2. Membrane Transporter/Ion Channel Neuronal Signaling
  3. iGluR
  4. (S)-Alaproclate

(S)-Alaproclate  (Synonyms: (S)-GEA 654; (S)-A03)

Cat. No.: HY-124779
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(S)-Alaproclate ((S)-GEA 654) is more potent than the R-(+)-enantiomer both in blocking the NMDA receptor currents in vitro and in antagonizing the cGMP increase in vivo.

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(S)-Alaproclate Chemical Structure

(S)-Alaproclate Chemical Structure

CAS No. : 66171-75-3

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Other Forms of (S)-Alaproclate:

(S)-Alaproclate Related Antibodies

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Description

(S)-Alaproclate ((S)-GEA 654) is more potent than the R-(+)-enantiomer both in blocking the NMDA receptor currents in vitro and in antagonizing the cGMP increase in vivo[1].

Molecular Weight

255.74

Formula

C13H18ClNO2
CAS No.
SMILES

C[C@H](N)C(OC(C)(C)CC1=CC=C(C=C1)Cl)=O
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Room temperature in continental US; may vary elsewhere.
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Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
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(S)-Alaproclate Related Classifications

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  • Do most proteins show cross-species activity?

    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.

Keywords:

(S)-Alaproclate66171-75-3(S)-GEA 654 (S)-A03iGluRIonotropic glutamate receptorsNMDAcGMPR-(+)-AlaproclatInhibitorinhibitorinhibit

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