Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H15N2O7.2Na.H |
Molecular Weight | 322.2228 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H+].[Na+].[Na+].OCCN(CCN(CC([O-])=O)CC([O-])=O)CC([O-])=O
InChI
InChIKey=HMMZUOFUYYDMNY-UHFFFAOYSA-L
InChI=1S/C10H18N2O7.2Na/c13-4-3-11(5-8(14)15)1-2-12(6-9(16)17)7-10(18)19;;/h13H,1-7H2,(H,14,15)(H,16,17)(H,18,19);;/q;2*+1/p-2
Molecular Formula | H |
Molecular Weight | 1.0079 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C10H15N2O7 |
Molecular Weight | 275.2353 |
Charge | -3 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
HYDROXYETHYLETHYLENEDIAMINETRIACETIC ACID (HEDTA) is used in cosmetics and care products. It’s a chelating agent, which in combination with selenium was effective in reducing the concentration of Al and level of DNA damage. In addition, experiments with rodents have shown that combination of HEDTA and propolis preserved histological features, mitigated oxidative stress and improved liver, kidney, and brain functions more profoundly.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Final report on the safety assessment of EDTA, calcium disodium EDTA, diammonium EDTA, dipotassium EDTA, disodium EDTA, TEA-EDTA, tetrasodium EDTA, tripotassium EDTA, trisodium EDTA, HEDTA, and trisodium HEDTA. | 2002 |
|
Effect of N-hydroxyethyl-ethylenediamine-triacetic acid (HEDTA) on Cr(VI) reduction by Fe(II). | 2003 Jun |
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Aluminum-induced oxidative stress in rat brain: response to combined administration of citric acid and HEDTA. | 2003 Mar |
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Isothermal titration calorimetric procedure to determine protein-metal ion binding parameters in the presence of excess metal ion or chelator. | 2003 Mar 15 |
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Immobilization of Fe chelators on sepharose gel and its effect on their chemical properties. | 2003 Sep 24 |
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Separation of yttrium from heavy lanthanide by CA-100 using the complexing agent. | 2004 May 28 |
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Speciation of chromium(III) and cobalt(III) (amino)carboxylate complexes using capillary electrophoresis. | 2005 Jan 1 |
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Macrocyclic lanthanide complexes as artificial nucleases and ribonucleases: effects of pH, metal ionic radii, number of coordinated water molecules, charge, and concentrations of the metal complexes. | 2005 Sep 19 |
|
Iron acquisition by phytosiderophores contributes to cadmium tolerance. | 2007 Apr |
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Influence of soil type on the mobility and bioavailability of chelated zinc. | 2007 May 2 |
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Homeostatic control of slow vacuolar channels by luminal cations and evaluation of the channel-mediated tonoplast Ca2+ fluxes in situ. | 2008 |
|
The dystrophin complex controls bk channel localization and muscle activity in Caenorhabditis elegans. | 2009 Dec |
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A novel manganese complex effective as superoxide anion scavenger and therapeutic agent against cell and tissue oxidative injury. | 2009 Nov 26 |
|
Development of a novel aluminum tolerance phenotyping platform used for comparisons of cereal aluminum tolerance and investigations into rice aluminum tolerance mechanisms. | 2010 Aug |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:38:14 GMT 2023
by
admin
on
Fri Dec 15 19:38:14 GMT 2023
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Record UNII |
KME849MC7A
|
Record Status |
Validated (UNII)
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Record Version |
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-
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1428868
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56841718
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KME849MC7A
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30718-90-2
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7578-42-9
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DTXSID2074401
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KME849MC7A
Created by
admin on Fri Dec 15 19:38:15 GMT 2023 , Edited by admin on Fri Dec 15 19:38:15 GMT 2023
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |