CYP17-IN-1

CAS No. 2093317-51-0

CYP17-IN-1( —— )

Catalog No. M26134 CAS No. 2093317-51-0

CYP17-IN-1 is an effective oral CYP17 inhibitor that can inhibit CYP17 in rats and humans with IC50 of 15.8 and 20.1 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 264 Get Quote
5MG 403 Get Quote
10MG 592 Get Quote
25MG 888 Get Quote
50MG 1242 Get Quote
100MG 1701 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    CYP17-IN-1
  • Note
    Research use only, not for human use.
  • Brief Description
    CYP17-IN-1 is an effective oral CYP17 inhibitor that can inhibit CYP17 in rats and humans with IC50 of 15.8 and 20.1 nM.
  • Description
    CYP17-IN-1 is an effective oral CYP17 inhibitor that can inhibit CYP17 in rats and humans with IC50 of 15.8 and 20.1 nM.(In Vitro):The IC50 value of CYP17-IN-1 for CYP3A4 is 8.5 μM.(In Vivo):CYP17-IN-1 dose-dependently reduced plasma testosterone levels in Sprague-Dawley rats.
  • In Vitro
    CYP17-IN-1 (compound 9c) exhibits an IC50 value of 8.5 μM against CYP3A4.
  • In Vivo
    CYP17-IN-1 (compound 9c) reduces plasma testosterone level in a dose-dependent manner in Sprague-Dawley rats.
  • Synonyms
    ——
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    P450
  • Recptor
    carbonic anhydrase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2093317-51-0
  • Formula Weight
    312.41
  • Molecular Formula
    C18H17FN2S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Cc1ccncc1CN1CCc2c(C1)sc1ccc(F)cc21
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Prete SD, et, al. Escherichia coli γ-carbonic anhydrase: characterisation and effects of simple aromatic/heterocyclic sulphonamide inhibitors. J Enzyme Inhib Med Chem. 2020 Dec;35(1):1545-1554.
molnova catalog
related products
  • Enerisant HCl

    Enerisant HCl is a novel potent and selective histamine H3 receptor antagonist, a substrate for P-gp, mediated by cytochrome P450 (CYP) and transporter proteins.

  • Beta-Tetralone

    2-Tetralone is an organic chemical compound with the molecular formula C10H10O.

  • TMS

    TMS is a very selective and potent competitive inhibitor of P450 1B1 (CYP1A1). It has strong selectivity among P450 family 1 enzymes.