Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H7NO2 |
| Molecular Weight | 101.1039 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C(\C)=N\O
InChI
InChIKey=FSEUPUDHEBLWJY-HWKANZROSA-N
InChI=1S/C4H7NO2/c1-3(5-7)4(2)6/h7H,1-2H3/b5-3+
| Molecular Formula | C4H7NO2 |
| Molecular Weight | 101.1039 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Mechanism of interaction of novel uncharged, centrally active reactivators with OP-hAChE conjugates. | 2013-03-25 |
|
| Centrally acting oximes in reactivation of tabun-phosphoramidated AChE. | 2013-03-25 |
|
| Cytoskeletal scaffolds regulate riboflavin endocytosis and recycling in placental trophoblasts. | 2006-12 |
|
| Actin and non-muscle myosin II facilitate apical exocytosis of tear proteins in rabbit lacrimal acinar epithelial cells. | 2005-10-15 |
|
| Modulation of acto-myosin contractility in skeletal muscle myoblasts uncouples growth arrest from differentiation. | 2004-08-01 |
|
| The catalytic domain of xPAK1 is sufficient to induce myosin II dependent in vivo cell fragmentation independently of other apoptotic events. | 2003-11-15 |
|
| ATPase inhibitors suppress actinomycin D-induced apoptosis in leukemia cells. | 2003-01-18 |
|
| [Effect of actomyosin contractility on focal contacts of myofibroblasts and structure of stress fibers]. | 2002 |
|
| Focal adhesion features during myofibroblastic differentiation are controlled by intracellular and extracellular factors. | 2001-09 |
|
| The influence of 2,3-butanedione monoxime on dichlorvos-induced enzymatic changes in buffalo calves. | 1992-06 |
|
| The therapeutic effects of 2,3-butanedione monoxime and atropine in severe dichlorvos intoxication in buffalo calves. | 1991 |
|
| Species differences in the reactivation of organophosphate-inhibited plasma esterases by diacetylmonoxime. | 1976-04 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:06:49 GMT 2025
by
admin
on
Mon Mar 31 21:06:49 GMT 2025
|
| Record UNII |
19SQ93LM6H
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
17019-25-9
Created by
admin on Mon Mar 31 21:06:49 GMT 2025 , Edited by admin on Mon Mar 31 21:06:49 GMT 2025
|
PRIMARY | |||
|
200-348-5
Created by
admin on Mon Mar 31 21:06:49 GMT 2025 , Edited by admin on Mon Mar 31 21:06:49 GMT 2025
|
PRIMARY | |||
|
116103
Created by
admin on Mon Mar 31 21:06:49 GMT 2025 , Edited by admin on Mon Mar 31 21:06:49 GMT 2025
|
PRIMARY | |||
|
DTXSID7024669
Created by
admin on Mon Mar 31 21:06:49 GMT 2025 , Edited by admin on Mon Mar 31 21:06:49 GMT 2025
|
PRIMARY | |||
|
Diacetyl monoxime
Created by
admin on Mon Mar 31 21:06:49 GMT 2025 , Edited by admin on Mon Mar 31 21:06:49 GMT 2025
|
PRIMARY | |||
|
19SQ93LM6H
Created by
admin on Mon Mar 31 21:06:49 GMT 2025 , Edited by admin on Mon Mar 31 21:06:49 GMT 2025
|
PRIMARY | |||
|
57-71-6
Created by
admin on Mon Mar 31 21:06:49 GMT 2025 , Edited by admin on Mon Mar 31 21:06:49 GMT 2025
|
NON-SPECIFIC STEREOCHEMISTRY | |||
|
660
Created by
admin on Mon Mar 31 21:06:49 GMT 2025 , Edited by admin on Mon Mar 31 21:06:49 GMT 2025
|
PRIMARY | |||
|
6409633
Created by
admin on Mon Mar 31 21:06:49 GMT 2025 , Edited by admin on Mon Mar 31 21:06:49 GMT 2025
|
PRIMARY |