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77086-22-7

77086-22-7 Structure

77086-22-7 Structure
IdentificationBack Directory
[Name]

(-)-MK-801 MALEATE
[CAS]

77086-22-7
[Synonyms]

mk801
(+)MK801
(+)MK108
MK 801 ;MK801
Dizocipine maleate
(-)-MK-801 MALEATE
(+)Mk801/MK801/MK-801
(+)-MK-801·Maleic acid
MK-801(Dizocilpine)Maleate
(+/-)-mk-801 hydrogen maleate
Dizocilpine hydrogen maleate
Dizocilpine Maleate [(+)-MK 801 maleate
(+)-MK 801 Maleate - CAS 77086-22-7 - Calbiochem
(+)-MK-801 HYDROGEN MALEATE (DIZOCILPINE MALEATE)
[5R,(-)]-10,11-Dihydro-5-methyl-5H-dibenzo[a,d]cyclohepten-5β,10β-imine
DIZOCILPINE MALEATE;DIZOCILPINE HYDROGEN MALEATE;(+)-MK 801;MK 801;MK801
[5R,10S,(-)]-10,11-Dihydro-5-methyl-5H-dibenzo[a,d]cyclohepten-5,10-imine
[5R,10S,(-)]-10,11-Dihydro-5-methyl-5H-dibenzo[a,d]cyclohepten-5β,10β-imine
(5S,10R)-5-Methyl-10,11-dihydro-5H-5,10-epiminodibenzo[a,d][7]annulene maleate
(+)-10,11-dihydro-5-methyl-5H-dibenzo[a,d]cyclohepten-5,10-diyldiammonium maleate
(+)-10,11-dihydro-5-methyl-5H-dibenzo[a,d]cyclohepten-5,10-diyldiammonium maleate
(5S,10R)-(-)-5-METHYL-10,11-DIHYDRO-5H-DIBENZO[A,D]CYCLOHEPTEN-5,10-IMINE MALEATE
d)cyclohepten-5,10-imine,10,11-dihydro-5-methyl-5h-dibenzo((5s)-5h-dibenzo((z)-2-b
5-Methyl-10,11-dihydro-5H-5,10-epiMinodibenzo[a,d][7]annulene (2Z)-but-2-enedioate
(5S,10R)-(+)-5-Methyl-10,11-dihydro-(5H)-dibenzo[a.d]cycloheptene-5,10-iminemaleate
(5S)-10,11-Dihydro-5-methyl-5H-dibenzo[a,d]cyclohepten-5,10-imine (Z)-2-butenedioate
Dizocilpine hydrogen maleate, (5R,10S)-(+)-5-Methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine hydrogen maleate
inhibit,anticonvulsant,neurotransmitter,noncompetitive,ambulation,MK-801,Dizocilpine Maleate,voltage,hyperlocomotion,Ionotropic glutamate receptors,Inhibitor,iGluR,MK801,Dizocilpine
[EINECS(EC#)]

278-614-5
[Molecular Formula]

C20H19NO4
[MDL Number]

MFCD00082465
[MOL File]

77086-22-7.mol
[Molecular Weight]

337.37
Chemical PropertiesBack Directory
[Melting point ]

208.5-210°
[alpha ]

D20 +114° (c = 0.0128 g/2 ml ethanol)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

DMSO: >20 mg/mL
[form ]

solid
[color ]

white
[optical activity]

[α]25/D +117°, c = 1 in methanol(lit.)
[InChIKey]

QLTXKCWMEZIHBJ-FWHYOZOBSA-N
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[RTECS ]

HP1093575
Hazard InformationBack Directory
[Uses]

(-)-MK-801 MALEATE acts as an NMDA receptor antagonist. It is selective and potent, but noncompetitive, used in various ischemia treatments.
[Uses]

(-)-MK-801 MALEATE is probe for NMDA receptors
[Definition]

ChEBI: Dizocilpine maleate is a maleate salt obtained by reaction of dizocilpine with one equivalent of maleic acid. It has a role as an anaesthetic, an anticonvulsant, a neuroprotective agent, a nicotinic antagonist and a NMDA receptor antagonist. It is a maleate salt and a tetracyclic antidepressant. It contains a dizocilpine(1+).
[General Description]

A highly potent, selective and non-competitive NMDA receptor antagonist that acts by binding to a site located within the NMDA associated ion channel, preventing Ca2+ flux. An effective anti-ischemic agent in several animal models. Has been used to develop an in vivo model of NMDA receptor-dependent apoptotic neurodegenerative disease in developing rat brains. Has also been used to develop an in vitro model of NMDA receptor-specific Ca2+ entry induced seizures.
[Biological Activity]

(-)-MK-801 MALEATE is a potent, selective and non-competitive NMDA receptor antagonist. Acts by binding to a site located within the NMDA associated ion channel and thus prevents Ca 2+ flux. An effective anti-ischemic agent in several animal models. Also available as part of the Mixed NMDA Receptor Tocriset™ .
[Biochem/physiol Actions]

Primary TargetNMDA receptor
[storage]

Store at -20°C
[References]

[1] wong eh, kemp ja, priestley t, knight ar, woodruff gn, iversen ll . the anticonvulsant mk-801 is a potent n-methyl-d-aspartate antagonist. proc natl acad sci u s a. 1986 sep;83(18):7104-8.
Spectrum DetailBack Directory
[Spectrum Detail]

(-)-MK-801 MALEATE(77086-22-7)1HNMR
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