Enzalutamide carboxylic acid

CAS No. 1242137-15-0

Enzalutamide carboxylic acid( —— )

Catalog No. M21564 CAS No. 1242137-15-0

Enzalutamide carboxylic acid is an antagonist of androgen receptor (AR) .

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 136 In Stock
2MG 81 In Stock
5MG 122 In Stock
10MG 187 In Stock
25MG 315 In Stock
50MG 431 In Stock
100MG 635 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Enzalutamide carboxylic acid
  • Note
    Research use only, not for human use.
  • Brief Description
    Enzalutamide carboxylic acid is an antagonist of androgen receptor (AR) .
  • Description
    Enzalutamide carboxylic acid is an antagonist of androgen receptor (AR) .
  • In Vitro
    Enzalutamide is converted into its major metabolites, N-desmethyl enzalutamide and carboxylic acid enzalutamide, by cytochrome P450 (CYP) 3A4/5 and CYP2C8, respectively. N-desmethyl enzalutamide has clinically relevant anti-androgen capacities similar to enzalutamide, whereas carboxylic acid enzalutamide is inactive.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Endocrinology/Hormones
  • Target
    Androgen Receptor (AR)
  • Recptor
    Androgen Receptor
  • Research Area
    cancer
  • Indication
    castration-resistant prostate cancer

Chemical Information

  • CAS Number
    1242137-15-0
  • Formula Weight
    451.4
  • Molecular Formula
    C20H13F4N3O3S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (276.92 mM)
  • SMILES
    CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1ccc(C(O)=O)c(F)c1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.van Nuland M et al. Exposure-Response Assessment of Enzalutamide and Its Major Metabolites in a Real-World Cohort of Patients with Metastatic Castration-Resistant Prostate Cancer. Pharmacotherapy. 2019 Dec;39(12):1137-1145.
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