Premarin

CAS No. 481-97-0

Premarin( Estrone 3-sulfate | Estrone sulfate )

Catalog No. M28099 CAS No. 481-97-0

Premarin is an an estrogen sulfate with neuroprotective actions during traumatic brain injury.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 393 Get Quote
10MG 581 Get Quote
25MG 888 Get Quote
50MG 1242 Get Quote
100MG 1674 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Premarin
  • Note
    Research use only, not for human use.
  • Brief Description
    Premarin is an an estrogen sulfate with neuroprotective actions during traumatic brain injury.
  • Description
    Premarin is an an estrogen sulfate with neuroprotective actions during traumatic brain injury.(In Vivo):In estrogen receptor-alpha blockade rats, Premarin therapy had less or no effect on fluid percussion injury-induced behavioral deficits, cerebral infarction and apoptosis, and activated inflammation. Premarin-induced angiogenesis and neurogenesis were estrogen receptor-alpha blockade-reduced.
  • In Vitro
    Endogenous metabolites is defined as those that are annotated by Kyoto Encyclopedia of Genes and Genomes as substrates or products of the ~1900 metabolic enzymes encoded in our genome. It is clear in the body of literature that there are documented toxic properties for many of these metabolites.
  • In Vivo
    ——
  • Synonyms
    Estrone 3-sulfate | Estrone sulfate
  • Pathway
    Endocrinology/Hormones
  • Target
    Estrogen Receptor/ERR
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    481-97-0
  • Formula Weight
    350.43
  • Molecular Formula
    C18H22O5S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C[C@@]12[C@]([C@]3([C@@](C=4C(CC3)=CC(OS(=O)(=O)O)=CC4)(CC1)[H])[H])(CCC2=O)[H]
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Gu G, et al.Synthesis of 2-chloro-4-nitrophenyl alpha-L-fucopyranoside: a substrate for alpha-L-fucosidase (AFU). Carbohydr Res. 2003 Jul 22;338(15):1603-7.
molnova catalog
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