Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H6NS2.Na |
| Molecular Weight | 143.206 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CN(C)C([S-])=S
InChI
InChIKey=VMSRVIHUFHQIAL-UHFFFAOYSA-M
InChI=1S/C3H7NS2.Na/c1-4(2)3(5)6;/h1-2H3,(H,5,6);/q;+1/p-1
| 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 |
| Molecular Formula | Na |
| Molecular Weight | 22.98976928 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Zinc- and oxidative property-dependent degradation of pro-caspase-1 and NLRP3 by ziram in mouse macrophages. | 2015-06-15 |
|
| Ziram and sodium N,N-dimethyldithiocarbamate inhibit ubiquitin activation through intracellular metal transport and increased oxidative stress in HEK293 cells. | 2015-04-20 |
|
| Prenatal treatment of mosaic mice (Atp7a mo-ms) mouse model for Menkes disease, with copper combined by dimethyldithiocarbamate (DMDTC). | 2012 |
|
| catena-Poly[cadmium-bis-(μ-N,N-dimethyl-dithio-carbamato-κS,S':S)]. | 2010-10-31 |
|
| Ziram causes dopaminergic cell damage by inhibiting E1 ligase of the proteasome. | 2008-12-12 |
|
| Suppression of the steroid-primed luteinizing hormone surge in the female rat by sodium dimethyldithiocarbamate: relationship to hypothalamic catecholamines and GnRH neuronal activation. | 2008-07 |
|
| 1,3-Butadiene and leukemia among synthetic rubber industry workers: exposure-response relationships. | 2007-03-20 |
|
| A novel anticancer gold(III) dithiocarbamate compound inhibits the activity of a purified 20S proteasome and 26S proteasome in human breast cancer cell cultures and xenografts. | 2006-11-01 |
|
| Dithiocarbamates have a common toxic effect on zebrafish body axis formation. | 2006-10-01 |
|
| The influence of co-exposure to dimethyldithiocarbamate on butadiene metabolism. | 2001-06-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:52:28 GMT 2025
by
admin
on
Mon Mar 31 19:52:28 GMT 2025
|
| Record UNII |
769GO8W6QQ
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Brand Name | English | ||
|
Brand Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Brand Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
EPA PESTICIDE CODE |
34804
Created by
admin on Mon Mar 31 19:52:28 GMT 2025 , Edited by admin on Mon Mar 31 19:52:28 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
6811
Created by
admin on Mon Mar 31 19:52:28 GMT 2025 , Edited by admin on Mon Mar 31 19:52:28 GMT 2025
|
PRIMARY | |||
|
128-04-1
Created by
admin on Mon Mar 31 19:52:28 GMT 2025 , Edited by admin on Mon Mar 31 19:52:28 GMT 2025
|
PRIMARY | |||
|
204-876-7
Created by
admin on Mon Mar 31 19:52:28 GMT 2025 , Edited by admin on Mon Mar 31 19:52:28 GMT 2025
|
PRIMARY | |||
|
769GO8W6QQ
Created by
admin on Mon Mar 31 19:52:28 GMT 2025 , Edited by admin on Mon Mar 31 19:52:28 GMT 2025
|
PRIMARY | |||
|
560256
Created by
admin on Mon Mar 31 19:52:28 GMT 2025 , Edited by admin on Mon Mar 31 19:52:28 GMT 2025
|
PRIMARY | |||
|
21 CFR 176.300
Created by
admin on Mon Mar 31 19:52:28 GMT 2025 , Edited by admin on Mon Mar 31 19:52:28 GMT 2025
|
PRIMARY | |||
|
85566
Created by
admin on Mon Mar 31 19:52:28 GMT 2025 , Edited by admin on Mon Mar 31 19:52:28 GMT 2025
|
PRIMARY | |||
|
DTXSID6027050
Created by
admin on Mon Mar 31 19:52:28 GMT 2025 , Edited by admin on Mon Mar 31 19:52:28 GMT 2025
|
PRIMARY |