P27100
N-Phenylmaleimide
97%
Synonym(s):
1-Phenyl-pyrrole-2,5-dione, 1-[4-(Acetoxy)phenyl]maleimide
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About This Item
Empirical Formula (Hill Notation):
C10H7NO2
CAS Number:
Molecular Weight:
173.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-382-0
Beilstein/REAXYS Number:
125098
MDL number:
Assay:
97%
Form:
solid
InChI key
HIDBROSJWZYGSZ-UHFFFAOYSA-N
InChI
1S/C10H7NO2/c12-9-6-7-10(13)11(9)8-4-2-1-3-5-8/h1-7H
SMILES string
O=C1C=CC(=O)N1c2ccccc2
assay
97%
form
solid
bp
162-163 °C/12 mmHg (lit.)
mp
85-87 °C (lit.)
Quality Level
Related Categories
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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S Xu et al.
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It is well established that in a skeletal muscle under relaxing conditions, cross-bridges exist in a mixture of four weak binding states in equilibrium (A*M*ATP, A*M*ADP*P(i), M*ATP, and M*ADP*P(i)). It has been shown that these four weak binding states are
M Salomon et al.
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I Velasco-Guillén et al.
Archives of biochemistry and biophysics, 372(1), 121-127 (1999-11-24)
The Ca(2+)-ATPase from sarcoplasmic reticulum reacts with phenylmaleimide, producing the inhibition of the ATPase activity following a pseudo-first-order kinetic with a rate constant of 19 M(-1) s(-1). Calcium and ATP binding are not altered upon phenylmaleimide inhibition. However, the presence
Michael L Vasil et al.
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The twin-arginine translocase (TAT) in some bacterial pathogens, including Pseudomonas aeruginosa, Burkholderia pseudomallei, and Mycobacterium tuberculosis, contributes to pathogenesis by translocating extracellular virulence determinants across the inner membrane into the periplasm, thereby allowing access to the Xcp (type II) secretory
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Asa D Melhado et al.
Journal of the American Chemical Society, 129(42), 12638-12639 (2007-09-29)
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