PU-02

CAS No. 313984-77-9

PU-02 ( 6-[(1-Naphthalenylmethyl)thio]-9H-purine )

Catalog No. M21984 CAS No. 313984-77-9

PU-02 is a potent and selective antagonist of 5-HT3 receptor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 50 In Stock
10MG 87 In Stock
25MG 170 In Stock
50MG 312 In Stock
100MG 500 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    PU-02
  • Note
    Research use only, not for human use.
  • Brief Description
    PU-02 is a potent and selective antagonist of 5-HT3 receptor.
  • Description
    PU-02 is a potent and selective antagonist of 5-HT3 receptor.
  • Synonyms
    6-[(1-Naphthalenylmethyl)thio]-9H-purine
  • Pathway
    Endocrinology/Hormones
  • Target
    5-HT Receptor
  • Recptor
    5-HT3
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    313984-77-9
  • Formula Weight
    292.36
  • Molecular Formula
    C16H12N4S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C(Sc1ncnc2nc[nH]c12)c1cccc2ccccc12
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Trattnig S M , Harpsoe K , Thygesen S B , et al. Discovery of a Novel Allosteric Modulator of 5-HT3 Receptors: INHIBITION AND POTENTIATION OF CYS-LOOP RECEPTOR SIGNALING THROUGH A CONSERVED TRANSMEMBRANE INTERSUBUNIT SITE[J]. Journal of Biological Chemistry, 2012, 287(30):25241-25254.
molnova catalog
related products
  • Fluvoxamine maleate

    Fluvoxamine maleate is a selective serotonin (5-HT) reuptake inhibitor (SSRI).

  • DSP-1053

    DSP-1053 is a novel potent serotonin reuptake (SERT) inhibitor with 5-HT1A partial agonistic activity that binds to human serotonin transporter and 5-HT1A receptor with Ki of 1.02 and 5.05 nM, respectively.

  • Prucalopride succina...

    Prucalopride succinate (R-108512) is a potent, selective 5-HT4 receptor agonist.