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Quercetin dihydrate - 97%, high purity , CAS No.6151-25-3

  • ≥97%
Item Number
Q104838
Grouped product items
SKUSizeAvailabilityPrice Qty
Q104838-5g
5g
In stock
$11.90
Q104838-10g
10g
In stock
$17.90
Q104838-25g
25g
In stock
$33.90
Q104838-50g
50g
In stock
$60.90
Q104838-100g
100g
In stock
$97.90
Q104838-250g
250g
In stock
$220.90
Q104838-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$418.90

Antioxidative flavonoid

Basic Description

SynonymsQuercetin dihydrate|6151-25-3|2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one dihydrate|MFCD00149487|Quercetine dihydrate|Quercetin (dihydrate)|3,3',4',5,7-Pentahydroxyflavone dihydrate|DTXSID9021219|Quercetin dihydrate (Sophoretin)|2-(3,4-Dihyd
Specifications & Purity≥97%
Biochemical and Physiological MechanismsQuercetin dihydrate is a flavonoid with anticancer activity. Quercetin is a mitochondrial ATPase and phosphodiesterase inhibitor. It Inhibits PI3-kinase activity and slightly inhibits PIP kinase activity. Quercetin has antiproliferative effects on cancer
Storage TempProtected from light
Shipped InNormal
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Quercetin is an antitrypanosomal and antileishmanial compound. Quercetin is a well-known bioflavonoid and its influence on tumour growth in vivo has been reported. Quercetic exhibits leishmanicidal effect on the amastigote stage of Leishmaniadonovani.

Associated Targets

CYP1A2 Tchem Cytochrome P450 1A2 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2D6 Tclin Cytochrome P450 2D6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2C19 Tchem Cytochrome P450 2C19 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2C9 Tchem Cytochrome P450 2C9 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RUNX1 Tbio Runt-related transcription factor 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HIF1A Tchem Hypoxia-inducible factor 1-alpha 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HSD17B10 Tchem 3-hydroxyacyl-CoA dehydrogenase type-2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KMT2A Tchem Histone-lysine N-methyltransferase 2A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GALC Tbio Galactocerebrosidase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

USP2 Tbio Ubiquitin carboxyl-terminal hydrolase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TSHR Tclin Thyrotropin receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

POLK Tbio DNA polymerase kappa 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RECQL Tbio ATP-dependent DNA helicase Q1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALOX15B Tchem Arachidonate 15-lipoxygenase B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALOX15 Tchem Arachidonate 15-lipoxygenase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

G6PD Tchem Glucose-6-phosphate 1-dehydrogenase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TP53 Tchem Cellular tumor antigen p53 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4E Tchem Lysine-specific demethylase 4E 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488195287
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488195287
IUPAC Name 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one;dihydrate
INCHI InChI=1S/C15H10O7.2H2O/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6;;/h1-5,16-19,21H;2*1H2
InChi Key GMGIWEZSKCNYSW-UHFFFAOYSA-N
Canonical SMILES C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O.O.O
Isomeric SMILES C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O.O.O
WGK Germany 3
RTECS LK8950000
Alternate CAS 849061-97-8
PubChem CID 5284452
UN Number 2811
Molecular Weight 338.27
Beilstein 317313

Certificates

Certificate of Analysis(COA)

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To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

36 results found

Lot NumberCertificate TypeDateItem
J2327639Certificate of AnalysisSep 28, 2023 Q104838
J2327642Certificate of AnalysisSep 20, 2023 Q104838
J2327640Certificate of AnalysisSep 20, 2023 Q104838
G2419020Certificate of AnalysisSep 20, 2023 Q104838
G2405077Certificate of AnalysisSep 20, 2023 Q104838
D2422073Certificate of AnalysisSep 20, 2023 Q104838
D2418084Certificate of AnalysisSep 20, 2023 Q104838
J2327641Certificate of AnalysisSep 20, 2023 Q104838
H2331041Certificate of AnalysisJul 04, 2023 Q104838
H2316039Certificate of AnalysisJul 04, 2023 Q104838
G2321923Certificate of AnalysisJul 04, 2023 Q104838
G2321902Certificate of AnalysisJul 04, 2023 Q104838
G2321901Certificate of AnalysisJul 04, 2023 Q104838
G2321889Certificate of AnalysisJul 04, 2023 Q104838
G2321888Certificate of AnalysisJul 04, 2023 Q104838
G2321884Certificate of AnalysisJul 04, 2023 Q104838
G2321879Certificate of AnalysisJul 04, 2023 Q104838
G2321880Certificate of AnalysisJul 04, 2023 Q104838
F2328839Certificate of AnalysisJun 12, 2023 Q104838
C2316363Certificate of AnalysisMar 04, 2023 Q104838
C2306368Certificate of AnalysisMar 04, 2023 Q104838
C2306369Certificate of AnalysisMar 04, 2023 Q104838
C2316330Certificate of AnalysisMar 04, 2023 Q104838
C2316343Certificate of AnalysisMar 04, 2023 Q104838
C2316374Certificate of AnalysisMar 04, 2023 Q104838
C2316373Certificate of AnalysisMar 04, 2023 Q104838
C2316372Certificate of AnalysisMar 04, 2023 Q104838
C2316371Certificate of AnalysisMar 04, 2023 Q104838
C2316370Certificate of AnalysisMar 04, 2023 Q104838
C2316364Certificate of AnalysisMar 04, 2023 Q104838
C2316344Certificate of AnalysisMar 04, 2023 Q104838
B2318464Certificate of AnalysisJun 08, 2022 Q104838
F2205294Certificate of AnalysisJun 08, 2022 Q104838
F2205297Certificate of AnalysisApr 06, 2022 Q104838
C2225055Certificate of AnalysisApr 06, 2022 Q104838
C2225054Certificate of AnalysisApr 06, 2022 Q104838

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Chemical and Physical Properties

SolubilitySoluble in DMSO (68 mg/ml at 25°C), Acetic Acid (1 mg/ml), Aqueous Alkali (1 mg/ml), water (<1 at 25°C), and ethanol (21 mg/ml at 25°C).
SensitivityLight sensitive.
Melt Point(°C)>300°C

Safety and Hazards(GHS)

Pictogram(s) GHS06
Signal Danger
Hazard Statements

H301:Toxic if swallowed

Precautionary Statements

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P330:Rinse mouth.

P301+P316:IF SWALLOWED: Get emergency medical help immediately.

WGK Germany 3
RTECS LK8950000

Related Documents

References

1. Ishida K et al..  (2017)  Inhibition of PI3K suppresses propagation of drug-tolerant cancer cell subpopulations enriched by 5-fluorouracil..  Sci Rep,  (2262).  [PMID:28536445]
2. Lin YJ et al..  (2019)  Network analysis and mechanisms of action of Chinese herb-related natural compounds in lung cancer cells..  Phytomedicine,  58  (152893).  [PMID:30901663]

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