Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C6H13NO2S |
| Molecular Weight | 163.238 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCSCC[C@H](N)C(O)=O
InChI
InChIKey=GGLZPLKKBSSKCX-YFKPBYRVSA-N
InChI=1S/C6H13NO2S/c1-2-10-4-3-5(7)6(8)9/h5H,2-4,7H2,1H3,(H,8,9)/t5-/m0/s1
| Molecular Formula | C6H13NO2S |
| Molecular Weight | 163.238 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Genomic models of short-term exposure accurately predict long-term chemical carcinogenicity and identify putative mechanisms of action. | 2014 |
|
| New short term prediction method for chemical carcinogenicity by hepatic transcript profiling following 28-day toxicity tests in rats. | 2011 |
|
| A medium-term, rapid rat bioassay model for the detection of carcinogenic potential of chemicals. | 2010-01 |
|
| Identification of genomic biomarkers for concurrent diagnosis of drug-induced renal tubular injury using a large-scale toxicogenomics database. | 2009-11-09 |
|
| Gene expression profiling in rat liver treated with various hepatotoxic-compounds inducing coagulopathy. | 2009-06 |
|
| An unusual S-adenosylmethionine synthetase gene from dinoflagellate is methylated. | 2007-10-04 |
|
| Silencing MAT2A gene by RNA interference inhibited cell growth and induced apoptosis in human hepatoma cells. | 2007-05 |
|
| Functional characterization of a methionine gamma-lyase in Arabidopsis and its implication in an alternative to the reverse trans-sulfuration pathway. | 2007-02 |
|
| Different effects of sulfur amino acids on prolidase and prolinase activity in normal and prolidase-deficient human erythrocytes. | 2007-01 |
|
| Selection and characterization of L-ethionine resistant mutants of Trichosporon cutaneum. | 2005-12-03 |
|
| Harnessing natural diversity to probe metabolic pathways. | 2005-12 |
|
| Single-gene knockout of a novel regulatory element confers ethionine resistance and elevates methionine production in Corynebacterium glutamicum. | 2005-08 |
|
| Cellular proliferation in the canine pancreas after d,l-ethionine dosage as detected by double immunohistochemical labelling. | 2003-09 |
|
| Physiologically relevant metal cofactor for methionine aminopeptidase-2 is manganese. | 2003-05-06 |
|
| Evaluation of d,l-ethionine as a mechanism for pancreatic islet regeneration in dogs. | 2002-08-16 |
|
| Effect of d,l-ethionine administration on the histomorphology of canine pancreatic acinar and beta-cells. | 2002-08 |
|
| Methionine deprivation and methionine analogs inhibit cell proliferation and growth of human xenografted gliomas. | 1997 |
|
| 13-cis-retinoic acid and hepatic steatosis in rats. | 1993-07-20 |
|
| Effects of the seleno-organic substance Ebselen in two different models of acute pancreatitis. | 1991-05 |
|
| Correlation between medium-term liver bioassay system data and results of long-term testing in rats. | 1990-04 |
|
| Hepatic levels of cytosolic, microsomal and 'mitochondrial' epoxide hydrolases and other drug-metabolizing enzymes after treatment of mice with various xenobiotics and endogenous compounds. | 1987 |
|
| Comparison of the promoting effects of various agents in induction of preneoplastic lesions in rat liver. | 1983-04 |
|
| Increased alpha1-fetoprotein production in rat liver injuries induced by various hepatotoxins. | 1976-04 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:56:08 GMT 2025
by
admin
on
Mon Mar 31 19:56:08 GMT 2025
|
| Record UNII |
WX1BN24WZT
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
25674
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | |||
|
235-966-4
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | |||
|
m5062
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | Merck Index | ||
|
5080
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | |||
|
4886
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | |||
|
WX1BN24WZT
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | |||
|
ETHIONINE
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | |||
|
68662
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | |||
|
D005001
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | |||
|
13073-35-3
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | |||
|
DTXSID5020578
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY | |||
|
82393
Created by
admin on Mon Mar 31 19:56:08 GMT 2025 , Edited by admin on Mon Mar 31 19:56:08 GMT 2025
|
PRIMARY |