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C8011

Sigma-Aldrich

Chelidamsäure Hydrat

≥95%, powder

Synonym(e):

1,4-Dihydro-4-oxo-2,6-pyridindicarbonsäure Hydrat, 4-Hydroxy-pyridin-2,6-dicarbonsäure

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About This Item

Empirische Formel (Hill-System):
C7H5NO5 · xH2O
CAS-Nummer:
138-60-3
Molekulargewicht:
183.12 (anhydrous basis)
Beilstein:
476229
EG-Nummer:
205-335-8
MDL-Nummer:
MFCD03818117
UNSPSC-Code:
12352202
PubChem Substanz-ID:
24278338
NACRES:
NA.77

Biologische Quelle

synthetic (organic)

Assay

≥95%

Form

powder

Farbe

brown

mp (Schmelzpunkt)

267 °C (dec.) (lit.)

Löslichkeit

1 M NH4OH: 50 mg/mL, clear to slightly hazy

SMILES String

O.OC(=O)C1=CC(=O)C=C(N1)C(O)=O

InChI

1S/C7H5NO5.H2O/c9-3-1-4(6(10)11)8-5(2-3)7(12)13;/h1-2H,(H,8,9)(H,10,11)(H,12,13);1H2

InChIKey

SNGPHFVJWBKEDG-UHFFFAOYSA-N

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Anwendung

Chelidamic acid hydrate has been used in eluent solution as a complexing additive in high-performance chelation ion chromatography (HPCIC) for speciation of iron. It has also been used as an organic ligand for the polyoxometalate (POM)-based lanthanoid hybrid compounds.

Biochem./physiol. Wirkung

Chelidamic acid (CDA), a hydroxylated derivative of 2,6-pyridine-dicarboxylic acid (DPA), is a trianionic chelating agent.
Among the most potent of the tested "conformationally restricted glutamate analogs" as an inhibitor of glutamate decarboxylase.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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Construction of a dinuclear cluster containing La (?) and 4-hydroxypyridine-2, 6-dicarboxylic acid to modify Keggin-type polyoxometalate
Taghipour F and Mirzaei M
Journal of Molecular Structure null
[Use of the radial hemolysis reaction for titrating antirabies sera].
G N Zgurskaia et al.
Voprosy virusologii, 29(3), 360-361 (1984-05-01)
Elvir Ramić et al.
The journal of physical chemistry. B, 110(41), 20655-20663 (2006-10-13)
Multifrequency electron paramagnetic resonance (EPR) and electron nuclear double resonance (ENDOR) techniques were used to obtain structural information about the copper(II)-chelidamate complex. Well-resolved nitrogen ENDOR spectra could be recorded from solid solution samples by using selective excitation of spin packets.
Maya Tutughamiarso et al.
Acta crystallographica. Section C, Crystal structure communications, 68(Pt 9), o344-o350 (2012-09-01)
Different tautomeric and zwitterionic forms of chelidamic acid (4-hydroxypyridine-2,6-dicarboxylic acid) are present in the crystal structures of chelidamic acid methanol monosolvate, C(7)H(5)NO(5)·CH(4)O, (Ia), dimethylammonium chelidamate (dimethylammonium 6-carboxy-4-hydroxypyridine-2-carboxylate), C(2)H(8)N(+)·C(7)H(4)NO(5)(-), (Ib), and chelidamic acid dimethyl sulfoxide monosolvate, C(7)H(5)NO(5)·C(2)H(6)OS, (Ic). While the zwitterionic
M Searcey et al.
Anti-cancer drug design, 13(8), 837-855 (1999-05-21)
We have explored the potential antitumour activity of DNA-intercalating free radical generators based on compounds constructed from 9-anilinoacridine and chelidamic acid as an iron (II) binding centre. Here we describe their synthesis, DNA cleaving ability and activity against a panel
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