Deacylketoconazole

CAS No. 67914-61-8

Deacylketoconazole( Deacyl ketoconazole )

Catalog No. M27360 CAS No. 67914-61-8

Deacylketoconazole is a Ketoconazole derivative and is also an antifungal agent.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 38 In Stock
10MG 53 In Stock
25MG 101 In Stock
50MG 141 In Stock
100MG 198 In Stock
200MG 296 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Deacylketoconazole
  • Note
    Research use only, not for human use.
  • Brief Description
    Deacylketoconazole is a Ketoconazole derivative and is also an antifungal agent.
  • Description
    Deacylketoconazole is a Ketoconazole derivative and is also an antifungal agent. Deacylketoconazole was 15- to 50-fold more active against Plasmodium falciparum than was ketoconazole.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Deacyl ketoconazole
  • Pathway
    GPCR/G Protein
  • Target
    Antibacterial
  • Recptor
    SETDB1-TTD
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    67914-61-8
  • Formula Weight
    489.4
  • Molecular Formula
    C24H26Cl2N4O3
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Clc1ccc(c(Cl)c1)[C@]1(Cn2ccnc2)OC[C@@H](COc2ccc(cc2)N2CCNCC2)O1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Guo Y, et, al. Structure-Guided Discovery of a Potent and Selective Cell-Active Inhibitor of SETDB1 Tudor Domain. Angew Chem Int Ed Engl. 2021 Apr 12;60(16):8760-8765.
molnova catalog
related products
  • TH-Z93

    TH-Z93 is a potent FPPS inhibitor (IC50:90 nM) and a lipophilic bisphosphonate.

  • ETX2514

    ETX2514 (ETX 2514, ETX-2514)?is a covalent, broad-spectrum β-lactamase inhibitor with IC50 of 4, 14 and 190 nM for class A KPC-2, class C AmpC and class D OXA-24, respectively.

  • RWJ-49815

    A potent bactericidal agent that inhibits the KinA autophosphorylation with IC50 of 1.6 uM.