55593
Aluminum Ionophore I
Selectophore™, function tested
Synonym(s):
Morin, 2′,3,4′,5,7-Pentahydroxyflavone
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About This Item
Empirical Formula (Hill Notation):
C15H10O7
CAS Number:
Molecular Weight:
302.24
EC Number:
207-542-9
UNSPSC Code:
26111700
PubChem Substance ID:
Colour Index Number:
75660
MDL number:
InChI key
YXOLAZRVSSWPPT-UHFFFAOYSA-N
InChI
1S/C15H10O7/c16-6-1-2-8(9(18)3-6)15-14(21)13(20)12-10(19)4-7(17)5-11(12)22-15/h1-5,16-19,21H
SMILES string
O=C1C(O)=C(C(C(O)=C2)=CC=C2O)OC3=CC(O)=CC(O)=C31
product line
Selectophore™
quality
function tested
General description
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Application
Application as aluminum(III) selective potentiometric sensor
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Legal Information
Selectophore is a trademark of Merck KGaA, Darmstadt, Germany
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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Radhika Kapoor et al.
PloS one, 7(8), e41663-e41663 (2012-08-18)
Apoptosis is an early event of liver damage in diabetes and oxidative stress has been linked to accelerate the apoptosis in hepatocytes. Therefore, the compounds that can scavenge ROS may confer regulatory effects on high-glucose induced apoptosis. In the present
Subash C Gupta et al.
Biochemical pharmacology, 85(7), 898-912 (2013-01-03)
The major goal of cancer drug discovery is to find an agent that is safe and affordable, yet effective against cancer. Here we show that morin (3,5,7,2',4'-pentahydroxyflavone) has potential against cancer cells through suppression of the signal transducer and activator
Vinod K Gupta et al.
Talanta, 72(4), 1469-1473 (2007-06-15)
Al(3+) selective sensor has been fabricated from poly(vinyl chloride) (PVC) matrix membranes containing neutral carrier morin as ionophore. Best performance was exhibited by the membrane having composition as morin:PVC:sodium tetraphenyl borate:tri-n-butylphosphate in the ratio 5:150:5:150 (w/w, mg). This membrane worked
Yan-Jun Hu et al.
Journal of photochemistry and photobiology. B, Biology, 112, 16-22 (2012-05-09)
The interaction between morin and bovine serum albumin (BSA) was studied using molecular spectroscopic approach at different temperatures under imitated physiological conditions. Quenching of intrinsic tryptophanyl fluorescence of BSA with increasing morin concentration is the actuating tool in the analysis.
Zoran Marković et al.
Food chemistry, 135(3), 2070-2077 (2012-09-08)
Due to intramolecular H-atom transfer, deprotonation of the most acidic 3-OH group of morin yields 2'-O(-) phenoxide anion. The reaction enthalpies related to mechanisms of free radical scavenging activity of this dominant species at a physiological pH of 7.4 were
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