Methiothepin mesylate

CAS No. 74611-28-2

Methiothepin mesylate ( —— )

Catalog No. M15847 CAS No. 74611-28-2

Metitepine (INN), also commonly known as methiothepin, is a drug that acts as an antagonist at various serotonin and dopamine receptors.

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 28 In Stock
10MG 45 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Methiothepin mesylate
  • Note
    Research use only, not for human use.
  • Brief Description
    Metitepine (INN), also commonly known as methiothepin, is a drug that acts as an antagonist at various serotonin and dopamine receptors.
  • Description
    Metitepine (INN), also commonly known as methiothepin, is a drug that acts as an antagonist at various serotonin and dopamine receptors. It is used as an antipsychotic.
  • Synonyms
    ——
  • Pathway
    Endocrinology/Hormones
  • Target
    5-HT Receptor
  • Recptor
    5-HT; Dopamine
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    74611-28-2
  • Formula Weight
    452.65
  • Molecular Formula
    C21H28N2O3S3
  • Purity
    >98%(HPLC)
  • Solubility
    DMSO: 10 mM
  • SMILES
    CS(O)(=O)=O.CSC1=CC2=C(SC3=CC=CC=C3CC2N2CCN(C)CC2)C=C1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Dall'Olio R, et al. Pharmacol Biochem Behav. 1985 Jul;23(1):43-8.
molnova catalog
related products
  • LP-211

    LP-211 is a brain penetrant selective agonist for a 5-HT7 receptor (Ki: 0.58 nM) and >300-fold selectivity over the 5-HT1A receptor.

  • SB-616234-A

    SB-616234-A is a selective and orally bioavailable antagonist of 5-HT1B receptor, with anxiolytic and antidepressant activity.

  • SUVN-502 mesylate hy...

    SUVN-502 (SUVN502)is apotent, selective, brain penetrant and orally active 5-HT6 receptor antagonist with Ki of 2.04 nM.