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  3. Amino Acid Derivatives
  4. 61337-87-9

61337-87-9

(S)-Mirtazapine Chemical Structure

61337-87-9

Chemical Structure

  • (S)-Mirtazapine
  • Synonym(s): (S)-Org3770; (S)-6-Azamianserin
  • CAS No: 61337-87-9
    Formula: C17H19N3
    Molecular Weight: 265.35
  • IUPAC Name: (S)-2-methyl-1,2,3,4,10,14b-hexahydrobenzo[c]pyrazino[1,2-a]pyrido[3,2-f]azepine
  • InChIKey: RONZAEMNMFQXRA-MRXNPFEDSA-N
  • SMILES: CN1C[C@]2([H])C3=CC=CC=C3CC4=CC=CN=C4N2CC1

Biological Activity: (S)-Mirtazapine ((S)-Org3770) is a S(+)-enantiomer of Mirtazapine with pronociceptive properties in an animal model of acute thermal nociception. (S)-Mirtazapine is a stereoselective 5-HT2 receptor antagonist. (S)-Mirtazapine is metabolized by CYP2D6 and CYP1A2[1].

Cat. No. Product Name Purity Description
HY-B0352A (S)-Mirtazapine 99.76% (S)-Mirtazapine ((S)-Org3770) is a S(+)-enantiomer of Mirtazapine with pronociceptive properties in an animal model of acute thermal nociception. (S)-Mirtazapine is a stereoselective 5-HT2 receptor antagonist. (S)-Mirtazapine is metabolized by CYP2D6 and CYP1A2.
HY-B0352AS (S)-Mirtazapine-d3 ≥99.0% (S)-Mirtazapine-d3 is a deuterium labeled (S)-Mirtazapine. (S)-Mirtazapine is a S(+)-enantiomer of Mirtazapine with pronociceptive properties in an animal model of acute thermal nociception.(S)-Mirtazapine is a stereoselective 5-HT2 receptor antagonist. (S)-Mirtazapine is metabolized by CYP2D6 and CYP1A2.

References

[1]. Muth-Selbach U, et al. Racemic intrathecal mirtazapine but not its enantiomers acts anti-neuropathic after chronic constriction injury in rats. Brain Res Bull. 2009 Apr 6;79(1):63-8. [Content Brief]

Keywords:

(S)-Mirtazapine(S)-Mirtazapine-d3