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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
Structure of DIACETYL MONOXIME

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+

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Species differences in the reactivation of organophosphate-inhibited plasma esterases by diacetylmonoxime.
1976 Apr
The therapeutic effects of 2,3-butanedione monoxime and atropine in severe dichlorvos intoxication in buffalo calves.
1991
Focal adhesion features during myofibroblastic differentiation are controlled by intracellular and extracellular factors.
2001 Sep
[Effect of actomyosin contractility on focal contacts of myofibroblasts and structure of stress fibers].
2002
ATPase inhibitors suppress actinomycin D-induced apoptosis in leukemia cells.
2002 Sep-Oct
The catalytic domain of xPAK1 is sufficient to induce myosin II dependent in vivo cell fragmentation independently of other apoptotic events.
2003 Nov 15
Modulation of acto-myosin contractility in skeletal muscle myoblasts uncouples growth arrest from differentiation.
2004 Aug 1
Actin and non-muscle myosin II facilitate apical exocytosis of tear proteins in rabbit lacrimal acinar epithelial cells.
2005 Oct 15
Cytoskeletal scaffolds regulate riboflavin endocytosis and recycling in placental trophoblasts.
2006 Dec
Mechanism of interaction of novel uncharged, centrally active reactivators with OP-hAChE conjugates.
2013 Mar 25
Centrally acting oximes in reactivation of tabun-phosphoramidated AChE.
2013 Mar 25
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:01:52 GMT 2023
Edited
by admin
on Sat Dec 16 02:01:52 GMT 2023
Record UNII
19SQ93LM6H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIACETYL MONOXIME
Common Name English
NSC-660
Code English
3-OXIMINO-2-BUTANONE
Systematic Name English
NSC-116103
Code English
BIACETYL MONOOXIME
Systematic Name English
2,3-BUTANEDIONE, 2-OXIME
Systematic Name English
2,3-BUTANEDIONE, MONOOXIME, (2E)-
Systematic Name English
(2E)-BUTANE-2,3-DIONE OXIME
Systematic Name English
DIACETYLMONOXIME
Common Name English
2,3-BUTANEDIONE MONOXIME
Common Name English
2,3-BUTANEDIONE, MONOOXIME, (E)-
Systematic Name English
ISONITROSOETHYL METHYL KETONE
Common Name English
2,3-BUTANEDIONE, 2-OXIME, (2E)-
Systematic Name English
2-OXIMINO-3-BUTANONE
Systematic Name English
Code System Code Type Description
CAS
17019-25-9
Created by admin on Sat Dec 16 02:01:52 GMT 2023 , Edited by admin on Sat Dec 16 02:01:52 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-348-5
Created by admin on Sat Dec 16 02:01:52 GMT 2023 , Edited by admin on Sat Dec 16 02:01:52 GMT 2023
PRIMARY
NSC
116103
Created by admin on Sat Dec 16 02:01:52 GMT 2023 , Edited by admin on Sat Dec 16 02:01:52 GMT 2023
PRIMARY
EPA CompTox
DTXSID7024669
Created by admin on Sat Dec 16 02:01:52 GMT 2023 , Edited by admin on Sat Dec 16 02:01:52 GMT 2023
PRIMARY
WIKIPEDIA
Diacetyl monoxime
Created by admin on Sat Dec 16 02:01:52 GMT 2023 , Edited by admin on Sat Dec 16 02:01:52 GMT 2023
PRIMARY
FDA UNII
19SQ93LM6H
Created by admin on Sat Dec 16 02:01:52 GMT 2023 , Edited by admin on Sat Dec 16 02:01:52 GMT 2023
PRIMARY
CAS
57-71-6
Created by admin on Sat Dec 16 02:01:52 GMT 2023 , Edited by admin on Sat Dec 16 02:01:52 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
NSC
660
Created by admin on Sat Dec 16 02:01:52 GMT 2023 , Edited by admin on Sat Dec 16 02:01:52 GMT 2023
PRIMARY
PUBCHEM
6409633
Created by admin on Sat Dec 16 02:01:52 GMT 2023 , Edited by admin on Sat Dec 16 02:01:52 GMT 2023
PRIMARY