Weight | 148.276 g/mol |
---|---|
Formula | C5H10NS2- |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
Diethyldithiocarbamate (392-74-5)
Score:
#1083 in Biology
,
#1216 in Chemistry
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- In vivo inhibition of superoxide dismutase in mice by diethyldithiocarbamate. (Journal of Biological Chemistry, 1976)
- Evaluation of Triacetyloleandomycin, -Nasymphthoflavone and Diethyldithiocarbamate as Selective Chemical Probes for Inhibition of Human Cytochromes P450 (Archives of Biochemistry and Biophysics, 1994)
- Metabolism of disulfiram and diethyldithiocarbamate in rats with demonstration of an in vivo ethanol-induced inhibition of the glucuronic acid conjugation of the thiol (Biochemical Pharmacology, 1965)
- Structural studies of metal dithiocarbamates. II. The crystal and molecular structure of copper diethyldithiocarbamate (Acta Crystallographica, 1965)
- Inhibition of cis-platinum nephrotoxicity by diethyldithiocarbamate rescue in a rat model (Proceedings of the National Academy of Sciences of the United States of America, 1979)
- Mechanism of the Inhibition of Aldehyde Dehydrogenase in Vivo by Disulfiram and Diethyldithiocarbamate (Molecular Pharmacology, 1971)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCN(CC)C(=S)[S-]
-
InChIKeyLMBWSYZSUOEYSN-UHFFFAOYSA-M
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Synthesis
Ethylboronic acid
+
Reactant
(Chan-Lam coupling reaction)
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