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Details

Stereochemistry ACHIRAL
Molecular Formula C14H8N2O4
Molecular Weight 268.2243
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N,N'-4-PHENYLENEDIMALEIMIDE

SMILES

O=C1C=CC(=O)N1C2=CC=C(C=C2)N3C(=O)C=CC3=O

InChI

InChIKey=AQGZJQNZNONGKY-UHFFFAOYSA-N
InChI=1S/C14H8N2O4/c17-11-5-6-12(18)15(11)9-1-2-10(4-3-9)16-13(19)7-8-14(16)20/h1-8H

HIDE SMILES / InChI

Molecular Formula C14H8N2O4
Molecular Weight 268.2243
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Cross-bridge cooperativity during isometric contraction and unloaded shortening of skeletal muscle.
2001
Changes in the thermal unfolding of p-phenylenedimaleimide-modified myosin subfragment 1 induced by its 'weak' binding to F-actin.
2001 Feb 2
Identification of functionally important cysteines in the alpha-subunit of transducin by chemical cross-linking techniques.
2002 Jan
Helices VII and X in the lactose permease of Escherichia coli: proximity and ligand-induced distance changes.
2002 Jan 4
Evidence for disaggregation of oligomeric G(o)alpha induced by guanosine-5;-3-O-(thio)triphosphate activation.
2003 Jan
New aspects of the spontaneous polymerization of actin in the presence of salts.
2009 Apr 10
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:17:46 GMT 2023
Edited
by admin
on Fri Dec 15 18:17:46 GMT 2023
Record UNII
BEC7P1E6J1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N,N'-4-PHENYLENEDIMALEIMIDE
Common Name English
NSC-81257
Code English
P-PHENYLENE DIMALEIMIDE
Common Name English
1H-PYRROLE-2,5-DIONE, 1,1'-(1,4-PHENYLENE)BIS-
Systematic Name English
Code System Code Type Description
PUBCHEM
76765
Created by admin on Fri Dec 15 18:17:46 GMT 2023 , Edited by admin on Fri Dec 15 18:17:46 GMT 2023
PRIMARY
ECHA (EC/EINECS)
221-910-6
Created by admin on Fri Dec 15 18:17:46 GMT 2023 , Edited by admin on Fri Dec 15 18:17:46 GMT 2023
PRIMARY
CAS
3278-31-7
Created by admin on Fri Dec 15 18:17:46 GMT 2023 , Edited by admin on Fri Dec 15 18:17:46 GMT 2023
PRIMARY
FDA UNII
BEC7P1E6J1
Created by admin on Fri Dec 15 18:17:46 GMT 2023 , Edited by admin on Fri Dec 15 18:17:46 GMT 2023
PRIMARY
EPA CompTox
DTXSID70186446
Created by admin on Fri Dec 15 18:17:46 GMT 2023 , Edited by admin on Fri Dec 15 18:17:46 GMT 2023
PRIMARY
NSC
81257
Created by admin on Fri Dec 15 18:17:46 GMT 2023 , Edited by admin on Fri Dec 15 18:17:46 GMT 2023
PRIMARY