N-Desmethyl-Apalutamide

CAS No. 1332391-11-3

N-Desmethyl-Apalutamide( N-Desmethyl Apalutamide )

Catalog No. M26314 CAS No. 1332391-11-3

N-Desmethyl-Apalutamide is a less potent antagonist of the androgen receptor, is an active Apalutamide metabolite.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 278 In Stock
5MG 259 In Stock
10MG 373 In Stock
25MG 562 In Stock
50MG 759 In Stock
100MG 1014 In Stock
200MG 1376 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    N-Desmethyl-Apalutamide
  • Note
    Research use only, not for human use.
  • Brief Description
    N-Desmethyl-Apalutamide is a less potent antagonist of the androgen receptor, is an active Apalutamide metabolite.
  • Description
    N-Desmethyl-Apalutamide is a less potent antagonist of the androgen receptor, is an active Apalutamide metabolite.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    N-Desmethyl Apalutamide
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    P450
  • Recptor
    CYP2C9| HIV
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1332391-11-3
  • Formula Weight
    463.41
  • Molecular Formula
    C20H13F4N5O2S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (215.79 mM)
  • SMILES
    NC(=O)c1ccc(cc1F)N1C(=S)N(C(=O)C11CCC1)c1cnc(C#N)c(c1)C(F)(F)F
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Chen DF, et al. Anti-AIDS agents--XXVI. Structure-activity correlations of gomisin-G-related anti-HIV lignans from Kadsura interior and of related synthetic analogues. Bioorg Med Chem. 1997 Aug;5(8):1715-23.
molnova catalog
related products
  • Ginsenoside F1

    Ginsenoside F1,an enzymatically modified derivative of ginsenoside Rg1, protection from ultraviolet-B-induced apoptosis is tightly correlated with ginsenoside-F1-mediated inhibition of ultraviolet-B-induced downregulation of Bcl-2 and Brn-3a expression.

  • Chamaechromone

    Chamaechromone is a natural product isolated from the roots of Stellera chamaejasme L.. Chamaechromone has anti-HBV and insecticidal activity.

  • Glabrol

    Glabrol is a PTP1B inhibitor it is also a CYP1B1 inhibitor it shows inhibition of CYP1B1 in live cell assay with the IC50 value of 15uM.