ChemicalBook--->CAS DataBase List--->244101-03-9

244101-03-9

244101-03-9 Structure

244101-03-9 Structure
IdentificationBack Directory
[Name]

L-826,266
[CAS]

244101-03-9
[Synonyms]

266
L-826
L-826,266
[Molecular Formula]

C27H21BrClNO4S
[MDL Number]

MFCD09970777
[MOL File]

244101-03-9.mol
[Molecular Weight]

570.88
Chemical PropertiesBack Directory
[density ]

1.470±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 20 mg/ml; DMSO: 10 mg/ml
[form ]

A crystalline solid
[pka]

4.19±0.10(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Description]

L-826266 is a EP(1) receptor antagonist.
[Uses]

L-826266 is a selective and competitive EP3 receptor antagonist. L-826266 can be used for convulsive disorders research[1].
[in vivo]

L-826266 (0.01-1 nmol/site; i.c.v.; once) delays seizures, and increases the latency for clonic and generalized tonic-clonic seizures induced by PTZ[1].

Animal Model:Adult male Wistar rats (250-300 g) injected with Pentylenetetrazol (PTZ)[1]
Dosage:0.01 nmol/site, 0.1 nmol/site or 1 nmol/site
Administration:i.c.v.; once
Result:Increased the latency for clonic and generalized tonic-clonic seizures induced by PTZ.
[IC 50]

EP3
[References]

[1] M S Oliveira, et al. Modulation of pentylenetetrazol-induced seizures by prostaglandin E2 receptors. Neuroscience. 2008 Apr 9;152(4):1110-8. DOI:10.1016/j.neuroscience.2008.01.005
[2] Mauro Schneider Oliveira, et al. Prostaglandin E2 modulates Na+,K+-ATPase activity in rat hippocampus: implications for neurological diseases. J Neurochem. 2009 Apr;109(2):416-26. DOI:10.1111/j.1471-4159.2009.05961.x
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