin
@sh
Afzelin
@sr
Afzéline
@fr
afzelin
@en
afzelina
@pl
altLabel
3,4',5,7-Tetrahydroxyflavone-3-L-rhamnoside
@en
Kaempferin
@en
Kaempferol 3-O-alpha-L-rhamnoside
@en
Kaempferol 3-rhamnoside
@en
kaempferol 3-O-α-L-rhamnopyranoside
@en
prefLabel
Afzelin
@sh
Afzelin
@sr
Afzéline
@fr
afzelin
@en
afzelina
@pl
P4964
P6689
P592
P6366
P638
P661
P662
P665
P683
P117
P1579
P2017
C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O
P2063
LMPK12111842
P2064
P2067
P231
P233
CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O
P234
1S/C21H20O10/c1-8-15(25)17(27) ...... ,1H3/t8-,15-,17+,18+,21-/m0/s1
P235
SOSLMHZOJATCCP-AEIZVZFYSA-N
P274
P3117
DTXSID50197459