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PNU-120596

Catalog No. P0043 Name Sigma Aldrich
CAS Number 501925-31-1 Website http://www.sigmaaldrich.com
M. F. C13H14ClN3O4 Telephone 1-800-521-8956
M. W. 311.72096 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 73122

SYNONYMS

IUPAC name
1-(5-chloro-2,4-dimethoxyphenyl)-3-(5-methyl-1,2-oxazol-3-yl)urea
IUPAC Traditional name
1-(5-chloro-2,4-dimethoxyphenyl)-3-(5-methyl-1,2-oxazol-3-yl)urea
Synonyms
NSC 216666
N-(5-Chloro-2,4-dimethoxyphenyl)-N′-(5-methyl-3-isoxazolyl)-urea

DATABASE IDS

CAS Number 501925-31-1
MDL Number MFCD00095313

PROPERTIES

Empirical Formula (Hill Notation) C13H14ClN3O4
Purity ≥98% (HPLC)
Apperance white to off-white
Solubility DMSO: >10 mg/mL
MSDS Link Download
Storage Temperature room temp
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
An allosteric modulator of α7 nicotinic receptors, N-(5-chloro-2,4-dimethoxyphenyl)-N′-(5-methyl-3-isoxazolyl)-urea (PNU-120596), causes conformational changes in the extracellular ligand binding domain similar to those caused by acetylcholinePNU-120596 is a positive allosteric modulator selective for the α7 nicotinic acetylcholine receptor.1 PNU-120596 produces no detectable change in currents mediated by α4β2, α3β4, α9α10 nAChRs. It increases channel mean open time, but does not affect ion selectivity. It does not bind at the agonist binding site, but induces conformational changes similar to the natural effector.1
Description (简体中文)
Biochem/physiol Actions
An allosteric modulator of α7 nicotinic receptors, N-(5-chloro-2,4-dimethoxyphenyl)-N′-(5-methyl-3-isoxazolyl)-urea (PNU-120596), causes conformational changes in the extracellular ligand binding domain similar to those caused by acetylcholinePNU-120596 is a positive allosteric modulator selective for the α7 nicotinic acetylcholine receptor.1 PNU-120596 produces no detectable change in currents mediated by α4β2, α3β4, α9α10 nAChRs. It increases channel mean open time, but does not affect ion selectivity. It does not bind at the agonist binding site, but induces conformational changes similar to the natural effector.1

REFERENCES