Abbolactone

CAS No. 52-01-7

Abbolactone( SC9420 | SC-9420 | Spironolactone | Spiresis )

Catalog No. M17714 CAS No. 52-01-7

Spironolactone is an Aldosterone Antagonist. The mechanism of action of spironolactone is as an Aldosterone Antagonist.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 48 In Stock
50MG 30 In Stock
100MG 41 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Abbolactone
  • Note
    Research use only, not for human use.
  • Brief Description
    Spironolactone is an Aldosterone Antagonist. The mechanism of action of spironolactone is as an Aldosterone Antagonist.
  • Description
    Spironolactone is a medication primarily used to treat fluid build-up due to heart failure, liver scarring, or kidney disease. Other uses include high blood pressure, low blood potassium that does not improve with supplementation, early puberty, excessive hair growth in women, and as a component of hormone replacement therapy for trans women.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    SC9420 | SC-9420 | Spironolactone | Spiresis
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Phospholipase
  • Recptor
    Androgen Receptor
  • Research Area
    Metabolic Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    52-01-7
  • Formula Weight
    416.57
  • Molecular Formula
    C24H32O4S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 50 mg/mL 120.03 mM; H2O : < 0.1 mg/mL
  • SMILES
    CC(=O)S[C@@H]1CC2=CC(=O)CC[C@@]2([C@@H]3[C@@H]1[C@@H]4CC[C@]5([C@]4(CC3)C)CCC(=O)O5)C
  • Chemical Name
    S-((7R,8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3,5'-dioxo-1,2,3,4',5',6,7,8,9,10,11,12,13,14,15,16-hexadecahydro-3'H-spiro[cyclopenta[a]phenanthrene-17,2'-furan]-7-yl) ethanethioate

Shipping & Storage Information

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

Reference

1. Ye P, et al. Horm Metab Res. 2009 Jan;41(1):35-9.
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