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P7908

Sigma-Aldrich

N-(1-Pyrenyl)maleimide

Sinonimo/i:

1-(1-Pyrenyl)-1H-pyrrole-2,5-dione

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About This Item

Formula empirica (notazione di Hill):
C20H11NO2
Numero CAS:
42189-56-0
Peso molecolare:
297.31
Beilstein:
1542661
Numero CE:
255-702-1
Numero MDL:
MFCD00049301
Codice UNSPSC:
12352100
ID PubChem:
24898892
NACRES:
NA.22

Forma fisica

powder

Punto di fusione

235-237 °C (lit.)

Stringa SMILE

O=C1C=CC(=O)N1c2ccc3ccc4cccc5ccc2c3c45

InChI

1S/C20H11NO2/c22-17-10-11-18(23)21(17)16-9-7-14-5-4-12-2-1-3-13-6-8-15(16)20(14)19(12)13/h1-11H
YXKWRQLPBHVBRP-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

Reactant used in synthesis of:
  • Oligodeoxynucleotide derivatives
  • Polymer conjugates of immunogenic peptides
  • Modified oligonucleotides for biosensing applications,

Reactant:
  • Involved in synthesis of thermally stable fluorescent maleimide/isobutene alternating copolymers
  • Used as derivitizing agent for determination of glutathione disulfide levels in biological samples

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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1-Pyrenebutyric hydrazide for fluorescence, ≥97.0% (T)

Sigma-Aldrich

82669

1-Pyrenebutyric hydrazide

N-tert-Butylmaleimide 97%

Sigma-Aldrich

386421

N-tert-Butylmaleimide

N-Phenylmaleimide 97%

Sigma-Aldrich

P27100

N-Phenylmaleimide

E I Slobozhanina et al.
Journal of applied toxicology : JAT, 25(2), 109-114 (2005-03-04)
In the present work we studied, by chemiluminescence measurements, the influence of lead on the production of reactive oxygen species (ROS) in haemolysates obtained from human erythrocytes incubated in the presence of different concentrations of lead acetate. Moreover, we evaluated
V G Panse et al.
The Journal of biological chemistry, 276(36), 33681-33688 (2001-07-04)
SecB is a homotetrameric, cytosolic chaperone that forms part of the protein translocation machinery in Escherichia coli. We have investigated the bound-state conformation of a model protein substrate of SecB, bovine pancreatic trypsin inhibitor (BPTI) as well as the conformation
Mengmeng Wang et al.
Biochemistry, 45(25), 7778-7786 (2006-06-21)
Domain motions of S-adenosyl-l-homocysteine (AdoHcy) hydrolase have been detected by time-resolved fluorescence anisotropy measurements. Time constants for reorientational motions in the native enzyme were compared with those for enzymes where key residues were altered by site-directed mutation. Mutations M351P, H353A
T Inobe et al.
Biochimica et biophysica acta, 1545(1-2), 160-173 (2001-05-09)
Chaperonin-assisted protein folding proceeds through cycles of ATP binding and hydrolysis by GroEL, which undergoes a large structural change by the ATP binding or hydrolysis. One of the main concerns of GroEL is the mechanism of the productive and cooperative
Jinhui Li et al.
Biochemistry, 42(36), 10674-10682 (2003-09-10)
We have used frequency-domain fluorescence spectroscopy to investigate the structural linkage between the transmembrane and cytosolic domains of the regulatory protein phospholamban (PLB). Using an engineered PLB having a single cysteine (Cys(24)) derivatized with the fluorophore N-(1-pyrenyl)maleimide (PMal), we have
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