Udenafil

CAS No. 268203-93-6

Udenafil( DA-8159 )

Catalog No. M13819 CAS No. 268203-93-6

A potent and selective phosphodiesterase 5 (PDE5) inhibitor for treat erectile dysfunction.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 46 In Stock
5MG 41 In Stock
10MG 69 In Stock
25MG 136 In Stock
50MG 214 In Stock
100MG 312 In Stock
200MG 448 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Udenafil
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent and selective phosphodiesterase 5 (PDE5) inhibitor for treat erectile dysfunction.
  • Description
    A potent and selective phosphodiesterase 5 (PDE5) inhibitor for treat erectile dysfunction.Sexual Dysfunction Approved(In Vitro):Udenafil is an oral PDE5 inhibitor. Udenafil significantly increases cAMP and cGMP levels and are more highly distributed in the prostate than plasma.
  • In Vitro
    Udenafil is an oral PDE5 inhibitor. Udenafil significantly increases cAMP and cGMP levels and are more highly distributed in the prostate than plasma.
  • In Vivo
    ——
  • Synonyms
    DA-8159
  • Pathway
    Angiogenesis
  • Target
    PDE
  • Recptor
    PDE
  • Research Area
    Endocrinology
  • Indication
    Sexual Dysfunction

Chemical Information

  • CAS Number
    268203-93-6
  • Formula Weight
    516.6561
  • Molecular Formula
    C25H36N6O4S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 33 mg/mL
  • SMILES
    O=S(C1=CC=C(OCCC)C(C(NC2=C3N(C)N=C2CCC)=NC3=O)=C1)(NCCC4N(C)CCC4)=O
  • Chemical Name
    Benzenesulfonamide, 3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-5-yl)-N-[2-(1-methyl-2-pyrrolidinyl)ethyl]-4-propoxy-

Shipping & Storage Information

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

Reference

1. Salem EA, et al. Curr Opin Investig Drugs. 2006 Jul;7(7):661-9. 2. Lee CH, et al. J Sex Med. 2010 Jul;7(7):2564-71. 3. Kang HE, et al. Br J Pharmacol. 2009 Mar;156(6):1009-18.
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