Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H7NS2 |
| Molecular Weight | 121.224 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)C(S)=S
InChI
InChIKey=MZGNSEAPZQGJRB-UHFFFAOYSA-N
InChI=1S/C3H7NS2/c1-4(2)3(5)6/h1-2H3,(H,5,6)
| Molecular Formula | C3H7NS2 |
| Molecular Weight | 121.224 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Ziram causes dopaminergic cell damage by inhibiting E1 ligase of the proteasome. | 2008 Dec 12 |
|
| catena-Poly[cadmium-bis-(μ-N,N-dimethyl-dithio-carbamato-κS,S':S)]. | 2010 Oct 31 |
|
| Prenatal treatment of mosaic mice (Atp7a mo-ms) mouse model for Menkes disease, with copper combined by dimethyldithiocarbamate (DMDTC). | 2012 |
|
| Ziram and sodium N,N-dimethyldithiocarbamate inhibit ubiquitin activation through intracellular metal transport and increased oxidative stress in HEK293 cells. | 2015 Apr 20 |
|
| Zinc- and oxidative property-dependent degradation of pro-caspase-1 and NLRP3 by ziram in mouse macrophages. | 2015 Jun 15 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:16:39 GMT 2023
by
admin
on
Sat Dec 16 09:16:39 GMT 2023
|
| Record UNII |
2IMH4383Z4
|
| Record Status |
Validated (UNII)
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| Record Version |
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