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About This Item
Empirical Formula (Hill Notation):
C14H8O6
CAS Number:
Molecular Weight:
272.21
UNSPSC Code:
12171500
NACRES:
NA.77
PubChem Substance ID:
EC Number:
201-366-6
MDL number:
Colour Index Number:
58500
Beilstein/REAXYS Number:
1889617
Assay:
≥95% (HPLC)
Form:
powder
Product Name
Quinalizarin, ≥95% (HPLC)
Quality Segment
assay
≥95% (HPLC)
form
powder
color
red
mp
≥300 °C
storage temp.
room temp
SMILES string
Oc1ccc2C(=O)c3c(O)ccc(O)c3C(=O)c2c1O
InChI
1S/C14H8O6/c15-6-3-4-7(16)11-10(6)12(18)5-1-2-8(17)13(19)9(5)14(11)20/h1-4,15-17,19H
InChI key
VBHKTXLEJZIDJF-UHFFFAOYSA-N
Application
Quinalizarin has been used:
- as a casein kinase II (CKII) inhibitor to study its effect on CKII-mediated phosphorylation of importin α on subcellular scaling in sperm chromosomes and egg extract
- as a CKII inhibitor to study its ability to block parasite multiplication in a [3H]-hypoxanthine incorporation assay
- to study its effect on colorectal cancer (CRC) cell cycle arrest, cell apoptosis, and reactive oxygen species (ROS) generation in SW480 and HCT-116 cell lines
Biochem/physiol Actions
Quinalizarin is a potent (IC50 = 110 nM), ATP-competitive, and highly selective (IC50 >1μM against CK1 and 72 other kinases) casein Kinase II (CK2) inhibitor.
Quinalizarin is a potent, ATP-competitive, and highly selective casein Kinase II (CK2) inhibitor.
Studies show that quinalizarin can prevent the in vitro activity of recombinant Plasmodium falciparum casein kinase 2α (PfCK2α) catalytic subunit with an IC50 of 2μM.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Global Trade Item Number
| SKU | GTIN |
|---|---|
| Q2763-25MG | 04061835307937 |
| Q2763-5MG | 04061836687892 |

