Chlorprothixene

CAS No. 113-59-7

Chlorprothixene ( —— )

Catalog No. M10478 CAS No. 113-59-7

Chlorprothixene is a typical antipsychotic drug of the thioxanthene class and was the first of the series to be synthesized.

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 34 In Stock
100MG 57 In Stock
200MG 79 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Chlorprothixene
  • Note
    Research use only, not for human use.
  • Brief Description
    Chlorprothixene is a typical antipsychotic drug of the thioxanthene class and was the first of the series to be synthesized.
  • Description
    Chlorprothixene is a typical antipsychotic drug of the thioxanthene class and was the first of the series to be synthesized.
  • Synonyms
    ——
  • Pathway
    Endocrinology/Hormones
  • Target
    5-HT Receptor
  • Recptor
    5-HT6; 5-HT7; D2; D3; H1 receptor
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    113-59-7
  • Formula Weight
    315.86
  • Molecular Formula
    C18H18ClNS
  • Purity
    >98%(HPLC)
  • Solubility
    Ethanol: 28 mg/mL (88.64 mM); DMSO: 6 mg/mL (18.99 mM)
  • SMILES
    CN(C)CC/C=C\1/C2=CC=CC=C2SC3=C1C=C(C=C3)Cl
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Froimowitz M, Cody V. J Med Chem. 1993 Jul 23;36(15):2219-27.
molnova catalog
related products
  • 4-((5-cyclopropyl-3-...

    4-((5-cyclopropyl-3-methyl-1-((methylsulfonyl)methyl)-1H-pyrazol-4-yl)oxy)-2,6-dimethylbenzonitrile is an agonist of 5-HT Receptor with anti-Alzheimer and antidepressant activities.

  • Sodium ascorbate

    Sodium Ascorbate is a more bioavailable form of vitamin C that is an alternative to taking ascorbic acid as a supplement.

  • Lasmiditan hydrochlo...

    Lasmiditan hydrochloride is a novel centrally acting highly selective 5-HT(1F) receptor agonist (K1:2.21 μM).