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Midafotel (SDZ-EAA 494) is a potent and comprtitive NMDA antagonist with an ED50 value of 39 nM. Midafotel causes intense stereotyped behaviors. Midafotel shows neuroprotective effects.

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Midafotel Chemical Structure

Midafotel Chemical Structure

CAS No. : 117414-74-1

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Based on 1 publication(s) in Google Scholar

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Description

Midafotel (SDZ-EAA 494) is a potent and comprtitive NMDA antagonist with an ED50 value of 39 nM. Midafotel causes intense stereotyped behaviors. Midafotel shows neuroprotective effects[1][2][3].

IC50 & Target[1]

NMDA Receptor

39 nM ()

In Vivo

Midafotel (15 mg/kg; i.p.) causes intense stereotyped behaviors in rats[2].
Midafotel (1.5, 4.5, 15 mg/kg; i.v.; initiated 15 min prior to MCA occlusion (followed by constant infusion at 1, 3 or 10 mg/kg/h)) produces dose-dependent reductions in the volumes of infarction; the dose of 4.5 mg/kg being the most effective in focal cerebral ischemia in the rat[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Adult female Wistar rats[2]
Dosage: 15 mg/kg
Administration: I.p.
Result: Induced the typical PCP-like behavioral syndrome with ataxia, hyperlocomotion and stereotyped behaviors, i.e., head weaving, stereotyped sniffing, face washing and grooming, significantly increased extracellular levels of HVA and 5-HIAA in the striatum.
Molecular Weight

250.19

Formula

C8H15N2O5P

CAS No.
SMILES

OC([C@H]1CN(CCN1)C/C=C/P(O)(O)=O)=O

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Room temperature in continental US; may vary elsewhere.

Storage

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References
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Midafotel Related Classifications

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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Midafotel
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HY-107718
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