Adoprazine

CAS No. 222551-17-9

Adoprazine ( SLV313 )

Catalog No. M26047 CAS No. 222551-17-9

Adoprazine is a potential atypical antipsychotic bearing potent D2 receptor antagonist and 5-HT1A receptor agonist properties.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 106 Get Quote
5MG 177 Get Quote
10MG 303 Get Quote
25MG 530 Get Quote
50MG 755 Get Quote
100MG 1044 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Adoprazine
  • Note
    Research use only, not for human use.
  • Brief Description
    Adoprazine is a potential atypical antipsychotic bearing potent D2 receptor antagonist and 5-HT1A receptor agonist properties.
  • Description
    Adoprazine is a potential atypical antipsychotic bearing potent D2 receptor antagonist and 5-HT1A receptor agonist properties.
  • Synonyms
    SLV313
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    222551-17-9
  • Formula Weight
    405.5
  • Molecular Formula
    C24H24FN3O2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Fc1ccc(cc1)-c1cncc(CN2CCN(CC2)c2cccc3OCCOc23)c1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Zhang Z, Lunter DJ. Confocal Raman microspectroscopy as an alternative to differential scanning calorimetry to detect the impact of emulsifiers and formulations on stratum corneum lipid conformation. Eur J Pharm Sci. 2018 May 15. pii: S0928-0987(18)30232-X. doi: 10.1016/j.ejps.2018.05.013. [Epub ahead of print] PubMed PMID: 29775655.
molnova catalog
related products
  • Phlorizin

    Phlorizin is a non-selective SGLT inhibitor found in apple, for hSGLT1( Ki=300 nM) and hSGLT2( Ki=39 nM) .

  • Urantide

    Selective and competitive urotensin-II (UT) receptor antagonist (pKB = 8.3). Blocks hU-II induced contractions in thoracic aorta ex vivo. Exhibits no effect on noradrenaline or endothelin 1-induced contraction or on acetylcholine-induced relaxation. Behaves as a partial agonist in a calcium mobilization assay (in CHO cells expressing hUT receptors).

  • 3-Adenylic acid

    3'-Adenylic acid is an agent of bioactive chemical.