CGP 35949

CAS No. 111130-13-3

CGP 35949( —— )

Catalog No. M34546 CAS No. 111130-13-3

CGP 35949 is an LTD4 antagonist with phospholipase inhibitory activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 178 Get Quote
5MG 255 Get Quote
10MG 375 Get Quote
25MG 545 Get Quote
50MG 762 Get Quote
100MG 1017 Get Quote
500MG 2043 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    CGP 35949
  • Note
    Research use only, not for human use.
  • Brief Description
    CGP 35949 is an LTD4 antagonist with phospholipase inhibitory activity.
  • Description
    CGP-35949 sodium is a LTD4 antagonist with phospholipase inhibitory activity. CGP-35949 sodium can be used for research of asthma.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Leukotriene Receptor
  • Recptor
    Leukotriene Receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    111130-13-3
  • Formula Weight
    509.92
  • Molecular Formula
    C23H25ClN5NaO5
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CCCC1=C(OCCCOC2=C(Cl)C=C(C)C(NC(C3=NN=N[N-]3)=O)=C2)C=CC(C(C)=O)=C1O.[Na+]
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Beck A, et al. CGP 35949, an LTD4 antagonist with phospholipase inhibitory activity: a new approach to the treatment of asthma. Adv Prostaglandin Thromboxane Leukot Res. 1987;17B:771-4.?
molnova catalog
related products
  • SR 2640 hydrochlorid...

    SR 2640 hydrochloride is a competitive antagonist of leukotriene D4 and E4 and can be used in studies about leukotrienes in human asthma.

  • Masilukast

    Masilukast(MCC-847) is an oral leukotriene D4 (LTD4) receptor antagonist for the study of diseases associated with inflammation.

  • Pobilukast

    Pobilukast (SKF 104353) is a selective cysteinyl leukotriene receptor antagonist that blocks phosphatidylinositol metabolism and leukotriene D-induced thromboxane synthesis, and can be used to study limiting myocardial damage in excessively myocardial reperfusion-injured (MI/R) rats.