Details
Stereochemistry | ACHIRAL |
Molecular Formula | 2C2H8N2.Cu |
Molecular Weight | 183.743 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 2 |
SHOW SMILES / InChI
SMILES
[Cu++].NCCN.NCCN
InChI
InChIKey=ATSGLBOJGVTHHC-UHFFFAOYSA-N
InChI=1S/2C2H8N2.Cu/c2*3-1-2-4;/h2*1-4H2;/q;;+2
Molecular Formula | Cu |
Molecular Weight | 63.546 |
Charge | 2 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C2H8N2 |
Molecular Weight | 60.0983 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionCurator's Comment: description was created based on several sources, including:
https://www.ncbi.nlm.nih.gov/pubmed/9735163 | https://www.ncbi.nlm.nih.gov/pubmed/1667723 | Pohanish, R.P. (2011) "Sittig's Handbook of Toxic and Hazardous Chemicals and Carcinogens", p.790 Retrieved from https://books.google.ru/books?id=RYt0Wzb60b4C
Curator's Comment: description was created based on several sources, including:
https://www.ncbi.nlm.nih.gov/pubmed/9735163 | https://www.ncbi.nlm.nih.gov/pubmed/1667723 | Pohanish, R.P. (2011) "Sittig's Handbook of Toxic and Hazardous Chemicals and Carcinogens", p.790 Retrieved from https://books.google.ru/books?id=RYt0Wzb60b4C
CUPRIC ETHYLENEDIAMINE is a purple liquid with an ammoniacal odor. It is used to dissolve cellulose products to give a cuprammonium-type solution. Superoxide ion is generated as an intermediate at the first reaction step between CUPRIC ETHYLENEDIAMINE and H2O2. DNA strand scission may be caused by hydroxyl radicals generated from the reaction of CUPRIC ETHYLENEDIAMINE with biological reductants under aerobic conditions. Since ascorbic acid, is present in living cells, CUPRIC ETHYLENEDIAMINE may be capable of initiating DNA damage in the presence of this reductant. Inhalation of vapor CUPRIC ETHYLENEDIAMINE irritates mucous membrane and may cause asthma. Liquid causes severe irritation of eyes and possible corneal injury. Contact with skin causes irritation. Ingestion causes irritation of mouth and stomach.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2311221 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9735163 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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PubMed
Title | Date | PubMed |
---|---|---|
Evidence for the formation of superoxide ion from the reaction of Cu(II)-ethylenediamine complex with hydrogen peroxide. | 1991 Nov |
|
Reactive oxygen species generated from the reaction of copper(II) complexes with biological reductants cause DNA strand scission. | 1998 Sep 15 |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9735163
Cupriethylene diamine (0.25 mM) plus hydroquinone did not cause any DNA strand scission, irrespective of the concentration of hydroquinone used (0.25, 0.5, 1.25, 2.5 mM).
Substance Class |
Chemical
Created
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admin
on
Edited
Sat Dec 16 08:52:57 GMT 2023
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admin
on
Sat Dec 16 08:52:57 GMT 2023
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Record UNII |
NIP4I4LVCC
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Record Status |
Validated (UNII)
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Record Version |
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EPA PESTICIDE CODE |
24407
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