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ChemicalBook--->CAS DataBase List--->122955-42-4

122955-42-4

122955-42-4 Structure

122955-42-4 Structure
IdentificationBack Directory
[Name]

10,10-BIS(4-PYRIDINYLMETHYL)-9(10H)-ANTHRACENONE DIHYDROCHLORIDE
[CAS]

122955-42-4
[Synonyms]

XE 991
XE9912HCl
XE 991 DIHYDROCHLORIDE
9(10H)-Anthracenone, 10,10-bis(4-pyridinylmethyl)-
10-bis(4-Pyridinylmethyl)-9(10H)-anthracenone dihydrochloride
10,10-BIS(4-PYRIDINYLMETHYL)-9(10H)-ANTHRACENONE DIHYDROCHLORIDE
[Molecular Formula]

C26H20N2O
[MDL Number]

MFCD05662331
[MOL File]

122955-42-4.mol
[Molecular Weight]

376.45
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

DMSO: >20mg/mL
[form ]

solid
[color ]

white to beige
[Water Solubility ]

Soluble in water (100mM)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[RTECS ]

CB1530000
Hazard InformationBack Directory
[Uses]

XE-991 has been used as a KCNQ (Kv7.2/7.3) inhibitor to examine whether M-current inhibition affects oxytocin receptor (TGOT) mediated depolarization. It has also been used as an KCNQ inhibitor to study the ionic mechanism responsible for the overshoot/undershoot in membrane potential in mouse cholinergic interneurons (ChIs) in the presence of tetrodotoxin (TTX).
[Biological Activity]

Potent and selective blocker of KCNQ voltage-gated potassium channels. Blocks KCNQ2+3/M-currents (IC 50 = 0.6-0.98 μ M) and KCNQ1 homomeric channels (IC 50 = 0.75 μ M) but is less potent against KCNQ1/minK channels (IC 50 = 11.1 μ M). Augments hippocampal ACh release and is a cognitive enhancer following oral administration in vivo .
[Biochem/physiol Actions]

XE-991 is a KCNQ channel blocker; which is more potent than linopiridine (Cat. No. L-134).
[storage]

Room temperature (desiccate)
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