CGP 52432

CAS No. 139667-74-6

CGP 52432( Cgp 52432 | Cgp52432 | Cgp52432 )

Catalog No. M17994 CAS No. 139667-74-6

CGP52432 is a very potent antagonist of GABAB receptors (IC50 = 85 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 84 In Stock
5MG 75 In Stock
10MG 136 In Stock
25MG 255 In Stock
50MG 365 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
    CGP 52432
  • Note
    Research use only, not for human use.
  • Brief Description
    CGP52432 is a very potent antagonist of GABAB receptors (IC50 = 85 nM).
  • Description
    Cgp 52432 is a GABA-A receptor antagonist.
  • In Vitro
    CGP52432 is a GABAB receptor antagonist, with an IC50 of 85 nM, 35- and 100-fold lower than at the receptors regulating somatostatin and glutamate overflow, respectively.
  • In Vivo
    CGP52432 (10, 30 mg/kg) shows no effect on the total arm entries and total head dips of mice on the elevated-plus maze. CGP52432 (100 nmol/kg, i.v., or 1 nmol/kg, i.c.v.) abolishes the suppressive effects of GABA ( 50 μmol/kg, i.v.) on enhanced renal sympathetic nerve activity (RSNA) during ischaemia, causeing elimination of the renoprotective effects of GABA in rats.
  • Synonyms
    Cgp 52432 | Cgp52432 | Cgp52432
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    GABAB
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    139667-74-6
  • Formula Weight
    384.23
  • Molecular Formula
    C15H24Cl2NO4P
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 5 mg/mL 13.01 mM;
  • SMILES
    CCOC(OCC)P(=O)(CCCNCC1=CC(=C(C=C1)Cl)Cl)O
  • Chemical Name
    Phosphinic acid, (3-(((3,4-dichlorophenyl)methyl)amino)propyl)(diethoxymethyl)-

Shipping & Storage Information

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

Reference

1.Bonanno G,etal.GABA(B) receptors as potential targets for drugs able to prevent excessive excitatory amino acid transmission in the spinal cord.Eur J Pharmacol. 1998 Dec 4;362(2-3):143-8.
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