2. GPCR/G Protein Neuronal Signaling
  3. 5-HT Receptor
  4. (S)-Mirtazapine

(S)-Mirtazapine  (Synonyms: (S)-Org3770; (S)-6-Azamianserin)

Cat. No.: HY-B0352A Purity: 99.76% ee.: 98.35%
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(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.

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(S)-Mirtazapine Chemical Structure

(S)-Mirtazapine Chemical Structure

CAS No. : 61337-87-9

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Based on 1 publication(s) in Google Scholar

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(S)-Mirtazapine Related Antibodies

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Description

(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].

IC50 & Target

5-HT2 Receptor

 

5-HT3 Receptor

 

Molecular Weight

265.35

Formula

C17H19N3
CAS No.
Appearance

Solid

Color

Off-white to light yellow

SMILES

CN1C[C@]2([H])C3=CC=CC=C3CC4=CC=CN=C4N2CC1
Shipping

Room temperature in continental US; may vary elsewhere.
Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Purity & Documentation
References
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(S)-Mirtazapine Related Classifications

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
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Help & FAQs
  • 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)-Mirtazapine61337-87-9(S)-Org3770 (S)-6-Azamianserin5-HT ReceptorSerotonin Receptor5-hydroxytryptamine ReceptorS(+)-enantiomerpronociceptiveCYP2D6CYP1A2metabolized5-HT2Inhibitorinhibitorinhibit

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